Variant report

Variant	nsv1061864
Chromosome Location	chr22:22794082-23255556
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:12299)
CpG islands
(count:3235)
Chromatin interactive
region (count:759)
LncRNA
region (count:51)
Mature miRNA
region (count: 3)
miRNA target
sites (count:8)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:23226039-23226556	K562	blood:	n/a	n/a
2	ARID3A	chr22:23122421-23122441	K562	blood:	n/a	n/a
3	ARID3A	chr22:22901601-22901802	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:23035299-23035558	K562	blood:	n/a	n/a
5	ARID3A	chr22:22863051-22863422	HepG2	liver:	n/a	n/a
6	ARID3A	chr22:23088195-23088474	K562	blood:	n/a	n/a
7	ARID3A	chr22:22829197-22829446	HepG2	liver:	n/a	n/a
8	ARID3A	chr22:22874015-22874868	HepG2	liver:	n/a	n/a
9	ARID3A	chr22:23062845-23063144	HepG2	liver:	n/a	n/a
10	ARID3A	chr22:23071123-23071265	K562	blood:	n/a	n/a
11	ARID3A	chr22:23030066-23030494	K562	blood:	n/a	n/a
12	ARID3A	chr22:23185588-23185620	K562	blood:	n/a	n/a
13	ARID3A	chr22:23096142-23096349	HepG2	liver:	n/a	n/a
14	ARID3A	chr22:22818443-22818683	HepG2	liver:	n/a	n/a
15	ARID3A	chr22:22871218-22871395	K562	blood:	n/a	n/a
16	ARID3A	chr22:23035867-23036079	HepG2	liver:	n/a	n/a
17	ARID3A	chr22:22815687-22815688	K562	blood:	n/a	n/a
18	ARID3A	chr22:22899261-22900164	K562	blood:	n/a	n/a
19	ARID3A	chr22:22894947-22895370	K562	blood:	n/a	n/a
20	ARID3A	chr22:22815096-22815412	K562	blood:	n/a	n/a
21	ARID3A	chr22:22958671-22958917	K562	blood:	n/a	n/a
22	ARID3A	chr22:23123576-23123779	K562	blood:	n/a	n/a
23	ARID3A	chr22:23008889-23009175	K562	blood:	n/a	n/a
24	ARID3A	chr22:23095901-23096393	K562	blood:	n/a	n/a
25	ARID3A	chr22:23062560-23063183	K562	blood:	n/a	n/a
26	ARID3A	chr22:23112680-23113069	K562	blood:	n/a	n/a
27	ARID3A	chr22:23119431-23119566	K562	blood:	n/a	n/a
28	ARID3A	chr22:23052055-23052419	K562	blood:	n/a	n/a
29	ARID3A	chr22:22929379-22929733	K562	blood:	n/a	n/a
30	ARID3A	chr22:22873765-22876064	K562	blood:	n/a	n/a
31	ARID3A	chr22:23232773-23233217	K562	blood:	n/a	n/a
32	ARID3A	chr22:22921648-22921857	K562	blood:	n/a	n/a
33	ARID3A	chr22:22818370-22818848	K562	blood:	n/a	n/a
34	ARID3A	chr22:22862879-22863439	K562	blood:	n/a	n/a
35	ARID3A	chr22:22936496-22936877	K562	blood:	n/a	n/a
36	ARID3A	chr22:22901376-22901941	K562	blood:	n/a	n/a
37	ARID3A	chr22:22861960-22862639	K562	blood:	n/a	n/a
38	ARID3A	chr22:22918856-22919113	K562	blood:	n/a	n/a
39	ATF1	chr22:23050906-23051024	K562	blood:	n/a	n/a
40	ATF1	chr22:23105060-23105238	K562	blood:	n/a	n/a
41	ATF1	chr22:23125167-23125353	K562	blood:	n/a	n/a
42	ATF1	chr22:23125944-23126543	K562	blood:	n/a	n/a
43	ATF1	chr22:23158393-23159026	K562	blood:	n/a	n/a
44	ATF1	chr22:23023316-23024282	K562	blood:	n/a	n/a
45	ATF1	chr22:23208195-23208865	K562	blood:	n/a	n/a
46	ATF1	chr22:23047401-23047568	K562	blood:	n/a	n/a
47	ATF1	chr22:23055701-23055768	K562	blood:	n/a	n/a
48	ATF1	chr22:23169293-23169433	K562	blood:	n/a	n/a
49	ATF1	chr22:23013723-23013930	K562	blood:	n/a	n/a
50	ATF1	chr22:23144811-23145247	K562	blood:	n/a	n/a

(count:3235 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:22863293-22863343	Caco-2	colon:	n/a
2	chr22:22989254-22989304	AG09309	skin:	n/a
3	chr22:22863293-22863343	Caco-2	colon:	n/a
4	chr22:22989254-22989304	AG09309	skin:	n/a
5	chr22:22843648-22843698	A549	lung:	n/a
6	chr22:23003332-23003382	K562	blood:	n/a
7	chr22:22918718-22918768	SKMC	muscle:	n/a
8	chr22:22843648-22843698	HMEC	breast:	n/a
9	chr22:23196971-23197021	CMK	blood:	n/a
10	chr22:22986350-22986400	AG10803	skin:	n/a
11	chr22:22987124-22987174	HPAEpiC	pulmonary alveolar:	n/a
12	chr22:22839645-22839695	HNPCEpiC	eye:	n/a
13	chr22:22862884-22862934	GM19239	blood:	n/a
14	chr22:22877746-22877796	Jurkat	blood:	n/a
15	chr22:22901830-22901880	BJ	skin:	n/a
16	chr22:22875038-22875088	HMEC	breast:	n/a
17	chr22:22986350-22986400	SK-N-MC	brain:	n/a
18	chr22:22986350-22986400	NB4	blood:	n/a
19	chr22:22862884-22862934	NH-A	brain:	n/a
20	chr22:22868585-22868635	GM19239	blood:	n/a
21	chr22:22989254-22989304	PrEC	prostate:	n/a
22	chr22:22901267-22901317	MCF-7	breast:	n/a
23	chr22:22987072-22987122	ECC-1	luminal epithelium:	n/a
24	chr22:22901880-22901930	HL-60	blood:	n/a
25	chr22:22863663-22863713	HAEpiC	amniotic membrane:	n/a
26	chr22:22862802-22862852	T-47D	breast:	n/a
27	chr22:22863655-22863705	ovcar-3	ovarian:	n/a
28	chr22:23196862-23196912	HL-60	blood:	n/a
29	chr22:22877746-22877796	HMEC	breast:	n/a
30	chr22:22875038-22875088	SKMC	muscle:	n/a
31	chr22:22863219-22863269	NB4	blood:	n/a
32	chr22:22874447-22874497	ProgFib	skin:	n/a
33	chr22:22863293-22863343	LNCaP	prostate:	n/a
34	chr22:22901880-22901930	LNCaP	prostate:	n/a
35	chr22:22988798-22988848	PrEC	prostate:	n/a
36	chr22:22874590-22874640	AG09309	skin:	n/a
37	chr22:22901596-22901646	RPTEC	kidney:	n/a
38	chr22:22862802-22862852	BE2_C	brain:	n/a
39	chr22:22863663-22863713	HMEC	breast:	n/a
40	chr22:22983403-22983453	BE2_C	brain:	n/a
41	chr22:22986667-22986717	AG10803	skin:	n/a
42	chr22:22987059-22987109	HRCEpiC	kidney:	n/a
43	chr22:22859162-22859212	LNCaP	prostate:	n/a
44	chr22:23196971-23197021	LNCaP	prostate:	n/a
45	chr22:22901857-22901907	PANC-1	pancreas:	n/a
46	chr22:22988798-22988848	A549	lung:	n/a
47	chr22:22904270-22904320	SK-N-MC	brain:	n/a
48	chr22:22868585-22868635	BJ	skin:	n/a
49	chr22:22901857-22901907	PFSK-1	brain:	n/a
50	chr22:22902237-22902287	A549	lung:	n/a

(count:759 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Distal block	Cell Line	Cell type
1	chr22:23008854..23009551-chr22:23029940..23030690,2	MCF-7	breast:
2	chr22:23080532..23082933-chr22:23093316..23095424,2	K562	blood:
3	chr22:22901665..22902179-chr22:22909894..22910753,3	K562	blood:
4	chr22:23034627..23035920-chr22:23062552..23063228,3	K562	blood:
5	chr22:22815066..22815979-chr22:23225208..23226122,2	K562	blood:
6	chr22:22929529..22931977-chr22:23035772..23037370,2	K562	blood:
7	chr22:22802243..22804145-chr22:22815235..22817257,2	K562	blood:
8	chr22:23071304..23074253-chr22:23078346..23081293,2	K562	blood:
9	chr22:23237287..23240210-chr22:23254703..23257164,2	K562	blood:
10	chr22:23095720..23096793-chr22:23225681..23226777,7	K562	blood:
11	chr22:22818512..22819047-chr22:22929119..22929840,3	K562	blood:
12	chr22:23190706..23191213-chr22:23623766..23624457,2	K562	blood:
13	chr22:23095784..23096610-chr22:23233130..23233640,2	K562	blood:
14	chr22:23130308..23131793-chr22:23219322..23220417,8	K562	blood:
15	chr22:23221267..23223203-chr22:23236416..23239424,3	K562	blood:
16	chr22:22818502..22819097-chr22:23225816..23226413,3	K562	blood:
17	chr22:23152221..23152901-chr22:23190288..23191157,3	K562	blood:
18	chr22:23130817..23133388-chr22:23167138..23169692,2	K562	blood:
19	chr22:22818125..22818946-chr22:22894855..22895468,2	MCF-7	breast:
20	chr22:22510850..22511523-chr22:23029816..23030698,2	K562	blood:
21	chr22:23025457..23028332-chr22:23029232..23031511,3	K562	blood:
22	chr22:22932799..22934322-chr22:22954672..22956825,2	K562	blood:
23	chr22:22711103..22713710-chr22:22892140..22893898,2	K562	blood:
24	chr22:23197561..23198498-chr22:23225909..23226760,4	MCF-7	breast:
25	chr22:22823437..22825876-chr22:22832174..22833684,2	K562	blood:
26	chr22:23112324..23114387-chr22:23139146..23140685,2	K562	blood:
27	chr22:22872350..22874493-chr5:57759289..57762269,2	K562	blood:
28	chr22:23152570..23153090-chr22:23180111..23180906,2	K562	blood:
29	chr22:22818443..22819012-chr22:22929528..22930033,2	MCF-7	breast:
30	chr22:23112382..23113353-chr22:23225822..23226588,5	K562	blood:
31	chr12:7519897..7522502-chr22:22898699..22901020,2	K562	blood:
32	chr22:23129985..23132046-chr22:23176209..23178175,2	K562	blood:
33	chr22:22869194..22871714-chr22:23521389..23524203,2	K562	blood:
34	chr22:22901204..22902181-chr22:22936191..22937061,2	K562	blood:
35	chr22:22815195..22816024-chr22:22918500..22919019,2	K562	blood:
36	chr22:22711086..22713329-chr22:22894770..22898200,3	K562	blood:
37	chr22:23144551..23145511-chr22:23470374..23471293,4	K562	blood:
38	chr22:23054239..23055029-chr22:23225832..23226341,2	K562	blood:
39	chr22:23061644..23064154-chr22:23089157..23090984,2	K562	blood:
40	chr22:23095758..23096682-chr22:23190267..23191347,4	K562	blood:
41	chr22:23054391..23056750-chr22:23065881..23068203,2	K562	blood:
42	chr22:22811413..22813356-chr22:22840248..22842971,2	K562	blood:
43	chr22:22823832..22826164-chr22:22828089..22830611,2	K562	blood:
44	chr22:22817463..22819380-chr22:22957921..22959383,14	K562	blood:
45	chr22:23117086..23119817-chr22:23129556..23132183,2	K562	blood:
46	chr22:23029744..23030755-chr22:23090478..23091090,6	K562	blood:
47	chr22:22955844..22957349-chr22:22958037..22960847,2	K562	blood:
48	chr22:22817987..22818671-chr22:23088295..23088910,2	K562	blood:
49	chr22:23112678..23113353-chr22:23153551..23154062,2	K562	blood:
50	chr22:23024129..23024811-chr22:23034990..23035498,2	K562	blood:

(count:51 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POM121L1P-1	chr22:23035462-23035547	NONHSAT083808
2	lnc-GGTLC2-10	chr22:23104787-23105009	NONHSAT083819
3	lnc-POM121L1P-5	chr22:23186421-23186739	refGeneNc_260_NR_028483
4	lnc-GGTLC2-5	chr22:22961042-22961081	NONHSAT083792
5	lnc-GGTLC2-3	chr22:23007120-23007377	NONHSAT083803
6	lnc-POM121L1P-5	chr22:23220658-23220783	refGeneNc_260_NR_028483
7	lnc-LL22NC03-63E9.3.1-2	chr22:22922478-22922760	NONHSAT083790
8	lnc-POM121L1P-5	chr22:23200951-23201121	refGeneNc_260_NR_028483
9	lnc-POM121L1P-1	chr22:23038799-23038911	NONHSAT083808
10	lnc-POM121L1P-1	chr22:23035263-23035547	ENSG00000223999
11	lnc-LL22NC03-63E9.3.1-4	chr22:22828865-22829110	expReg_chr22_1075_+
12	lnc-RTDR1-6	chr22:23221233-23221684	NONHSAT083832
13	lnc-POM121L1P-3	chr22:23053951-23054068	NONHSAT083813
14	lnc-RTDR1-4	chr22:23242926-23243073	NONHSAT083834
15	lnc-POM121L1P-1	chr22:23035358-23035378	NONHSAT083808
16	lnc-POM121L1P-4	chr22:23155178-23156344	ucscGeneNc_uc002zzz_1
17	lnc-IGLL5-5	chr22:23180779-23181049	NONHSAT083827
18	lnc-RTDR1-6	chr22:23220011-23220059	NONHSAT083832
19	lnc-POM121L1P-5	chr22:23164245-23164726	refGeneNc_260_NR_028483
20	lnc-POM121L1P-5	chr22:23178179-23178296	refGeneNc_260_NR_028483
21	lnc-D87017.1-3	chr22:23252998-23253245	NONHSAT083835
22	lnc-IGLL5-4	chr22:23192550-23192799	NONHSAT083828
23	lnc-POM121L1P-5	chr22:23167960-23168108	refGeneNc_260_NR_028483
24	lnc-POM121L1P-5	chr22:23165262-23165535	refGeneNc_260_NR_028483
25	lnc-LL22NC03-63E9.3.1-6	chr22:22804685-22804990	NONHSAT083786
26	lnc-LL22NC03-63E9.3.1-1	chr22:22906072-22909007	NR_027426
27	lnc-GGTLC2-4	chr22:23015622-23015679	NONHSAT083804
28	lnc-RTDR1-1	chr22:23248506-23248831	NONHSAT083775
29	lnc-POM121L1P-1	chr22:23045057-23045160	NONHSAT083808
30	lnc-GGTLC2-4	chr22:23015829-23016072	NONHSAT083804
31	lnc-GGTLC2-5	chr22:22961376-22961633	NONHSAT083792
32	lnc-LL22NC03-63E9.3.1-5	chr22:22819996-22820323	NONHSAT083787
33	lnc-POM121L1P-1	chr22:23045437-23045463	NONHSAT083808
34	lnc-POM121L1P-1	chr22:23035632-23035797	ENSG00000223999
35	lnc-GGTLC2-6	chr22:23021570-23021818	NONHSAT083805
36	lnc-POM121L1P-5	chr22:23197736-23197863	refGeneNc_260_NR_028483
37	lnc-GGTLC2-3	chr22:23006943-23006988	NONHSAT083803
38	lnc-POM121L1P-1	chr22:23045057-23045160	NONHSAT083810
39	lnc-GGTLC2-9	chr22:23098043-23098286	NONHSAT083817
40	lnc-LL22NC03-63E9.3.1-6	chr22:22804540-22804573	NONHSAT083786
41	lnc-RTDR1-4	chr22:23243305-23243327	NONHSAT083834
42	lnc-GGTLC2-8	chr22:23081432-23081675	NONHSAT083816
43	lnc-LL22NC03-63E9.3.1-1	chr22:22901756-22901814	NR_027426
44	lnc-POM121L1P-3	chr22:23048732-23048890	NONHSAT083813
45	lnc-IGLL5-7	chr22:23157168-23157423	NONHSAT083824
46	lnc-GGTLC2-7	chr22:23043245-23043455	NONHSAT083812
47	lnc-RTDR1-4	chr22:23243491-23243570	NONHSAT083834
48	lnc-POM121L1P-1	chr22:23038579-23038911	NONHSAT083810
49	lnc-LL22NC03-63E9.3.1-1	chr22:22905268-22905377	NR_027426
50	lnc-POM121L1P-1	chr22:23045437-23045463	NONHSAT083810

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5571-5p	chr22:23228471-23228491	MIMAT0022257
hsa-miR-650	chr22:23165285-23165305	MIMAT0003320
hsa-miR-5571-3p	chr22:23228511-23228529	MIMAT0022258

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ZNF280B	hsa-let-7d-5p	chr22:22838970-22838991
2	ZNF280B	hsa-let-7d-5p	chr22:22839482-22839476
3	ZNF280B	hsa-let-7f-5p	chr22:22839295-22839316
4	ZNF280B	hsa-let-7f-5p	chr22:22839482-22839476
5	ZNF280B	hsa-let-7d-5p	chr22:22839295-22839316
6	ZNF280B	hsa-let-7f-5p	chr22:22839301-22839294
7	ZNF280B	hsa-let-7d-5p	chr22:22839301-22839294
8	ZNF280B	hsa-let-7f-5p	chr22:22838970-22838990

Variant related genes	Relation type
ENSG00000264824	TF binding region
IGLV3-7	TF binding region
ENSG00000207833	TF binding region
MIR650	TF binding region
ENSG00000226477	TF binding region
ENSG00000207832	TF binding region
IGLV4-3	TF binding region
IGLJ5	TF binding region
ZNF280B	TF binding region
IGLV3-2	TF binding region
IGLV2-34	TF binding region
ENSG00000220891	TF binding region
IGLV3-32	TF binding region
IGLV3-13	TF binding region
IGLV3-4	TF binding region
ENSG00000237127	TF binding region
ENSG00000232350	TF binding region
IGLC1	TF binding region
IGLV3-6	TF binding region
IGLV2-5	TF binding region
IGLV3-16	TF binding region
IGLV2-18	TF binding region
IGLV3-17	TF binding region
ENSG00000264629	TF binding region
IGLJ6	TF binding region
IGLV3-31	TF binding region
IGLVVI-22-1	TF binding region
BCRP4	TF binding region
IGLJ4	TF binding region
ENSG00000207830	TF binding region
IGLC4	TF binding region
IGLV3-12	TF binding region
IGLV3-25	TF binding region
ENSG00000207835	TF binding region
ENSG00000231392	TF binding region
IGLV2-23	TF binding region
IGLV3-30	TF binding region
POM121L1P	TF binding region
IGLJ2	TF binding region
ENSG00000207834	TF binding region
ENSG00000226595	TF binding region
IGLV2-8	TF binding region
IGLC5	TF binding region
IGLV2-28	TF binding region
IGLV7-35	TF binding region
IGLV3-10	TF binding region
IGLV2-11	TF binding region
ENSG00000239066	TF binding region
IGLVVI-25-1	TF binding region
IGLV3-15	TF binding region
IGLV3-26	TF binding region
IGLL5	TF binding region
IGLJ3	TF binding region
IGLV3-19	TF binding region
IGLV3-24	TF binding region
ENSG00000223999	TF binding region
IGLV3-22	TF binding region
IGLV3-27	TF binding region
GGTLC2	TF binding region
IGLC3	TF binding region
IGLV3-9	TF binding region
IGLV2-14	TF binding region
PRAME	TF binding region
IGLVI-20	TF binding region
ZNF280A	TF binding region
IGLV3-1	TF binding region
ENSG00000230821	TF binding region
IGLJ1	TF binding region
IGLV3-21	TF binding region
IGLV3-29	TF binding region
IGLV2-33	TF binding region
IGLC2	TF binding region
ENSG00000264824	CpG island
IGLV3-7	CpG island
ENSG00000207833	CpG island
MIR650	CpG island
ENSG00000226477	CpG island
ENSG00000207832	CpG island
IGLV4-3	CpG island
IGLJ5	CpG island
ZNF280B	CpG island
IGLV3-2	CpG island
IGLV2-34	CpG island
ENSG00000220891	CpG island
IGLV3-32	CpG island
IGLV3-13	CpG island
IGLV3-4	CpG island
ENSG00000237127	CpG island
ENSG00000232350	CpG island
IGLC1	CpG island
IGLV3-6	CpG island
IGLV2-5	CpG island
IGLV3-16	CpG island
IGLV2-18	CpG island
IGLV3-17	CpG island
ENSG00000264629	CpG island
IGLJ6	CpG island
IGLV3-31	CpG island
IGLVVI-22-1	CpG island
BCRP4	CpG island
IGLJ4	CpG island
ENSG00000207830	CpG island
IGLC4	CpG island
IGLV3-12	CpG island
IGLV3-25	CpG island
ENSG00000207835	CpG island
ENSG00000231392	CpG island
IGLV2-23	CpG island
IGLV3-30	CpG island
POM121L1P	CpG island
IGLJ2	CpG island
ENSG00000207834	CpG island
ENSG00000226595	CpG island
IGLV2-8	CpG island
IGLC5	CpG island
IGLV2-28	CpG island
IGLV7-35	CpG island
IGLV3-10	CpG island
IGLV2-11	CpG island
ENSG00000239066	CpG island
IGLVVI-25-1	CpG island
IGLV3-15	CpG island
IGLV3-26	CpG island
IGLL5	CpG island
IGLJ3	CpG island
IGLV3-19	CpG island
IGLV3-24	CpG island
ENSG00000223999	CpG island
IGLV3-22	CpG island
IGLV3-27	CpG island
GGTLC2	CpG island
IGLC3	CpG island
IGLV3-9	CpG island
IGLV2-14	CpG island
PRAME	CpG island
IGLVI-20	CpG island
ZNF280A	CpG island
IGLV3-1	CpG island
ENSG00000230821	CpG island
IGLJ1	CpG island
IGLV3-21	CpG island
IGLV3-29	CpG island
IGLV2-33	CpG island
IGLC2	CpG island
ENSG00000211656	chromatin interactions
ENSG00000236794	chromatin interactions
ENSG00000215456	chromatin interactions
ENSG00000211653	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000231392	chromatin interactions
ENSG00000223350	chromatin interactions
ENSG00000253329	chromatin interactions
ENSG00000198477	chromatin interactions
ENSG00000211649	chromatin interactions
ENSG00000206652	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000211681	chromatin interactions
ENSG00000232603	chromatin interactions
ENSG00000253546	chromatin interactions
ENSG00000253631	chromatin interactions
ENSG00000220891	chromatin interactions
ENSG00000211675	chromatin interactions
ENSG00000169548	chromatin interactions
ENSG00000100030	chromatin interactions
ENSG00000211655	chromatin interactions
ENSG00000211657	chromatin interactions
ENSG00000211685	chromatin interactions
ENSG00000100027	chromatin interactions
ENSG00000223999	chromatin interactions
ENSG00000253338	chromatin interactions
ENSG00000253234	chromatin interactions
ENSG00000211669	chromatin interactions
ENSG00000253448	chromatin interactions
ENSG00000264824	chromatin interactions
ENSG00000230821	chromatin interactions
ENSG00000168288	chromatin interactions
ENSG00000254077	chromatin interactions
ENSG00000211670	chromatin interactions
ENSG00000254030	chromatin interactions
ENSG00000211678	chromatin interactions
ENSG00000211676	chromatin interactions
ENSG00000253920	chromatin interactions
ENSG00000207834	chromatin interactions
ENSG00000211680	chromatin interactions
ENSG00000207832	chromatin interactions
ENSG00000215417	chromatin interactions
ENSG00000253913	chromatin interactions
ENSG00000211679	chromatin interactions
ENSG00000253451	chromatin interactions
ENSG00000128228	chromatin interactions
ENSG00000253963	chromatin interactions
ENSG00000273342	chromatin interactions
ENSG00000211658	chromatin interactions
ENSG00000211682	chromatin interactions
ENSG00000252622	chromatin interactions
ENSG00000226420	chromatin interactions
ENSG00000211665	chromatin interactions
ENSG00000211674	chromatin interactions
ENSG00000237127	chromatin interactions
ENSG00000211663	chromatin interactions
ENSG00000100034	chromatin interactions
ENSG00000212102	chromatin interactions
ENSG00000211660	chromatin interactions
ENSG00000253822	chromatin interactions
ENSG00000177675	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000222037	chromatin interactions
ENSG00000231969	chromatin interactions
ENSG00000126883	chromatin interactions
ENSG00000211664	chromatin interactions
ENSG00000100038	chromatin interactions
ENSG00000100023	chromatin interactions
ENSG00000254240	chromatin interactions
ENSG00000211641	chromatin interactions
ENSG00000211659	chromatin interactions
ENSG00000207830	chromatin interactions
ENSG00000211662	chromatin interactions
ENSG00000100218	chromatin interactions
ENSG00000100228	chromatin interactions
ENSG00000211677	chromatin interactions
ENSG00000186716	chromatin interactions
ENSG00000253786	chromatin interactions
ENSG00000211672	chromatin interactions
ENSG00000211667	chromatin interactions
ENSG00000207835	chromatin interactions
ENSG00000226595	chromatin interactions
ENSG00000211684	chromatin interactions
ENSG00000261135	chromatin interactions
ENSG00000211671	chromatin interactions
ENSG00000226477	chromatin interactions
ENSG00000254709	chromatin interactions
ENSG00000211673	chromatin interactions
ENSG00000253889	chromatin interactions
ENSG00000211648	chromatin interactions
ENSG00000211666	chromatin interactions
ENSG00000224144	chromatin interactions
ENSG00000185686	chromatin interactions
ENSG00000254029	chromatin interactions
ENSG00000207751	chromatin interactions
ENSG00000253590	chromatin interactions
ENSG00000264629	chromatin interactions
ENSG00000187556	chromatin interactions
ENSG00000253779	chromatin interactions
ENSG00000207836	chromatin interactions
ENSG00000232350	chromatin interactions
ENSG00000253152	chromatin interactions
ENSG00000211661	chromatin interactions
ING4	Mature miRNA region

Extended variants
information (count: 24352 )
Associated
traits (count: 221 )

Variant overlapped rSNPs/rCNVs (count:24352 , 50 per page) page: 1 2 3 4 5 6 7 ... 488

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372972830	chr22:22794093-22794094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs9607881	chr22:22794110-22794111	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs377485319	chr22:22794128-22794129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191222951	chr22:22794160-22794161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145796821	chr22:22794196-22794197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140676192	chr22:22794198-22794199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533423045	chr22:22794269-22794270	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs115537133	chr22:22794355-22794356	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs183510680	chr22:22794358-22794359	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs374286254	chr22:22794450-22794451	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs113096169	chr22:22794469-22794470	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs562110387	chr22:22794495-22794496	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs189415742	chr22:22794553-22794554	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145851037	chr22:22794571-22794572	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs570561200	chr22:22794573-22794574	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs202066766	chr22:22794671-22794672	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs532964030	chr22:22794676-22794677	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs576779955	chr22:22794698-22794699	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs549759599	chr22:22794729-22794730	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs569950422	chr22:22794756-22794757	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs146638660	chr22:22794796-22794797	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181727351	chr22:22794827-22794828	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs187001341	chr22:22794877-22794878	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561253301	chr22:22795493-22795494	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs546777524	chr22:22795512-22795513	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs529082532	chr22:22795530-22795531	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs6002339	chr22:22795542-22795543	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs207477915	chr22:22795554-22795555	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs414296	chr22:22795589-22795590	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs141210264	chr22:22795628-22795629	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs114270317	chr22:22795691-22795692	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs75222818	chr22:22795704-22795705	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs372666621	chr22:22795708-22795709	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs143261093	chr22:22795739-22795740	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs539517648	chr22:22795756-22795757	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs113305317	chr22:22795763-22795764	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs367937003	chr22:22795772-22795773	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs556596830	chr22:22795775-22795776	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs11912989	chr22:22795784-22795785	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs542207106	chr22:22795812-22795813	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs201843740	chr22:22795822-22795823	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs555790785	chr22:22795824-22795825	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs551716662	chr22:22795834-22795835	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs186253612	chr22:22795835-22795836	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs9620029	chr22:22795846-22795847	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs564860736	chr22:22795937-22795938	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs372435132	chr22:22795951-22795952	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs533545264	chr22:22795958-22795959	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs543188191	chr22:22795963-22795964	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs550392818	chr22:22795970-22795971	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:221)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Emanuel syndrome	21549014	CNVD
Digeorge syndrome	22283845	CNVD
Schizophrenia	17504246	CNVD
Digeorge syndrome	18033723	CNVD
22q11 deletion syndrome	17034021	CNVD
22q11 deletion syndrome	22511897	CNVD
22q11 deletion syndrome	16829213	CNVD
Autism	22067053	CNVD
Autism	19218893	CNVD
Biliary cancer	22067053	CNVD
Congenital heart defect	21390462	CNVD
Digeorge syndrome	16617304	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Obsessive-compulsive disorder	22067053	CNVD
Psychosis	22067053	CNVD
Schizophrenia	19415332	CNVD
Schizophrenia	20587603	CNVD
Shprintzen syndrome	19443537	CNVD
absent pulmonary valve syndrome	16795129	CNVD
language delay	22067053	CNVD
periventricular nodular heterotopia	20648244	CNVD
renal disease	17924346	CNVD
Schizophrenia	20433910	CNVD
22q11 deletion syndrome	17028864	CNVD
Schizophrenia	16969581	CNVD
Non-syndromic sensorineural hearing loss	17135275	CNVD
velo-cardio-facial syndrome	17135275	CNVD
Digeorge syndrome	18787571	CNVD
Autism	18925931	CNVD
Non-small cell lung cancer	21829676	CNVD
22q11.2 microdeletion syndrome	21547621	CNVD
Congenital heart defect	21308838	CNVD
Digeorge syndrome	16512914	CNVD
Digeorge syndrome	20954168	CNVD
Nuchal translucency	21837766	CNVD
Right aortic arch in the fetus	17066500	CNVD
Shprintzen syndrome	17117043	CNVD
Tetralogy of fallot	17405110	CNVD
Velocardiofacial syndrome	20140301	CNVD
Velocardiofacial syndrome	16512914	CNVD
bone mass and metabolism	20516202	CNVD
choanal atresia	18209138	CNVD
extracardiac malformations	17086578	CNVD
fetal heart defects	21308838	CNVD
parathyroid gland dysfunction	16793949	CNVD
prenatal diagnosis	20453657	CNVD
velopharyngeal insufficiency	19620585	CNVD
Prader-willi syndrome	20942916	CNVD
22q11 deletion syndrome	17653112	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Cat eye syndrome	21549014	CNVD
Digeorge syndrome	21549014	CNVD
22q11.2 microdeletion syndrome	22051516	CNVD
22q11.2 microdeletion syndrome	18483005	CNVD
22q11.2 microdeletion syndrome	19565140	CNVD
22q11.2 microdeletion syndrome	20396437	CNVD
22q11.2 microdeletion syndrome	21390462	CNVD
22q11.2 microdeletion syndrome	21573985	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Congenital heart defect	21257016	CNVD
Developmental delay	18414209	CNVD
DiGeorge-Velo cardiofacial	19284877	CNVD
Epilepsy	20970697	CNVD
Heart disease	20551144	CNVD
Hughes'' syndrome	16595601	CNVD
Mental retardation	18414209	CNVD
Okamoto syndrome	19046188	CNVD
Primary immunodeficiency	22566803	CNVD
Schizophrenia	20877625	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Tetralogy of Fallot	22912587	CNVD
Velocardiofacial syndrome	17556857	CNVD
Velocardiofacial syndrome	20206275	CNVD
Velocardiofacial syndrome	20970697	CNVD
delayed speech development	21274400	CNVD
velo-cardio-facial syndrome	16511839	CNVD
velo-cardio-facial syndrome	21763005	CNVD
22q11.2 microdeletion syndrome	18799940	CNVD
Digeorge syndrome	20877625	CNVD
22q11.2 microdeletion syndrome	18923514	CNVD
Congenital heart defect	22185286	CNVD
DiGeorge-Velo cardiofacial	16773131	CNVD
Digeorge syndrome	20186050	CNVD
velo-cardio-facial conotruncal-face syndrome	20186050	CNVD
22q11.2 microdeletion syndrome	22116936	CNVD
Disorders of sex development	22290220	CNVD
22q11.2 duplication syndrome	18923514	CNVD
Autism	22095694	CNVD
Mental retardation	19951919	CNVD
Honadal dysgenesis	21048976	CNVD
Mental retardation	16773131	CNVD
22q11.2 microdeletion syndrome	22395003	CNVD
22q11.2 microdeletion syndrome	18691436	CNVD
22q11.2 microdeletion syndrome	18053182	CNVD
22q11.2 microdeletion syndrome	18324686	CNVD
22q11.2 microdeletion syndrome	20074913	CNVD
Congenital heart defect	20802965	CNVD
Congenital heart defect	21134246	CNVD
DiGeorge syndrome	19040613	CNVD
DiGeorge-Velo cardiofacial	18179902	CNVD
Digeorge syndrome	18172682	CNVD
Digeorge syndrome	22470819	CNVD
Digeorge syndrome	21364285	CNVD
Neuroendocrine carcinoma	22470819	CNVD
Non-syndromic sensorineural hearing loss	20069674	CNVD
Smith-Magenis syndrome	18301319	CNVD
Tetralogy of fallot	19144126	CNVD
Velo-cardio-facial syndrome	21364285	CNVD
Velocardiofacial syndrome	18788013	CNVD
cardiac malformation	20573211	CNVD
cardiac malformation	18172682	CNVD
velo-cardio-facial syndrome	18636631	CNVD
Schizophrenia	21822266	CNVD
synaptic plasticity	21368174	CNVD
Schizophrenia	18043741	CNVD
sporadic birth defects	19047251	CNVD
Autism	19046189	CNVD
DiGeorge-Velo cardiofacial	19047251	CNVD
Hypernasal speech	21968682	CNVD
Mental retardation	17339581	CNVD
diverse phenotype	16760730	CNVD
Mental retardation	20152051	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
DiGeorge-Velo cardiofacial	17597781	CNVD
Digeorge syndrome	17576883	CNVD
Schizophrenia	18806272	CNVD
Schizophrenia	18990708	CNVD
Velocardiofacial syndrome	17576883	CNVD
Schizophrenia	20075378	CNVD
Neurodevelopmental disorder	17015230	CNVD
Neuropsychiatric disorder	20069037	CNVD
Williams-beuren syndrome	18553513	CNVD
Emphysema	19352772	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Disease	21346257	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Developmental delay	21147756	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Asthma	21956041	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	21128281	CNVD
Systemic lupus erythematosus	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
22q11.23 microdeletion syndrome	19193630	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Autism	20841430	CNVD
Cancer	20164919	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	17989066	CNVD

Chromatin state (count:3008 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:22793800-22794400	Enhancers	Primary B cells from peripheral blood	blood
2	chr22:22795400-22796000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr22:22800600-22801400	Enhancers	HSMM	muscle
4	chr22:22800600-22801800	Enhancers	HSMMtube	muscle
5	chr22:22800800-22801000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr22:22800800-22801000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr22:22801200-22801800	Enhancers	Fetal Muscle Leg	muscle
8	chr22:22803600-22806600	Enhancers	Primary B cells from cord blood	blood
9	chr22:22803600-22807000	Enhancers	Primary B cells from peripheral blood	blood
10	chr22:22804200-22805400	Enhancers	GM12878-XiMat	blood
11	chr22:22804400-22805000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr22:22804600-22804800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
13	chr22:22804600-22805000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
14	chr22:22804600-22805000	Enhancers	Spleen	Spleen
15	chr22:22804600-22805400	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr22:22804800-22805000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
17	chr22:22804800-22805000	Enhancers	Right Atrium	heart
18	chr22:22804800-22805400	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr22:22804800-22805400	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr22:22805000-22805200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr22:22805200-22807200	Weak transcription	Right Atrium	heart
22	chr22:22806600-22806800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
23	chr22:22809000-22809200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
24	chr22:22812800-22813000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr22:22813400-22814400	ZNF genes & repeats	Right Atrium	heart
26	chr22:22813600-22815000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
27	chr22:22814000-22814200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
28	chr22:22814400-22814600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr22:22815800-22832800	Weak transcription	Right Atrium	heart
30	chr22:22817000-22818800	Enhancers	Primary B cells from cord blood	blood
31	chr22:22817200-22818800	Enhancers	Primary B cells from peripheral blood	blood
32	chr22:22817800-22818400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
33	chr22:22818000-22818200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
34	chr22:22818000-22818600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr22:22818200-22818400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
36	chr22:22818200-22818400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr22:22818200-22818400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
38	chr22:22818200-22818600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
39	chr22:22818200-22818600	Bivalent Enhancer	Fetal Brain Female	brain
40	chr22:22818200-22818600	Enhancers	HSMMtube	muscle
41	chr22:22818200-22818800	Enhancers	Brain Anterior Caudate	brain
42	chr22:22818400-22818600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
43	chr22:22818600-22818800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
44	chr22:22818600-22818800	Flanking Active TSS	A549	lung
45	chr22:22818600-22818800	Flanking Active TSS	HSMMtube	muscle
46	chr22:22818600-22819000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr22:22818600-22819000	Bivalent Enhancer	HSMM	muscle
48	chr22:22818600-22819000	Flanking Bivalent TSS/Enh	K562	blood
49	chr22:22818800-22819000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
50	chr22:22818800-22819000	Bivalent/Poised TSS	A549	lung

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