Variant report

Variant	nsv834172
Chromosome Location	chr22:29899036-30057948
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3978)
CpG islands
(count:2688)
Chromatin interactive
region (count:166)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3978 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:29949703-29950243	K562	blood:	n/a	n/a
2	ARID3A	chr22:29986014-29986221	K562	blood:	n/a	n/a
3	ARID3A	chr22:29984476-29984562	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:29967049-29967249	HepG2	liver:	n/a	n/a
5	ARID3A	chr22:29981088-29981110	HepG2	liver:	n/a	n/a
6	ARID3A	chr22:29985931-29986205	HepG2	liver:	n/a	n/a
7	ARID3A	chr22:29990096-29990144	K562	blood:	n/a	n/a
8	ARID3A	chr22:29970861-29971504	HepG2	liver:	n/a	n/a
9	ARID3A	chr22:29949715-29950069	HepG2	liver:	n/a	n/a
10	ARID3A	chr22:29999369-29999506	HepG2	liver:	n/a	n/a
11	ARID3A	chr22:29999159-29999616	K562	blood:	n/a	chr22:29999225-29999240
12	ATF1	chr22:29999113-29999668	K562	blood:	n/a	n/a
13	ATF1	chr22:29949568-29950038	K562	blood:	n/a	n/a
14	ATF2	chr22:29976050-29976575	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr22:29999237-29999535	GM12878	blood:	n/a	n/a
16	ATF2	chr22:29949462-29950001	GM12878	blood:	n/a	n/a
17	ATF2	chr22:29949526-29950104	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr22:29949534-29950280	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr22:29999217-29999588	GM12878	blood:	n/a	n/a
20	ATF3	chr22:29999232-29999626	K562	blood:	n/a	chr22:29999557-29999566
21	ATF3	chr22:30018029-30018545	A549	lung:	n/a	n/a
22	ATF3	chr22:29999382-29999689	K562	blood:	n/a	chr22:29999557-29999566
23	ATF3	chr22:30017908-30018534	A549	lung:	n/a	n/a
24	BACH1	chr22:29916887-29917108	K562	blood:	n/a	n/a
25	BACH1	chr22:29899941-29900344	K562	blood:	n/a	n/a
26	BACH1	chr22:29949883-29949894	K562	blood:	n/a	n/a
27	BACH1	chr22:29999147-29999764	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr22:29900044-29900280	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr22:29916867-29917110	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr22:30014184-30014487	GM12878	blood:	n/a	n/a
31	BATF	chr22:29992442-29992649	GM12878	blood:	n/a	chr22:29992560-29992571
32	BCL11A	chr22:29977136-29977349	GM12878	blood:	n/a	n/a
33	BCL3	chr22:29914890-29915258	GM12878	blood:	n/a	n/a
34	BCL3	chr22:29914952-29915274	GM12878	blood:	n/a	n/a
35	BCL3	chr22:29949555-29950270	A549	lung:	n/a	chr22:29949738-29949747 chr22:29949763-29949772
36	BCL3	chr22:29949498-29950354	A549	lung:	n/a	chr22:29949738-29949747 chr22:29949763-29949772
37	BCL3	chr22:29949471-29950011	GM12878	blood:	n/a	chr22:29949738-29949747 chr22:29949763-29949772
38	BCL3	chr22:30017900-30018585	A549	lung:	n/a	n/a
39	BCLAF1	chr22:29976888-29977336	GM12878	blood:	n/a	n/a
40	BCLAF1	chr22:29949548-29950016	GM12878	blood:	n/a	chr22:29949738-29949747 chr22:29949763-29949772
41	BCLAF1	chr22:29949544-29950140	GM12878	blood:	n/a	chr22:29949738-29949747 chr22:29949763-29949772
42	BCLAF1	chr22:29949543-29950133	K562	blood:	n/a	chr22:29949738-29949747 chr22:29949763-29949772
43	BCLAF1	chr22:29999465-30000097	GM12878	blood:	n/a	chr22:29999873-29999886
44	BHLHE40	chr22:29949643-29950033	HepG2	liver:	n/a	n/a
45	BHLHE40	chr22:29949349-29950246	K562	blood:	n/a	n/a
46	BHLHE40	chr22:29949521-29950072	GM12878	blood:	n/a	n/a
47	BHLHE40	chr22:29977068-29977320	K562	blood:	n/a	n/a
48	BHLHE40	chr22:30021663-30021734	K562	blood:	n/a	n/a
49	BHLHE40	chr22:30021689-30021932	GM12878	blood:	n/a	n/a
50	BHLHE40	chr22:29984423-29984679	HepG2	liver:	n/a	n/a

(count:2688 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29977203-29977253	HIPEpiC	eye:	n/a
2	chr22:29977262-29977312	A549	lung:	n/a
3	chr22:30003603-30003653	HCT-116	colon:	n/a
4	chr22:29999407-29999457	HEEpiC	esophagus:	n/a
5	chr22:29977203-29977253	HIPEpiC	eye:	n/a
6	chr22:29977262-29977312	A549	lung:	n/a
7	chr22:30003603-30003653	HCT-116	colon:	n/a
8	chr22:29999407-29999457	HEEpiC	esophagus:	n/a
9	chr22:29949986-29950036	HNPCEpiC	eye:	n/a
10	chr22:30000194-30000244	HRCEpiC	kidney:	n/a
11	chr22:29976923-29976973	HIPEpiC	eye:	n/a
12	chr22:29999402-29999452	AG09309	skin:	n/a
13	chr22:29920546-29920596	NHDF-neo	bronchial:	n/a
14	chr22:29977742-29977792	GM12892	blood:	n/a
15	chr22:29977253-29977303	HPAEpiC	pulmonary alveolar:	n/a
16	chr22:29977203-29977253	H1-hESC	embryonic stem cell:	embryo
17	chr22:30000107-30000157	HEK293	kidney:	embryo
18	chr22:29999118-29999168	HCF	heart:	n/a
19	chr22:29999402-29999452	MCF-7	breast:	n/a
20	chr22:29977063-29977113	U87	brain:	n/a
21	chr22:29949913-29949963	SKMC	muscle:	n/a
22	chr22:29946559-29946609	BE2_C	brain:	n/a
23	chr22:29974709-29974759	RPTEC	kidney:	n/a
24	chr22:29949725-29949775	PrEC	prostate:	n/a
25	chr22:29999969-30000019	HL-60	blood:	n/a
26	chr22:29999969-30000019	HPAEpiC	pulmonary alveolar:	n/a
27	chr22:29978158-29978208	CMK	blood:	n/a
28	chr22:29999516-29999566	HCF	heart:	n/a
29	chr22:29977322-29977372	ProgFib	skin:	n/a
30	chr22:29999402-29999452	GM06990	blood:	n/a
31	chr22:29999554-29999604	A549	lung:	n/a
32	chr22:29977322-29977372	HMEC	breast:	n/a
33	chr22:29949725-29949775	MCF10A-Er-Src	breast:	n/a
34	chr22:29977322-29977372	AG04449	skin:	fetal
35	chr22:29977203-29977253	CMK	blood:	n/a
36	chr22:29978158-29978208	AG09309	skin:	n/a
37	chr22:29977742-29977792	IMR90	lung:	fetal
38	chr22:29977162-29977212	SAEC	small airway:	n/a
39	chr22:29977677-29977727	NH-A	brain:	n/a
40	chr22:29950936-29950986	U87	brain:	n/a
41	chr22:29999554-29999604	NHDF-neo	bronchial:	n/a
42	chr22:29920546-29920596	HCT-116	colon:	n/a
43	chr22:29999883-29999933	GM19239	blood:	n/a
44	chr22:29999883-29999933	HepG2	liver:	n/a
45	chr22:30000194-30000244	SKMC	muscle:	n/a
46	chr22:29977677-29977727	HCM	heart:	n/a
47	chr22:29974709-29974759	HCPEpiC	choroid plexus:	n/a
48	chr22:29999444-29999494	HRCEpiC	kidney:	n/a
49	chr22:29952103-29952153	HepG2	liver:	n/a
50	chr22:29977228-29977278	SK-N-MC	brain:	n/a

(count:166 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr22:30001741..30005693-chr22:30010044..30012563,3	K562	blood:
2	chr22:29783150..29785946-chr22:29944649..29946343,2	MCF-7	breast:
3	chr22:29913237..29914759-chr22:29922102..29924091,2	K562	blood:
4	chr22:29940656..29942248-chr22:29948423..29951166,2	MCF-7	breast:
5	chr22:29947295..29951735-chr22:29976015..29980297,4	K562	blood:
6	chr22:29998884..29999633-chr3:23958298..23958926,2	NB4	blood:
7	chr22:29921497..29923019-chr22:29929067..29931805,2	MCF-7	breast:
8	chr22:29907526..29909424-chr22:29918736..29921432,2	MCF-7	breast:
9	chr22:30019261..30020777-chr22:30025452..30026983,2	K562	blood:
10	chr22:29924148..29926700-chr22:29944225..29946425,2	MCF-7	breast:
11	chr22:29974628..29977179-chr22:29983583..29986095,3	MCF-7	breast:
12	chr22:30045640..30047901-chr22:30049009..30050786,2	MCF-7	breast:
13	chr22:30047107..30049570-chr22:30052178..30054357,2	K562	blood:
14	chr22:29877422..29878326-chr22:29912754..29914005,18	MCF-7	breast:
15	chr22:29907835..29909461-chr22:29910820..29913528,2	MCF-7	breast:
16	chr22:29947295..29951735-chr22:29976015..29980297,4	K562	blood:
17	chr22:29935861..29937892-chr22:29938918..29941318,2	K562	blood:
18	chr22:29928796..29930893-chr22:29932516..29935444,2	K562	blood:
19	chr22:29993439..29997077-chr22:29997568..30000829,3	MCF-7	breast:
20	chr22:29953914..29956563-chr22:29957184..29959467,2	K562	blood:
21	chr22:30031527..30032428-chr22:30484594..30485517,5	K562	blood:
22	chr13:52026823..52027558-chr22:29999049..30000022,2	HCT-116	colon:
23	chr22:30019261..30020777-chr22:30025452..30026983,2	K562	blood:
24	chr22:30013839..30015515-chr22:30021150..30023734,2	MCF-7	breast:
25	chr22:29663275..29666008-chr22:29976454..29978804,2	K562	blood:
26	chr22:29948193..29950224-chr22:29975940..29978547,6	MCF-7	breast:
27	chr22:29877043..29879359-chr22:29911623..29914922,6	MCF-7	breast:
28	chr22:29782601..29785697-chr22:29975164..29978533,5	MCF-7	breast:
29	chr22:29945702..29947218-chr22:29948273..29950145,2	MCF-7	breast:
30	chr22:29790656..29791686-chr22:29920171..29921137,10	MCF-7	breast:
31	chr22:29946832..29952460-chr22:29954697..29959036,10	MCF-7	breast:
32	chr22:29961562..29963537-chr22:29964937..29966766,2	MCF-7	breast:
33	chr22:30019747..30021747-chr22:30036683..30039570,2	MCF-7	breast:
34	chr22:29998526..30000327-chr22:30030498..30033329,2	MCF-7	breast:
35	chr22:29774141..29774748-chr22:29913157..29913945,3	MCF-7	breast:
36	chr22:29975560..29978145-chr22:29998416..30001350,4	MCF-7	breast:
37	chr22:29949841..29950776-chr7:5631996..5632681,2	Hela-S3	cervix:
38	chr22:29999797..30002683-chr22:30006391..30009061,4	K562	blood:
39	chr22:29790720..29791562-chr22:29920209..29921282,4	MCF-7	breast:
40	chr22:29935399..29937361-chr22:29938539..29940418,2	K562	blood:
41	chr22:29975483..29978642-chr22:29996311..30000725,6	MCF-7	breast:
42	chr22:29935333..29937514-chr22:29945069..29947567,2	K562	blood:
43	chr11:129334906..129335676-chr22:29997138..29998015,2	Hela-S3	cervix:
44	chr22:29976905..29978704-chr22:29988519..29990911,2	MCF-7	breast:
45	chr22:30036794..30038709-chr22:30046357..30049323,2	MCF-7	breast:
46	chr22:29900180..29902259-chr22:29906979..29909604,2	MCF-7	breast:
47	chr22:29991169..29993450-chr22:30000929..30002699,2	K562	blood:
48	chr22:29907526..29909424-chr22:29918736..29921432,2	MCF-7	breast:
49	chr22:30010110..30012415-chr22:30019753..30021534,2	K562	blood:
50	chr22:30021415..30023125-chr22:30030680..30033150,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEFH-1	chr22:29999564-29999796	NONHSAT084714
2	lnc-THOC5-2	chr22:29976974-29977015	NONHSAT084712
3	lnc-NIPSNAP1-1	chr22:29909878-29910005	ENSG00000234208.1
4	lnc-NIPSNAP1-1	chr22:29931219-29931379	ENSG00000234208.1
5	lnc-NEFH-1	chr22:29999564-29999811	NONHSAT084713
6	lnc-THOC5-2	chr22:29975746-29976144	NONHSAT084712
7	lnc-CABP7-2	chr22:30004889-30005490	NONHSAT084715

No data

Variant related genes	Relation type
THOC5	TF binding region
RPEP4	TF binding region
NF2	TF binding region
NIPSNAP1	TF binding region
ENSG00000234208	TF binding region
THOC5	CpG island
RPEP4	CpG island
NF2	CpG island
NIPSNAP1	CpG island
ENSG00000234208	CpG island
ENSG00000100263	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000100296	chromatin interactions
ENSG00000075618	chromatin interactions
ENSG00000186575	chromatin interactions
ENSG00000225465	chromatin interactions
ENSG00000234208	chromatin interactions
ENSG00000197885	chromatin interactions
ENSG00000185340	chromatin interactions
ENSG00000100285	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000100280	chromatin interactions
ENSG00000182944	chromatin interactions
ENSG00000184117	chromatin interactions
ENSG00000174748	chromatin interactions
ENSG00000233010	chromatin interactions

Extended variants
information (count: 6043 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:6043 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567624724	chr22:29899133-29899134	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs189117792	chr22:29899147-29899148	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530222659	chr22:29899261-29899262	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550005415	chr22:29899264-29899265	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571769880	chr22:29899277-29899278	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs540913613	chr22:29899280-29899281	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs144926269	chr22:29899355-29899356	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs28698037	chr22:29899394-29899395	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs181162809	chr22:29899427-29899428	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs73156596	chr22:29899552-29899553	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs574881873	chr22:29899562-29899563	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184018492	chr22:29899615-29899616	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs187961650	chr22:29899629-29899630	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs530620993	chr22:29899682-29899683	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545565916	chr22:29899695-29899696	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs564055321	chr22:29899718-29899719	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs5763284	chr22:29899724-29899725	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs202030315	chr22:29899735-29899736	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs28633341	chr22:29899736-29899737	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs538840664	chr22:29899805-29899806	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs180982412	chr22:29899838-29899839	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs528843631	chr22:29899839-29899840	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs550701377	chr22:29899841-29899842	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs568946899	chr22:29899888-29899889	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs537659960	chr22:29899949-29899950	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575350756	chr22:29900067-29900068	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559182225	chr22:29900215-29900216	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs187036869	chr22:29900257-29900258	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531737841	chr22:29900306-29900307	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs67419835	chr22:29900342-29900343	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs71700489	chr22:29900344-29900345	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs192209447	chr22:29900352-29900353	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs73407057	chr22:29900355-29900356	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs574783822	chr22:29900364-29900365	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs71329491	chr22:29900370-29900371	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs542203447	chr22:29900380-29900381	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs562201787	chr22:29900382-29900383	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs377051425	chr22:29900383-29900384	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs140706304	chr22:29900425-29900426	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs5997483	chr22:29900450-29900451	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs557054735	chr22:29900451-29900452	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs142876210	chr22:29900454-29900455	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs575299260	chr22:29900468-29900469	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs545621477	chr22:29900469-29900470	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs71329492	chr22:29900486-29900487	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs5763285	chr22:29900513-29900514	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs148138299	chr22:29900565-29900566	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs376050165	chr22:29900566-29900567	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs540530791	chr22:29900614-29900615	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs9625812	chr22:29900622-29900623	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
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
Hodgkin''s lymphoma	17606441	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
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Recurrent pregnancy loss	19789632	CNVD
Cancer	17440070	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	20824076	CNVD

Chromatin state (count:5827 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29877400-29900600	Weak transcription	Right Atrium	heart
2	chr22:29878000-29900800	Weak transcription	Fetal Brain Female	brain
3	chr22:29878000-29903000	Weak transcription	Pancreas	Pancrea
4	chr22:29878400-29899800	Weak transcription	Fetal Intestine Large	intestine
5	chr22:29878400-29899800	Weak transcription	NH-A	brain
6	chr22:29878800-29902600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr22:29879000-29899600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr22:29879200-29901200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr22:29879600-29899400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr22:29880400-29901000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr22:29882000-29899200	Weak transcription	Brain Angular Gyrus	brain
12	chr22:29882800-29903200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr22:29883600-29899800	Weak transcription	Brain Germinal Matrix	brain
14	chr22:29883800-29904000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr22:29884000-29902200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr22:29884800-29901200	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr22:29885000-29902600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr22:29885600-29904000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr22:29886000-29903400	Weak transcription	Gastric	stomach
20	chr22:29886200-29899600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr22:29886200-29902800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr22:29886800-29899800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr22:29887400-29902000	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr22:29887600-29902000	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr22:29888800-29901000	Weak transcription	Thymus	Thymus
26	chr22:29888800-29901200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr22:29889000-29900800	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr22:29889400-29899800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr22:29889600-29899800	Weak transcription	NHLF	lung
30	chr22:29889800-29899800	Weak transcription	NHDF-Ad	bronchial
31	chr22:29890000-29899800	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr22:29890400-29900800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr22:29890800-29901800	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr22:29890800-29902200	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr22:29891000-29899800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr22:29891000-29900200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr22:29891000-29901400	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr22:29891000-29901400	Weak transcription	Primary B cells from cord blood	blood
39	chr22:29891000-29902600	Weak transcription	Primary hematopoietic stem cells	blood
40	chr22:29891000-29903600	Weak transcription	Spleen	Spleen
41	chr22:29891000-29904000	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr22:29891200-29899800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr22:29891200-29899800	Weak transcription	Adipose Nuclei	Adipose
44	chr22:29891200-29901200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr22:29891200-29901200	Weak transcription	NHEK	skin
46	chr22:29891200-29902600	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr22:29891200-29902600	Weak transcription	Fetal Lung	lung
48	chr22:29891200-29903000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr22:29891400-29899800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr22:29891400-29899800	Weak transcription	Fetal Muscle Leg	muscle

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