Variant report

Variant	esv2752017
Chromosome Location	chr3:75392373-75754704
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6712)
CpG islands
(count:5742)
Chromatin interactive
region (count:15)
LncRNA
region (count:42)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:6712 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75710659-75710674	K562	blood:	n/a	n/a
2	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
6	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
7	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
8	ARID3A	chr3:75693851-75694060	K562	blood:	n/a	n/a
9	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
10	ARID3A	chr3:75601426-75601483	K562	blood:	n/a	n/a
11	ARID3A	chr3:75482025-75482381	HepG2	liver:	n/a	n/a
12	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
13	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
14	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
15	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
16	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
17	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
18	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
19	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
20	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
21	ATF1	chr3:75690145-75690820	K562	blood:	n/a	n/a
22	ATF1	chr3:75442553-75442767	K562	blood:	n/a	n/a
23	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
24	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
25	ATF1	chr3:75484451-75484710	K562	blood:	n/a	n/a
26	ATF1	chr3:75703512-75703565	K562	blood:	n/a	n/a
27	ATF1	chr3:75482136-75482245	K562	blood:	n/a	n/a
28	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
29	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
30	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
31	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
32	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
33	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
34	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
35	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
36	ATF1	chr3:75689319-75689814	K562	blood:	n/a	n/a
37	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
38	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a
39	ATF1	chr3:75691118-75692520	K562	blood:	n/a	n/a
40	ATF3	chr3:75718289-75718505	K562	blood:	n/a	n/a
41	ATF3	chr3:75482021-75482341	K562	blood:	n/a	n/a
42	ATF3	chr3:75482035-75482349	A549	lung:	n/a	n/a
43	ATF3	chr3:75717987-75718165	K562	blood:	n/a	n/a
44	BACH1	chr3:75691900-75692752	K562	blood:	n/a	n/a
45	BACH1	chr3:75744812-75745060	K562	blood:	n/a	n/a
46	BACH1	chr3:75736972-75737792	K562	blood:	n/a	n/a
47	BACH1	chr3:75739253-75739499	K562	blood:	n/a	n/a
48	BACH1	chr3:75704919-75705249	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr3:75740483-75740494	K562	blood:	n/a	n/a
50	BACH1	chr3:75689184-75689642	K562	blood:	n/a	n/a

(count:5742 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75414693-75414743	HPAEpiC	pulmonary alveolar:	n/a
2	chr3:75658552-75658602	GM19239	blood:	n/a
3	chr3:75714447-75714497	T-47D	breast:	n/a
4	chr3:75445095-75445145	RPTEC	kidney:	n/a
5	chr3:75708104-75708154	MCF-7	breast:	n/a
6	chr3:75668369-75668419	Caco-2	colon:	n/a
7	chr3:75555938-75555988	PANC-1	pancreas:	n/a
8	chr3:75410789-75410839	Jurkat	blood:	n/a
9	chr3:75414693-75414743	HPAEpiC	pulmonary alveolar:	n/a
10	chr3:75658552-75658602	GM19239	blood:	n/a
11	chr3:75714447-75714497	T-47D	breast:	n/a
12	chr3:75445095-75445145	RPTEC	kidney:	n/a
13	chr3:75708104-75708154	MCF-7	breast:	n/a
14	chr3:75668369-75668419	Caco-2	colon:	n/a
15	chr3:75555938-75555988	PANC-1	pancreas:	n/a
16	chr3:75410789-75410839	Jurkat	blood:	n/a
17	chr3:75555994-75556044	SK-N-SH_RA	brain:	n/a
18	chr3:75668924-75668974	GM06990	blood:	n/a
19	chr3:75411038-75411088	GM19239	blood:	n/a
20	chr3:75701993-75702043	HNPCEpiC	eye:	n/a
21	chr3:75485448-75485498	HCPEpiC	choroid plexus:	n/a
22	chr3:75631426-75631476	MCF10A-Er-Src	breast:	n/a
23	chr3:75707560-75707610	PFSK-1	brain:	n/a
24	chr3:75720876-75720926	K562	blood:	n/a
25	chr3:75719158-75719208	ovcar-3	ovarian:	n/a
26	chr3:75553762-75553812	GM12892	blood:	n/a
27	chr3:75628819-75628869	Jurkat	blood:	n/a
28	chr3:75666392-75666442	H1-hESC	embryonic stem cell:	embryo
29	chr3:75664059-75664109	IMR90	lung:	fetal
30	chr3:75669109-75669159	NH-A	brain:	n/a
31	chr3:75708104-75708154	NT2-D1	testis:	n/a
32	chr3:75658490-75658540	HAEpiC	amniotic membrane:	n/a
33	chr3:75484516-75484566	MCF-7	breast:	n/a
34	chr3:75661799-75661849	GM06990	blood:	n/a
35	chr3:75441804-75441854	HCM	heart:	n/a
36	chr3:75484516-75484566	BE2_C	brain:	n/a
37	chr3:75712695-75712745	GM12878	blood:	n/a
38	chr3:75484516-75484566	GM12878	blood:	n/a
39	chr3:75720876-75720926	HUVEC	blood vessel:	n/a
40	chr3:75679024-75679074	CMK	blood:	n/a
41	chr3:75679454-75679504	K562	blood:	n/a
42	chr3:75704951-75705001	SAEC	small airway:	n/a
43	chr3:75556027-75556077	BJ	skin:	n/a
44	chr3:75679454-75679504	MCF-7	breast:	n/a
45	chr3:75658410-75658460	HRE	kidney:	n/a
46	chr3:75668627-75668677	H1-hESC	embryonic stem cell:	embryo
47	chr3:75444752-75444802	ProgFib	skin:	n/a
48	chr3:75553294-75553344	HL-60	blood:	n/a
49	chr3:75653319-75653369	Caco-2	colon:	n/a
50	chr3:75664059-75664109	MCF-7	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:75717548..75719836-chr9:68411784..68414340,4	MCF-7	breast:
2	chr3:75390707..75391392-chr3:75471007..75471537,3	MCF-7	breast:
3	chr3:75693392..75694000-chr5:103852101..103852601,2	MCF-7	breast:
4	chr16:33943186..33943816-chr3:75719164..75719883,2	MCF-7	breast:
5	chr3:75466672..75467412-chr3:129812592..129813394,2	NB4	blood:
6	chr3:75484863..75485638-chr6:26156199..26156944,2	HCT-116	colon:
7	chr3:75718137..75719895-chr9:68411990..68414461,3	MCF-7	breast:
8	chr3:75343052..75344300-chr3:75470848..75471840,6	MCF-7	breast:
9	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:
10	chr3:75692090..75692596-chr7:138578273..138578773,2	K562	blood:
11	chr3:75343239..75343917-chr3:75478470..75479360,2	MCF-7	breast:
12	chr3:75343035..75343810-chr3:75470999..75471871,7	MCF-7	breast:
13	chr19:22025273..22026773-chr3:75695462..75697658,2	MCF-7	breast:
14	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
15	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:

(count:42 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF717-1	chr3:75679231-75679352	NONHSAT090540
2	lnc-FRG2C-2	chr3:75608026-75608398	XLOC_002712
3	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545
4	lnc-FRG2C-3	chr3:75485367-75485503	XLOC_002710
5	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
6	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
7	lnc-FRG2C-3	chr3:75501683-75501794	NONHSAT090533
8	lnc-FRG2C-10	chr3:75694930-75696049	NONHSAT090542
9	lnc-FRG2C-3	chr3:75497520-75500553	NONHSAT090533
10	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
11	lnc-FRG2C-2	chr3:75606117-75606146	XLOC_002712
12	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
13	lnc-FRG2C-3	chr3:75501683-75501802	ENSG00000272690.1
14	lnc-FRG2C-3	chr3:75488905-75488997	XLOC_002710
15	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925
16	lnc-FRG2C-10	chr3:75691156-75691895	NONHSAT090542
17	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
18	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
19	lnc-FRG2C-3	chr3:75484499-75484564	ENSG00000272690.1
20	lnc-FRG2C-3	chr3:75496316-75496447	ENSG00000272690.1
21	lnc-FRG2C-3	chr3:75488905-75488988	XLOC_002710
22	lnc-FRG2C-3	chr3:75485928-75486426	XLOC_002710
23	lnc-FRG2C-3	chr3:75492659-75492797	ENSG00000272690.1
24	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
25	lnc-FRG2C-3	chr3:75500361-75500553	ENSG00000272690.1
26	lnc-FRG2C-3	chr3:75486207-75486426	XLOC_002710
27	lnc-ZNF717-3	chr3:75589200-75589378	ENSG00000272710.1
28	lnc-FRG2C-3	chr3:75492659-75492775	XLOC_002710
29	lnc-FRG2C-3	chr3:75501348-75501809	ENSG00000272690.1
30	lnc-FRG2C-3	chr3:75505768-75506637	ENSG00000272690.1
31	lnc-FRG2C-3	chr3:75500361-75500553	ENSG00000272690.1
32	lnc-FRG2C-2	chr3:75608026-75608433	XLOC_002712
33	lnc-ZNF717-1	chr3:75674122-75674304	NONHSAT090540
34	lnc-ZNF717-3	chr3:75629129-75629150	ENSG00000272710.1
35	lnc-ZNF717-2	chr3:75691158-75691575	XLOC_003164
36	lnc-ZNF717-2	chr3:75695572-75695597	XLOC_003164
37	lnc-FRG2C-11	chr3:75570954-75571163	NONHSAT090534
38	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
39	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
40	lnc-FRG2C-10	chr3:75687750-75688507	NONHSAT090542
41	lnc-FRG2C-2	chr3:75606223-75606260	XLOC_002712
42	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1324	chr3:75679974-75679997	MIMAT0005956

No data

Variant related genes	Relation type
UNC93B3	TF binding region
FRG2C	TF binding region
ENSG00000243422	TF binding region
ENSG00000239383	TF binding region
OR7E66P	TF binding region
LINC00960	TF binding region
MYLKP1	TF binding region
RPS3AP15	TF binding region
ENSG00000243794	TF binding region
OR7E121P	TF binding region
RARRES2P1	TF binding region
ENSG00000272690	TF binding region
FAM86DP	TF binding region
ENSG00000266685	TF binding region
ENSG00000242953	TF binding region
OR7E55P	TF binding region
ENSG00000221602	TF binding region
AGGF1P3	TF binding region
OR7E22P	TF binding region
LSP1P2	TF binding region
ENSG00000263782	TF binding region
ENPP7P2	TF binding region
ALG1L6P	TF binding region
ENSG00000236138	TF binding region
ENSG00000244699	TF binding region
ENSG00000272710	TF binding region
MIR1324	TF binding region
UNC93B3	CpG island
FRG2C	CpG island
ENSG00000243422	CpG island
ENSG00000239383	CpG island
OR7E66P	CpG island
LINC00960	CpG island
MYLKP1	CpG island
RPS3AP15	CpG island
ENSG00000243794	CpG island
OR7E121P	CpG island
RARRES2P1	CpG island
ENSG00000272690	CpG island
FAM86DP	CpG island
ENSG00000266685	CpG island
ENSG00000242953	CpG island
OR7E55P	CpG island
ENSG00000221602	CpG island
AGGF1P3	CpG island
OR7E22P	CpG island
LSP1P2	CpG island
ENSG00000263782	CpG island
ENPP7P2	CpG island
ALG1L6P	CpG island
ENSG00000236138	CpG island
ENSG00000244699	CpG island
ENSG00000272710	CpG island
MIR1324	CpG island
ENSG00000232815	chromatin interactions
ENSG00000251287	chromatin interactions
ENSG00000129925	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000248243	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000236829	chromatin interactions
SFRS5	miRNA target sites
ITGB1	miRNA target sites

Extended variants
information (count: 18098 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:18098 , 50 per page) page: 1 2 3 4 5 6 7 ... 362

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7618408	chr3:75392373-75392374	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566084233	chr3:75392374-75392375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545224017	chr3:75392405-75392406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78732643	chr3:75392445-75392446	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs17028115	chr3:75392451-75392452	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs538021500	chr3:75392490-75392491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs28568610	chr3:75392557-75392558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575711246	chr3:75392585-75392586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546294686	chr3:75392587-75392588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs193098939	chr3:75392617-75392618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564478494	chr3:75392624-75392625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573234653	chr3:75392627-75392628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77970097	chr3:75392660-75392661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs6419792	chr3:75392689-75392690	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs140996233	chr3:75392717-75392718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs115339130	chr3:75392730-75392731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562911397	chr3:75392733-75392734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369351181	chr3:75392734-75392735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs5850223	chr3:75392777-75392778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11283402	chr3:75392796-75392797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373544589	chr3:75392804-75392805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528874220	chr3:75392819-75392820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533049744	chr3:75392920-75392921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150181332	chr3:75392972-75392973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111868786	chr3:75392983-75392984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533538305	chr3:75392991-75392992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149110009	chr3:75393001-75393002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567538441	chr3:75393041-75393042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537716666	chr3:75393045-75393046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556347724	chr3:75393055-75393056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565498623	chr3:75393057-75393058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539949212	chr3:75393126-75393127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146238404	chr3:75393135-75393136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185745243	chr3:75393144-75393145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189145615	chr3:75393152-75393153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs55666371	chr3:75393230-75393231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566391110	chr3:75393244-75393245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74657613	chr3:75393262-75393263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138808816	chr3:75393301-75393302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs180877312	chr3:75393318-75393319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184940163	chr3:75393336-75393337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544748071	chr3:75393367-75393368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559165859	chr3:75393368-75393369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559792844	chr3:75393438-75393439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188630194	chr3:75393515-75393516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548981404	chr3:75393537-75393538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs17028077	chr3:75393547-75393548	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs531641127	chr3:75393589-75393590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549768753	chr3:75393605-75393606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571461735	chr3:75393606-75393607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Melanoma	20877625	CNVD
Ollier disease	21235737	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21858162	CNVD

Chromatin state (count:3705 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75389800-75392800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr3:75391000-75393200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr3:75391000-75400600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:75391200-75392400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr3:75391200-75392600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:75392600-75392800	Enhancers	Lung	lung
7	chr3:75393200-75395000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr3:75394400-75394600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:75399400-75400800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:75400600-75400800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr3:75400800-75401800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr3:75403200-75403600	Enhancers	Stomach Mucosa	stomach
13	chr3:75411000-75411400	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr3:75411000-75412000	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr3:75411000-75412200	Enhancers	Pancreas	Pancrea
16	chr3:75411000-75413400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr3:75411200-75411600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr3:75411200-75411600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:75411600-75412400	Enhancers	Placenta	Placenta
20	chr3:75411600-75412800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr3:75411800-75412200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr3:75412000-75413400	Enhancers	Stomach Mucosa	stomach
23	chr3:75413000-75413200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:75420200-75421800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr3:75421400-75423000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr3:75421800-75422600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr3:75422000-75422200	Flanking Active TSS	Osteobl	bone
28	chr3:75422000-75422400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr3:75422000-75422400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr3:75422000-75423000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr3:75422200-75422800	Enhancers	Osteobl	bone
32	chr3:75422600-75423000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr3:75423000-75423600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr3:75427600-75427800	Enhancers	Fetal Lung	lung
35	chr3:75427800-75428000	Enhancers	Fetal Heart	heart
36	chr3:75427800-75428200	Enhancers	Fetal Muscle Leg	muscle
37	chr3:75427800-75429000	Weak transcription	Fetal Lung	lung
38	chr3:75428000-75429000	Weak transcription	Fetal Heart	heart
39	chr3:75429000-75429200	Enhancers	Fetal Lung	lung
40	chr3:75429000-75429600	Enhancers	Fetal Heart	heart
41	chr3:75429000-75429600	Enhancers	Gastric	stomach
42	chr3:75429000-75429800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr3:75429000-75429800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:75429000-75429800	ZNF genes & repeats	Fetal Kidney	kidney
45	chr3:75429000-75429800	Enhancers	Pancreas	Pancrea
46	chr3:75429200-75429800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr3:75429200-75429800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr3:75429200-75429800	Active TSS	Fetal Lung	lung
49	chr3:75429200-75429800	ZNF genes & repeats	Dnd41	blood
50	chr3:75429400-75429800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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