Variant report

Variant	nsv878598
Chromosome Location	chr4:8195705-8254784
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2582)
CpG islands
(count:2754)
Chromatin interactive
region (count:86)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2582 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8202213-8202581	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:8240304-8240605	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:8254490-8254732	K562	blood:	n/a	n/a
4	ARID3A	chr4:8244040-8244260	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:8244929-8245080	K562	blood:	n/a	n/a
6	ARID3A	chr4:8200832-8201080	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:8227773-8228124	HepG2	liver:	n/a	n/a
8	ATF1	chr4:8254361-8254786	K562	blood:	n/a	n/a
9	ATF1	chr4:8223428-8223513	K562	blood:	n/a	n/a
10	ATF1	chr4:8220182-8220394	K562	blood:	n/a	n/a
11	ATF1	chr4:8202225-8202706	K562	blood:	n/a	n/a
12	ATF2	chr4:8200447-8201221	GM12878	blood:	n/a	n/a
13	ATF2	chr4:8243931-8244274	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr4:8243931-8244299	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr4:8200545-8201122	GM12878	blood:	n/a	n/a
16	ATF2	chr4:8203146-8203570	GM12878	blood:	n/a	n/a
17	ATF2	chr4:8230227-8230995	GM12878	blood:	n/a	n/a
18	ATF2	chr4:8203157-8203703	GM12878	blood:	n/a	n/a
19	ATF2	chr4:8230182-8231087	GM12878	blood:	n/a	n/a
20	ATF3	chr4:8243980-8244184	K562	blood:	n/a	chr4:8244062-8244071 chr4:8244108-8244116
21	ATF3	chr4:8202500-8202669	K562	blood:	n/a	n/a
22	BACH1	chr4:8230123-8230900	H1-hESC	embryonic stem cell:	n/a	chr4:8230476-8230490
23	BACH1	chr4:8227896-8228237	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr4:8244014-8244385	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr4:8230293-8230668	K562	blood:	n/a	chr4:8230476-8230490
26	BACH1	chr4:8254579-8254646	K562	blood:	n/a	n/a
27	BACH1	chr4:8244170-8244172	K562	blood:	n/a	n/a
28	BATF	chr4:8223336-8223630	GM12878	blood:	n/a	n/a
29	BATF	chr4:8230352-8230584	GM12878	blood:	n/a	chr4:8230476-8230486
30	BATF	chr4:8230281-8230848	GM12878	blood:	n/a	chr4:8230476-8230486
31	BATF	chr4:8223277-8223584	GM12878	blood:	n/a	n/a
32	BCL11A	chr4:8200742-8201148	GM12878	blood:	n/a	chr4:8200963-8200972 chr4:8200816-8200829 chr4:8200751-8200760
33	BCL11A	chr4:8230171-8231050	GM12878	blood:	n/a	n/a
34	BCL11A	chr4:8203102-8203453	GM12878	blood:	n/a	chr4:8203444-8203453
35	BCL11A	chr4:8200750-8201203	GM12878	blood:	n/a	chr4:8200963-8200972 chr4:8200816-8200829 chr4:8200751-8200760
36	BCL11A	chr4:8230278-8230620	GM12878	blood:	n/a	n/a
37	BCL11A	chr4:8203313-8203587	GM12878	blood:	n/a	chr4:8203444-8203453
38	BCL3	chr4:8230261-8231421	GM12878	blood:	n/a	n/a
39	BCLAF1	chr4:8200397-8201149	GM12878	blood:	n/a	chr4:8200963-8200972 chr4:8200816-8200829 chr4:8200751-8200760
40	BCLAF1	chr4:8203140-8203628	GM12878	blood:	n/a	chr4:8203444-8203453
41	BCLAF1	chr4:8200346-8201218	GM12878	blood:	n/a	chr4:8200963-8200972 chr4:8200816-8200829 chr4:8200751-8200760
42	BCLAF1	chr4:8230183-8231019	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:8200406-8201154	K562	blood:	n/a	chr4:8200519-8200540
44	BHLHE40	chr4:8201709-8202500	GM12878	blood:	n/a	chr4:8201905-8201921
45	BHLHE40	chr4:8217197-8217387	K562	blood:	n/a	n/a
46	BHLHE40	chr4:8197835-8198032	K562	blood:	n/a	n/a
47	BHLHE40	chr4:8245861-8246051	K562	blood:	n/a	chr4:8245988-8245997 chr4:8245989-8245998 chr4:8245988-8245997 chr4:8245982-8246003 chr4:8245987-8245996
48	BHLHE40	chr4:8211333-8211402	K562	blood:	n/a	n/a
49	BHLHE40	chr4:8241105-8241392	K562	blood:	n/a	n/a
50	BHLHE40	chr4:8230103-8231100	GM12878	blood:	n/a	n/a

(count:2754 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8248444-8248494	HIPEpiC	eye:	n/a
2	chr4:8221101-8221151	H1-hESC	embryonic stem cell:	embryo
3	chr4:8230829-8230879	GM06990	blood:	n/a
4	chr4:8201560-8201610	GM12892	blood:	n/a
5	chr4:8233126-8233176	HRCEpiC	kidney:	n/a
6	chr4:8207250-8207300	GM12892	blood:	n/a
7	chr4:8230053-8230103	SK-N-SH	brain:	n/a
8	chr4:8221132-8221182	T-47D	breast:	n/a
9	chr4:8239254-8239304	NH-A	brain:	n/a
10	chr4:8248444-8248494	HIPEpiC	eye:	n/a
11	chr4:8221101-8221151	H1-hESC	embryonic stem cell:	embryo
12	chr4:8230829-8230879	GM06990	blood:	n/a
13	chr4:8201560-8201610	GM12892	blood:	n/a
14	chr4:8233126-8233176	HRCEpiC	kidney:	n/a
15	chr4:8207250-8207300	GM12892	blood:	n/a
16	chr4:8230053-8230103	SK-N-SH	brain:	n/a
17	chr4:8221132-8221182	T-47D	breast:	n/a
18	chr4:8239254-8239304	NH-A	brain:	n/a
19	chr4:8253322-8253372	GM12878	blood:	n/a
20	chr4:8248877-8248927	HEK293	kidney:	embryo
21	chr4:8200852-8200902	HEK293	kidney:	embryo
22	chr4:8202280-8202330	NB4	blood:	n/a
23	chr4:8248912-8248962	AoSMC	blood vessel:	n/a
24	chr4:8230847-8230897	HMEC	breast:	n/a
25	chr4:8230847-8230897	GM12892	blood:	n/a
26	chr4:8253707-8253757	ovcar-3	ovarian:	n/a
27	chr4:8200774-8200824	MCF-7	breast:	n/a
28	chr4:8239220-8239270	H1-hESC	embryonic stem cell:	embryo
29	chr4:8216813-8216863	AoSMC	blood vessel:	n/a
30	chr4:8207058-8207108	HCT-116	colon:	n/a
31	chr4:8202280-8202330	AG09309	skin:	n/a
32	chr4:8248877-8248927	ECC-1	luminal epithelium:	n/a
33	chr4:8242745-8242795	HIPEpiC	eye:	n/a
34	chr4:8200774-8200824	HCM	heart:	n/a
35	chr4:8221101-8221151	HCF	heart:	n/a
36	chr4:8233126-8233176	H1-hESC	embryonic stem cell:	embryo
37	chr4:8230689-8230739	AG10803	skin:	n/a
38	chr4:8230829-8230879	GM12892	blood:	n/a
39	chr4:8216813-8216863	Jurkat	blood:	n/a
40	chr4:8242745-8242795	BJ	skin:	n/a
41	chr4:8200549-8200599	K562	blood:	n/a
42	chr4:8201125-8201175	HRPEpiC	eye:	n/a
43	chr4:8207325-8207375	HepG2	liver:	n/a
44	chr4:8231787-8231837	LNCaP	prostate:	n/a
45	chr4:8239254-8239304	MCF10A-Er-Src	breast:	n/a
46	chr4:8253707-8253757	PrEC	prostate:	n/a
47	chr4:8230053-8230103	GM12892	blood:	n/a
48	chr4:8239303-8239353	HMEC	breast:	n/a
49	chr4:8207250-8207300	Jurkat	blood:	n/a
50	chr4:8239220-8239270	ovcar-3	ovarian:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:8202634..8204375-chr4:8204383..8206592,2	MCF-7	breast:
2	chr4:8238966..8241301-chr4:8261569..8263591,2	MCF-7	breast:
3	chr4:8201531..8203736-chr4:8237028..8240221,3	MCF-7	breast:
4	chr4:8252940..8255402-chr4:8411571..8414054,2	K562	blood:
5	chr4:8243862..8244409-chr4:8407695..8408313,2	MCF-7	breast:
6	chr4:8244003..8244602-chr4:8267775..8268462,2	MCF-7	breast:
7	chr4:8246169..8248159-chr4:8249694..8252255,2	K562	blood:
8	chr4:8202937..8205415-chr4:8232393..8234006,2	K562	blood:
9	chr4:8177372..8179736-chr4:8243215..8245049,2	K562	blood:
10	chr4:8205263..8208734-chr4:8209545..8212035,3	MCF-7	breast:
11	chr4:8199393..8202510-chr4:8203198..8206188,4	MCF-7	breast:
12	chr4:8195725..8198126-chr4:8238876..8240631,2	MCF-7	breast:
13	chr4:8243635..8244141-chr4:8412098..8412912,2	K562	blood:
14	chr4:8178683..8179355-chr4:8239861..8240827,2	K562	blood:
15	chr17:41464854..41467656-chr4:8218806..8220306,2	MCF-7	breast:
16	chr4:8204604..8207320-chr4:8213479..8215268,2	K562	blood:
17	chr4:8181697..8186152-chr4:8199354..8203571,7	MCF-7	breast:
18	chr4:8203500..8205646-chr4:8217325..8220224,2	MCF-7	breast:
19	chr4:8243586..8244597-chr4:8404569..8406088,15	MCF-7	breast:
20	chr4:8178239..8179222-chr4:8243368..8244103,2	K562	blood:
21	chr4:8196365..8198460-chr4:8203921..8207190,4	K562	blood:
22	chr11:62609146..62609723-chr4:8218786..8219286,2	HCT-116	colon:
23	chr4:8252135..8254748-chr4:8262223..8264616,3	K562	blood:
24	chr4:8243618..8244524-chr4:8268726..8269548,3	MCF-7	breast:
25	chr4:8193914..8196178-chr4:8208983..8211317,3	MCF-7	breast:
26	chr17:41464192..41465862-chr4:8218786..8220286,2	K562	blood:
27	chr4:8193914..8196178-chr4:8208983..8211317,3	MCF-7	breast:
28	chr2:74258378..74259054-chr4:8199921..8200797,2	MCF-7	breast:
29	chr4:8204604..8207320-chr4:8213479..8215268,2	K562	blood:
30	chr4:8209569..8211422-chr4:8212311..8214321,2	K562	blood:
31	chr4:8018368..8020892-chr4:8193998..8196693,2	MCF-7	breast:
32	chr4:8201008..8201849-chr4:156775894..156776553,2	MCF-7	breast:
33	chr17:41398862..41401693-chr4:8218786..8220306,3	K562	blood:
34	chr4:8233606..8235264-chr4:8235764..8238250,2	MCF-7	breast:
35	chr4:8252135..8255007-chr4:8262927..8264616,3	K562	blood:
36	chr4:8219379..8221157-chr4:8375226..8376743,2	MCF-7	breast:
37	chr4:8243346..8245051-chr4:8408250..8411036,2	K562	blood:
38	chr11:62607698..62610640-chr4:8218786..8220306,3	K562	blood:
39	chr4:8178298..8179365-chr4:8239616..8240695,4	MCF-7	breast:
40	chr4:8217481..8219669-chr4:8436164..8438381,2	MCF-7	breast:
41	chr17:41466254..41467859-chr4:8218786..8220306,2	MCF-7	breast:
42	chr4:8247491..8249787-chr4:8251476..8253386,2	MCF-7	breast:
43	chr4:8196058..8199736-chr4:8201784..8203810,3	K562	blood:
44	chr4:8206620..8209251-chr4:8213740..8215490,2	MCF-7	breast:
45	chr4:8194111..8197514-chr4:8198468..8201950,4	K562	blood:
46	chr4:8199821..8202591-chr4:8203028..8206014,3	K562	blood:
47	chr4:8183544..8186316-chr4:8238695..8241218,2	MCF-7	breast:
48	chr4:8247491..8249787-chr4:8251476..8253386,2	MCF-7	breast:
49	chr3:73158604..73161603-chr4:8218786..8220306,4	K562	blood:
50	chr11:62609126..62610640-chr4:8218786..8220306,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HTRA3-5	chr4:8203113-8203274	NONHSAT095079
2	lnc-HTRA3-5	chr4:8201025-8201132	NONHSAT095078
3	lnc-HTRA3-5	chr4:8206894-8207339	NONHSAT095078
4	lnc-HTRA3-5	chr4:8206894-8206990	NONHSAT095079

No data

Variant related genes	Relation type
SH3TC1	TF binding region
SH3TC1	CpG island
ENSG00000163995	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000151790	chromatin interactions
ENSG00000125089	chromatin interactions
ENSG00000155275	chromatin interactions
ENSG00000087008	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 3413 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3413 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1281117	chr4:8195705-8195706	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140951159	chr4:8195717-8195718	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs538852719	chr4:8195737-8195738	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs554004134	chr4:8195738-8195739	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs116542014	chr4:8195769-8195770	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs375057556	chr4:8195792-8195793	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs561314637	chr4:8195807-8195808	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs143153407	chr4:8195810-8195811	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543889226	chr4:8195829-8195830	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs184835462	chr4:8195850-8195851	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs116122592	chr4:8195861-8195862	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs545230741	chr4:8195894-8195895	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs59350156	chr4:8195909-8195910	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs527603908	chr4:8195969-8195970	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs376075725	chr4:8195971-8195972	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs376601678	chr4:8195976-8195977	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs57164699	chr4:8196068-8196069	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs567245869	chr4:8196073-8196074	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs1281118	chr4:8196081-8196082	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs146653375	chr4:8196101-8196102	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs571022818	chr4:8196104-8196105	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs538814152	chr4:8196120-8196121	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs553967940	chr4:8196141-8196142	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs74550231	chr4:8196145-8196146	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs398092146	chr4:8196147-8196148	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs565962942	chr4:8196154-8196155	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs536937757	chr4:8196163-8196164	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs114869470	chr4:8196172-8196173	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs189292143	chr4:8196307-8196308	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs543455923	chr4:8196308-8196309	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs572180041	chr4:8196329-8196330	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs559053635	chr4:8196338-8196339	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs180888988	chr4:8196360-8196361	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs185490847	chr4:8196371-8196372	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs374627346	chr4:8196379-8196380	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs190977213	chr4:8196388-8196389	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs58572623	chr4:8196393-8196394	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs140237458	chr4:8196468-8196469	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561032291	chr4:8196480-8196481	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs143590405	chr4:8196518-8196519	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs554246769	chr4:8196526-8196527	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs116142849	chr4:8196586-8196587	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs570982189	chr4:8196587-8196588	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs16841879	chr4:8196592-8196593	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs547126504	chr4:8196630-8196631	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs148065325	chr4:8196645-8196646	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536491322	chr4:8196763-8196764	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs374659608	chr4:8196797-8196798	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs1281119	chr4:8196800-8196801	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs182011748	chr4:8196808-8196809	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Oligozoospermia	20877625	CNVD
Autism	20841430	CNVD

Chromatin state (count:2367 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8185200-8202600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:8189600-8199200	Enhancers	HUVEC	blood vessel
3	chr4:8190200-8200400	Enhancers	Fetal Thymus	thymus
4	chr4:8191400-8199800	Weak transcription	Liver	Liver
5	chr4:8191800-8196000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr4:8191800-8200800	Enhancers	Placenta	Placenta
7	chr4:8192000-8196400	Weak transcription	Right Atrium	heart
8	chr4:8192200-8200400	Weak transcription	Brain Anterior Caudate	brain
9	chr4:8192400-8197600	Weak transcription	Colonic Mucosa	Colon
10	chr4:8192400-8200600	Weak transcription	Brain Substantia Nigra	brain
11	chr4:8193000-8200600	Weak transcription	Brain Cingulate Gyrus	brain
12	chr4:8193600-8196000	Weak transcription	HMEC	breast
13	chr4:8193600-8196000	Weak transcription	NHEK	skin
14	chr4:8193600-8196600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:8193600-8196600	Weak transcription	Left Ventricle	heart
16	chr4:8193600-8200400	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr4:8193600-8200600	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr4:8194000-8196600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr4:8194200-8198000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:8194200-8199200	Enhancers	Thymus	Thymus
21	chr4:8194200-8201000	Weak transcription	Psoas Muscle	Psoas
22	chr4:8194600-8195800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr4:8194600-8195800	Enhancers	Placenta Amnion	Placenta Amnion
24	chr4:8194800-8195800	Enhancers	Right Ventricle	heart
25	chr4:8194800-8196000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr4:8194800-8196400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr4:8194800-8197600	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr4:8194800-8198200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr4:8195000-8195800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:8195000-8196000	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr4:8195000-8196200	Weak transcription	Adipose Nuclei	Adipose
32	chr4:8195000-8199600	Weak transcription	Gastric	stomach
33	chr4:8195000-8200000	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr4:8195000-8200000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr4:8195000-8200000	Weak transcription	Fetal Heart	heart
36	chr4:8195000-8200200	Weak transcription	Brain Hippocampus Middle	brain
37	chr4:8195000-8200400	Weak transcription	Colon Smooth Muscle	Colon
38	chr4:8195200-8196200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:8195200-8196600	Weak transcription	Lung	lung
40	chr4:8195200-8197600	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr4:8195200-8197600	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr4:8195200-8197800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr4:8195200-8199000	Weak transcription	A549	lung
44	chr4:8195200-8199800	Weak transcription	Fetal Kidney	kidney
45	chr4:8195200-8199800	Weak transcription	GM12878-XiMat	blood
46	chr4:8195200-8200000	Weak transcription	Hela-S3	cervix
47	chr4:8195400-8196000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr4:8195400-8196600	Enhancers	Fetal Lung	lung
49	chr4:8195400-8197000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr4:8195400-8197200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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