Variant report

Variant	nsv869928
Chromosome Location	chr4:8195069-8214848
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:916)
CpG islands
(count:917)
Chromatin interactive
region (count:31)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8200832-8201080	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:8202213-8202581	HepG2	liver:	n/a	n/a
3	ATF1	chr4:8202225-8202706	K562	blood:	n/a	n/a
4	ATF2	chr4:8200447-8201221	GM12878	blood:	n/a	n/a
5	ATF2	chr4:8203146-8203570	GM12878	blood:	n/a	n/a
6	ATF2	chr4:8203157-8203703	GM12878	blood:	n/a	n/a
7	ATF2	chr4:8200545-8201122	GM12878	blood:	n/a	n/a
8	ATF3	chr4:8202500-8202669	K562	blood:	n/a	n/a
9	BCL11A	chr4:8203102-8203453	GM12878	blood:	n/a	chr4:8203444-8203453
10	BCL11A	chr4:8203313-8203587	GM12878	blood:	n/a	chr4:8203444-8203453
11	BCL11A	chr4:8200742-8201148	GM12878	blood:	n/a	chr4:8200963-8200972 chr4:8200816-8200829 chr4:8200751-8200760
12	BCL11A	chr4:8200750-8201203	GM12878	blood:	n/a	chr4:8200963-8200972 chr4:8200816-8200829 chr4:8200751-8200760
13	BCLAF1	chr4:8203140-8203628	GM12878	blood:	n/a	chr4:8203444-8203453
14	BCLAF1	chr4:8200397-8201149	GM12878	blood:	n/a	chr4:8200963-8200972 chr4:8200816-8200829 chr4:8200751-8200760
15	BCLAF1	chr4:8200346-8201218	GM12878	blood:	n/a	chr4:8200963-8200972 chr4:8200816-8200829 chr4:8200751-8200760
16	BHLHE40	chr4:8201709-8202500	GM12878	blood:	n/a	chr4:8201905-8201921
17	BHLHE40	chr4:8200267-8201188	GM12878	blood:	n/a	chr4:8200519-8200540
18	BHLHE40	chr4:8203297-8203306	K562	blood:	n/a	n/a
19	BHLHE40	chr4:8200406-8201154	K562	blood:	n/a	chr4:8200519-8200540
20	BHLHE40	chr4:8211333-8211402	K562	blood:	n/a	n/a
21	BHLHE40	chr4:8197835-8198032	K562	blood:	n/a	n/a
22	BHLHE40	chr4:8204556-8204938	HepG2	liver:	n/a	n/a
23	BHLHE40	chr4:8202796-8203608	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:8207826-8208041	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:8204521-8205184	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:8203836-8204202	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:8202103-8202647	K562	blood:	n/a	n/a
28	BHLHE40	chr4:8201877-8202438	HepG2	liver:	n/a	chr4:8201905-8201921
29	BHLHE40	chr4:8200385-8201166	HepG2	liver:	n/a	chr4:8200519-8200540
30	BRCA1	chr4:8201901-8201954	GM12878	blood:	n/a	n/a
31	BRCA1	chr4:8203334-8203337	GM12878	blood:	n/a	n/a
32	BRCA1	chr4:8200750-8200841	GM12878	blood:	n/a	n/a
33	CCNT2	chr4:8200771-8201248	K562	blood:	n/a	n/a
34	CCNT2	chr4:8201852-8202620	K562	blood:	n/a	n/a
35	CEBPB	chr4:8200350-8201205	GM12878	blood:	n/a	n/a
36	CEBPB	chr4:8209197-8209341	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:8202470-8202637	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:8212384-8212584	Hela-S3	cervix:	n/a	chr4:8212532-8212540
39	CEBPB	chr4:8202465-8202607	K562	blood:	n/a	n/a
40	CEBPB	chr4:8212349-8212549	A549	lung:	n/a	chr4:8212532-8212540
41	CEBPB	chr4:8212361-8212674	ECC-1	luminal epithelium:	n/a	chr4:8212532-8212540
42	CEBPB	chr4:8202186-8202719	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:8204419-8204820	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:8212340-8212687	ECC-1	luminal epithelium:	n/a	chr4:8212532-8212540
45	CEBPB	chr4:8212287-8212510	IMR90	lung:	n/a	n/a
46	CEBPB	chr4:8204470-8204783	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:8200908-8200914	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr4:8204463-8204671	HepG2	liver:	n/a	n/a
49	CEBPB	chr4:8202399-8202713	IMR90	lung:	n/a	n/a
50	CEBPB	chr4:8202428-8202686	K562	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8200549-8200599	AG04449	skin:	fetal
2	chr4:8200974-8201024	HMEC	breast:	n/a
3	chr4:8200549-8200599	AG04449	skin:	fetal
4	chr4:8200974-8201024	HMEC	breast:	n/a
5	chr4:8207250-8207300	HUVEC	blood vessel:	n/a
6	chr4:8200549-8200599	U87	brain:	n/a
7	chr4:8202491-8202541	SKMC	muscle:	n/a
8	chr4:8200774-8200824	SAEC	small airway:	n/a
9	chr4:8207058-8207108	Jurkat	blood:	n/a
10	chr4:8201560-8201610	T-47D	breast:	n/a
11	chr4:8202531-8202581	IMR90	lung:	fetal
12	chr4:8200974-8201024	GM06990	blood:	n/a
13	chr4:8201560-8201610	NHBE	bronchial:	n/a
14	chr4:8206575-8206625	HL-60	blood:	n/a
15	chr4:8207325-8207375	NH-A	brain:	n/a
16	chr4:8202491-8202541	HEK293	kidney:	embryo
17	chr4:8202491-8202541	Hela-S3	cervix:	n/a
18	chr4:8207250-8207300	SKMC	muscle:	n/a
19	chr4:8207250-8207300	SAEC	small airway:	n/a
20	chr4:8200549-8200599	BJ	skin:	n/a
21	chr4:8200852-8200902	MCF-7	breast:	n/a
22	chr4:8207325-8207375	HUVEC	blood vessel:	n/a
23	chr4:8207058-8207108	HCPEpiC	choroid plexus:	n/a
24	chr4:8201125-8201175	A549	lung:	n/a
25	chr4:8207325-8207375	U87	brain:	n/a
26	chr4:8200774-8200824	H1-hESC	embryonic stem cell:	embryo
27	chr4:8201128-8201178	ovcar-3	ovarian:	n/a
28	chr4:8207058-8207108	Caco-2	colon:	n/a
29	chr4:8201125-8201175	HepG2	liver:	n/a
30	chr4:8200774-8200824	Hepatocyte	liver:	n/a
31	chr4:8202531-8202581	AG04449	skin:	fetal
32	chr4:8200852-8200902	Hepatocyte	liver:	n/a
33	chr4:8207250-8207300	BJ	skin:	n/a
34	chr4:8202491-8202541	AG04449	skin:	fetal
35	chr4:8207058-8207108	RPTEC	kidney:	n/a
36	chr4:8201128-8201178	Jurkat	blood:	n/a
37	chr4:8202531-8202581	AG09319	gingival:	n/a
38	chr4:8207119-8207169	HMEC	breast:	n/a
39	chr4:8207058-8207108	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:8207325-8207375	SK-N-SH	brain:	n/a
41	chr4:8201125-8201175	HCPEpiC	choroid plexus:	n/a
42	chr4:8207119-8207169	GM12878	blood:	n/a
43	chr4:8206575-8206625	AG04449	skin:	fetal
44	chr4:8207325-8207375	AG09319	gingival:	n/a
45	chr4:8207250-8207300	CMK	blood:	n/a
46	chr4:8202280-8202330	PrEC	prostate:	n/a
47	chr4:8201128-8201178	SK-N-MC	brain:	n/a
48	chr4:8202531-8202581	NHBE	bronchial:	n/a
49	chr4:8207058-8207108	AG04450	lung:	fetal
50	chr4:8202531-8202581	A549	lung:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8204604..8207320-chr4:8213479..8215268,2	K562	blood:
2	chr4:8195725..8198126-chr4:8238876..8240631,2	MCF-7	breast:
3	chr4:8199821..8202591-chr4:8203028..8206014,3	K562	blood:
4	chr4:8206620..8209251-chr4:8213740..8215490,2	MCF-7	breast:
5	chr4:8202937..8205415-chr4:8232393..8234006,2	K562	blood:
6	chr4:8206620..8209251-chr4:8213740..8215490,2	MCF-7	breast:
7	chr4:8196365..8198460-chr4:8203921..8207190,4	K562	blood:
8	chr4:8199821..8202591-chr4:8203028..8206014,3	K562	blood:
9	chr4:8211892..8215889-chr4:8218251..8222766,5	MCF-7	breast:
10	chr4:8178126..8179213-chr4:8194505..8195435,5	MCF-7	breast:
11	chr2:74258378..74259054-chr4:8199921..8200797,2	MCF-7	breast:
12	chr4:8209569..8211422-chr4:8212311..8214321,2	K562	blood:
13	chr4:8205263..8208734-chr4:8209545..8212035,3	MCF-7	breast:
14	chr4:8193914..8196178-chr4:8208983..8211317,3	MCF-7	breast:
15	chr4:8202798..8206403-chr4:8207013..8209683,3	K562	blood:
16	chr4:8189199..8191768-chr4:8203536..8206206,2	MCF-7	breast:
17	chr4:8203500..8205646-chr4:8217325..8220224,2	MCF-7	breast:
18	chr4:8196365..8198460-chr4:8203921..8207190,4	K562	blood:
19	chr4:8201008..8201849-chr4:156775894..156776553,2	MCF-7	breast:
20	chr4:8193914..8196178-chr4:8208983..8211317,3	MCF-7	breast:
21	chr4:8202634..8204375-chr4:8204383..8206592,2	MCF-7	breast:
22	chr4:8201150..8205648-chr4:8206751..8210488,5	MCF-7	breast:
23	chr4:8204604..8207320-chr4:8213479..8215268,2	K562	blood:
24	chr4:8196058..8199736-chr4:8201784..8203810,3	K562	blood:
25	chr4:8199393..8202510-chr4:8203198..8206188,4	MCF-7	breast:
26	chr4:8158369..8164233-chr4:8200767..8204083,4	MCF-7	breast:
27	chr4:8199393..8202510-chr4:8203198..8206188,4	MCF-7	breast:
28	chr4:8178210..8179173-chr4:8194105..8195549,8	MCF-7	breast:
29	chr4:8018368..8020892-chr4:8193998..8196693,2	MCF-7	breast:
30	chr4:8181697..8186152-chr4:8199354..8203571,7	MCF-7	breast:
31	chr4:8194111..8197514-chr4:8198468..8201950,4	K562	blood:

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

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

No data

Variant related genes	Relation type
SH3TC1	TF binding region
SH3TC1	CpG island
ENSG00000163995	chromatin interactions
ENSG00000151790	chromatin interactions
ENSG00000125089	chromatin interactions

Extended variants
information (count: 1042 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1281116	chr4:8195075-8195076	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73220410	chr4:8195125-8195126	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs150044036	chr4:8195157-8195158	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs190089999	chr4:8195167-8195168	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs573686558	chr4:8195189-8195190	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs115042516	chr4:8195196-8195197	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs556737810	chr4:8195277-8195278	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs578136053	chr4:8195297-8195298	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545289522	chr4:8195354-8195355	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560497619	chr4:8195396-8195397	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369997081	chr4:8195402-8195403	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs76260495	chr4:8195439-8195440	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs572064175	chr4:8195450-8195451	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs144934680	chr4:8195455-8195456	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs199741862	chr4:8195458-8195459	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs200703857	chr4:8195461-8195462	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs376877565	chr4:8195462-8195463	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs531855075	chr4:8195484-8195485	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs111925588	chr4:8195489-8195490	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550036244	chr4:8195516-8195517	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs562686555	chr4:8195527-8195528	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs533202318	chr4:8195555-8195556	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551697564	chr4:8195584-8195585	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs566775225	chr4:8195586-8195587	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs181164967	chr4:8195609-8195610	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs58214166	chr4:8195628-8195629	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs567219771	chr4:8195646-8195647	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs537931894	chr4:8195686-8195687	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs1281117	chr4:8195705-8195706	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs140951159	chr4:8195717-8195718	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs538852719	chr4:8195737-8195738	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs554004134	chr4:8195738-8195739	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs116542014	chr4:8195769-8195770	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs375057556	chr4:8195792-8195793	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs561314637	chr4:8195807-8195808	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143153407	chr4:8195810-8195811	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs543889226	chr4:8195829-8195830	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs184835462	chr4:8195850-8195851	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs116122592	chr4:8195861-8195862	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545230741	chr4:8195894-8195895	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs59350156	chr4:8195909-8195910	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs527603908	chr4:8195969-8195970	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs376075725	chr4:8195971-8195972	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs376601678	chr4:8195976-8195977	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	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
46	rs567245869	chr4:8196073-8196074	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	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
48	rs146653375	chr4:8196101-8196102	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs571022818	chr4:8196104-8196105	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs538814152	chr4:8196120-8196121	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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

Chromatin state (count:1001 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

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	chr4:8191800-8195400	Weak transcription	Fetal Lung	lung
6	chr4:8191800-8196000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr4:8191800-8200800	Enhancers	Placenta	Placenta
8	chr4:8192000-8195600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr4:8192000-8196400	Weak transcription	Right Atrium	heart
10	chr4:8192200-8200400	Weak transcription	Brain Anterior Caudate	brain
11	chr4:8192400-8197600	Weak transcription	Colonic Mucosa	Colon
12	chr4:8192400-8200600	Weak transcription	Brain Substantia Nigra	brain
13	chr4:8192800-8195400	Enhancers	Primary B cells from peripheral blood	blood
14	chr4:8193000-8200600	Weak transcription	Brain Cingulate Gyrus	brain
15	chr4:8193400-8195400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr4:8193600-8195200	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr4:8193600-8195200	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr4:8193600-8195600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:8193600-8195600	Weak transcription	Esophagus	oesophagus
20	chr4:8193600-8196000	Weak transcription	HMEC	breast
21	chr4:8193600-8196000	Weak transcription	NHEK	skin
22	chr4:8193600-8196600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:8193600-8196600	Weak transcription	Left Ventricle	heart
24	chr4:8193600-8200400	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr4:8193600-8200600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr4:8194000-8195200	Enhancers	Lung	lung
27	chr4:8194000-8196600	Weak transcription	Primary hematopoietic stem cells	blood
28	chr4:8194200-8195200	Enhancers	Hela-S3	cervix
29	chr4:8194200-8195600	Enhancers	Primary B cells from cord blood	blood
30	chr4:8194200-8198000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:8194200-8199200	Enhancers	Thymus	Thymus
32	chr4:8194200-8201000	Weak transcription	Psoas Muscle	Psoas
33	chr4:8194600-8195200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:8194600-8195200	Enhancers	Fetal Kidney	kidney
35	chr4:8194600-8195200	Enhancers	Ovary	ovary
36	chr4:8194600-8195200	Enhancers	A549	lung
37	chr4:8194600-8195200	Enhancers	GM12878-XiMat	blood
38	chr4:8194600-8195400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr4:8194600-8195400	Enhancers	Stomach Mucosa	stomach
40	chr4:8194600-8195400	Enhancers	Spleen	Spleen
41	chr4:8194600-8195600	Enhancers	Fetal Intestine Large	intestine
42	chr4:8194600-8195600	Enhancers	Fetal Intestine Small	intestine
43	chr4:8194600-8195600	Enhancers	Pancreas	Pancrea
44	chr4:8194600-8195800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:8194600-8195800	Enhancers	Placenta Amnion	Placenta Amnion
46	chr4:8194800-8195200	Bivalent Enhancer	Fetal Stomach	stomach
47	chr4:8194800-8195200	Bivalent Enhancer	HepG2	liver
48	chr4:8194800-8195400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr4:8194800-8195600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr4:8194800-8195800	Enhancers	Right Ventricle	heart

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