Variant report

Variant	nsv971151
Chromosome Location	chr7:4915196-4928162
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:4922017-4922353	K562	blood:	n/a	n/a
2	ATF3	chr7:4923175-4923421	K562	blood:	n/a	chr7:4923236-4923244 chr7:4923240-4923249 chr7:4923342-4923351
3	BACH1	chr7:4923070-4923417	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr7:4922044-4922193	K562	blood:	n/a	chr7:4922057-4922073
5	BHLHE40	chr7:4923175-4923369	A549	lung:	n/a	chr7:4923312-4923328
6	BHLHE40	chr7:4923166-4923608	HepG2	liver:	n/a	chr7:4923312-4923328
7	BHLHE40	chr7:4922963-4923635	K562	blood:	n/a	chr7:4923312-4923328 chr7:4923148-4923164
8	CBX3	chr7:4923136-4923846	K562	blood:	n/a	n/a
9	CCNT2	chr7:4922509-4923651	K562	blood:	n/a	chr7:4923466-4923475 chr7:4923590-4923599 chr7:4923551-4923560
10	CEBPB	chr7:4920676-4920699	H1-hESC	embryonic stem cell:	n/a	chr7:4920681-4920692
11	CEBPB	chr7:4920672-4920706	K562	blood:	n/a	chr7:4920681-4920692
12	CEBPB	chr7:4920647-4920713	HepG2	liver:	n/a	chr7:4920681-4920692
13	CEBPB	chr7:4920617-4920692	A549	lung:	n/a	chr7:4920681-4920692
14	CEBPD	chr7:4923209-4923440	HepG2	liver:	n/a	n/a
15	CHD2	chr7:4923470-4923600	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr7:4921804-4922311	K562	blood:	n/a	n/a
17	CREB1	chr7:4923204-4923686	A549	lung:	n/a	n/a
18	CREB1	chr7:4923021-4923782	HepG2	liver:	n/a	n/a
19	CREB1	chr7:4923273-4923760	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr7:4923268-4923748	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr7:4923207-4923393	A549	lung:	n/a	n/a
22	CREB1	chr7:4921888-4922412	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr7:4922014-4922409	K562	blood:	n/a	n/a
24	CREB1	chr7:4921941-4922388	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:4923440-4923590	SK-N-SH_RA	brain:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
26	CTCF	chr7:4923420-4923570	SAEC	small airway:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
27	CTCF	chr7:4923480-4923630	GM12872	blood:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923545-4923558
28	CTCF	chr7:4923460-4923610	SK-N-SH_RA	brain:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923545-4923558
29	CTCF	chr7:4923460-4923610	A549	lung:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923545-4923558
30	CTCF	chr7:4928088-4928250	MCF-7	breast:	n/a	chr7:4928159-4928177
31	CTCF	chr7:4928120-4928200	HepG2	liver:	n/a	chr7:4928159-4928177
32	CTCF	chr7:4923420-4923570	HUVEC	blood vessel:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
33	CTCF	chr7:4923420-4923570	WERI-Rb-1	eye:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
34	CTCF	chr7:4923440-4923590	AG10803	skin:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
35	CTCF	chr7:4923212-4923651	GM19239	blood:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
36	CTCF	chr7:4923520-4923670	WI-38	lung:	n/a	chr7:4923542-4923560 chr7:4923545-4923558
37	CTCF	chr7:4923202-4923367	ECC-1	luminal epithelium:	n/a	chr7:4923315-4923331 chr7:4923316-4923329 chr7:4923316-4923329 chr7:4923319-4923332 chr7:4923314-4923332
38	CTCF	chr7:4923216-4923598	A549	lung:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
39	CTCF	chr7:4923240-4923390	GM12868	blood:	n/a	chr7:4923315-4923331 chr7:4923316-4923329 chr7:4923316-4923329 chr7:4923319-4923332 chr7:4923314-4923332
40	CTCF	chr7:4922800-4922950	HCM	heart:	n/a	n/a
41	CTCF	chr7:4922100-4922250	BJ	skin:	n/a	n/a
42	CTCF	chr7:4923197-4923683	A549	lung:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
43	CTCF	chr7:4923207-4923650	A549	lung:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
44	CTCF	chr7:4923122-4923741	MCF-7	breast:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
45	CTCF	chr7:4923380-4923530	HA-sp	spinal cord:	n/a	chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453
46	CTCF	chr7:4922460-4922610	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr7:4923226-4923366	GM10266	blood:	n/a	chr7:4923315-4923331 chr7:4923316-4923329 chr7:4923316-4923329 chr7:4923319-4923332 chr7:4923314-4923332
48	CTCF	chr7:4923200-4923632	LNCaP	prostate:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
49	CTCF	chr7:4923440-4923590	HBMEC	blood vessel:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
50	CTCF	chr7:4923460-4923610	GM12866	blood:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923545-4923558

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4917385-4917435	Hepatocyte	liver:	n/a
2	chr7:4917385-4917435	Hepatocyte	liver:	n/a
3	chr7:4917307-4917357	NHBE	bronchial:	n/a
4	chr7:4919428-4919478	A549	lung:	n/a
5	chr7:4923383-4923433	HMEC	breast:	n/a
6	chr7:4922708-4922758	HIPEpiC	eye:	n/a
7	chr7:4922039-4922089	HEK293	kidney:	embryo
8	chr7:4922944-4922994	NHBE	bronchial:	n/a
9	chr7:4918779-4918829	HRCEpiC	kidney:	n/a
10	chr7:4922708-4922758	SK-N-SH	brain:	n/a
11	chr7:4922039-4922089	HRE	kidney:	n/a
12	chr7:4922039-4922089	SAEC	small airway:	n/a
13	chr7:4923615-4923665	HEEpiC	esophagus:	n/a
14	chr7:4925830-4925880	NHBE	bronchial:	n/a
15	chr7:4917385-4917435	HMEC	breast:	n/a
16	chr7:4922565-4922615	HEK293	kidney:	embryo
17	chr7:4917530-4917580	PrEC	prostate:	n/a
18	chr7:4922196-4922246	IMR90	lung:	fetal
19	chr7:4923383-4923433	HL-60	blood:	n/a
20	chr7:4924010-4924060	MCF10A-Er-Src	breast:	n/a
21	chr7:4922039-4922089	AG04449	skin:	fetal
22	chr7:4923383-4923433	AG09309	skin:	n/a
23	chr7:4918779-4918829	K562	blood:	n/a
24	chr7:4917385-4917435	PANC-1	pancreas:	n/a
25	chr7:4923615-4923665	K562	blood:	n/a
26	chr7:4924002-4924052	HEK293	kidney:	embryo
27	chr7:4918906-4918956	HEEpiC	esophagus:	n/a
28	chr7:4918779-4918829	ECC-1	luminal epithelium:	n/a
29	chr7:4919428-4919478	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:4924002-4924052	GM19239	blood:	n/a
31	chr7:4922565-4922615	BE2_C	brain:	n/a
32	chr7:4924010-4924060	AG10803	skin:	n/a
33	chr7:4922196-4922246	SK-N-SH	brain:	n/a
34	chr7:4923383-4923433	HAEpiC	amniotic membrane:	n/a
35	chr7:4922039-4922089	SK-N-SH_RA	brain:	n/a
36	chr7:4924010-4924060	AG04449	skin:	fetal
37	chr7:4925830-4925880	NHDF-neo	bronchial:	n/a
38	chr7:4922565-4922615	Jurkat	blood:	n/a
39	chr7:4922565-4922615	K562	blood:	n/a
40	chr7:4922039-4922089	RPTEC	kidney:	n/a
41	chr7:4923140-4923190	SK-N-SH	brain:	n/a
42	chr7:4924010-4924060	NH-A	brain:	n/a
43	chr7:4917307-4917357	HMEC	breast:	n/a
44	chr7:4922944-4922994	AG09309	skin:	n/a
45	chr7:4922039-4922089	AG09309	skin:	n/a
46	chr7:4921975-4922025	ProgFib	skin:	n/a
47	chr7:4917385-4917435	PrEC	prostate:	n/a
48	chr7:4923575-4923625	SAEC	small airway:	n/a
49	chr7:4921827-4921877	PrEC	prostate:	n/a
50	chr7:4923615-4923665	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:4911970..4915387-chr7:4918422..4922936,4	K562	blood:
2	chr7:4927849..4928583-chr7:5124843..5125774,2	MCF-7	breast:
3	chr7:4918185..4921025-chr7:4922421..4926916,4	K562	blood:
4	chr7:4916304..4918012-chr7:4921729..4924082,2	MCF-7	breast:
5	chr7:4923091..4923826-chr7:5013336..5013934,3	K562	blood:
6	chr7:4915943..4917939-chr7:4918278..4920161,2	MCF-7	breast:
7	chr7:4869433..4870053-chr7:4923355..4923936,3	MCF-7	breast:
8	chr7:4909223..4912201-chr7:4926426..4928312,2	MCF-7	breast:
9	chr7:4915943..4917939-chr7:4918278..4920161,2	MCF-7	breast:
10	chr7:4916690..4918497-chr7:4922375..4924359,2	K562	blood:
11	chr7:4920631..4924250-chr7:4926781..4929390,5	K562	blood:
12	chr7:4914075..4917883-chr7:4920628..4924428,4	K562	blood:
13	chr7:4920954..4923771-chr7:5084405..5086180,2	K562	blood:

Variant related genes	Relation type
RADIL	TF binding region
RADIL	CpG island
ENSG00000272968	chromatin interactions
ENSG00000146587	chromatin interactions
ENSG00000196204	chromatin interactions
ENSG00000157927	chromatin interactions

Extended variants
information (count: 705 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:705 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs430376	chr7:4915225-4915226	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs138258275	chr7:4915232-4915233	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs149616159	chr7:4915263-4915264	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs75531682	chr7:4915267-4915268	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs114194843	chr7:4915296-4915297	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs148374804	chr7:4915297-4915298	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs536521351	chr7:4915299-4915300	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs181113414	chr7:4915305-4915306	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs185962210	chr7:4915306-4915307	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs214126	chr7:4915322-4915323	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs561096852	chr7:4915353-4915354	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs448602	chr7:4915369-4915370	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs79870519	chr7:4915370-4915371	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566305571	chr7:4915377-4915378	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs540497016	chr7:4915383-4915384	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs188509	chr7:4915389-4915390	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549694362	chr7:4915390-4915391	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs571514432	chr7:4915425-4915426	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs190915491	chr7:4915453-4915454	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs182175586	chr7:4915461-4915462	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs550958786	chr7:4915487-4915488	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540024215	chr7:4915495-4915496	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs562832571	chr7:4915499-4915500	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs530179377	chr7:4915501-4915502	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs548351940	chr7:4915523-4915524	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs566756379	chr7:4915530-4915531	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs4724130	chr7:4915536-4915537	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs569646948	chr7:4915573-4915574	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs571133629	chr7:4915612-4915613	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs538247418	chr7:4915621-4915622	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs554119434	chr7:4915637-4915638	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs556967045	chr7:4915666-4915667	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs568954871	chr7:4915745-4915746	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs536389148	chr7:4915757-4915758	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs554722990	chr7:4915793-4915794	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs148723074	chr7:4915808-4915809	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs187606013	chr7:4915857-4915858	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540428571	chr7:4915908-4915909	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs142295934	chr7:4915916-4915917	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs190795042	chr7:4915930-4915931	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs73318140	chr7:4915941-4915942	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs562928368	chr7:4915985-4915986	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs369110671	chr7:4916048-4916049	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs146295716	chr7:4916071-4916072	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs541885693	chr7:4916076-4916077	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs183061013	chr7:4916093-4916094	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs527839559	chr7:4916114-4916115	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139552275	chr7:4916123-4916124	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs111805813	chr7:4916142-4916143	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532061949	chr7:4916181-4916182	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4905200-4921800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:4906800-4916400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:4906800-4919200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr7:4906800-4921600	Weak transcription	Gastric	stomach
5	chr7:4908400-4916600	Weak transcription	Ovary	ovary
6	chr7:4909000-4918400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr7:4909800-4915200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr7:4910400-4917600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr7:4910400-4918400	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr7:4911400-4919200	Weak transcription	Esophagus	oesophagus
11	chr7:4911600-4921600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr7:4911800-4921600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr7:4912000-4916400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:4912000-4917200	Weak transcription	Brain Germinal Matrix	brain
15	chr7:4912000-4919200	Weak transcription	Fetal Intestine Small	intestine
16	chr7:4912000-4921400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr7:4912200-4916600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:4912200-4921600	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr7:4912200-4921800	Weak transcription	K562	blood
20	chr7:4912600-4915200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:4912600-4916400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr7:4912600-4921400	Weak transcription	Colon Smooth Muscle	Colon
23	chr7:4913200-4915200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr7:4913200-4917600	Strong transcription	Fetal Brain Female	brain
25	chr7:4913400-4918800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr7:4913400-4921600	Weak transcription	Brain Cingulate Gyrus	brain
27	chr7:4913600-4916400	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr7:4913600-4918000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:4914000-4915200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr7:4914000-4916400	Weak transcription	Lung	lung
31	chr7:4914000-4920000	Weak transcription	Brain Substantia Nigra	brain
32	chr7:4914000-4921600	Weak transcription	Brain Anterior Caudate	brain
33	chr7:4914200-4915800	Enhancers	Fetal Heart	heart
34	chr7:4914200-4916200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr7:4914200-4916400	Weak transcription	Stomach Smooth Muscle	stomach
36	chr7:4914200-4919600	Weak transcription	Left Ventricle	heart
37	chr7:4914400-4915200	Weak transcription	Fetal Muscle Leg	muscle
38	chr7:4914400-4916400	Weak transcription	Fetal Muscle Trunk	muscle
39	chr7:4914400-4917800	Strong transcription	Fetal Stomach	stomach
40	chr7:4914400-4918400	Weak transcription	Right Ventricle	heart
41	chr7:4914400-4919600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr7:4914600-4916800	Weak transcription	Adipose Nuclei	Adipose
43	chr7:4914600-4917400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:4914600-4919000	Weak transcription	Rectal Smooth Muscle	rectum
45	chr7:4914800-4915400	Strong transcription	Aorta	Aorta
46	chr7:4914800-4919000	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr7:4915000-4915400	Enhancers	Spleen	Spleen
48	chr7:4915000-4917800	Strong transcription	Fetal Lung	lung
49	chr7:4915000-4918000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr7:4915000-4918400	Weak transcription	Brain Hippocampus Middle	brain

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