Variant report

Variant	esv3357410
Chromosome Location	chr4:8159277-8161825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:326)
CpG islands
(count:793)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:326 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8160518-8160811	HepG2	liver:	n/a	n/a
2	ATF3	chr4:8160572-8160865	K562	blood:	n/a	n/a
3	ATF3	chr4:8160566-8160839	HepG2	liver:	n/a	n/a
4	BACH1	chr4:8160434-8161068	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr4:8160437-8160887	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:8160344-8161077	K562	blood:	n/a	n/a
7	CCNT2	chr4:8160162-8160844	K562	blood:	n/a	n/a
8	CEBPB	chr4:8160491-8161101	K562	blood:	n/a	n/a
9	CEBPB	chr4:8160501-8161324	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:8160435-8161166	MCF-7	breast:	n/a	n/a
11	CEBPB	chr4:8160624-8161081	A549	lung:	n/a	n/a
12	CEBPB	chr4:8160618-8161004	K562	blood:	n/a	n/a
13	CEBPB	chr4:8160527-8161087	GM12878	blood:	n/a	n/a
14	CEBPB	chr4:8160542-8161183	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr4:8160446-8161178	MCF-7	breast:	n/a	n/a
16	CEBPB	chr4:8160585-8161038	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:8160444-8161220	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr4:8160370-8161059	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr4:8160423-8161226	HCT-116	colon:	n/a	n/a
20	CEBPB	chr4:8160504-8161209	K562	blood:	n/a	n/a
21	CEBPB	chr4:8160608-8160979	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:8160576-8161015	A549	lung:	n/a	n/a
23	CEBPB	chr4:8160447-8160988	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:8160424-8161196	A549	lung:	n/a	n/a
25	CEBPB	chr4:8160662-8160841	GM12878	blood:	n/a	n/a
26	CEBPB	chr4:8160556-8161062	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr4:8160620-8160903	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:8160328-8161337	HCT-116	colon:	n/a	n/a
29	CEBPD	chr4:8160679-8160930	HepG2	liver:	n/a	n/a
30	CEBPD	chr4:8160494-8161053	K562	blood:	n/a	n/a
31	CEBPD	chr4:8160473-8161008	K562	blood:	n/a	n/a
32	CEBPD	chr4:8160506-8160977	HepG2	liver:	n/a	n/a
33	CHD2	chr4:8159592-8159684	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr4:8160299-8160861	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr4:8160412-8161135	GM12878	blood:	n/a	n/a
36	CHD2	chr4:8160601-8160914	HepG2	liver:	n/a	n/a
37	CREB1	chr4:8160405-8160996	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr4:8160254-8161005	HepG2	liver:	n/a	n/a
39	CREB1	chr4:8160428-8160928	A549	lung:	n/a	n/a
40	CTBP2	chr4:8160303-8160865	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr4:8160591-8160603	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr4:8161360-8161510	NHDF-neo	bronchial:	n/a	chr4:8161375-8161384
43	CTCF	chr4:8160523-8160608	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:8160469-8160595	GM10248	blood:	n/a	n/a
45	CTCF	chr4:8160518-8160676	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr4:8160840-8160990	GM12875	blood:	n/a	n/a
47	CTCF	chr4:8159840-8159990	NHEK	skin:	n/a	n/a
48	CTCF	chr4:8159840-8159990	GM12871	blood:	n/a	n/a
49	CTCF	chr4:8160472-8160878	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr4:8160300-8160450	GM12875	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8160571-8160621	NH-A	brain:	n/a
2	chr4:8160569-8160619	RPTEC	kidney:	n/a
3	chr4:8161776-8161826	H1-hESC	embryonic stem cell:	embryo
4	chr4:8160088-8160138	HRPEpiC	eye:	n/a
5	chr4:8160379-8160429	H1-hESC	embryonic stem cell:	embryo
6	chr4:8160571-8160621	HNPCEpiC	eye:	n/a
7	chr4:8160584-8160634	SAEC	small airway:	n/a
8	chr4:8160591-8160641	NHDF-neo	bronchial:	n/a
9	chr4:8160088-8160138	PFSK-1	brain:	n/a
10	chr4:8160088-8160138	NH-A	brain:	n/a
11	chr4:8160088-8160138	U87	brain:	n/a
12	chr4:8160295-8160345	Caco-2	colon:	n/a
13	chr4:8160591-8160641	Hela-S3	cervix:	n/a
14	chr4:8160566-8160616	BJ	skin:	n/a
15	chr4:8159729-8159779	Jurkat	blood:	n/a
16	chr4:8160584-8160634	SKMC	muscle:	n/a
17	chr4:8160088-8160138	HAEpiC	amniotic membrane:	n/a
18	chr4:8160566-8160616	HNPCEpiC	eye:	n/a
19	chr4:8160566-8160616	HCPEpiC	choroid plexus:	n/a
20	chr4:8160088-8160138	NHBE	bronchial:	n/a
21	chr4:8160295-8160345	GM19239	blood:	n/a
22	chr4:8160295-8160345	K562	blood:	n/a
23	chr4:8160571-8160621	AG10803	skin:	n/a
24	chr4:8160295-8160345	PrEC	prostate:	n/a
25	chr4:8160892-8160942	ECC-1	luminal epithelium:	n/a
26	chr4:8160892-8160942	MCF-7	breast:	n/a
27	chr4:8161093-8161143	NHBE	bronchial:	n/a
28	chr4:8160892-8160942	PANC-1	pancreas:	n/a
29	chr4:8160591-8160641	Hepatocyte	liver:	n/a
30	chr4:8160892-8160942	ProgFib	skin:	n/a
31	chr4:8159729-8159779	HNPCEpiC	eye:	n/a
32	chr4:8160591-8160641	RPTEC	kidney:	n/a
33	chr4:8161093-8161143	GM12878	blood:	n/a
34	chr4:8160892-8160942	HCF	heart:	n/a
35	chr4:8161776-8161826	HCPEpiC	choroid plexus:	n/a
36	chr4:8160580-8160630	K562	blood:	n/a
37	chr4:8160892-8160942	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:8160566-8160616	NHBE	bronchial:	n/a
39	chr4:8160584-8160634	HEEpiC	esophagus:	n/a
40	chr4:8160295-8160345	MCF-7	breast:	n/a
41	chr4:8160379-8160429	AG09309	skin:	n/a
42	chr4:8160379-8160429	PANC-1	pancreas:	n/a
43	chr4:8160892-8160942	HRPEpiC	eye:	n/a
44	chr4:8160379-8160429	HRE	kidney:	n/a
45	chr4:8160088-8160138	MCF10A-Er-Src	breast:	n/a
46	chr4:8160580-8160630	ovcar-3	ovarian:	n/a
47	chr4:8160295-8160345	GM12892	blood:	n/a
48	chr4:8161776-8161826	SK-N-SH_RA	brain:	n/a
49	chr4:8160892-8160942	SKMC	muscle:	n/a
50	chr4:8160571-8160621	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:43008550..43011275-chr4:8161727..8163687,2	MCF-7	breast:
2	chr4:8158369..8164233-chr4:8200767..8204083,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABLIM2-1	chr4:8160852-8162635	XLOC_003874

No data

Variant related genes	Relation type
ABLIM2	TF binding region
ABLIM2	CpG island
ENSG00000270022	chromatin interactions
ENSG00000100227	chromatin interactions
ENSG00000125089	chromatin interactions

Extended variants
information (count: 106 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:106 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549500579	chr4:8159291-8159292	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs568132233	chr4:8159300-8159301	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs562731911	chr4:8159307-8159308	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs535652085	chr4:8159316-8159317	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs556910872	chr4:8159320-8159321	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs569111400	chr4:8159327-8159328	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539395460	chr4:8159329-8159330	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs557320149	chr4:8159346-8159347	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs187427121	chr4:8159367-8159368	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs144762017	chr4:8159400-8159401	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192233968	chr4:8159405-8159406	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs35633902	chr4:8159423-8159424	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555456279	chr4:8159446-8159447	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145220591	chr4:8159476-8159477	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544773261	chr4:8159487-8159488	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs562989094	chr4:8159489-8159490	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs34202591	chr4:8159492-8159493	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs536840467	chr4:8159508-8159509	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs374412454	chr4:8159514-8159515	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs368897587	chr4:8159515-8159516	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs545723758	chr4:8159561-8159562	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs560478212	chr4:8159591-8159592	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182816232	chr4:8159595-8159596	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs372064055	chr4:8159607-8159608	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs575537204	chr4:8159703-8159704	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs567733544	chr4:8159733-8159734	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs531740364	chr4:8159753-8159754	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs35429656	chr4:8159759-8159760	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550747497	chr4:8159807-8159808	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188277938	chr4:8159821-8159822	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs546224462	chr4:8159860-8159861	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs539303114	chr4:8159915-8159916	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs112911552	chr4:8159936-8159937	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs566098313	chr4:8159952-8159953	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533530734	chr4:8159978-8159979	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs530142701	chr4:8160031-8160032	Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573680230	chr4:8160057-8160058	Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs144885928	chr4:8160159-8160160	Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs192798368	chr4:8160224-8160225	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs578218948	chr4:8160254-8160255	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs545687120	chr4:8160269-8160270	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs184439790	chr4:8160353-8160354	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572807683	chr4:8160417-8160418	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs541936559	chr4:8160473-8160474	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs561171637	chr4:8160494-8160495	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs189314494	chr4:8160513-8160514	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs550015688	chr4:8160525-8160526	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs562315922	chr4:8160531-8160532	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs532977459	chr4:8160539-8160540	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs551197038	chr4:8160553-8160554	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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

Chromatin state (count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8157600-8160400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
2	chr4:8158000-8159400	Bivalent Enhancer	Fetal Muscle Leg	muscle
3	chr4:8158000-8159400	Enhancers	Left Ventricle	heart
4	chr4:8158000-8159600	Enhancers	Gastric	stomach
5	chr4:8158200-8159400	Enhancers	Aorta	Aorta
6	chr4:8158200-8159600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:8158200-8159600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr4:8158200-8159800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr4:8158400-8159400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:8158400-8159600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
11	chr4:8158600-8159400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:8158600-8159400	Enhancers	Brain Substantia Nigra	brain
13	chr4:8158600-8159400	Weak transcription	HSMMtube	muscle
14	chr4:8158600-8159600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
15	chr4:8158600-8159600	Active TSS	Brain Inferior Temporal Lobe	brain
16	chr4:8158600-8162000	Active TSS	Psoas Muscle	Psoas
17	chr4:8158800-8159600	Active TSS	Brain Cingulate Gyrus	brain
18	chr4:8158800-8160000	Flanking Active TSS	Brain Hippocampus Middle	brain
19	chr4:8158800-8160200	Bivalent Enhancer	Fetal Brain Male	brain
20	chr4:8158800-8161200	Active TSS	Brain Angular Gyrus	brain
21	chr4:8159000-8159400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
22	chr4:8159000-8159400	Bivalent Enhancer	Fetal Intestine Small	intestine
23	chr4:8159000-8159600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr4:8159000-8159600	Bivalent Enhancer	Stomach Mucosa	stomach
25	chr4:8159000-8160400	Flanking Active TSS	Stomach Smooth Muscle	stomach
26	chr4:8159200-8159400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
27	chr4:8159200-8159400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr4:8159200-8159400	Bivalent/Poised TSS	Primary T helper 17 cells PMA-I stimulated	--
29	chr4:8159200-8159400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:8159200-8159400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
31	chr4:8159200-8159400	Bivalent Enhancer	Fetal Stomach	stomach
32	chr4:8159200-8159400	Enhancers	Lung	lung
33	chr4:8159200-8159400	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr4:8159200-8159400	Enhancers	Right Atrium	heart
35	chr4:8159200-8159400	Flanking Bivalent TSS/Enh	Thymus	Thymus
36	chr4:8159200-8159600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
37	chr4:8159200-8159600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
38	chr4:8159200-8159600	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr4:8159200-8159600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr4:8159200-8159600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:8159200-8159600	Enhancers	Duodenum Mucosa	Duodenum
42	chr4:8159200-8159800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr4:8159200-8159800	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr4:8159200-8159800	Flanking Active TSS	Brain Anterior Caudate	brain
45	chr4:8159200-8159800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr4:8159200-8159800	Flanking Active TSS	Hela-S3	cervix
47	chr4:8159200-8160000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
48	chr4:8159200-8160000	Flanking Active TSS	Esophagus	oesophagus
49	chr4:8159200-8160000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
50	chr4:8159200-8160000	Enhancers	Fetal Heart	heart

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