Variant report

Variant	esv3437185
Chromosome Location	chr20:1164977-1167825
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	ARID3A	chr20:1166469-1166713	K562	blood:	n/a	n/a
2	ARID3A	chr20:1166535-1166710	HepG2	liver:	n/a	n/a
3	BACH1	chr20:1166477-1166774	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr20:1165128-1165647	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr20:1165353-1165553	K562	blood:	n/a	chr20:1165393-1165409
6	BHLHE40	chr20:1164932-1165009	K562	blood:	n/a	n/a
7	BHLHE40	chr20:1166473-1166846	K562	blood:	n/a	n/a
8	BRCA1	chr20:1166513-1166701	HepG2	liver:	n/a	n/a
9	BRCA1	chr20:1167369-1167388	HepG2	liver:	n/a	n/a
10	CCNT2	chr20:1165384-1166670	K562	blood:	n/a	chr20:1166606-1166615 chr20:1165723-1165732 chr20:1166265-1166274
11	CEBPD	chr20:1166377-1166849	HepG2	liver:	n/a	n/a
12	CHD2	chr20:1166464-1166869	K562	blood:	n/a	n/a
13	CHD2	chr20:1166546-1166764	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr20:1167070-1167706	HepG2	liver:	n/a	n/a
15	CHD2	chr20:1166532-1166642	GM12878	blood:	n/a	n/a
16	CHD2	chr20:1165112-1165264	HepG2	liver:	n/a	n/a
17	CHD2	chr20:1166473-1166742	HepG2	liver:	n/a	n/a
18	CHD2	chr20:1164914-1165308	K562	blood:	n/a	chr20:1165058-1165068
19	CREB1	chr20:1166460-1166733	A549	lung:	n/a	n/a
20	CTCF	chr20:1166500-1166650	HCFaa	heart:	n/a	chr20:1166567-1166585
21	CTCF	chr20:1166500-1166650	NB4	blood:	n/a	chr20:1166567-1166585
22	CTCF	chr20:1166464-1166705	Pancreas_OC	pancreas:	n/a	chr20:1166567-1166585
23	CTCF	chr20:1166540-1166690	GM12867	blood:	n/a	chr20:1166567-1166585
24	CTCF	chr20:1166520-1166670	K562	blood:	n/a	chr20:1166567-1166585
25	CTCF	chr20:1166101-1167263	A549	lung:	n/a	chr20:1166567-1166585 chr20:1166162-1166175
26	CTCF	chr20:1166500-1166650	HCPEpiC	choroid plexus:	n/a	chr20:1166567-1166585
27	CTCF	chr20:1166458-1166719	MCF-7	breast:	n/a	chr20:1166567-1166585
28	CTCF	chr20:1166450-1166685	LNCaP	prostate:	n/a	chr20:1166567-1166585
29	CTCF	chr20:1166499-1166661	Kidney_OC	kidney:	n/a	chr20:1166567-1166585
30	CTCF	chr20:1166802-1166868	GM19238	blood:	n/a	n/a
31	CTCF	chr20:1166451-1166747	GM12892	blood:	n/a	chr20:1166567-1166585
32	CTCF	chr20:1166460-1166754	MCF-7	breast:	n/a	chr20:1166567-1166585
33	CTCF	chr20:1166500-1166650	HRPEpiC	eye:	n/a	chr20:1166567-1166585
34	CTCF	chr20:1166453-1166734	K562	blood:	n/a	chr20:1166567-1166585
35	CTCF	chr20:1166460-1166610	GM12868	blood:	n/a	chr20:1166567-1166585
36	CTCF	chr20:1166459-1166716	MCF-7	breast:	n/a	chr20:1166567-1166585
37	CTCF	chr20:1166500-1166650	HEEpiC	esophagus:	n/a	chr20:1166567-1166585
38	CTCF	chr20:1166520-1166670	HMF	breast:	n/a	chr20:1166567-1166585
39	CTCF	chr20:1166500-1166650	GM12871	blood:	n/a	chr20:1166567-1166585
40	CTCF	chr20:1166480-1166630	RPTEC	kidney:	n/a	chr20:1166567-1166585
41	CTCF	chr20:1166520-1166670	AG10803	skin:	n/a	chr20:1166567-1166585
42	CTCF	chr20:1166860-1167010	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr20:1166480-1166630	HAc	cerebellar:	n/a	chr20:1166567-1166585
44	CTCF	chr20:1166454-1166711	A549	lung:	n/a	chr20:1166567-1166585
45	CTCF	chr20:1166500-1166650	HBMEC	blood vessel:	n/a	chr20:1166567-1166585
46	CTCF	chr20:1166460-1166610	HVMF	connective:	n/a	chr20:1166567-1166585
47	CTCF	chr20:1166448-1166690	MCF-7	breast:	n/a	chr20:1166567-1166585
48	CTCF	chr20:1166480-1166630	HA-sp	spinal cord:	n/a	chr20:1166567-1166585
49	CTCF	chr20:1166501-1166664	GM20000	blood:	n/a	chr20:1166567-1166585
50	CTCF	chr20:1166520-1166670	HEEpiC	esophagus:	n/a	chr20:1166567-1166585

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1165703-1165753	RPTEC	kidney:	n/a
2	chr20:1166329-1166379	HEEpiC	esophagus:	n/a
3	chr20:1165703-1165753	RPTEC	kidney:	n/a
4	chr20:1166329-1166379	HEEpiC	esophagus:	n/a
5	chr20:1165435-1165485	ECC-1	luminal epithelium:	n/a
6	chr20:1166481-1166531	HIPEpiC	eye:	n/a
7	chr20:1165206-1165256	AG04449	skin:	fetal
8	chr20:1165404-1165454	AG04450	lung:	fetal
9	chr20:1165206-1165256	H1-hESC	embryonic stem cell:	embryo
10	chr20:1165404-1165454	MCF-7	breast:	n/a
11	chr20:1166481-1166531	AG09309	skin:	n/a
12	chr20:1165703-1165753	HIPEpiC	eye:	n/a
13	chr20:1166329-1166379	HCPEpiC	choroid plexus:	n/a
14	chr20:1165065-1165115	HEEpiC	esophagus:	n/a
15	chr20:1165228-1165278	NHBE	bronchial:	n/a
16	chr20:1165703-1165753	HUVEC	blood vessel:	n/a
17	chr20:1165065-1165115	PrEC	prostate:	n/a
18	chr20:1165228-1165278	NB4	blood:	n/a
19	chr20:1165228-1165278	HNPCEpiC	eye:	n/a
20	chr20:1165435-1165485	MCF-7	breast:	n/a
21	chr20:1165228-1165278	GM12892	blood:	n/a
22	chr20:1165065-1165115	U87	brain:	n/a
23	chr20:1166481-1166531	HCF	heart:	n/a
24	chr20:1165228-1165278	ovcar-3	ovarian:	n/a
25	chr20:1166481-1166531	HMEC	breast:	n/a
26	chr20:1165404-1165454	AG09319	gingival:	n/a
27	chr20:1166481-1166531	HNPCEpiC	eye:	n/a
28	chr20:1165228-1165278	CMK	blood:	n/a
29	chr20:1165065-1165115	HRPEpiC	eye:	n/a
30	chr20:1165065-1165115	HCF	heart:	n/a
31	chr20:1165404-1165454	HCF	heart:	n/a
32	chr20:1165435-1165485	HCM	heart:	n/a
33	chr20:1165065-1165115	H1-hESC	embryonic stem cell:	embryo
34	chr20:1165065-1165115	CMK	blood:	n/a
35	chr20:1165065-1165115	NB4	blood:	n/a
36	chr20:1165065-1165115	HRE	kidney:	n/a
37	chr20:1165404-1165454	HPAEpiC	pulmonary alveolar:	n/a
38	chr20:1165065-1165115	HepG2	liver:	n/a
39	chr20:1165228-1165278	HIPEpiC	eye:	n/a
40	chr20:1165065-1165115	Hepatocyte	liver:	n/a
41	chr20:1165703-1165753	ovcar-3	ovarian:	n/a
42	chr20:1165703-1165753	NT2-D1	testis:	n/a
43	chr20:1165404-1165454	HRPEpiC	eye:	n/a
44	chr20:1165065-1165115	Jurkat	blood:	n/a
45	chr20:1165206-1165256	GM12892	blood:	n/a
46	chr20:1165404-1165454	GM12891	blood:	n/a
47	chr20:1166481-1166531	T-47D	breast:	n/a
48	chr20:1165206-1165256	HCPEpiC	choroid plexus:	n/a
49	chr20:1165228-1165278	GM06990	blood:	n/a
50	chr20:1166329-1166379	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:796367..797247-chr20:1166167..1167087,2	K562	blood:
2	chr20:1166329..1168074-chr20:1189249..1191383,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM74B-2	chr20:1165782-1166059	NONHSAT078092

Variant related genes	Relation type
TMEM74B	TF binding region
TMEM74B	CpG island

Extended variants
information (count: 104 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:104 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538098155	chr20:1164987-1164988	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs550395952	chr20:1165019-1165020	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs117485047	chr20:1165122-1165123	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs114405198	chr20:1165175-1165176	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs576063121	chr20:1165183-1165184	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs566003948	chr20:1165238-1165239	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs534963576	chr20:1165239-1165240	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs909881	chr20:1165258-1165259	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs151290870	chr20:1165266-1165267	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs549756555	chr20:1165289-1165290	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs66669236	chr20:1165297-1165298	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs554906284	chr20:1165337-1165338	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs571736537	chr20:1165354-1165355	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs374791212	chr20:1165408-1165409	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs537595932	chr20:1165420-1165421	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs80093090	chr20:1165450-1165451	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs573990940	chr20:1165454-1165455	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs536617363	chr20:1165490-1165491	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs553328399	chr20:1165556-1165557	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs573205796	chr20:1165585-1165586	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs13036311	chr20:1165593-1165594	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs540438134	chr20:1165626-1165627	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs565129635	chr20:1165630-1165631	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs545078432	chr20:1165662-1165663	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs544298420	chr20:1165721-1165722	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs560786346	chr20:1165864-1165865	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs190365650	chr20:1165884-1165885	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs550087496	chr20:1165894-1165895	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs13041890	chr20:1165928-1165929	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs13040743	chr20:1165939-1165940	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs13040745	chr20:1165946-1165947	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs909880	chr20:1166037-1166038	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs528797289	chr20:1166091-1166092	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs182242287	chr20:1166131-1166132	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs547996936	chr20:1166133-1166134	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs571811628	chr20:1166142-1166143	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs191955920	chr20:1166164-1166165	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs184064587	chr20:1166174-1166175	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs551071295	chr20:1166192-1166193	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs567738116	chr20:1166220-1166221	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs536724555	chr20:1166295-1166296	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs188211208	chr20:1166448-1166449	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs573265461	chr20:1166463-1166464	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs193170118	chr20:1166465-1166466	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs558525029	chr20:1166516-1166517	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs575411830	chr20:1166530-1166531	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs74272318	chr20:1166533-1166534	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs545787030	chr20:1166538-1166539	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs574226425	chr20:1166539-1166540	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs539928743	chr20:1166542-1166543	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1152800-1165000	Weak transcription	Brain Substantia Nigra	brain
2	chr20:1153800-1165400	Weak transcription	A549	lung
3	chr20:1156400-1165000	Weak transcription	Brain Angular Gyrus	brain
4	chr20:1156600-1165000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr20:1157200-1165200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr20:1157800-1165000	Weak transcription	Brain Anterior Caudate	brain
7	chr20:1157800-1165000	Weak transcription	Duodenum Mucosa	Duodenum
8	chr20:1158000-1165200	Weak transcription	Pancreas	Pancrea
9	chr20:1158400-1165200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr20:1159000-1165000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr20:1159000-1165000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr20:1159800-1165000	Weak transcription	Liver	Liver
13	chr20:1162000-1165200	Weak transcription	Gastric	stomach
14	chr20:1162000-1165200	Weak transcription	Left Ventricle	heart
15	chr20:1163400-1165000	Bivalent Enhancer	Fetal Lung	lung
16	chr20:1163800-1165200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
17	chr20:1164400-1165000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr20:1164400-1165200	Enhancers	Right Ventricle	heart
19	chr20:1164600-1165200	Bivalent Enhancer	Brain Hippocampus Middle	brain
20	chr20:1164600-1165200	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
21	chr20:1164600-1165600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr20:1164800-1165000	Bivalent Enhancer	Fetal Brain Male	brain
23	chr20:1164800-1165200	Bivalent Enhancer	Spleen	Spleen
24	chr20:1164800-1165200	Flanking Active TSS	K562	blood
25	chr20:1164800-1165400	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
26	chr20:1164800-1165600	Flanking Bivalent TSS/Enh	HepG2	liver
27	chr20:1164800-1166800	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr20:1165000-1165200	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr20:1165000-1165200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
30	chr20:1165000-1165200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
31	chr20:1165000-1165200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr20:1165000-1165200	Enhancers	Liver	Liver
33	chr20:1165000-1165200	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
34	chr20:1165000-1165200	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
35	chr20:1165000-1165200	Active TSS	Lung	lung
36	chr20:1165000-1165200	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
37	chr20:1165000-1165200	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
38	chr20:1165000-1165200	Bivalent Enhancer	Stomach Mucosa	stomach
39	chr20:1165000-1165400	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
40	chr20:1165000-1165400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
41	chr20:1165000-1165400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
42	chr20:1165000-1165400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
43	chr20:1165000-1165400	Active TSS	Brain Angular Gyrus	brain
44	chr20:1165000-1165400	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain
45	chr20:1165000-1165400	Bivalent Enhancer	Brain Substantia Nigra	brain
46	chr20:1165000-1165400	Flanking Bivalent TSS/Enh	Fetal Lung	lung
47	chr20:1165000-1165600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
48	chr20:1165000-1165600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr20:1165000-1165600	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
50	chr20:1165000-1165600	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum

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