Variant report

Variant	esv3351020
Chromosome Location	chr10:116851912-116854210
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:245)
CpG islands
(count:673)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr10:116853916-116854116	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr10:116852386-116853318	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr10:116852842-116853079	HepG2	liver:	n/a	chr10:116852939-116852955 chr10:116852927-116852943
4	BHLHE40	chr10:116852859-116853122	GM12878	blood:	n/a	chr10:116852939-116852955 chr10:116852927-116852943
5	CEBPB	chr10:116852024-116852345	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr10:116852817-116853116	GM12878	blood:	n/a	chr10:116853005-116853015 chr10:116852845-116852855
7	CHD1	chr10:116852152-116853647	H1-hESC	embryonic stem cell:	n/a	chr10:116853005-116853015 chr10:116852397-116852407 chr10:116852845-116852855
8	CHD1	chr10:116852789-116853538	IMR90	lung:	n/a	chr10:116853005-116853015 chr10:116852845-116852855
9	CHD2	chr10:116852230-116852612	H1-hESC	embryonic stem cell:	n/a	chr10:116852397-116852407
10	CHD2	chr10:116852987-116853055	H1-hESC	embryonic stem cell:	n/a	chr10:116853005-116853015
11	CHD2	chr10:116853349-116853692	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr10:116852936-116852947	GM12878	blood:	n/a	n/a
13	CTBP2	chr10:116852969-116853677	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr10:116853600-116853750	RPTEC	kidney:	n/a	n/a
15	CTCF	chr10:116853540-116853690	MCF-7	breast:	n/a	n/a
16	CTCF	chr10:116853500-116853650	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr10:116853540-116853690	RPTEC	kidney:	n/a	n/a
18	CTCF	chr10:116853540-116853690	GM12874	blood:	n/a	n/a
19	CTCF	chr10:116853580-116853730	HRE	kidney:	n/a	n/a
20	CTCF	chr10:116853492-116853723	IMR90	lung:	n/a	n/a
21	CTCF	chr10:116853472-116853773	GM12891	blood:	n/a	n/a
22	CTCF	chr10:116853520-116853670	BE2_C	brain:	n/a	n/a
23	CTCF	chr10:116853620-116853770	GM12867	blood:	n/a	n/a
24	CTCF	chr10:116853507-116853715	GM10266	blood:	n/a	n/a
25	CTCF	chr10:116853560-116853710	MCF-7	breast:	n/a	n/a
26	CTCF	chr10:116853480-116853630	HMEC	breast:	n/a	n/a
27	CTCF	chr10:116853492-116853698	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr10:116853540-116853690	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr10:116853580-116853730	GM12869	blood:	n/a	n/a
30	CTCF	chr10:116853620-116853770	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr10:116853482-116853793	MCF-7	breast:	n/a	n/a
32	CTCF	chr10:116853560-116853710	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr10:116853480-116853630	HAc	cerebellar:	n/a	n/a
34	CTCF	chr10:116853502-116853777	A549	lung:	n/a	n/a
35	CTCF	chr10:116853527-116853723	GM10248	blood:	n/a	n/a
36	CTCF	chr10:116853560-116853710	SAEC	small airway:	n/a	n/a
37	CTCF	chr10:116853540-116853690	GM12870	blood:	n/a	n/a
38	CTCF	chr10:116853560-116853710	GM12874	blood:	n/a	n/a
39	CTCF	chr10:116853580-116853730	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr10:116853540-116853690	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr10:116852240-116852390	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr10:116853580-116853730	GM12866	blood:	n/a	n/a
43	CTCF	chr10:116853489-116853711	HepG2	liver:	n/a	n/a
44	CTCF	chr10:116853624-116853668	HepG2	liver:	n/a	n/a
45	CTCF	chr10:116853600-116853750	BJ	skin:	n/a	n/a
46	CTCF	chr10:116853560-116853710	HepG2	liver:	n/a	n/a
47	CTCF	chr10:116853553-116853695	GM20000	blood:	n/a	n/a
48	CTCF	chr10:116853560-116853710	GM12871	blood:	n/a	n/a
49	CTCF	chr10:116853500-116853650	GM12872	blood:	n/a	n/a
50	CTCF	chr10:116853620-116853770	HPF	lung:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:116853118-116853168	HEK293	kidney:	embryo
2	chr10:116852687-116852737	AG04449	skin:	fetal
3	chr10:116853118-116853168	HEK293	kidney:	embryo
4	chr10:116852687-116852737	AG04449	skin:	fetal
5	chr10:116852865-116852915	H1-hESC	embryonic stem cell:	embryo
6	chr10:116853118-116853168	AG10803	skin:	n/a
7	chr10:116853118-116853168	AG09309	skin:	n/a
8	chr10:116854028-116854078	SK-N-SH_RA	brain:	n/a
9	chr10:116852865-116852915	SK-N-MC	brain:	n/a
10	chr10:116854028-116854078	HCPEpiC	choroid plexus:	n/a
11	chr10:116852865-116852915	HIPEpiC	eye:	n/a
12	chr10:116852687-116852737	Jurkat	blood:	n/a
13	chr10:116852470-116852520	BE2_C	brain:	n/a
14	chr10:116853118-116853168	BE2_C	brain:	n/a
15	chr10:116853664-116853714	HMEC	breast:	n/a
16	chr10:116853814-116853864	HIPEpiC	eye:	n/a
17	chr10:116853814-116853864	AG09309	skin:	n/a
18	chr10:116852811-116852861	HUVEC	blood vessel:	n/a
19	chr10:116853814-116853864	RPTEC	kidney:	n/a
20	chr10:116853814-116853864	Hela-S3	cervix:	n/a
21	chr10:116854028-116854078	HCF	heart:	n/a
22	chr10:116852186-116852236	PrEC	prostate:	n/a
23	chr10:116853814-116853864	IMR90	lung:	fetal
24	chr10:116852811-116852861	HCT-116	colon:	n/a
25	chr10:116852865-116852915	Hela-S3	cervix:	n/a
26	chr10:116853468-116853518	SK-N-SH_RA	brain:	n/a
27	chr10:116852811-116852861	Hepatocyte	liver:	n/a
28	chr10:116853814-116853864	SK-N-SH_RA	brain:	n/a
29	chr10:116852186-116852236	HepG2	liver:	n/a
30	chr10:116852687-116852737	T-47D	breast:	n/a
31	chr10:116852470-116852520	IMR90	lung:	fetal
32	chr10:116852791-116852841	GM12878	blood:	n/a
33	chr10:116852470-116852520	HL-60	blood:	n/a
34	chr10:116854028-116854078	HUVEC	blood vessel:	n/a
35	chr10:116853664-116853714	HRCEpiC	kidney:	n/a
36	chr10:116853118-116853168	AG09319	gingival:	n/a
37	chr10:116853118-116853168	ovcar-3	ovarian:	n/a
38	chr10:116852791-116852841	NHDF-neo	bronchial:	n/a
39	chr10:116854028-116854078	GM12878	blood:	n/a
40	chr10:116853118-116853168	Hepatocyte	liver:	n/a
41	chr10:116852687-116852737	AG09309	skin:	n/a
42	chr10:116853814-116853864	BE2_C	brain:	n/a
43	chr10:116852687-116852737	HUVEC	blood vessel:	n/a
44	chr10:116854028-116854078	NHBE	bronchial:	n/a
45	chr10:116852791-116852841	HEK293	kidney:	embryo
46	chr10:116852186-116852236	GM12878	blood:	n/a
47	chr10:116854028-116854078	PrEC	prostate:	n/a
48	chr10:116853468-116853518	GM19239	blood:	n/a
49	chr10:116852470-116852520	SAEC	small airway:	n/a
50	chr10:116852865-116852915	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:116696953..116700606-chr10:116852065..116855116,4	MCF-7	breast:

No data

Variant related genes	Relation type
ATRNL1	TF binding region
ATRNL1	CpG island
ENSG00000165832	chromatin interactions

Extended variants
information (count: 74 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:74 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111921247	chr10:116851921-116851922	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs554371917	chr10:116851974-116851975	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs187075321	chr10:116852067-116852068	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs529462665	chr10:116852068-116852069	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs200775974	chr10:116852070-116852071	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs543392605	chr10:116852140-116852141	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs372003556	chr10:116852145-116852146	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs139124296	chr10:116852151-116852152	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs377285451	chr10:116852181-116852182	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs149901275	chr10:116852211-116852212	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs541045004	chr10:116852233-116852234	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs35589005	chr10:116852256-116852257	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs3086111	chr10:116852259-116852260	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs397801352	chr10:116852260-116852261	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs564427254	chr10:116852310-116852311	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs368299222	chr10:116852315-116852316	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs112656967	chr10:116852317-116852318	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs577272601	chr10:116852329-116852330	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs144956465	chr10:116852348-116852349	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs561366196	chr10:116852353-116852354	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs375358071	chr10:116852388-116852389	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs541130131	chr10:116852457-116852458	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs550161715	chr10:116852458-116852459	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs571927744	chr10:116852475-116852476	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs376162928	chr10:116852502-116852503	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs111428697	chr10:116852548-116852549	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs538619488	chr10:116852557-116852558	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs547419788	chr10:116852565-116852566	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs12776132	chr10:116852592-116852593	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs565811310	chr10:116852594-116852595	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs559779669	chr10:116852678-116852679	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs71484968	chr10:116852723-116852724	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs576114355	chr10:116852745-116852746	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs541814524	chr10:116852761-116852762	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs558539311	chr10:116852774-116852775	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs577103497	chr10:116852777-116852778	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs569169743	chr10:116852809-116852810	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs541006307	chr10:116852822-116852823	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs559438111	chr10:116852904-116852905	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs574578929	chr10:116852998-116852999	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs541909211	chr10:116853021-116853022	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs192237837	chr10:116853112-116853113	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113159037	chr10:116853130-116853131	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs149907321	chr10:116853169-116853170	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs2484265	chr10:116853177-116853178	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs565421073	chr10:116853263-116853264	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs532691886	chr10:116853329-116853330	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs142406851	chr10:116853469-116853470	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs565776554	chr10:116853486-116853487	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs530044425	chr10:116853532-116853533	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Barrett''s syndrome	19417022	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neuroticism	17667963	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17133270	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116851000-116852000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr10:116851000-116852000	Enhancers	Colon Smooth Muscle	Colon
3	chr10:116851200-116852000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:116851400-116852000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
5	chr10:116851400-116852000	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
6	chr10:116851400-116853400	Active TSS	Stomach Smooth Muscle	stomach
7	chr10:116851600-116852000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
8	chr10:116851600-116852000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
9	chr10:116851600-116852000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr10:116851600-116852000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr10:116851600-116852000	Bivalent Enhancer	Fetal Intestine Small	intestine
12	chr10:116851600-116852200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr10:116851600-116852200	Enhancers	Placenta	Placenta
14	chr10:116851600-116852600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
15	chr10:116851600-116853200	Active TSS	Brain Cingulate Gyrus	brain
16	chr10:116851600-116854200	Active TSS	Brain Inferior Temporal Lobe	brain
17	chr10:116851600-116855800	Active TSS	Ovary	ovary
18	chr10:116851600-116856200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
19	chr10:116851800-116852000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
20	chr10:116851800-116852000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr10:116851800-116852000	Flanking Active TSS	Fetal Stomach	stomach
22	chr10:116851800-116852000	Bivalent Enhancer	Rectal Smooth Muscle	rectum
23	chr10:116851800-116852000	Active TSS	Skeletal Muscle Male	skeletal muscle
24	chr10:116851800-116852000	Bivalent/Poised TSS	Dnd41	blood
25	chr10:116851800-116852000	Bivalent Enhancer	NH-A	brain
26	chr10:116851800-116852200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr10:116851800-116852200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
28	chr10:116851800-116852200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
29	chr10:116851800-116852200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
30	chr10:116851800-116852200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
31	chr10:116851800-116852200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
32	chr10:116851800-116852200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr10:116851800-116852200	Active TSS	Brain Germinal Matrix	brain
34	chr10:116851800-116852200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
35	chr10:116851800-116852200	Flanking Active TSS	Fetal Brain Male	brain
36	chr10:116851800-116852200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr10:116851800-116852200	Flanking Active TSS	Fetal Lung	lung
38	chr10:116851800-116852600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr10:116851800-116852600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr10:116851800-116852600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
41	chr10:116851800-116854200	Active TSS	Fetal Brain Female	brain
42	chr10:116851800-116854400	Active TSS	Fetal Kidney	kidney
43	chr10:116851800-116854800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr10:116851800-116856200	Active TSS	Brain Anterior Caudate	brain
45	chr10:116852000-116852200	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr10:116852000-116852200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr10:116852000-116852200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
48	chr10:116852000-116852200	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr10:116852000-116852200	Bivalent/Poised TSS	Primary B cells from cord blood	blood
50	chr10:116852000-116852200	Bivalent Enhancer	Primary B cells from peripheral blood	blood

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