Variant report

Variant	esv3332511
Chromosome Location	chr10:118030012-118035110
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:238)
CpG islands
(count:1893)
Chromatin interactive
region (count:15)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:238 , 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	chr10:118032561-118032688	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr10:118033184-118033509	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD1	chr10:118030531-118031243	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr10:118031497-118031571	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD1	chr10:118031968-118033015	H1-hESC	embryonic stem cell:	n/a	chr10:118032701-118032711
6	CHD1	chr10:118033394-118033487	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr10:118033829-118034564	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTBP2	chr10:118030332-118033128	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr10:118033640-118033790	HMEC	breast:	n/a	n/a
10	CTCF	chr10:118032476-118032573	MCF-7	breast:	n/a	n/a
11	CTCF	chr10:118033660-118033810	BJ	skin:	n/a	n/a
12	CTCF	chr10:118033700-118033850	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr10:118032380-118032530	GM12864	blood:	n/a	n/a
14	CTCF	chr10:118033600-118033750	HRE	kidney:	n/a	n/a
15	CTCF	chr10:118034060-118034210	HAc	cerebellar:	n/a	n/a
16	CTCF	chr10:118032523-118032550	MCF-7	breast:	n/a	n/a
17	CTCF	chr10:118033137-118033217	ProgFib	skin:	n/a	n/a
18	CTCF	chr10:118032200-118032350	SK-N-SH_RA	brain:	n/a	chr10:118032301-118032314
19	CTCF	chr10:118033620-118033770	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr10:118033700-118033787	A549	lung:	n/a	n/a
21	CTCF	chr10:118032980-118033130	AG04449	skin:	n/a	n/a
22	CTCF	chr10:118032460-118032610	HMEC	breast:	n/a	n/a
23	CTCF	chr10:118031840-118031990	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr10:118032160-118032310	BJ	skin:	n/a	n/a
25	CTCF	chr10:118030440-118030590	AG04449	skin:	n/a	n/a
26	CTCF	chr10:118032160-118032310	AG04449	skin:	n/a	n/a
27	CTCF	chr10:118032480-118032630	GM12864	blood:	n/a	n/a
28	CTCF	chr10:118033620-118033770	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr10:118033620-118033770	AG04449	skin:	n/a	n/a
30	CTCF	chr10:118032540-118032690	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr10:118032720-118032870	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr10:118033680-118033830	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr10:118032520-118032670	HEK293	kidney:	n/a	n/a
34	CTCF	chr10:118033040-118033190	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr10:118033620-118033770	AG09319	gingival:	n/a	n/a
36	CTCF	chr10:118033000-118033150	BJ	skin:	n/a	n/a
37	CTCF	chr10:118032440-118032590	AG09309	skin:	n/a	n/a
38	CTCF	chr10:118033687-118033887	IMR90	lung:	n/a	n/a
39	CTCF	chr10:118033840-118033990	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr10:118032400-118032550	GM12866	blood:	n/a	n/a
41	CTCF	chr10:118033640-118033790	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr10:118033620-118033770	HRE	kidney:	n/a	n/a
43	CTCF	chr10:118033800-118033950	RPTEC	kidney:	n/a	n/a
44	CTCF	chr10:118030491-118030533	MCF-7	breast:	n/a	n/a
45	CTCF	chr10:118032500-118032650	AG04449	skin:	n/a	n/a
46	CTCF	chr10:118033644-118033809	Gliobla	brain:	n/a	n/a
47	CTCF	chr10:118032460-118032610	A549	lung:	n/a	n/a
48	CTCF	chr10:118032387-118032600	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr10:118032460-118032610	GM12871	blood:	n/a	n/a
50	CTCF	chr10:118030660-118030810	SK-N-SH_RA	brain:	n/a	chr10:118030792-118030802

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:118032905-118032955	GM06990	blood:	n/a
2	chr10:118032330-118032380	AG04450	lung:	fetal
3	chr10:118032905-118032955	GM06990	blood:	n/a
4	chr10:118032330-118032380	AG04450	lung:	fetal
5	chr10:118031864-118031914	SKMC	muscle:	n/a
6	chr10:118033115-118033165	MCF10A-Er-Src	breast:	n/a
7	chr10:118031864-118031914	NHBE	bronchial:	n/a
8	chr10:118034031-118034081	NB4	blood:	n/a
9	chr10:118033370-118033420	GM12878	blood:	n/a
10	chr10:118034031-118034081	HAEpiC	amniotic membrane:	n/a
11	chr10:118032872-118032922	HepG2	liver:	n/a
12	chr10:118032987-118033037	PFSK-1	brain:	n/a
13	chr10:118031950-118032000	BE2_C	brain:	n/a
14	chr10:118030848-118030898	HIPEpiC	eye:	n/a
15	chr10:118031256-118031306	HEEpiC	esophagus:	n/a
16	chr10:118033290-118033340	GM19239	blood:	n/a
17	chr10:118031632-118031682	HEK293	kidney:	embryo
18	chr10:118031950-118032000	HRE	kidney:	n/a
19	chr10:118031632-118031682	PANC-1	pancreas:	n/a
20	chr10:118031950-118032000	HCPEpiC	choroid plexus:	n/a
21	chr10:118032879-118032929	HL-60	blood:	n/a
22	chr10:118032626-118032676	HIPEpiC	eye:	n/a
23	chr10:118033370-118033420	NB4	blood:	n/a
24	chr10:118033370-118033420	SK-N-MC	brain:	n/a
25	chr10:118031632-118031682	MCF-7	breast:	n/a
26	chr10:118031153-118031203	SAEC	small airway:	n/a
27	chr10:118032626-118032676	PFSK-1	brain:	n/a
28	chr10:118034031-118034081	U87	brain:	n/a
29	chr10:118031950-118032000	NHDF-neo	bronchial:	n/a
30	chr10:118031950-118032000	HRCEpiC	kidney:	n/a
31	chr10:118032879-118032929	SAEC	small airway:	n/a
32	chr10:118031632-118031682	H1-hESC	embryonic stem cell:	embryo
33	chr10:118032948-118032998	Hepatocyte	liver:	n/a
34	chr10:118033273-118033323	NHDF-neo	bronchial:	n/a
35	chr10:118032355-118032405	SK-N-SH_RA	brain:	n/a
36	chr10:118032626-118032676	CMK	blood:	n/a
37	chr10:118032626-118032676	GM06990	blood:	n/a
38	chr10:118033370-118033420	HIPEpiC	eye:	n/a
39	chr10:118031870-118031920	ProgFib	skin:	n/a
40	chr10:118033902-118033952	GM19239	blood:	n/a
41	chr10:118034357-118034407	H1-hESC	embryonic stem cell:	embryo
42	chr10:118032879-118032929	SK-N-MC	brain:	n/a
43	chr10:118032626-118032676	HRPEpiC	eye:	n/a
44	chr10:118032905-118032955	PrEC	prostate:	n/a
45	chr10:118031870-118031920	U87	brain:	n/a
46	chr10:118033115-118033165	NB4	blood:	n/a
47	chr10:118034031-118034081	HepG2	liver:	n/a
48	chr10:118033115-118033165	ECC-1	luminal epithelium:	n/a
49	chr10:118034031-118034081	MCF10A-Er-Src	breast:	n/a
50	chr10:118032905-118032955	ovcar-3	ovarian:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:117465313..117467973-chr10:118033324..118035057,2	MCF-7	breast:
2	chr10:118006561..118008463-chr10:118028900..118031732,2	MCF-7	breast:
3	chr10:117759144..117761162-chr10:118033564..118036485,2	MCF-7	breast:
4	chr10:117427698..117429252-chr10:118029636..118031173,2	MCF-7	breast:
5	chr10:117840235..117842704-chr10:118029621..118031631,2	MCF-7	breast:
6	chr10:117466869..117469113-chr10:118028705..118031024,3	MCF-7	breast:
7	chr10:117902634..117903478-chr10:118030267..118031232,2	MCF-7	breast:
8	chr10:117894623..117897026-chr10:118030243..118031768,2	MCF-7	breast:
9	chr10:118029653..118031249-chr10:118045197..118046929,2	MCF-7	breast:
10	chr10:118014146..118017027-chr10:118028962..118031890,3	MCF-7	breast:
11	chr10:117858148..117861915-chr10:118033235..118035636,3	MCF-7	breast:
12	chr10:117464567..117466683-chr10:118027769..118030068,2	MCF-7	breast:
13	chr10:117892801..117895046-chr10:118029774..118031284,2	MCF-7	breast:
14	chr10:117902736..117903478-chr10:118030267..118031114,2	MCF-7	breast:
15	chr10:117851031..117852800-chr10:118033043..118034663,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf82-2	chr10:118032073-118032155	NONHSAT016482
2	lnc-C10orf82-2	chr10:118031516-118031787	NONHSAT016482

No data

Variant related genes	Relation type
GFRA1	TF binding region
GFRA1	CpG island
ENSG00000151892	chromatin interactions

Extended variants
information (count: 185 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:185 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181422727	chr10:118030023-118030024	Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs539632486	chr10:118030073-118030074	Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557930500	chr10:118030091-118030092	Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs184136054	chr10:118030106-118030107	Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536555715	chr10:118030119-118030120	Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs144903899	chr10:118030144-118030145	Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573536617	chr10:118030185-118030186	Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542171817	chr10:118030191-118030192	Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs567656284	chr10:118030199-118030200	Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs564001658	chr10:118030277-118030278	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs531059578	chr10:118030280-118030281	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs545967508	chr10:118030281-118030282	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs189185685	chr10:118030284-118030285	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs373964412	chr10:118030293-118030294	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201490354	chr10:118030296-118030297	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34626044	chr10:118030318-118030319	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs371257858	chr10:118030321-118030322	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs34371262	chr10:118030386-118030387	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs148946370	chr10:118030395-118030396	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs8192662	chr10:118030415-118030416	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs561939618	chr10:118030479-118030480	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs375878951	chr10:118030480-118030481	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529247195	chr10:118030504-118030505	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs968390	chr10:118030523-118030524	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs75680382	chr10:118030524-118030525	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs147661837	chr10:118030545-118030546	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs372829201	chr10:118030546-118030547	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs539670236	chr10:118030566-118030567	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs377281268	chr10:118030590-118030591	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200978034	chr10:118030598-118030599	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs76531145	chr10:118030627-118030628	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs372156491	chr10:118030633-118030634	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533656942	chr10:118030649-118030650	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs555403632	chr10:118030661-118030662	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs573597834	chr10:118030699-118030700	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs537847861	chr10:118030734-118030735	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs556362225	chr10:118030745-118030746	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs11197617	chr10:118030775-118030776	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs538822073	chr10:118030913-118030914	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1362217	chr10:118030928-118030929	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs546055545	chr10:118030940-118030941	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs146833397	chr10:118030951-118030952	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs545484754	chr10:118030988-118030989	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs181672651	chr10:118031023-118031024	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs562202646	chr10:118031058-118031059	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs563682458	chr10:118031070-118031071	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs550928032	chr10:118031083-118031084	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs373344339	chr10:118031162-118031163	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533279126	chr10:118031197-118031198	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs186600359	chr10:118031206-118031207	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Breast cancer	21509527	CNVD

Chromatin state (count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:118020600-118030200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr10:118023400-118030400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr10:118023800-118030200	Weak transcription	HSMMtube	muscle
4	chr10:118026600-118030400	Weak transcription	Brain Angular Gyrus	brain
5	chr10:118028000-118030200	Weak transcription	HSMM	muscle
6	chr10:118028400-118030200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr10:118028600-118030600	Enhancers	Liver	Liver
8	chr10:118029600-118030400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
9	chr10:118029600-118030600	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr10:118029600-118034200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
11	chr10:118029800-118030600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr10:118029800-118030600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
13	chr10:118029800-118030800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
14	chr10:118029800-118032800	Active TSS	Fetal Kidney	kidney
15	chr10:118030000-118030200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr10:118030000-118030200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
17	chr10:118030000-118030200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr10:118030000-118030200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
19	chr10:118030000-118030400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr10:118030000-118030600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
21	chr10:118030000-118032000	Bivalent Enhancer	Fetal Brain Male	brain
22	chr10:118030000-118034200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
23	chr10:118030000-118034400	Active TSS	Rectal Smooth Muscle	rectum
24	chr10:118030000-118034600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
25	chr10:118030200-118030400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr10:118030200-118030400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
27	chr10:118030200-118030400	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
28	chr10:118030200-118030400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr10:118030200-118030400	Bivalent Enhancer	Brain Germinal Matrix	brain
30	chr10:118030200-118030400	Bivalent Enhancer	Spleen	Spleen
31	chr10:118030200-118030600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
32	chr10:118030200-118030600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr10:118030200-118030600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
34	chr10:118030200-118031000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr10:118030200-118032600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr10:118030200-118033800	Active TSS	HSMM	muscle
37	chr10:118030200-118033800	Active TSS	HSMMtube	muscle
38	chr10:118030200-118034000	Active TSS	Muscle Satellite Cultured Cells	--
39	chr10:118030200-118034200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
40	chr10:118030200-118034200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr10:118030200-118034400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
42	chr10:118030200-118034400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
43	chr10:118030200-118034400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
44	chr10:118030200-118034400	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
45	chr10:118030200-118034600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
46	chr10:118030400-118030600	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr10:118030400-118030600	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr10:118030400-118030600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr10:118030400-118030600	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:118030400-118030600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast

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