Variant report

Variant	nsv826796
Chromosome Location	chr13:110430886-110442431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1081)
CpG islands
(count:1831)
Chromatin interactive
region (count:45)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1081 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:110439189-110439250	K562	blood:	n/a	n/a
2	BACH1	chr13:110439610-110439935	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:110436949-110437136	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:110437536-110437689	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:110439162-110439355	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr13:110438037-110438193	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr13:110430608-110430953	K562	blood:	n/a	n/a
8	BHLHE40	chr13:110438776-110439348	K562	blood:	n/a	n/a
9	BHLHE40	chr13:110438833-110439061	GM12878	blood:	n/a	n/a
10	BRCA1	chr13:110432478-110433039	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr13:110438824-110439391	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr13:110437026-110437199	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr13:110434393-110434406	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr13:110438770-110439071	K562	blood:	n/a	n/a
15	CBX3	chr13:110430306-110430919	HCT-116	colon:	n/a	n/a
16	CCNT2	chr13:110438073-110440307	K562	blood:	n/a	chr13:110440103-110440112 chr13:110439148-110439157 chr13:110439278-110439287
17	CEBPB	chr13:110439589-110439732	K562	blood:	n/a	n/a
18	CEBPB	chr13:110439228-110439244	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr13:110438769-110439370	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr13:110438821-110439107	IMR90	lung:	n/a	n/a
21	CEBPB	chr13:110438162-110438328	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr13:110436946-110437196	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr13:110438849-110439087	K562	blood:	n/a	n/a
24	CEBPB	chr13:110438843-110439089	A549	lung:	n/a	n/a
25	CEBPB	chr13:110441297-110441305	Hela-S3	cervix:	n/a	n/a
26	CEBPD	chr13:110438727-110439506	K562	blood:	n/a	n/a
27	CHD1	chr13:110437579-110437779	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr13:110436801-110438434	IMR90	lung:	n/a	n/a
29	CHD1	chr13:110438877-110438980	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr13:110436949-110438473	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr13:110435922-110435936	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr13:110438864-110439256	GM12878	blood:	n/a	chr13:110439010-110439020
33	CHD2	chr13:110438856-110439323	K562	blood:	n/a	chr13:110439010-110439020 chr13:110439279-110439289
34	CHD2	chr13:110439696-110440040	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr13:110435963-110436155	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr13:110438718-110440183	Hela-S3	cervix:	n/a	chr13:110439684-110439694 chr13:110439010-110439020 chr13:110439279-110439289
37	CHD2	chr13:110433880-110434411	Hela-S3	cervix:	n/a	chr13:110434340-110434350
38	CHD2	chr13:110439772-110439902	K562	blood:	n/a	n/a
39	CHD2	chr13:110438857-110439319	H1-hESC	embryonic stem cell:	n/a	chr13:110439010-110439020 chr13:110439279-110439289
40	CREB1	chr13:110438766-110439273	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr13:110438768-110439230	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr13:110438778-110439142	HepG2	liver:	n/a	n/a
43	CREB1	chr13:110436877-110437326	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr13:110438800-110439246	K562	blood:	n/a	n/a
45	CREB1	chr13:110437576-110438325	A549	lung:	n/a	n/a
46	CREB1	chr13:110436531-110437309	A549	lung:	n/a	n/a
47	CREB1	chr13:110438661-110439476	A549	lung:	n/a	n/a
48	CREB1	chr13:110434893-110435575	A549	lung:	n/a	n/a
49	CREB1	chr13:110438804-110439309	K562	blood:	n/a	n/a
50	CREB1	chr13:110438822-110439083	HepG2	liver:	n/a	n/a

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:110440179-110440229	AG09309	skin:	n/a
2	chr13:110440179-110440229	AG09309	skin:	n/a
3	chr13:110432220-110432270	HEEpiC	esophagus:	n/a
4	chr13:110436780-110436830	HUVEC	blood vessel:	n/a
5	chr13:110438578-110438628	PANC-1	pancreas:	n/a
6	chr13:110437561-110437611	AG10803	skin:	n/a
7	chr13:110440179-110440229	U87	brain:	n/a
8	chr13:110431691-110431741	Hela-S3	cervix:	n/a
9	chr13:110440179-110440229	GM12878	blood:	n/a
10	chr13:110440179-110440229	MCF10A-Er-Src	breast:	n/a
11	chr13:110440352-110440402	T-47D	breast:	n/a
12	chr13:110436111-110436161	AG09309	skin:	n/a
13	chr13:110439006-110439056	ECC-1	luminal epithelium:	n/a
14	chr13:110431612-110431662	HL-60	blood:	n/a
15	chr13:110438935-110438985	NHDF-neo	bronchial:	n/a
16	chr13:110437561-110437611	AG04449	skin:	fetal
17	chr13:110436780-110436830	BJ	skin:	n/a
18	chr13:110438578-110438628	H1-hESC	embryonic stem cell:	embryo
19	chr13:110440175-110440225	SK-N-MC	brain:	n/a
20	chr13:110438937-110438987	BJ	skin:	n/a
21	chr13:110438578-110438628	U87	brain:	n/a
22	chr13:110436780-110436830	PANC-1	pancreas:	n/a
23	chr13:110433636-110433686	NHDF-neo	bronchial:	n/a
24	chr13:110440175-110440225	NHDF-neo	bronchial:	n/a
25	chr13:110433784-110433834	SK-N-MC	brain:	n/a
26	chr13:110434016-110434066	SK-N-SH_RA	brain:	n/a
27	chr13:110434682-110434732	HEK293	kidney:	embryo
28	chr13:110434682-110434732	HCPEpiC	choroid plexus:	n/a
29	chr13:110434016-110434066	BJ	skin:	n/a
30	chr13:110439234-110439284	HRE	kidney:	n/a
31	chr13:110437093-110437143	NHBE	bronchial:	n/a
32	chr13:110435424-110435474	HL-60	blood:	n/a
33	chr13:110438288-110438338	GM12891	blood:	n/a
34	chr13:110432935-110432985	GM12891	blood:	n/a
35	chr13:110434016-110434066	HRE	kidney:	n/a
36	chr13:110437561-110437611	ECC-1	luminal epithelium:	n/a
37	chr13:110436111-110436161	GM19239	blood:	n/a
38	chr13:110437759-110437809	SAEC	small airway:	n/a
39	chr13:110432935-110432985	AG04450	lung:	fetal
40	chr13:110434682-110434732	HEEpiC	esophagus:	n/a
41	chr13:110438935-110438985	NHBE	bronchial:	n/a
42	chr13:110438906-110438956	HEK293	kidney:	embryo
43	chr13:110440179-110440229	NB4	blood:	n/a
44	chr13:110436111-110436161	HCM	heart:	n/a
45	chr13:110436780-110436830	Caco-2	colon:	n/a
46	chr13:110437093-110437143	PrEC	prostate:	n/a
47	chr13:110440175-110440225	K562	blood:	n/a
48	chr13:110435424-110435474	MCF10A-Er-Src	breast:	n/a
49	chr13:110439234-110439284	NB4	blood:	n/a
50	chr13:110436780-110436830	HCM	heart:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:110336875..110340182-chr13:110433980..110437911,3	K562	blood:
2	chr13:110438627..110439624-chr2:32502857..32503409,2	NB4	blood:
3	chr13:110348737..110350886-chr13:110432945..110435656,2	K562	blood:
4	chr13:110438443..110438962-chr16:2285162..2286129,2	NB4	blood:
5	chr13:110413885..110415752-chr13:110436312..110438893,2	MCF-7	breast:
6	chr13:110436751..110439259-chr13:111364404..111367804,3	K562	blood:
7	chr13:110435545..110437326-chr13:110470827..110473616,2	K562	blood:
8	chr13:110439033..110439968-chr7:104653218..104653931,2	NB4	blood:
9	chr13:110372327..110374107-chr13:110434766..110436742,2	K562	blood:
10	chr13:45010548..45011431-chr13:110438404..110439086,2	Hela-S3	cervix:
11	chr13:110438834..110439674-chr3:197686852..197687479,2	Hela-S3	cervix:
12	chr13:110433484..110434398-chr6:26157776..26158704,2	Hela-S3	cervix:
13	chr13:110308109..110310593-chr13:110433626..110436596,2	K562	blood:
14	chr13:52026999..52027561-chr13:110438389..110438889,2	NB4	blood:
15	chr12:52448921..52449564-chr13:110433424..110434327,2	Hela-S3	cervix:
16	chr13:110355569..110358710-chr13:110439541..110442319,3	MCF-7	breast:
17	chr13:110438846..110439621-chr8:125485961..125486658,2	Hela-S3	cervix:
18	chr13:110414170..110416819-chr13:110432906..110435378,2	K562	blood:
19	chr13:110436747..110437632-chr2:157188777..157189594,2	Hela-S3	cervix:
20	chr13:110403771..110406116-chr13:110433660..110436383,2	K562	blood:
21	chr13:110372207..110373827-chr13:110434766..110436789,2	K562	blood:
22	chr13:109797639..109798548-chr13:110436659..110437260,3	MCF-7	breast:
23	chr13:110173341..110174851-chr13:110433335..110435967,2	MCF-7	breast:
24	chr13:110262551..110263536-chr13:110436991..110438083,3	MCF-7	breast:
25	chr13:110437769..110438360-chr13:111365491..111366397,2	NB4	blood:
26	chr13:110359448..110362939-chr13:110431472..110434391,4	K562	blood:
27	chr13:110439300..110440162-chr3:50336111..50336962,2	Hela-S3	cervix:
28	chr13:110336875..110339890-chr13:110432636..110435480,3	K562	blood:
29	chr13:110438490..110439006-chr6:26216450..26217232,2	Hela-S3	cervix:
30	chr13:110406850..110408586-chr13:110434989..110436543,2	K562	blood:
31	chr13:21347448..21348138-chr13:110438450..110439192,2	NB4	blood:
32	chr13:110397775..110399986-chr13:110436393..110438798,2	MCF-7	breast:
33	chr13:110367353..110370316-chr13:110433831..110435383,2	K562	blood:
34	chr13:110387460..110391261-chr13:110433185..110436412,3	K562	blood:
35	chr13:110079830..110080650-chr13:110436980..110437762,2	MCF-7	breast:
36	chr13:110437609..110438511-chr2:70520669..70521396,2	Hela-S3	cervix:
37	chr13:110437931..110439923-chr13:110442337..110443965,2	MCF-7	breast:
38	chr13:110438522..110439383-chr7:23221250..23222004,2	NB4	blood:
39	chr13:110430383..110434613-chr13:110438487..110441138,4	MCF-7	breast:
40	chr13:110437956..110438456-chr2:100106242..100106983,2	K562	blood:
41	chr13:110436751..110439195-chr13:111365292..111367804,2	K562	blood:
42	chr1:145382581..145383105-chr13:110438820..110439782,2	Hela-S3	cervix:
43	chr13:110404473..110407455-chr13:110429957..110432658,3	K562	blood:
44	chr13:110439408..110440218-chr17:26368504..26369181,2	Hela-S3	cervix:
45	chr13:110431371..110432927-chr13:111365497..111367425,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL4A2-3	chr13:110440328-110440912	NONHSAT035119
2	lnc-COL4A2-3	chr13:110433655-110433753	NONHSAT035119
3	lnc-COL4A2-3	chr13:110439457-110442761	NONHSAT035120
4	lnc-COL4A2-3	chr13:110439709-110439792	NONHSAT035121

No data

Variant related genes	Relation type
IRS2	TF binding region
IRS2	CpG island
ENSG00000135945	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000119820	chromatin interactions
ENSG00000185621	chromatin interactions
ENSG00000102804	chromatin interactions
ENSG00000225727	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000136243	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000087095	chromatin interactions
ENSG00000186792	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000255813	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000114473	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000167968	chromatin interactions
ENSG00000243477	chromatin interactions
ENSG00000150456	chromatin interactions
ENSG00000185950	chromatin interactions
ENSG00000245149	chromatin interactions
ENSG00000153234	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000143977	chromatin interactions
ENSG00000168274	chromatin interactions

Extended variants
information (count: 374 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:374 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78005022	chr13:110430898-110430899	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs190512190	chr13:110430928-110430929	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530242557	chr13:110430970-110430971	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550030068	chr13:110430974-110430975	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs563666955	chr13:110431033-110431034	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs532411028	chr13:110431137-110431138	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs377053509	chr13:110431149-110431150	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs552006547	chr13:110431187-110431188	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs550561775	chr13:110431204-110431205	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs143374752	chr13:110431220-110431221	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528260772	chr13:110431248-110431249	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs548013934	chr13:110431287-110431288	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs182732325	chr13:110431288-110431289	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537119156	chr13:110431348-110431349	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34692120	chr13:110431365-110431366	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs201314494	chr13:110431367-110431368	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs116384618	chr13:110431495-110431496	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs371485870	chr13:110431544-110431545	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs570383398	chr13:110431554-110431555	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs77857362	chr13:110431561-110431562	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs7981170	chr13:110431574-110431575	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs538318389	chr13:110431604-110431605	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs4771648	chr13:110431626-110431627	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs541618495	chr13:110431642-110431643	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs555175187	chr13:110431650-110431651	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs574951408	chr13:110431659-110431660	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs543858814	chr13:110431691-110431692	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs141498920	chr13:110431710-110431711	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs188415180	chr13:110431724-110431725	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs570867509	chr13:110431741-110431742	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs568715552	chr13:110431742-110431743	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs191160271	chr13:110431789-110431790	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs557364707	chr13:110431794-110431795	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs559205640	chr13:110431828-110431829	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs182953660	chr13:110431876-110431877	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs7981705	chr13:110431891-110431892	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs145361364	chr13:110431912-110431913	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs530625299	chr13:110431920-110431921	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs36045512	chr13:110431972-110431973	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs76724577	chr13:110431984-110431985	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs199630638	chr13:110431999-110432000	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs137953696	chr13:110432097-110432098	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs539406448	chr13:110432116-110432117	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs115220486	chr13:110432130-110432131	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs142433480	chr13:110432151-110432152	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs187552563	chr13:110432347-110432348	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs535302941	chr13:110432377-110432378	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs9555634	chr13:110432411-110432412	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs555312183	chr13:110432448-110432449	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs574929641	chr13:110432450-110432451	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:1337 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110409000-110431200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr13:110417000-110432400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr13:110417200-110431600	Weak transcription	Fetal Muscle Leg	muscle
4	chr13:110423000-110433400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr13:110423200-110433200	Weak transcription	Gastric	stomach
6	chr13:110423600-110431000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr13:110424800-110431000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr13:110424800-110433200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr13:110425000-110431000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr13:110425000-110431400	Weak transcription	Placenta	Placenta
11	chr13:110425000-110432000	Weak transcription	Fetal Stomach	stomach
12	chr13:110425000-110433400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr13:110425000-110433400	Weak transcription	Esophagus	oesophagus
14	chr13:110425000-110433400	Weak transcription	Pancreas	Pancrea
15	chr13:110425000-110433400	Weak transcription	Spleen	Spleen
16	chr13:110425400-110432600	Weak transcription	Fetal Intestine Small	intestine
17	chr13:110428200-110433400	Active TSS	Right Ventricle	heart
18	chr13:110428600-110431800	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr13:110428600-110434200	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr13:110428800-110431200	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr13:110428800-110431400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr13:110428800-110431400	Enhancers	Dnd41	blood
23	chr13:110428800-110431600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr13:110428800-110433600	Enhancers	Fetal Heart	heart
25	chr13:110428800-110437800	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
26	chr13:110429000-110431400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr13:110429000-110431400	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr13:110429000-110431400	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr13:110429000-110431600	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr13:110429000-110432000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr13:110429600-110431400	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr13:110429600-110431400	Active TSS	Psoas Muscle	Psoas
33	chr13:110429600-110431600	Active TSS	Left Ventricle	heart
34	chr13:110429600-110431600	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr13:110429600-110433400	Weak transcription	Fetal Muscle Trunk	muscle
36	chr13:110429800-110431000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr13:110429800-110431000	Enhancers	Stomach Mucosa	stomach
38	chr13:110430000-110431000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
39	chr13:110430000-110431600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr13:110430000-110431600	Flanking Active TSS	Liver	Liver
41	chr13:110430000-110432400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr13:110430000-110433200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr13:110430000-110433600	Enhancers	Primary T cells fromperipheralblood	blood
44	chr13:110430000-110434000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr13:110430200-110431000	Flanking Active TSS	Brain Anterior Caudate	brain
46	chr13:110430200-110431000	Flanking Active TSS	Brain Substantia Nigra	brain
47	chr13:110430200-110431000	Flanking Active TSS	Hela-S3	cervix
48	chr13:110430200-110431200	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr13:110430200-110431200	Flanking Active TSS	Brain Hippocampus Middle	brain
50	chr13:110430200-110431600	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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