Variant report

Variant	nsv904358
Chromosome Location	chr15:74708461-74716609
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:377)
CpG islands
(count:183)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:74715318-74715492	HepG2	liver:	n/a	n/a
2	BACH1	chr15:74715730-74716028	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr15:74715311-74715511	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr15:74708452-74709073	GM12878	blood:	n/a	n/a
5	BCL3	chr15:74708516-74709009	GM12878	blood:	n/a	n/a
6	BHLHE40	chr15:74716460-74716593	K562	blood:	n/a	n/a
7	BHLHE40	chr15:74715185-74715213	K562	blood:	n/a	n/a
8	BHLHE40	chr15:74714990-74715773	HepG2	liver:	n/a	chr15:74715008-74715024
9	BHLHE40	chr15:74715011-74715309	GM12878	blood:	n/a	n/a
10	BRCA1	chr15:74716073-74716075	HepG2	liver:	n/a	n/a
11	BRCA1	chr15:74712549-74712574	GM12878	blood:	n/a	n/a
12	CEBPB	chr15:74715024-74715461	IMR90	lung:	n/a	chr15:74715131-74715148
13	CEBPB	chr15:74714996-74715499	HepG2	liver:	n/a	chr15:74715131-74715148
14	CEBPB	chr15:74715338-74715511	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr15:74715316-74715323	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPD	chr15:74713862-74714212	HepG2	liver:	n/a	n/a
17	CHD2	chr15:74716293-74716548	K562	blood:	n/a	n/a
18	CHD2	chr15:74708721-74708763	GM12878	blood:	n/a	n/a
19	CHD2	chr15:74715354-74715573	HepG2	liver:	n/a	n/a
20	CHD2	chr15:74715122-74715364	GM12878	blood:	n/a	n/a
21	CTCF	chr15:74712740-74712890	AG04449	skin:	n/a	n/a
22	CTCF	chr15:74708634-74708727	GM19239	blood:	n/a	n/a
23	CTCF	chr15:74716000-74716150	AG09309	skin:	n/a	chr15:74716114-74716123
24	CTCF	chr15:74716060-74716210	NHEK	skin:	n/a	chr15:74716114-74716123
25	CTCF	chr15:74709860-74710010	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr15:74709920-74710070	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr15:74712760-74712910	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr15:74716080-74716230	HMF	breast:	n/a	chr15:74716114-74716123
29	CTCF	chr15:74709940-74710090	HMF	breast:	n/a	n/a
30	CTCF	chr15:74716080-74716230	HAc	cerebellar:	n/a	chr15:74716114-74716123
31	CTCF	chr15:74716080-74716230	HFF	foreskin:	n/a	chr15:74716114-74716123
32	CTCF	chr15:74709880-74710030	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr15:74715940-74716090	HMEC	breast:	n/a	chr15:74715940-74715947
34	CTCF	chr15:74716120-74716270	HCT-116	colon:	n/a	n/a
35	CTCF	chr15:74716020-74716170	HEEpiC	esophagus:	n/a	chr15:74716114-74716123
36	CTCF	chr15:74716100-74716250	NHEK	skin:	n/a	chr15:74716114-74716123
37	CTCF	chr15:74716060-74716210	HBMEC	blood vessel:	n/a	chr15:74716114-74716123
38	CTCF	chr15:74709840-74709990	HRE	kidney:	n/a	n/a
39	CTCF	chr15:74716060-74716210	HMEC	breast:	n/a	chr15:74716114-74716123
40	CTCF	chr15:74708771-74708843	GM19239	blood:	n/a	n/a
41	CTCF	chr15:74715940-74716090	SAEC	small airway:	n/a	chr15:74715940-74715947
42	CUX1	chr15:74714577-74714619	GM12878	blood:	n/a	n/a
43	CUX1	chr15:74712567-74712569	GM12878	blood:	n/a	n/a
44	E2F6	chr15:74716228-74716444	K562	blood:	n/a	n/a
45	EBF1	chr15:74712660-74712817	GM12878	blood:	n/a	n/a
46	EBF1	chr15:74709100-74709409	GM12878	blood:	n/a	chr15:74709315-74709324 chr15:74709314-74709325
47	EBF1	chr15:74712151-74712344	GM12878	blood:	n/a	chr15:74712218-74712229
48	EBF1	chr15:74712468-74712801	GM12878	blood:	n/a	n/a
49	EBF1	chr15:74709161-74709393	GM12878	blood:	n/a	chr15:74709315-74709324 chr15:74709314-74709325
50	EBF1	chr15:74709200-74709439	GM12878	blood:	n/a	chr15:74709315-74709324 chr15:74709314-74709325

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74715105-74715155	HCPEpiC	choroid plexus:	n/a
2	chr15:74714463-74714513	ECC-1	luminal epithelium:	n/a
3	chr15:74709717-74709767	AG09309	skin:	n/a
4	chr15:74714463-74714513	PFSK-1	brain:	n/a
5	chr15:74709717-74709767	PFSK-1	brain:	n/a
6	chr15:74709717-74709767	GM06990	blood:	n/a
7	chr15:74715105-74715155	SKMC	muscle:	n/a
8	chr15:74714463-74714513	HEK293	kidney:	embryo
9	chr15:74715105-74715155	HRCEpiC	kidney:	n/a
10	chr15:74714463-74714513	HRE	kidney:	n/a
11	chr15:74715105-74715155	SK-N-SH_RA	brain:	n/a
12	chr15:74709717-74709767	BJ	skin:	n/a
13	chr15:74709717-74709767	HEK293	kidney:	embryo
14	chr15:74709717-74709767	NB4	blood:	n/a
15	chr15:74709717-74709767	HUVEC	blood vessel:	n/a
16	chr15:74714463-74714513	AG04449	skin:	fetal
17	chr15:74714463-74714513	K562	blood:	n/a
18	chr15:74714463-74714513	MCF10A-Er-Src	breast:	n/a
19	chr15:74714463-74714513	T-47D	breast:	n/a
20	chr15:74714463-74714513	HRCEpiC	kidney:	n/a
21	chr15:74714463-74714513	NT2-D1	testis:	n/a
22	chr15:74715105-74715155	HNPCEpiC	eye:	n/a
23	chr15:74715105-74715155	U87	brain:	n/a
24	chr15:74715105-74715155	HMEC	breast:	n/a
25	chr15:74714463-74714513	AG09309	skin:	n/a
26	chr15:74714463-74714513	RPTEC	kidney:	n/a
27	chr15:74714463-74714513	SAEC	small airway:	n/a
28	chr15:74709717-74709767	BE2_C	brain:	n/a
29	chr15:74715105-74715155	SK-N-SH	brain:	n/a
30	chr15:74714463-74714513	GM12892	blood:	n/a
31	chr15:74709717-74709767	T-47D	breast:	n/a
32	chr15:74715105-74715155	GM12892	blood:	n/a
33	chr15:74709717-74709767	HRE	kidney:	n/a
34	chr15:74715105-74715155	AG09309	skin:	n/a
35	chr15:74715105-74715155	IMR90	lung:	fetal
36	chr15:74709717-74709767	SAEC	small airway:	n/a
37	chr15:74715105-74715155	MCF-7	breast:	n/a
38	chr15:74715105-74715155	CMK	blood:	n/a
39	chr15:74714463-74714513	HRPEpiC	eye:	n/a
40	chr15:74715105-74715155	HUVEC	blood vessel:	n/a
41	chr15:74714463-74714513	GM06990	blood:	n/a
42	chr15:74709717-74709767	U87	brain:	n/a
43	chr15:74715105-74715155	T-47D	breast:	n/a
44	chr15:74715105-74715155	NB4	blood:	n/a
45	chr15:74709717-74709767	ovcar-3	ovarian:	n/a
46	chr15:74714463-74714513	HCT-116	colon:	n/a
47	chr15:74714463-74714513	HNPCEpiC	eye:	n/a
48	chr15:74714463-74714513	HPAEpiC	pulmonary alveolar:	n/a
49	chr15:74715105-74715155	HRE	kidney:	n/a
50	chr15:74714463-74714513	PANC-1	pancreas:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:74712692..74714612-chr15:74714775..74716965,2	MCF-7	breast:
2	chr15:74709055..74711069-chr15:74716225..74718265,2	MCF-7	breast:
3	chr15:74665724..74666602-chr15:74716103..74717034,2	K562	blood:
4	chr15:74711706..74714244-chr15:74719320..74721195,2	K562	blood:
5	chr15:74674587..74678748-chr15:74711681..74714409,4	K562	blood:
6	chr15:74715058..74717919-chr15:74753629..74755415,2	K562	blood:
7	chr15:74706547..74708360-chr15:74715336..74717632,2	K562	blood:
8	chr15:74712355..74714244-chr15:74719225..74721195,3	K562	blood:
9	chr15:74688261..74689838-chr15:74715380..74717091,2	K562	blood:
10	chr15:74710571..74713498-chr15:74715208..74717540,3	K562	blood:
11	chr15:74713352..74715766-chr15:74724000..74726928,3	MCF-7	breast:
12	chr15:74683786..74686291-chr15:74709517..74711848,2	K562	blood:
13	chr15:74703939..74707088-chr15:74707597..74710860,4	K562	blood:
14	chr15:74680306..74681854-chr15:74712615..74715350,2	MCF-7	breast:
15	chr15:74675641..74677310-chr15:74711681..74714409,2	K562	blood:
16	chr15:74675805..74678192-chr15:74715315..74717229,2	MCF-7	breast:
17	chr15:74708483..74711346-chr15:74713083..74715062,3	MCF-7	breast:
18	chr15:74711559..74715833-chr15:74724252..74727151,6	K562	blood:
19	chr15:74692322..74695920-chr15:74711238..74714934,4	K562	blood:
20	chr15:74710597..74712982-chr15:75051460..75053643,2	K562	blood:
21	chr15:74693785..74695419-chr15:74712435..74714990,2	MCF-7	breast:
22	chr15:74698938..74701316-chr15:74711313..74715118,3	MCF-7	breast:
23	chr15:74716409..74721225-chr15:74724454..74727081,9	K562	blood:
24	chr15:74706143..74707711-chr15:74709343..74712295,2	K562	blood:
25	chr15:74715079..74717127-chr15:74720885..74723638,2	MCF-7	breast:
26	chr15:74710571..74713498-chr15:74715208..74717540,3	K562	blood:
27	chr15:74712461..74714565-chr15:74744762..74746348,2	MCF-7	breast:
28	chr15:74712692..74714612-chr15:74714775..74716965,2	MCF-7	breast:
29	chr15:74708765..74710665-chr15:74717275..74720280,3	K562	blood:
30	chr15:74689719..74694435-chr15:74706184..74713253,9	MCF-7	breast:
31	chr15:74708430..74711665-chr15:74722964..74726115,3	K562	blood:
32	chr15:74709055..74711069-chr15:74716225..74718265,2	MCF-7	breast:
33	chr15:74682079..74683871-chr15:74715405..74717396,2	MCF-7	breast:
34	chr15:74709821..74711608-chr15:74905554..74908094,2	MCF-7	breast:
35	chr15:74709534..74711192-chr15:74725861..74727762,2	MCF-7	breast:
36	chr15:74708483..74711346-chr15:74713083..74715062,3	MCF-7	breast:

No data

Variant related genes	Relation type
SEMA7A	TF binding region
SEMA7A	CpG island
ENSG00000179335	chromatin interactions
ENSG00000138623	chromatin interactions
ENSG00000260919	chromatin interactions
ENSG00000247240	chromatin interactions

Extended variants
information (count: 386 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:386 , 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	rs28362920	chr15:74708461-74708462	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs2734631	chr15:74708505-74708506	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs575965456	chr15:74708510-74708511	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs78087478	chr15:74708525-74708526	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs79910850	chr15:74708526-74708527	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs370037703	chr15:74708542-74708543	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs541634241	chr15:74708551-74708552	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs138845632	chr15:74708558-74708559	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs575210912	chr15:74708563-74708564	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs542509891	chr15:74708583-74708584	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs563545650	chr15:74708593-74708594	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs2577114	chr15:74708621-74708622	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs2577115	chr15:74708630-74708631	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs542402335	chr15:74708632-74708633	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs552130673	chr15:74708660-74708661	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs552420806	chr15:74708661-74708662	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs564603335	chr15:74708669-74708670	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs374906393	chr15:74708672-74708673	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs532216757	chr15:74708682-74708683	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs547200110	chr15:74708683-74708684	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs565492091	chr15:74708697-74708698	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs536162824	chr15:74708715-74708716	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs561994023	chr15:74708716-74708717	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538291161	chr15:74708789-74708790	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs556293009	chr15:74708792-74708793	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs566571850	chr15:74708799-74708800	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs141463797	chr15:74708811-74708812	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs150441958	chr15:74708815-74708816	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558408117	chr15:74708819-74708820	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs555180497	chr15:74708827-74708828	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs199732833	chr15:74708874-74708875	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs28362919	chr15:74708876-74708877	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs371507166	chr15:74708885-74708886	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs375784064	chr15:74708886-74708887	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs577961502	chr15:74708903-74708904	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs2734630	chr15:74708908-74708909	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs2577116	chr15:74708911-74708912	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs368853845	chr15:74708936-74708937	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs34238219	chr15:74708938-74708939	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs150057109	chr15:74708978-74708979	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs372879846	chr15:74708984-74708985	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140707085	chr15:74709008-74709009	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs144656616	chr15:74709009-74709010	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs147891683	chr15:74709017-74709018	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs2974974	chr15:74709070-74709071	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs28362918	chr15:74709071-74709072	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs563989584	chr15:74709072-74709073	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs55774452	chr15:74709073-74709074	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2734629	chr15:74709075-74709076	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs373620148	chr15:74709080-74709081	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74696200-74710400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr15:74696200-74711400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr15:74696200-74712600	Weak transcription	Right Atrium	heart
4	chr15:74696400-74712200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr15:74696800-74709400	Weak transcription	Left Ventricle	heart
6	chr15:74697000-74712400	Weak transcription	Fetal Heart	heart
7	chr15:74697000-74712600	Weak transcription	Fetal Lung	lung
8	chr15:74699600-74716600	Weak transcription	Fetal Kidney	kidney
9	chr15:74700000-74713800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr15:74700200-74711200	Weak transcription	Fetal Intestine Large	intestine
11	chr15:74700400-74710800	Weak transcription	Ovary	ovary
12	chr15:74700600-74712200	Weak transcription	Fetal Brain Male	brain
13	chr15:74700800-74712400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr15:74701200-74714600	Genic enhancers	Spleen	Spleen
15	chr15:74701400-74712600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr15:74701600-74709200	Strong transcription	NHLF	lung
17	chr15:74701600-74709600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr15:74702000-74710800	Strong transcription	Brain Germinal Matrix	brain
19	chr15:74702000-74712400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr15:74702200-74710800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr15:74702200-74710800	Strong transcription	Placenta Amnion	Placenta Amnion
22	chr15:74702200-74715000	Weak transcription	Colonic Mucosa	Colon
23	chr15:74702400-74708600	Weak transcription	Right Ventricle	heart
24	chr15:74702400-74709200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr15:74702400-74710400	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr15:74702400-74711000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr15:74702400-74711200	Strong transcription	Fetal Stomach	stomach
28	chr15:74702600-74710400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr15:74702600-74711000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr15:74702600-74712200	Strong transcription	NHEK	skin
31	chr15:74702800-74709200	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr15:74702800-74709600	Weak transcription	Adipose Nuclei	Adipose
33	chr15:74702800-74712200	Weak transcription	Pancreas	Pancrea
34	chr15:74703000-74710800	Strong transcription	HepG2	liver
35	chr15:74703200-74712600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr15:74703200-74713000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr15:74703800-74713000	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr15:74704000-74708600	Weak transcription	Rectal Smooth Muscle	rectum
39	chr15:74704000-74708600	Weak transcription	NHDF-Ad	bronchial
40	chr15:74704400-74710800	Strong transcription	K562	blood
41	chr15:74704600-74711200	Weak transcription	Liver	Liver
42	chr15:74705200-74709000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr15:74705200-74712800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr15:74705400-74710400	Strong transcription	Primary T helper cells PMA-I stimulated	--
45	chr15:74705800-74709400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
46	chr15:74705800-74711200	Strong transcription	Fetal Brain Female	brain
47	chr15:74705800-74711400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr15:74706000-74708800	Genic enhancers	Muscle Satellite Cultured Cells	--
49	chr15:74706200-74708600	Strong transcription	Brain Cingulate Gyrus	brain
50	chr15:74706200-74709000	Strong transcription	iPS-15b Cell Line	embryonic stem cell

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