Variant report

Variant	esv1849253
Chromosome Location	chr15:77327571-77332606
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr15:77326463-77328028	A549	lung:	n/a	n/a
2	BCL3	chr15:77327427-77328043	A549	lung:	n/a	n/a
3	BHLHE40	chr15:77327273-77327720	K562	blood:	n/a	chr15:77327366-77327387 chr15:77327372-77327381 chr15:77327370-77327383 chr15:77327371-77327380 chr15:77327372-77327381
4	CEBPB	chr15:77330718-77330925	Hela-S3	cervix:	n/a	chr15:77330791-77330804
5	CHD2	chr15:77329799-77329867	Hela-S3	cervix:	n/a	n/a
6	CHD2	chr15:77327435-77327673	Hela-S3	cervix:	n/a	n/a
7	CHD2	chr15:77327460-77327662	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr15:77327544-77327607	HepG2	liver:	n/a	n/a
9	CTCF	chr15:77327540-77327690	HMEC	breast:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
10	CTCF	chr15:77327500-77327650	AG10803	skin:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
11	CTCF	chr15:77327520-77327670	GM12866	blood:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
12	CTCF	chr15:77327520-77327670	HEEpiC	esophagus:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
13	CTCF	chr15:77327460-77327610	WI-38	lung:	n/a	n/a
14	CTCF	chr15:77327540-77327690	SK-N-SH_RA	brain:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
15	CTCF	chr15:77327490-77327755	MCF-7	breast:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
16	CTCF	chr15:77327480-77327630	HRE	kidney:	n/a	chr15:77327607-77327620 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
17	CTCF	chr15:77327523-77327648	A549	lung:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
18	CTCF	chr15:77327434-77327754	GM19240	blood:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
19	CTCF	chr15:77327660-77327810	HAc	cerebellar:	n/a	chr15:77327788-77327797 chr15:77327784-77327797
20	CTCF	chr15:77327520-77327670	GM12871	blood:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
21	CTCF	chr15:77327560-77327710	GM12868	blood:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
22	CTCF	chr15:77327520-77327670	GM12870	blood:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
23	CTCF	chr15:77327540-77327690	NHDF-neo	bronchial:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
24	CTCF	chr15:77327540-77327690	HFF-Myc	foreskin:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
25	CTCF	chr15:77327441-77327734	A549	lung:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
26	CTCF	chr15:77327560-77327710	HepG2	liver:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
27	CTCF	chr15:77327560-77327710	HFF-Myc	foreskin:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
28	CTCF	chr15:77327540-77327690	GM12872	blood:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
29	CTCF	chr15:77327520-77327670	HCPEpiC	choroid plexus:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
30	CTCF	chr15:77327560-77327710	GM12864	blood:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
31	CTCF	chr15:77327405-77327789	IMR90	lung:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
32	CTCF	chr15:77327540-77327690	BJ	skin:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
33	CTCF	chr15:77327520-77327670	HVMF	connective:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
34	CTCF	chr15:77327292-77327734	ProgFib	skin:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327324-77327337 chr15:77327605-77327621
35	CTCF	chr15:77327600-77327750	BJ	skin:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
36	CTCF	chr15:77327502-77327689	GM20000	blood:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
37	CTCF	chr15:77327421-77327736	HepG2	liver:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
38	CTCF	chr15:77327540-77327690	HFF	foreskin:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
39	CTCF	chr15:77327460-77327610	RPTEC	kidney:	n/a	n/a
40	CTCF	chr15:77327345-77327931	K562	blood:	n/a	chr15:77327788-77327797 chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327784-77327797 chr15:77327605-77327621
41	CTCF	chr15:77327520-77327670	WERI-Rb-1	eye:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
42	CTCF	chr15:77327491-77327682	HepG2	liver:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
43	CTCF	chr15:77326963-77328000	SK-N-SH	brain:	n/a	chr15:77327788-77327797 chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327000-77327008 chr15:77327604-77327622 chr15:77327784-77327797 chr15:77327324-77327337 chr15:77327605-77327621 chr15:77326982-77327000
44	CTCF	chr15:77327500-77327650	HCM	heart:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
45	CTCF	chr15:77327535-77327716	LNCaP	prostate:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
46	CTCF	chr15:77327560-77327710	WI-38	lung:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
47	CTCF	chr15:77327540-77327690	GM12864	blood:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
48	CTCF	chr15:77327560-77327710	GM12867	blood:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
49	CTCF	chr15:77327500-77327650	HepG2	liver:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621
50	CTCF	chr15:77327580-77327730	AG04450	lung:	n/a	chr15:77327607-77327620 chr15:77327618-77327634 chr15:77327606-77327627 chr15:77327604-77327622 chr15:77327605-77327621

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77327887-77327937	MCF-7	breast:	n/a
2	chr15:77327887-77327937	RPTEC	kidney:	n/a
3	chr15:77327887-77327937	HRE	kidney:	n/a
4	chr15:77327887-77327937	HCF	heart:	n/a
5	chr15:77327887-77327937	BJ	skin:	n/a
6	chr15:77327887-77327937	SAEC	small airway:	n/a
7	chr15:77327887-77327937	AoSMC	blood vessel:	n/a
8	chr15:77327887-77327937	LNCaP	prostate:	n/a
9	chr15:77327887-77327937	HMEC	breast:	n/a
10	chr15:77327887-77327937	A549	lung:	n/a
11	chr15:77327887-77327937	AG04450	lung:	fetal
12	chr15:77327887-77327937	NHBE	bronchial:	n/a
13	chr15:77327887-77327937	NH-A	brain:	n/a
14	chr15:77327887-77327937	SK-N-SH_RA	brain:	n/a
15	chr15:77327887-77327937	HUVEC	blood vessel:	n/a
16	chr15:77327887-77327937	NT2-D1	testis:	n/a
17	chr15:77327887-77327937	Hela-S3	cervix:	n/a
18	chr15:77327887-77327937	HCPEpiC	choroid plexus:	n/a
19	chr15:77327887-77327937	GM12878	blood:	n/a
20	chr15:77327887-77327937	BE2_C	brain:	n/a
21	chr15:77327887-77327937	HL-60	blood:	n/a
22	chr15:77327887-77327937	MCF10A-Er-Src	breast:	n/a
23	chr15:77327887-77327937	GM12892	blood:	n/a
24	chr15:77327887-77327937	Jurkat	blood:	n/a
25	chr15:77327887-77327937	NHDF-neo	bronchial:	n/a
26	chr15:77327887-77327937	HRCEpiC	kidney:	n/a
27	chr15:77327887-77327937	Caco-2	colon:	n/a
28	chr15:77327887-77327937	ECC-1	luminal epithelium:	n/a
29	chr15:77327887-77327937	HPAEpiC	pulmonary alveolar:	n/a
30	chr15:77327887-77327937	SK-N-MC	brain:	n/a
31	chr15:77327887-77327937	NB4	blood:	n/a
32	chr15:77327887-77327937	GM06990	blood:	n/a
33	chr15:77327887-77327937	ovcar-3	ovarian:	n/a
34	chr15:77327887-77327937	HCM	heart:	n/a
35	chr15:77327887-77327937	T-47D	breast:	n/a
36	chr15:77327887-77327937	Hepatocyte	liver:	n/a
37	chr15:77327887-77327937	HepG2	liver:	n/a
38	chr15:77327887-77327937	GM12891	blood:	n/a
39	chr15:77327887-77327937	PrEC	prostate:	n/a
40	chr15:77327887-77327937	HNPCEpiC	eye:	n/a
41	chr15:77327887-77327937	HRPEpiC	eye:	n/a
42	chr15:77327887-77327937	CMK	blood:	n/a
43	chr15:77327887-77327937	HIPEpiC	eye:	n/a
44	chr15:77327887-77327937	AG09319	gingival:	n/a
45	chr15:77327887-77327937	GM19239	blood:	n/a
46	chr15:77327887-77327937	H1-hESC	embryonic stem cell:	embryo
47	chr15:77327887-77327937	ProgFib	skin:	n/a
48	chr15:77327887-77327937	SK-N-SH	brain:	n/a
49	chr15:77327887-77327937	K562	blood:	n/a
50	chr15:77327887-77327937	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:77327656..77329511-chr15:77332033..77335172,3	K562	blood:
2	chr15:77325493..77328166-chr15:77329882..77331634,3	MCF-7	breast:
3	chr15:77327656..77330194-chr15:77332164..77335172,3	K562	blood:
4	chr15:77332598..77335104-chr15:77338074..77339723,2	MCF-7	breast:
5	chr15:77328280..77330879-chr15:77355103..77356921,2	K562	blood:
6	chr15:77320466..77323005-chr15:77324460..77327682,3	MCF-7	breast:

Variant related genes	Relation type
PSTPIP1	TF binding region
ENSG00000259652	TF binding region
PSTPIP1	CpG island
ENSG00000259652	CpG island
ENSG00000140368	chromatin interactions

Extended variants
information (count: 338 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9806416	chr15:77327571-77327572	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs9707978	chr15:77327577-77327578	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs559758018	chr15:77327584-77327585	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573951876	chr15:77327643-77327644	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs369033286	chr15:77327666-77327667	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs188548246	chr15:77327692-77327693	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs548824408	chr15:77327721-77327722	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs146024481	chr15:77327734-77327735	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs531132774	chr15:77327739-77327740	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs551894330	chr15:77327751-77327752	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs570198100	chr15:77327800-77327801	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs369324680	chr15:77327803-77327804	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs374490916	chr15:77327814-77327815	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs367828460	chr15:77327815-77327816	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs200876675	chr15:77327835-77327836	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs201582038	chr15:77327859-77327860	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs535394390	chr15:77327861-77327862	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs557172402	chr15:77327868-77327869	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs202234078	chr15:77327873-77327874	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs369205216	chr15:77327888-77327889	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs139552419	chr15:77327910-77327911	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs192912170	chr15:77327923-77327924	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs143536570	chr15:77327952-77327953	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs559126311	chr15:77327960-77327961	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs115368425	chr15:77327971-77327972	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs531755708	chr15:77328004-77328005	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs567893030	chr15:77328018-77328019	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs182793342	chr15:77328059-77328060	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs536945992	chr15:77328065-77328066	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs574731012	chr15:77328074-77328075	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs114366335	chr15:77328080-77328081	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs374768418	chr15:77328106-77328107	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs368099765	chr15:77328107-77328108	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs372009472	chr15:77328108-77328109	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs397813104	chr15:77328110-77328111	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs79288253	chr15:77328111-77328112	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs369498554	chr15:77328143-77328144	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs377721832	chr15:77328165-77328166	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs368838637	chr15:77328171-77328172	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs372468528	chr15:77328172-77328173	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs377214787	chr15:77328175-77328176	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs370404621	chr15:77328184-77328185	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs531047131	chr15:77328194-77328195	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs374682350	chr15:77328197-77328198	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs370740664	chr15:77328201-77328202	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs187211142	chr15:77328202-77328203	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs368482922	chr15:77328205-77328206	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs201186216	chr15:77328211-77328212	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs367643394	chr15:77328228-77328229	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs528187669	chr15:77328243-77328244	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	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
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77308800-77327600	Weak transcription	Esophagus	oesophagus
2	chr15:77312200-77328400	Weak transcription	Aorta	Aorta
3	chr15:77313000-77327800	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr15:77314600-77328000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr15:77314800-77330000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr15:77315400-77330400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr15:77315400-77330600	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr15:77316800-77327600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr15:77316800-77327800	Weak transcription	GM12878-XiMat	blood
10	chr15:77316800-77330200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr15:77317400-77329800	Strong transcription	Primary T cells from cord blood	blood
12	chr15:77317400-77330600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr15:77317600-77330400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr15:77318400-77350600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr15:77321000-77328200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr15:77321000-77328200	Weak transcription	Right Ventricle	heart
17	chr15:77321000-77328600	Weak transcription	Rectal Smooth Muscle	rectum
18	chr15:77321200-77328200	Weak transcription	Pancreas	Pancrea
19	chr15:77321200-77330200	Weak transcription	Brain Germinal Matrix	brain
20	chr15:77321200-77331000	Weak transcription	Fetal Brain Female	brain
21	chr15:77321200-77335400	Weak transcription	Left Ventricle	heart
22	chr15:77321200-77362000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr15:77322000-77328000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr15:77322200-77327800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr15:77322400-77328200	Enhancers	Fetal Muscle Leg	muscle
26	chr15:77322800-77328000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr15:77322800-77328200	Weak transcription	A549	lung
28	chr15:77322800-77328400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr15:77323000-77327600	Weak transcription	NHEK	skin
30	chr15:77323000-77328000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr15:77323000-77328400	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr15:77323000-77336000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr15:77323200-77327600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr15:77323200-77327600	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr15:77323200-77330600	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr15:77323200-77334200	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr15:77323400-77328400	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr15:77323400-77346000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr15:77323800-77328200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr15:77323800-77334200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr15:77324000-77327600	Enhancers	Fetal Intestine Large	intestine
42	chr15:77324000-77329800	Strong transcription	Primary T cells fromperipheralblood	blood
43	chr15:77324200-77327800	Weak transcription	Primary B cells from cord blood	blood
44	chr15:77324200-77328400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr15:77324200-77329600	Weak transcription	Primary hematopoietic stem cells	blood
46	chr15:77324200-77335200	Weak transcription	NH-A	brain
47	chr15:77324400-77327600	Weak transcription	Colonic Mucosa	Colon
48	chr15:77324400-77327600	Enhancers	Fetal Intestine Small	intestine
49	chr15:77324400-77328000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr15:77324400-77328200	Weak transcription	Fetal Thymus	thymus

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