Variant report

Variant	esv3338339
Chromosome Location	chr1:155159128-155163626
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	ARID3A	chr1:155163135-155163500	K562	blood:	n/a	n/a
2	ARID3A	chr1:155163429-155163588	HepG2	liver:	n/a	n/a
3	ATF2	chr1:155163180-155163620	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr1:155163143-155163855	A549	lung:	n/a	chr1:155163657-155163677
5	ATF3	chr1:155163200-155163730	A549	lung:	n/a	chr1:155163657-155163677
6	BACH1	chr1:155163141-155163800	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:155163286-155163675	K562	blood:	n/a	n/a
8	BCL3	chr1:155163030-155163766	A549	lung:	n/a	n/a
9	BCL3	chr1:155162937-155164820	A549	lung:	n/a	n/a
10	BCLAF1	chr1:155163190-155163678	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:155161078-155161718	HepG2	liver:	n/a	n/a
12	BHLHE40	chr1:155163064-155164834	K562	blood:	n/a	n/a
13	BRCA1	chr1:155163410-155163579	HepG2	liver:	n/a	n/a
14	BRCA1	chr1:155163005-155163071	GM12878	blood:	n/a	n/a
15	BRCA1	chr1:155162848-155163722	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr1:155163274-155163644	H1-hESC	embryonic stem cell:	n/a	n/a
17	CBX3	chr1:155162734-155164889	K562	blood:	n/a	n/a
18	CBX3	chr1:155163257-155163620	K562	blood:	n/a	n/a
19	CCNT2	chr1:155162883-155163703	K562	blood:	n/a	chr1:155162948-155162957 chr1:155162941-155162950
20	CEBPB	chr1:155163299-155163490	K562	blood:	n/a	n/a
21	CEBPB	chr1:155162858-155163005	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr1:155163237-155163665	Hela-S3	cervix:	n/a	n/a
23	CHD1	chr1:155163111-155163736	H1-hESC	embryonic stem cell:	n/a	chr1:155163428-155163438
24	CHD2	chr1:155163347-155163732	HepG2	liver:	n/a	chr1:155163428-155163438
25	CHD2	chr1:155162681-155163821	K562	blood:	n/a	chr1:155162743-155162753 chr1:155163428-155163438 chr1:155162947-155162957
26	CHD2	chr1:155162771-155163764	H1-hESC	embryonic stem cell:	n/a	chr1:155163428-155163438 chr1:155162947-155162957
27	CHD2	chr1:155162779-155163841	Hela-S3	cervix:	n/a	chr1:155163428-155163438 chr1:155162947-155162957
28	CHD2	chr1:155162872-155163732	GM12878	blood:	n/a	chr1:155163428-155163438 chr1:155162947-155162957
29	CREB1	chr1:155162981-155163810	A549	lung:	n/a	n/a
30	CTBP2	chr1:155162860-155163792	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr1:155163340-155163490	RPTEC	kidney:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
32	CTCF	chr1:155163247-155163650	HepG2	liver:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
33	CTCF	chr1:155162758-155163870	HCT-116	colon:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
34	CTCF	chr1:155163299-155163619	ProgFib	skin:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
35	CTCF	chr1:155163300-155163450	BE2_C	brain:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
36	CTCF	chr1:155163400-155163550	HCT-116	colon:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
37	CTCF	chr1:155163380-155163530	BJ	skin:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
38	CTCF	chr1:155163360-155163510	GM12865	blood:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
39	CTCF	chr1:155163333-155163581	HepG2	liver:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
40	CTCF	chr1:155163273-155163604	GM13977	blood:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
41	CTCF	chr1:155163183-155163699	GM12878	blood:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
42	CTCF	chr1:155163380-155163530	AoAF	blood vessel:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
43	CTCF	chr1:155163306-155163574	HUVEC	blood vessel:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
44	CTCF	chr1:155163360-155163510	HMEC	breast:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
45	CTCF	chr1:155163360-155163510	SK-N-SH_RA	brain:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
46	CTCF	chr1:155163420-155163570	HFF-Myc	foreskin:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
47	CTCF	chr1:155163340-155163490	BE2_C	brain:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
48	CTCF	chr1:155163360-155163510	GM12872	blood:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
49	CTCF	chr1:155163360-155163510	GM12875	blood:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
50	CTCF	chr1:155163309-155163608	Medullo	brain:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155161679-155161729	PANC-1	pancreas:	n/a
2	chr1:155163013-155163063	GM12878	blood:	n/a
3	chr1:155161679-155161729	PANC-1	pancreas:	n/a
4	chr1:155163013-155163063	GM12878	blood:	n/a
5	chr1:155161784-155161834	AG10803	skin:	n/a
6	chr1:155163240-155163290	T-47D	breast:	n/a
7	chr1:155162871-155162921	GM06990	blood:	n/a
8	chr1:155163013-155163063	GM12891	blood:	n/a
9	chr1:155161679-155161729	HRE	kidney:	n/a
10	chr1:155161833-155161883	AG09309	skin:	n/a
11	chr1:155163205-155163255	SK-N-MC	brain:	n/a
12	chr1:155163542-155163592	SK-N-SH_RA	brain:	n/a
13	chr1:155162871-155162921	SK-N-MC	brain:	n/a
14	chr1:155161211-155161261	GM12891	blood:	n/a
15	chr1:155161833-155161883	HRE	kidney:	n/a
16	chr1:155163240-155163290	H1-hESC	embryonic stem cell:	embryo
17	chr1:155162756-155162806	HCPEpiC	choroid plexus:	n/a
18	chr1:155163240-155163290	ProgFib	skin:	n/a
19	chr1:155161784-155161834	HRPEpiC	eye:	n/a
20	chr1:155161211-155161261	NHBE	bronchial:	n/a
21	chr1:155163240-155163290	RPTEC	kidney:	n/a
22	chr1:155163590-155163640	NB4	blood:	n/a
23	chr1:155162871-155162921	NHDF-neo	bronchial:	n/a
24	chr1:155163240-155163290	MCF-7	breast:	n/a
25	chr1:155161679-155161729	BE2_C	brain:	n/a
26	chr1:155162871-155162921	K562	blood:	n/a
27	chr1:155161784-155161834	Hepatocyte	liver:	n/a
28	chr1:155163013-155163063	HepG2	liver:	n/a
29	chr1:155162756-155162806	MCF-7	breast:	n/a
30	chr1:155163013-155163063	PANC-1	pancreas:	n/a
31	chr1:155162756-155162806	PrEC	prostate:	n/a
32	chr1:155161161-155161211	HCF	heart:	n/a
33	chr1:155161211-155161261	MCF-7	breast:	n/a
34	chr1:155163590-155163640	H1-hESC	embryonic stem cell:	embryo
35	chr1:155163013-155163063	H1-hESC	embryonic stem cell:	embryo
36	chr1:155163013-155163063	HCT-116	colon:	n/a
37	chr1:155161833-155161883	HAEpiC	amniotic membrane:	n/a
38	chr1:155162871-155162921	Caco-2	colon:	n/a
39	chr1:155161833-155161883	LNCaP	prostate:	n/a
40	chr1:155161161-155161211	BE2_C	brain:	n/a
41	chr1:155163205-155163255	SK-N-SH_RA	brain:	n/a
42	chr1:155161221-155161271	NHDF-neo	bronchial:	n/a
43	chr1:155162871-155162921	BE2_C	brain:	n/a
44	chr1:155163590-155163640	NH-A	brain:	n/a
45	chr1:155161211-155161261	Jurkat	blood:	n/a
46	chr1:155163240-155163290	HRPEpiC	eye:	n/a
47	chr1:155161161-155161211	ECC-1	luminal epithelium:	n/a
48	chr1:155161833-155161883	NH-A	brain:	n/a
49	chr1:155162756-155162806	GM06990	blood:	n/a
50	chr1:155163240-155163290	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:155055270..155058458-chr1:155162731..155164725,3	MCF-7	breast:
2	chr1:155106165..155110704-chr1:155161873..155165835,8	K562	blood:
3	chr1:155106788..155108939-chr1:155162594..155164354,3	MCF-7	breast:
4	chr1:155062500..155064343-chr1:155162863..155164814,2	K562	blood:
5	chr1:155163400..155164137-chr6:30584536..30585043,2	Hela-S3	cervix:
6	chr1:155163154..155164052-chr12:13044571..13045233,2	Hela-S3	cervix:
7	chr1:155162741..155164778-chr1:155231161..155233767,3	K562	blood:
8	chr1:155162847..155164513-chr1:155220020..155222402,2	K562	blood:
9	chr1:155162786..155163624-chr12:57482231..57482802,2	Hela-S3	cervix:
10	chr1:155162882..155163515-chr8:48873266..48874033,2	Hela-S3	cervix:
11	chr1:155090194..155092132-chr1:155163035..155164929,2	MCF-7	breast:
12	chr1:155163572..155164476-chr16:58553323..58553966,2	Hela-S3	cervix:
13	chr1:155148301..155150189-chr1:155162933..155164249,12	MCF-7	breast:
14	chr1:155162793..155163414-chr17:67323501..67324001,2	Hela-S3	cervix:
15	chr1:155162564..155164989-chr17:57968115..57970881,2	MCF-7	breast:
16	chr1:155163092..155163669-chr12:52445473..52446435,2	Hela-S3	cervix:
17	chr1:155163156..155164893-chr1:155532696..155534228,2	K562	blood:
18	chr1:155149492..155150044-chr1:155161179..155161836,3	MCF-7	breast:
19	chr1:155162738..155163669-chrX:48814765..48815662,3	Hela-S3	cervix:
20	chr1:155052798..155059451-chr1:155162483..155166744,9	K562	blood:
21	chr1:155162487..155164653-chr1:155579583..155581273,2	K562	blood:
22	chr1:155162882..155163604-chr6:26033354..26033888,2	Hela-S3	cervix:
23	chr1:155111495..155114008-chr1:155163515..155166006,3	K562	blood:
24	chr1:155162888..155163772-chr1:155196595..155197463,2	MCF-7	breast:
25	chr1:155163602..155164530-chr16:87424972..87425797,2	Hela-S3	cervix:
26	chr1:155163476..155164106-chr12:7052581..7053558,2	Hela-S3	cervix:
27	chr1:155163624..155164561-chr19:39899857..39900792,2	Hela-S3	cervix:
28	chr1:155148758..155149726-chr1:155162834..155163883,7	K562	blood:
29	chr1:155092552..155095095-chr1:155160179..155163739,4	MCF-7	breast:
30	chr1:155163393..155163958-chr2:101868707..101869452,2	Hela-S3	cervix:
31	chr1:155163169..155163906-chr1:155176359..155177228,4	MCF-7	breast:
32	chr1:154192824..154195193-chr1:155162794..155164640,2	K562	blood:
33	chr1:155162165..155164633-chr1:155276991..155278874,2	K562	blood:
34	chr1:155160377..155162781-chr1:155242739..155244795,2	MCF-7	breast:
35	chr1:155106609..155109409-chr1:155161242..155164268,3	MCF-7	breast:
36	chr1:155163009..155163576-chr5:43121348..43122173,2	Hela-S3	cervix:
37	chr1:155023801..155025386-chr1:155162454..155164656,2	MCF-7	breast:
38	chr1:155163394..155164688-chr5:39074461..39075271,3	Hela-S3	cervix:
39	chr1:155049427..155051718-chr1:155163518..155166382,2	K562	blood:
40	chr1:155163241..155165710-chr1:155212950..155214666,2	MCF-7	breast:
41	chr1:155098824..155101489-chr1:155162030..155163615,2	K562	blood:
42	chr1:155161598..155164529-chr1:155278690..155280381,2	MCF-7	breast:
43	chr1:155163315..155164121-chr2:178077192..178078037,2	Hela-S3	cervix:
44	chr1:154945649..154947897-chr1:155163027..155164595,2	K562	blood:
45	chr1:155157869..155162042-chr1:155196023..155198721,3	MCF-7	breast:
46	chr1:155162750..155164739-chr1:155293098..155295016,2	MCF-7	breast:
47	chr1:155162983..155163857-chr1:155292790..155293293,2	K562	blood:
48	chr1:154943189..154945318-chr1:155161226..155163403,2	K562	blood:
49	chr1:154192824..154194792-chr1:155163140..155164963,2	K562	blood:
50	chr1:155161998..155164147-chr1:155209813..155212664,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRTCAP2-2	chr1:155161654-155162101	NONHSAT006696
2	lnc-KRTCAP2-2	chr1:155162578-155162707	NONHSAT006698
3	lnc-KRTCAP2-2	chr1:155161994-155162065	NONHSAT006698
4	lnc-KRTCAP2-2	chr1:155162577-155162700	NONHSAT006696

Variant related genes	Relation type
MIR92B	TF binding region
ENSG00000231064	TF binding region
ENSG00000273088	TF binding region
MUC1	TF binding region
MIR92B	CpG island
ENSG00000231064	CpG island
ENSG00000273088	CpG island
MUC1	CpG island
ENSG00000163462	chromatin interactions
ENSG00000216109	chromatin interactions
ENSG00000164896	chromatin interactions
ENSG00000104738	chromatin interactions
ENSG00000068308	chromatin interactions
ENSG00000160767	chromatin interactions
ENSG00000116521	chromatin interactions
ENSG00000202027	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000169241	chromatin interactions
ENSG00000179085	chromatin interactions
ENSG00000143537	chromatin interactions
ENSG00000011275	chromatin interactions
ENSG00000143569	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000251246	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000170144	chromatin interactions
ENSG00000173207	chromatin interactions
ENSG00000143590	chromatin interactions
ENSG00000164327	chromatin interactions
ENSG00000103264	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000232519	chromatin interactions
ENSG00000123815	chromatin interactions
ENSG00000163463	chromatin interactions
ENSG00000100479	chromatin interactions
ENSG00000169242	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000125459	chromatin interactions
ENSG00000143612	chromatin interactions
ENSG00000243364	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000235919	chromatin interactions
ENSG00000160691	chromatin interactions
ENSG00000174374	chromatin interactions
ENSG00000158435	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000013588	chromatin interactions
ENSG00000266559	chromatin interactions
ENSG00000116539	chromatin interactions
ENSG00000140941	chromatin interactions
ENSG00000166886	chromatin interactions
ENSG00000263721	chromatin interactions
ENSG00000204634	chromatin interactions
ENSG00000203761	chromatin interactions
ENSG00000160685	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000168209	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000086544	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000229337	chromatin interactions
ENSG00000137259	chromatin interactions

Extended variants
information (count: 239 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:239 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566798251	chr1:155159155-155159156	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs28414349	chr1:155159188-155159189	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs559170904	chr1:155159250-155159251	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532965137	chr1:155159264-155159265	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs142159143	chr1:155159293-155159294	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs368083573	chr1:155159294-155159295	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs377291958	chr1:155159299-155159300	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs563457321	chr1:155159325-155159326	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs530880538	chr1:155159348-155159349	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs370083076	chr1:155159397-155159398	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs549386573	chr1:155159469-155159470	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs201219557	chr1:155159496-155159497	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs151187351	chr1:155159594-155159595	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs555426932	chr1:155159605-155159606	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201758571	chr1:155159658-155159659	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs148332231	chr1:155159708-155159709	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs191544901	chr1:155159717-155159718	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs372682991	chr1:155159718-155159719	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs572153326	chr1:155159745-155159746	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs200639498	chr1:155159773-155159774	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs557552446	chr1:155159798-155159799	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs1611771	chr1:155159895-155159896	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs367561217	chr1:155159896-155159897	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs371436760	chr1:155159907-155159908	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs374941067	chr1:155159914-155159915	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs369318053	chr1:155159918-155159919	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs199768496	chr1:155159932-155159933	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs183700327	chr1:155159944-155159945	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs141460657	chr1:155159955-155159956	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs200788986	chr1:155159959-155159960	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs373081136	chr1:155159990-155159991	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs375090196	chr1:155159991-155159992	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs371577379	chr1:155159995-155159996	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs369608212	chr1:155160010-155160011	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs369649894	chr1:155160016-155160017	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs199840128	chr1:155160019-155160020	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs11465207	chr1:155160049-155160050	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs559232741	chr1:155160085-155160086	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs199930906	chr1:155160095-155160096	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs541165815	chr1:155160105-155160106	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs544825247	chr1:155160114-155160115	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs372080499	chr1:155160128-155160129	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs200976316	chr1:155160159-155160160	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs373797308	chr1:155160160-155160161	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs377056857	chr1:155160168-155160169	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs531068248	chr1:155160182-155160183	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs35409840	chr1:155160185-155160186	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs201815857	chr1:155160198-155160199	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs201798179	chr1:155160214-155160215	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs146141676	chr1:155160215-155160216	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155146600-155163000	Weak transcription	Aorta	Aorta
2	chr1:155149600-155162000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr1:155149600-155162600	Weak transcription	Small Intestine	intestine
4	chr1:155149600-155162800	Weak transcription	NHDF-Ad	bronchial
5	chr1:155149800-155162000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr1:155149800-155162200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr1:155150000-155162000	Weak transcription	Stomach Smooth Muscle	stomach
8	chr1:155150000-155163000	Weak transcription	Fetal Brain Male	brain
9	chr1:155150200-155162400	Weak transcription	Dnd41	blood
10	chr1:155150400-155161800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr1:155150600-155162000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:155150800-155161800	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr1:155151000-155162000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr1:155151200-155162000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:155152200-155162800	Weak transcription	Osteobl	bone
16	chr1:155152400-155163000	Weak transcription	HUVEC	blood vessel
17	chr1:155152600-155161800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:155152600-155161800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr1:155152600-155162000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr1:155152600-155162200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr1:155152600-155162400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:155152600-155162800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr1:155152600-155163000	Weak transcription	Brain Substantia Nigra	brain
24	chr1:155152800-155162000	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr1:155152800-155162200	Weak transcription	Fetal Thymus	thymus
26	chr1:155152800-155162400	Weak transcription	Brain Anterior Caudate	brain
27	chr1:155152800-155163000	Weak transcription	NH-A	brain
28	chr1:155153000-155161800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:155153000-155162400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr1:155154800-155162200	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr1:155155000-155162200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:155155000-155162200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:155155000-155162800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr1:155155200-155161800	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr1:155155200-155162000	Weak transcription	NHLF	lung
36	chr1:155155400-155162200	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr1:155155400-155162400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr1:155156000-155159200	Enhancers	Primary B cells from peripheral blood	blood
39	chr1:155156400-155161000	Enhancers	Pancreas	Pancrea
40	chr1:155156400-155161800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr1:155156600-155159400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr1:155156600-155159400	Genic enhancers	Gastric	stomach
43	chr1:155156600-155162800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:155156600-155163000	Weak transcription	Brain Cingulate Gyrus	brain
45	chr1:155156800-155160000	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr1:155156800-155163000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr1:155157000-155159800	Enhancers	Fetal Intestine Small	intestine
48	chr1:155157000-155160000	Enhancers	Placenta	Placenta
49	chr1:155157000-155162000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr1:155157000-155162000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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