Variant report

Variant	nsv872464
Chromosome Location	chr1:155157853-155163181
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:488)
CpG islands
(count:671)
Chromatin interactive
region (count:66)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

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

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	ATF2	chr1:155163180-155163620	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr1:155163143-155163855	A549	lung:	n/a	chr1:155163657-155163677
4	BACH1	chr1:155158577-155158581	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:155163141-155163800	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr1:155157852-155158151	GM12878	blood:	n/a	n/a
7	BCL3	chr1:155162937-155164820	A549	lung:	n/a	n/a
8	BCL3	chr1:155163030-155163766	A549	lung:	n/a	n/a
9	BCL3	chr1:155157821-155158153	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:155157785-155158391	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	chr1:155163005-155163071	GM12878	blood:	n/a	n/a
14	BRCA1	chr1:155162848-155163722	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr1:155162734-155164889	K562	blood:	n/a	n/a
16	CCNT2	chr1:155162883-155163703	K562	blood:	n/a	chr1:155162948-155162957 chr1:155162941-155162950
17	CEBPB	chr1:155162858-155163005	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr1:155163111-155163736	H1-hESC	embryonic stem cell:	n/a	chr1:155163428-155163438
19	CHD2	chr1:155162771-155163764	H1-hESC	embryonic stem cell:	n/a	chr1:155163428-155163438 chr1:155162947-155162957
20	CHD2	chr1:155162779-155163841	Hela-S3	cervix:	n/a	chr1:155163428-155163438 chr1:155162947-155162957
21	CHD2	chr1:155157486-155158278	GM12878	blood:	n/a	n/a
22	CHD2	chr1:155162872-155163732	GM12878	blood:	n/a	chr1:155163428-155163438 chr1:155162947-155162957
23	CHD2	chr1:155162681-155163821	K562	blood:	n/a	chr1:155162743-155162753 chr1:155163428-155163438 chr1:155162947-155162957
24	CREB1	chr1:155162981-155163810	A549	lung:	n/a	n/a
25	CTBP2	chr1:155162860-155163792	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr1:155158009-155158226	GM19239	blood:	n/a	n/a
27	CTCF	chr1:155158120-155158270	HRE	kidney:	n/a	n/a
28	CTCF	chr1:155158020-155158170	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr1:155163107-155163206	GM12892	blood:	n/a	n/a
30	CTCF	chr1:155163107-155163658	A549	lung:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
31	CTCF	chr1:155163102-155163674	K562	blood:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
32	CTCF	chr1:155158100-155158250	GM12871	blood:	n/a	n/a
33	CTCF	chr1:155158060-155158210	GM12867	blood:	n/a	n/a
34	CTCF	chr1:155158060-155158210	HepG2	liver:	n/a	n/a
35	CTCF	chr1:155162768-155163981	SK-N-SH	brain:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449
36	CTCF	chr1:155158080-155158230	GM12870	blood:	n/a	n/a
37	CTCF	chr1:155157979-155158224	GM12891	blood:	n/a	n/a
38	CTCF	chr1:155158005-155158007	GM19239	blood:	n/a	n/a
39	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
40	CTCF	chr1:155158000-155158150	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr1:155158104-155158201	GM10248	blood:	n/a	n/a
42	CTCF	chr1:155158060-155158210	GM12872	blood:	n/a	n/a
43	CTCF	chr1:155158060-155158210	GM12878	blood:	n/a	n/a
44	CTCF	chr1:155158054-155158139	Lung_OC	lung:	n/a	n/a
45	CTCF	chr1:155158080-155158230	GM12872	blood:	n/a	n/a
46	CTCF	chr1:155158040-155158190	GM12865	blood:	n/a	n/a
47	CTCF	chr1:155158080-155158230	GM12878	blood:	n/a	n/a
48	CTCF	chr1:155158040-155158190	HL-60	blood:	n/a	n/a
49	CTCF	chr1:155158091-155158148	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr1:155162782-155163981	A549	lung:	n/a	chr1:155163434-155163447 chr1:155163432-155163450 chr1:155163437-155163445 chr1:155163434-155163447 chr1:155163427-155163448 chr1:155163433-155163449

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155161211-155161261	SKMC	muscle:	n/a
2	chr1:155162871-155162921	U87	brain:	n/a
3	chr1:155161833-155161883	ECC-1	luminal epithelium:	n/a
4	chr1:155162752-155162802	HRPEpiC	eye:	n/a
5	chr1:155162752-155162802	PANC-1	pancreas:	n/a
6	chr1:155158319-155158369	ProgFib	skin:	n/a
7	chr1:155161679-155161729	SK-N-SH_RA	brain:	n/a
8	chr1:155161211-155161261	HCM	heart:	n/a
9	chr1:155161161-155161211	BE2_C	brain:	n/a
10	chr1:155158319-155158369	Hepatocyte	liver:	n/a
11	chr1:155161211-155161261	AG04449	skin:	fetal
12	chr1:155161161-155161211	A549	lung:	n/a
13	chr1:155162756-155162806	SK-N-MC	brain:	n/a
14	chr1:155162756-155162806	HEEpiC	esophagus:	n/a
15	chr1:155162871-155162921	HCT-116	colon:	n/a
16	chr1:155161784-155161834	MCF10A-Er-Src	breast:	n/a
17	chr1:155161211-155161261	SK-N-MC	brain:	n/a
18	chr1:155162752-155162802	CMK	blood:	n/a
19	chr1:155161784-155161834	AG10803	skin:	n/a
20	chr1:155163013-155163063	GM12878	blood:	n/a
21	chr1:155161211-155161261	HL-60	blood:	n/a
22	chr1:155163013-155163063	SK-N-SH_RA	brain:	n/a
23	chr1:155163013-155163063	SAEC	small airway:	n/a
24	chr1:155161679-155161729	HUVEC	blood vessel:	n/a
25	chr1:155161679-155161729	ProgFib	skin:	n/a
26	chr1:155163013-155163063	BE2_C	brain:	n/a
27	chr1:155162871-155162921	ECC-1	luminal epithelium:	n/a
28	chr1:155161221-155161271	HUVEC	blood vessel:	n/a
29	chr1:155161211-155161261	HRE	kidney:	n/a
30	chr1:155162756-155162806	CMK	blood:	n/a
31	chr1:155161211-155161261	HRCEpiC	kidney:	n/a
32	chr1:155161833-155161883	ovcar-3	ovarian:	n/a
33	chr1:155161161-155161211	Jurkat	blood:	n/a
34	chr1:155162871-155162921	SK-N-SH_RA	brain:	n/a
35	chr1:155158319-155158369	HCM	heart:	n/a
36	chr1:155162752-155162802	Hepatocyte	liver:	n/a
37	chr1:155161784-155161834	ovcar-3	ovarian:	n/a
38	chr1:155161211-155161261	RPTEC	kidney:	n/a
39	chr1:155163013-155163063	CMK	blood:	n/a
40	chr1:155162752-155162802	AG09319	gingival:	n/a
41	chr1:155162756-155162806	SAEC	small airway:	n/a
42	chr1:155161161-155161211	NB4	blood:	n/a
43	chr1:155162871-155162921	NT2-D1	testis:	n/a
44	chr1:155161784-155161834	HAEpiC	amniotic membrane:	n/a
45	chr1:155161784-155161834	GM12891	blood:	n/a
46	chr1:155161211-155161261	Caco-2	colon:	n/a
47	chr1:155161833-155161883	RPTEC	kidney:	n/a
48	chr1:155161784-155161834	HUVEC	blood vessel:	n/a
49	chr1:155162756-155162806	A549	lung:	n/a
50	chr1:155162756-155162806	BE2_C	brain:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:155160177..155166575-chr1:155191666..155199927,14	MCF-7	breast:
2	chr1:155098824..155101489-chr1:155162030..155163615,2	K562	blood:
3	chr1:155148758..155149726-chr1:155162834..155163883,7	K562	blood:
4	chr1:155062500..155064343-chr1:155162863..155164814,2	K562	blood:
5	chr1:155090194..155092132-chr1:155163035..155164929,2	MCF-7	breast:
6	chr1:155162384..155165288-chr1:155195792..155197762,4	MCF-7	breast:
7	chr1:155163092..155163669-chr12:52445473..52446435,2	Hela-S3	cervix:
8	chr1:155055391..155058180-chr1:155162719..155165085,4	K562	blood:
9	chr1:155162741..155164778-chr1:155231161..155233767,3	K562	blood:
10	chr1:155099163..155101241-chr1:155155746..155158375,2	MCF-7	breast:
11	chr1:155162165..155164633-chr1:155276991..155278874,2	K562	blood:
12	chr1:155160377..155162781-chr1:155242739..155244795,2	MCF-7	breast:
13	chr1:155105295..155110704-chr1:155161873..155165835,7	K562	blood:
14	chr1:155163124..155163948-chr7:5820822..5821460,2	Hela-S3	cervix:
15	chr1:155023801..155025386-chr1:155162454..155164656,2	MCF-7	breast:
16	chr1:155106788..155108939-chr1:155162594..155164354,3	MCF-7	breast:
17	chr1:155163169..155163906-chr1:155176359..155177228,4	MCF-7	breast:
18	chr1:155162671..155164140-chr15:65588192..65588839,3	Hela-S3	cervix:
19	chr1:155106609..155109409-chr1:155161242..155164268,3	MCF-7	breast:
20	chr1:155055270..155058458-chr1:155162731..155164725,3	MCF-7	breast:
21	chr1:155162742..155164349-chr1:155205489..155207778,2	K562	blood:
22	chr1:155092552..155095095-chr1:155160179..155163739,4	MCF-7	breast:
23	chr1:154943189..154945318-chr1:155161226..155163403,2	K562	blood:
24	chr1:154192824..154194792-chr1:155163140..155164963,2	K562	blood:
25	chr1:155162487..155164653-chr1:155579583..155581273,2	K562	blood:
26	chr1:155162933..155163891-chr7:150777812..150778399,2	HCT-116	colon:
27	chr1:155160390..155165295-chr1:155194589..155199400,14	K562	blood:
28	chr1:155162899..155163747-chr11:65625244..65625902,2	Hela-S3	cervix:
29	chr1:155139118..155143025-chr1:155155964..155158470,4	MCF-7	breast:
30	chr1:155161236..155164985-chr1:155290580..155295192,7	K562	blood:
31	chr1:155163173..155164182-chr10:74032582..74033760,3	Hela-S3	cervix:
32	chr1:155161998..155164147-chr1:155209813..155212664,2	K562	blood:
33	chr1:154974390..154976020-chr1:155161759..155163515,2	MCF-7	breast:
34	chr1:155163156..155164893-chr1:155532696..155534228,2	K562	blood:
35	chr1:154192824..154195193-chr1:155162794..155164640,2	K562	blood:
36	chr1:155161598..155164529-chr1:155278690..155280381,2	MCF-7	breast:
37	chr1:155162888..155163772-chr1:155196595..155197463,2	MCF-7	breast:
38	chr1:155052798..155059451-chr1:155162483..155166744,9	K562	blood:
39	chr1:155162738..155163669-chrX:48814765..48815662,3	Hela-S3	cervix:
40	chr1:155148507..155150033-chr1:155162898..155164095,27	MCF-7	breast:
41	chr1:155163009..155163576-chr5:43121348..43122173,2	Hela-S3	cervix:
42	chr1:155161998..155167332-chr1:155208163..155212538,6	K562	blood:
43	chr1:155162847..155164513-chr1:155220020..155222402,2	K562	blood:
44	chr1:155163154..155164052-chr12:13044571..13045233,2	Hela-S3	cervix:
45	chr1:155162882..155163515-chr8:48873266..48874033,2	Hela-S3	cervix:
46	chr1:155149492..155150014-chr1:155161259..155161836,2	MCF-7	breast:
47	chr1:155163130..155164699-chr1:155531249..155533264,2	K562	blood:
48	chr1:155162793..155163414-chr17:67323501..67324001,2	Hela-S3	cervix:
49	chr1:155162750..155164739-chr1:155293098..155295016,2	MCF-7	breast:
50	chr1:155145302..155146232-chr1:155163021..155163628,3	K562	blood:

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

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

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MUC1	hsa-miR-145-5p	chr1:155158330-155158348

Variant related genes	Relation type
MIR92B	TF binding region
ENSG00000231064	TF binding region
MUC1	TF binding region
ENSG00000273088	TF binding region
MIR92B	CpG island
ENSG00000231064	CpG island
MUC1	CpG island
ENSG00000273088	CpG island
ENSG00000108443	chromatin interactions
ENSG00000164896	chromatin interactions
ENSG00000163462	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000160691	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000143537	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000202027	chromatin interactions
ENSG00000137259	chromatin interactions
ENSG00000011275	chromatin interactions
ENSG00000160685	chromatin interactions
ENSG00000013588	chromatin interactions
ENSG00000235919	chromatin interactions
ENSG00000125459	chromatin interactions
ENSG00000163463	chromatin interactions
ENSG00000160767	chromatin interactions
ENSG00000232519	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000169242	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000104738	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000143569	chromatin interactions
ENSG00000203761	chromatin interactions
ENSG00000216109	chromatin interactions
ENSG00000143612	chromatin interactions
ENSG00000143590	chromatin interactions
ENSG00000166886	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000168209	chromatin interactions
ENSG00000068308	chromatin interactions
ENSG00000173207	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000169241	chromatin interactions
ENSG00000116521	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000116539	chromatin interactions

Extended variants
information (count: 267 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1611774	chr1:155157853-155157854	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571550009	chr1:155157935-155157936	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs138935916	chr1:155157968-155157969	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs184190555	chr1:155157984-155157985	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs372375278	chr1:155157997-155157998	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs543012709	chr1:155158024-155158025	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs538758054	chr1:155158052-155158053	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562021864	chr1:155158060-155158061	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs557588596	chr1:155158061-155158062	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs11465211	chr1:155158068-155158069	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs11590286	chr1:155158081-155158082	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs574263015	chr1:155158261-155158262	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs149421473	chr1:155158275-155158276	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs376685656	chr1:155158276-155158277	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs533295118	chr1:155158304-155158305	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs112893627	chr1:155158345-155158346	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region miRNA target site	3 gene(s)	Overlapped CNVs	n/a
17	rs188749315	chr1:155158379-155158380	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs11465210	chr1:155158414-155158415	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs1611773	chr1:155158532-155158533	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs139043100	chr1:155158601-155158602	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs369597551	chr1:155158602-155158603	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs549073561	chr1:155158604-155158605	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs1611772	chr1:155158605-155158606	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs199968990	chr1:155158634-155158635	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs11465209	chr1:155158650-155158651	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs145965712	chr1:155158711-155158712	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs578209866	chr1:155158719-155158720	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs374314292	chr1:155158736-155158737	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs139881730	chr1:155158843-155158844	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
30	rs557887684	chr1:155158844-155158845	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
31	rs184988099	chr1:155158855-155158856	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
32	rs12566541	chr1:155158912-155158913	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs113989545	chr1:155158944-155158945	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
34	rs375269773	chr1:155158945-155158946	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
35	rs142212980	chr1:155158946-155158947	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
36	rs58446580	chr1:155158968-155158969	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
37	rs543430885	chr1:155159004-155159005	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
38	rs561508595	chr1:155159007-155159008	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
39	rs551247105	chr1:155159036-155159037	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
40	rs573915720	chr1:155159067-155159068	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
41	rs187046852	chr1:155159073-155159074	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	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

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:471 , 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	chr1:155149600-155158000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:155149600-155158200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:155149600-155158800	Weak transcription	A549	lung
5	chr1:155149600-155162000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr1:155149600-155162600	Weak transcription	Small Intestine	intestine
7	chr1:155149600-155162800	Weak transcription	NHDF-Ad	bronchial
8	chr1:155149800-155158400	Strong transcription	Brain Germinal Matrix	brain
9	chr1:155149800-155158800	Strong transcription	Fetal Stomach	stomach
10	chr1:155149800-155162000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr1:155149800-155162200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr1:155150000-155158400	Weak transcription	NHEK	skin
13	chr1:155150000-155162000	Weak transcription	Stomach Smooth Muscle	stomach
14	chr1:155150000-155163000	Weak transcription	Fetal Brain Male	brain
15	chr1:155150200-155162400	Weak transcription	Dnd41	blood
16	chr1:155150400-155161800	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr1:155150600-155162000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr1:155150800-155161800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr1:155151000-155162000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr1:155151200-155162000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr1:155152200-155162800	Weak transcription	Osteobl	bone
22	chr1:155152400-155163000	Weak transcription	HUVEC	blood vessel
23	chr1:155152600-155161800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:155152600-155161800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr1:155152600-155162000	Weak transcription	Primary hematopoietic stem cells	blood
26	chr1:155152600-155162200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr1:155152600-155162400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:155152600-155162800	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr1:155152600-155163000	Weak transcription	Brain Substantia Nigra	brain
30	chr1:155152800-155158000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr1:155152800-155162000	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr1:155152800-155162200	Weak transcription	Fetal Thymus	thymus
33	chr1:155152800-155162400	Weak transcription	Brain Anterior Caudate	brain
34	chr1:155152800-155163000	Weak transcription	NH-A	brain
35	chr1:155153000-155161800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:155153000-155162400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr1:155154800-155162200	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr1:155155000-155162200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:155155000-155162200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:155155000-155162800	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr1:155155200-155158400	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr1:155155200-155161800	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr1:155155200-155162000	Weak transcription	NHLF	lung
44	chr1:155155400-155158400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr1:155155400-155162200	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr1:155155400-155162400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:155155800-155158800	Enhancers	Spleen	Spleen
48	chr1:155156000-155158200	Enhancers	Stomach Mucosa	stomach
49	chr1:155156000-155159000	Enhancers	Fetal Muscle Leg	muscle
50	chr1:155156000-155159200	Enhancers	Primary B cells from peripheral blood	blood

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