Variant report

Variant	esv3381155
Chromosome Location	chr1:155160128-155162626
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:85)
CpG islands
(count:366)
Chromatin interactive
region (count:28)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:85 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:155161078-155161718	HepG2	liver:	n/a	n/a
2	EP300	chr1:155161095-155161636	GM12878	blood:	n/a	n/a
3	EP300	chr1:155161179-155161713	GM12878	blood:	n/a	n/a
4	ESR1	chr1:155160875-155161905	T-47D	breast:	n/a	chr1:155160982-155160997
5	FOSL2	chr1:155161037-155161718	HepG2	liver:	n/a	n/a
6	GABPA	chr1:155161165-155161758	Hela-S3	cervix:	n/a	n/a
7	GABPA	chr1:155161019-155161785	HepG2	liver:	n/a	n/a
8	GABPA	chr1:155160975-155161761	HepG2	liver:	n/a	n/a
9	GABPA	chr1:155161108-155161681	Hela-S3	cervix:	n/a	n/a
10	GATA3	chr1:155162479-155163053	T-47D	breast:	n/a	n/a
11	HEY1	chr1:155161025-155161780	K562	blood:	n/a	n/a
12	JUND	chr1:155161027-155161760	HepG2	liver:	n/a	n/a
13	MAX	chr1:155162394-155165027	K562	blood:	n/a	chr1:155164304-155164311 chr1:155164726-155164735 chr1:155163756-155163766 chr1:155164834-155164844 chr1:155162945-155162955 chr1:155164303-155164312
14	MAX	chr1:155162406-155165088	HCT-116	colon:	n/a	chr1:155164304-155164311 chr1:155164726-155164735 chr1:155163756-155163766 chr1:155164834-155164844 chr1:155162945-155162955 chr1:155164303-155164312
15	MAZ	chr1:155162533-155164983	Hela-S3	cervix:	n/a	chr1:155164304-155164311 chr1:155164726-155164735 chr1:155163756-155163766 chr1:155164834-155164844 chr1:155162945-155162955 chr1:155164303-155164312
16	MAZ	chr1:155162579-155163902	K562	blood:	n/a	chr1:155163756-155163766 chr1:155162945-155162955
17	MYC	chr1:155162526-155164884	MCF10A-Er-Src	breast:	n/a	chr1:155164304-155164311 chr1:155164726-155164735 chr1:155163756-155163766 chr1:155164834-155164844 chr1:155162945-155162955 chr1:155164303-155164312
18	NR3C1	chr1:155161090-155161648	A549	lung:	n/a	n/a
19	NR3C1	chr1:155161073-155161697	A549	lung:	n/a	n/a
20	NR3C1	chr1:155160931-155161824	A549	lung:	n/a	n/a
21	PAX5	chr1:155161170-155161634	GM12878	blood:	n/a	n/a
22	PAX5	chr1:155161072-155161682	GM12878	blood:	n/a	n/a
23	PAX5	chr1:155161197-155161597	GM12878	blood:	n/a	n/a
24	PAX5	chr1:155161144-155161601	GM12878	blood:	n/a	n/a
25	PBX3	chr1:155161038-155161763	GM12878	blood:	n/a	n/a
26	PBX3	chr1:155161175-155161585	GM12878	blood:	n/a	n/a
27	POLR2A	chr1:155161817-155168780	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr1:155162315-155165088	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr1:155162403-155162717	K562	blood:	n/a	n/a
30	POLR2A	chr1:155160974-155161793	GM12892	blood:	n/a	n/a
31	POLR2A	chr1:155162132-155164884	K562	blood:	n/a	n/a
32	POLR2A	chr1:155160974-155161792	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr1:155153389-155161077	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr1:155161754-155168618	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr1:155161721-155162735	H1-neurons	neurons:	n/a	n/a
36	POLR2A	chr1:155160983-155161838	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr1:155160682-155161162	H1-neurons	neurons:	n/a	n/a
38	POLR2A	chr1:155161035-155161786	A549	lung:	n/a	n/a
39	POLR2A	chr1:155161021-155161754	A549	lung:	n/a	n/a
40	POLR2A	chr1:155162272-155165472	K562	blood:	n/a	n/a
41	POLR2A	chr1:155162464-155162904	MCF-7	breast:	n/a	n/a
42	POLR2A	chr1:155161022-155161808	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr1:155160547-155160614	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr1:155161101-155161644	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr1:155162184-155165239	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr1:155160953-155161718	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr1:155159183-155160440	H1-neurons	neurons:	n/a	n/a
48	POLR2A	chr1:155162414-155164997	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr1:155161076-155161635	GM12878	blood:	n/a	n/a
50	POLR2A	chr1:155162497-155162843	MCF-7	breast:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155161161-155161211	HEEpiC	esophagus:	n/a
2	chr1:155161784-155161834	Hepatocyte	liver:	n/a
3	chr1:155161784-155161834	AG09319	gingival:	n/a
4	chr1:155161679-155161729	HEK293	kidney:	embryo
5	chr1:155161161-155161211	AG04450	lung:	fetal
6	chr1:155161221-155161271	K562	blood:	n/a
7	chr1:155161784-155161834	AoSMC	blood vessel:	n/a
8	chr1:155161833-155161883	A549	lung:	n/a
9	chr1:155161211-155161261	HL-60	blood:	n/a
10	chr1:155161221-155161271	H1-hESC	embryonic stem cell:	embryo
11	chr1:155161211-155161261	SK-N-SH	brain:	n/a
12	chr1:155161211-155161261	HEEpiC	esophagus:	n/a
13	chr1:155161161-155161211	AG04449	skin:	fetal
14	chr1:155161833-155161883	PrEC	prostate:	n/a
15	chr1:155161221-155161271	HMEC	breast:	n/a
16	chr1:155161221-155161271	AG09319	gingival:	n/a
17	chr1:155161211-155161261	BE2_C	brain:	n/a
18	chr1:155161211-155161261	GM19239	blood:	n/a
19	chr1:155161221-155161271	GM06990	blood:	n/a
20	chr1:155161784-155161834	GM19239	blood:	n/a
21	chr1:155161211-155161261	PrEC	prostate:	n/a
22	chr1:155161679-155161729	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:155161833-155161883	BJ	skin:	n/a
24	chr1:155161833-155161883	NB4	blood:	n/a
25	chr1:155161833-155161883	H1-hESC	embryonic stem cell:	embryo
26	chr1:155161679-155161729	HIPEpiC	eye:	n/a
27	chr1:155161833-155161883	ovcar-3	ovarian:	n/a
28	chr1:155161161-155161211	NB4	blood:	n/a
29	chr1:155161161-155161211	HepG2	liver:	n/a
30	chr1:155161833-155161883	PANC-1	pancreas:	n/a
31	chr1:155161221-155161271	GM12892	blood:	n/a
32	chr1:155161833-155161883	PFSK-1	brain:	n/a
33	chr1:155161161-155161211	HL-60	blood:	n/a
34	chr1:155161221-155161271	ovcar-3	ovarian:	n/a
35	chr1:155161211-155161261	HEK293	kidney:	embryo
36	chr1:155161161-155161211	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:155161211-155161261	HRCEpiC	kidney:	n/a
38	chr1:155161161-155161211	Caco-2	colon:	n/a
39	chr1:155161211-155161261	HAEpiC	amniotic membrane:	n/a
40	chr1:155161784-155161834	Caco-2	colon:	n/a
41	chr1:155161161-155161211	BJ	skin:	n/a
42	chr1:155161221-155161271	HepG2	liver:	n/a
43	chr1:155161161-155161211	HAEpiC	amniotic membrane:	n/a
44	chr1:155161833-155161883	GM12892	blood:	n/a
45	chr1:155161221-155161271	HEEpiC	esophagus:	n/a
46	chr1:155161161-155161211	GM12892	blood:	n/a
47	chr1:155161679-155161729	HCT-116	colon:	n/a
48	chr1:155161833-155161883	K562	blood:	n/a
49	chr1:155161211-155161261	ProgFib	skin:	n/a
50	chr1:155161221-155161271	PFSK-1	brain:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:155106165..155110704-chr1:155161873..155165835,8	K562	blood:
2	chr1:155157869..155162042-chr1:155196023..155198721,3	MCF-7	breast:
3	chr1:155105295..155110704-chr1:155161873..155165835,7	K562	blood:
4	chr1:155162165..155164633-chr1:155276991..155278874,2	K562	blood:
5	chr1:155092552..155095095-chr1:155160179..155163739,4	MCF-7	breast:
6	chr1:155149492..155150014-chr1:155161259..155161836,2	MCF-7	breast:
7	chr1:155149492..155150044-chr1:155161179..155161836,3	MCF-7	breast:
8	chr1:155023801..155025386-chr1:155162454..155164656,2	MCF-7	breast:
9	chr1:155160293..155162117-chr1:155291803..155294447,2	K562	blood:
10	chr1:155161236..155164985-chr1:155290580..155295192,7	K562	blood:
11	chr1:155162384..155165288-chr1:155195792..155197762,4	MCF-7	breast:
12	chr1:155161177..155163523-chr1:155219674..155222613,2	K562	blood:
13	chr1:154974390..154976020-chr1:155161759..155163515,2	MCF-7	breast:
14	chr1:155162564..155164989-chr17:57968115..57970881,2	MCF-7	breast:
15	chr1:155160377..155162781-chr1:155242739..155244795,2	MCF-7	breast:
16	chr1:154943189..154945318-chr1:155161226..155163403,2	K562	blood:
17	chr1:155162487..155164653-chr1:155579583..155581273,2	K562	blood:
18	chr1:155052798..155059451-chr1:155162483..155166744,9	K562	blood:
19	chr1:155160390..155165295-chr1:155194589..155199400,14	K562	blood:
20	chr1:155106788..155108939-chr1:155162594..155164354,3	MCF-7	breast:
21	chr1:155106609..155109409-chr1:155161242..155164268,3	MCF-7	breast:
22	chr1:155098824..155101489-chr1:155162030..155163615,2	K562	blood:
23	chr1:155160177..155166575-chr1:155191666..155199927,14	MCF-7	breast:
24	chr1:155161598..155164529-chr1:155278690..155280381,2	MCF-7	breast:
25	chr1:154944711..154947532-chr1:155161851..155164798,3	MCF-7	breast:
26	chr1:155096309..155104200-chr1:155157595..155166389,23	MCF-7	breast:
27	chr1:155161998..155167332-chr1:155208163..155212538,6	K562	blood:
28	chr1:155161998..155164147-chr1:155209813..155212664,2	K562	blood:

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

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

No data

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
ENSG00000125459	chromatin interactions
ENSG00000169242	chromatin interactions
ENSG00000160767	chromatin interactions
ENSG00000232519	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000143537	chromatin interactions
ENSG00000160685	chromatin interactions
ENSG00000203761	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000169241	chromatin interactions
ENSG00000160691	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000173207	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000143590	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000202027	chromatin interactions

Extended variants
information (count: 161 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:161 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	rs561379331	chr1:155160241-155160242	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
11	rs41264913	chr1:155160253-155160254	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs200411609	chr1:155160254-155160255	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs1611770	chr1:155160270-155160271	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs144273480	chr1:155160273-155160274	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs532835613	chr1:155160278-155160279	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs370391810	chr1:155160292-155160293	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs139620330	chr1:155160313-155160314	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs373382247	chr1:155160327-155160328	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs145224844	chr1:155160329-155160330	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs377536668	chr1:155160339-155160340	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs370532867	chr1:155160346-155160347	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs188283380	chr1:155160353-155160354	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs201857138	chr1:155160368-155160369	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs368178851	chr1:155160446-155160447	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs202177609	chr1:155160479-155160480	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs370819310	chr1:155160495-155160496	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs140871200	chr1:155160516-155160517	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs199973720	chr1:155160549-155160550	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs11465206	chr1:155160556-155160557	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs577718338	chr1:155160569-155160570	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs575326709	chr1:155160571-155160572	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs117506440	chr1:155160587-155160588	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs201962026	chr1:155160609-155160610	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs371252701	chr1:155160619-155160620	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs374807365	chr1:155160630-155160631	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs146950322	chr1:155160686-155160687	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs35819649	chr1:155160698-155160699	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs371485486	chr1:155160723-155160724	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs534337862	chr1:155160730-155160731	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs563563693	chr1:155160762-155160763	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs201308716	chr1:155160787-155160788	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs529196978	chr1:155160805-155160806	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs149945265	chr1:155160813-155160814	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs202108781	chr1:155160879-155160880	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs556778160	chr1:155160910-155160911	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs11465205	chr1:155160941-155160942	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs542758718	chr1:155160942-155160943	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs561232891	chr1:155160987-155160988	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs528549236	chr1:155160997-155160998	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs540649449	chr1:155161024-155161025	Weak transcription Active TSS	TF binding region Chromatin interactive region	9 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:269 , 50 per page) page: 1 2 3 4 5 6

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	chr1:155156400-155161000	Enhancers	Pancreas	Pancrea
39	chr1:155156400-155161800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr1:155156600-155162800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:155156600-155163000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr1:155156800-155163000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr1:155157000-155162000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr1:155157000-155162000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr1:155157000-155163000	Weak transcription	Brain Angular Gyrus	brain
46	chr1:155157200-155160400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:155157200-155161800	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr1:155157600-155162000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr1:155157600-155162200	Weak transcription	Primary T cells from cord blood	blood
50	chr1:155157800-155160600	Enhancers	H1 Cell Line	embryonic stem cell

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