Variant report

Variant	nsv1001918
Chromosome Location	chr1:180886750-180908005
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:646)
CpG islands
(count:489)
Chromatin interactive
region (count:49)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:180894667-180895049	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:180902429-180902690	K562	blood:	n/a	n/a
3	ATF1	chr1:180892225-180892497	K562	blood:	n/a	n/a
4	ATF2	chr1:180891990-180892734	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:180891953-180892859	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:180891910-180892776	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:180891428-180891599	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr1:180903757-180903955	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:180902335-180902681	K562	blood:	n/a	n/a
10	BHLHE40	chr1:180887694-180887836	K562	blood:	n/a	n/a
11	BHLHE40	chr1:180902895-180902952	K562	blood:	n/a	n/a
12	BHLHE40	chr1:180895744-180895986	K562	blood:	n/a	n/a
13	CBX3	chr1:180902215-180902707	K562	blood:	n/a	n/a
14	CBX3	chr1:180895683-180896087	K562	blood:	n/a	n/a
15	CBX3	chr1:180887683-180887995	K562	blood:	n/a	n/a
16	CCNT2	chr1:180902275-180902724	K562	blood:	n/a	chr1:180902500-180902520
17	CCNT2	chr1:180895690-180896030	K562	blood:	n/a	n/a
18	CCNT2	chr1:180904246-180904461	K562	blood:	n/a	n/a
19	CEBPB	chr1:180890007-180890212	A549	lung:	n/a	n/a
20	CEBPB	chr1:180900716-180900983	K562	blood:	n/a	chr1:180900833-180900846 chr1:180900833-180900844 chr1:180900835-180900846
21	CEBPB	chr1:180889613-180890162	IMR90	lung:	n/a	chr1:180889700-180889711
22	CEBPB	chr1:180889883-180890232	K562	blood:	n/a	n/a
23	CEBPB	chr1:180896546-180896757	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:180900750-180900976	IMR90	lung:	n/a	chr1:180900833-180900846 chr1:180900833-180900844 chr1:180900835-180900846
25	CEBPB	chr1:180889975-180890175	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr1:180892189-180892449	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:180898522-180898836	HepG2	liver:	n/a	chr1:180898655-180898666
28	CEBPB	chr1:180892216-180892467	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:180892049-180892608	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:180889944-180890155	K562	blood:	n/a	n/a
31	CEBPB	chr1:180889566-180890254	K562	blood:	n/a	chr1:180889700-180889711
32	CEBPB	chr1:180900790-180900970	A549	lung:	n/a	chr1:180900833-180900846 chr1:180900833-180900844 chr1:180900835-180900846
33	CEBPB	chr1:180900784-180900887	Hela-S3	cervix:	n/a	chr1:180900833-180900846 chr1:180900833-180900844 chr1:180900835-180900846
34	CEBPB	chr1:180892229-180892495	K562	blood:	n/a	n/a
35	CEBPB	chr1:180900681-180901015	HepG2	liver:	n/a	chr1:180900833-180900846 chr1:180900833-180900844 chr1:180900835-180900846
36	CEBPB	chr1:180900694-180900983	K562	blood:	n/a	chr1:180900833-180900846 chr1:180900833-180900844 chr1:180900835-180900846
37	CEBPB	chr1:180889561-180890169	HepG2	liver:	n/a	chr1:180889700-180889711
38	CEBPD	chr1:180902205-180902849	K562	blood:	n/a	n/a
39	CEBPD	chr1:180902253-180902800	K562	blood:	n/a	n/a
40	CHD1	chr1:180903917-180903926	GM12878	blood:	n/a	n/a
41	CHD2	chr1:180903843-180904028	GM12878	blood:	n/a	n/a
42	CHD2	chr1:180895965-180895974	HepG2	liver:	n/a	n/a
43	CHD2	chr1:180904845-180904868	HepG2	liver:	n/a	n/a
44	CHD2	chr1:180892383-180892443	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr1:180894701-180895029	HepG2	liver:	n/a	n/a
46	CHD2	chr1:180892771-180892966	Hela-S3	cervix:	n/a	n/a
47	CREB1	chr1:180892118-180892704	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTBP2	chr1:180892209-180893022	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr1:180889928-180890145	GM19240	blood:	n/a	chr1:180890025-180890046 chr1:180890030-180890048
50	CTCF	chr1:180889956-180890124	GM10248	blood:	n/a	chr1:180890025-180890046 chr1:180890030-180890048

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:180895868-180895918	AG09309	skin:	n/a
2	chr1:180895868-180895918	AG09309	skin:	n/a
3	chr1:180904018-180904068	AG09309	skin:	n/a
4	chr1:180904703-180904753	T-47D	breast:	n/a
5	chr1:180904914-180904964	HEK293	kidney:	embryo
6	chr1:180904703-180904753	HNPCEpiC	eye:	n/a
7	chr1:180904677-180904727	AG10803	skin:	n/a
8	chr1:180895868-180895918	Caco-2	colon:	n/a
9	chr1:180904703-180904753	HEEpiC	esophagus:	n/a
10	chr1:180904914-180904964	AG04450	lung:	fetal
11	chr1:180904018-180904068	SK-N-SH_RA	brain:	n/a
12	chr1:180895868-180895918	HPAEpiC	pulmonary alveolar:	n/a
13	chr1:180895868-180895918	GM19239	blood:	n/a
14	chr1:180892623-180892673	A549	lung:	n/a
15	chr1:180892623-180892673	HL-60	blood:	n/a
16	chr1:180894260-180894310	HRE	kidney:	n/a
17	chr1:180904018-180904068	NHBE	bronchial:	n/a
18	chr1:180904677-180904727	HAEpiC	amniotic membrane:	n/a
19	chr1:180901423-180901473	CMK	blood:	n/a
20	chr1:180904018-180904068	CMK	blood:	n/a
21	chr1:180894260-180894310	ProgFib	skin:	n/a
22	chr1:180904914-180904964	IMR90	lung:	fetal
23	chr1:180904703-180904753	AoSMC	blood vessel:	n/a
24	chr1:180901423-180901473	AG04449	skin:	fetal
25	chr1:180892623-180892673	HepG2	liver:	n/a
26	chr1:180895868-180895918	SKMC	muscle:	n/a
27	chr1:180904914-180904964	HNPCEpiC	eye:	n/a
28	chr1:180892623-180892673	AG10803	skin:	n/a
29	chr1:180895868-180895918	PrEC	prostate:	n/a
30	chr1:180901423-180901473	HL-60	blood:	n/a
31	chr1:180904703-180904753	HRE	kidney:	n/a
32	chr1:180904914-180904964	BJ	skin:	n/a
33	chr1:180894260-180894310	AG09309	skin:	n/a
34	chr1:180904703-180904753	HAEpiC	amniotic membrane:	n/a
35	chr1:180895868-180895918	SK-N-MC	brain:	n/a
36	chr1:180904677-180904727	BJ	skin:	n/a
37	chr1:180904018-180904068	NT2-D1	testis:	n/a
38	chr1:180904703-180904753	NT2-D1	testis:	n/a
39	chr1:180904914-180904964	HRCEpiC	kidney:	n/a
40	chr1:180892623-180892673	LNCaP	prostate:	n/a
41	chr1:180892623-180892673	NHBE	bronchial:	n/a
42	chr1:180895868-180895918	HRCEpiC	kidney:	n/a
43	chr1:180894260-180894310	PFSK-1	brain:	n/a
44	chr1:180895868-180895918	AG04450	lung:	fetal
45	chr1:180894260-180894310	GM12878	blood:	n/a
46	chr1:180901423-180901473	K562	blood:	n/a
47	chr1:180901423-180901473	HUVEC	blood vessel:	n/a
48	chr1:180894260-180894310	CMK	blood:	n/a
49	chr1:180894260-180894310	ovcar-3	ovarian:	n/a
50	chr1:180904018-180904068	NHDF-neo	bronchial:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:180893588..180895646-chr1:181053051..181055501,3	MCF-7	breast:
2	chr1:180471074..180472830-chr1:180903461..180905741,2	MCF-7	breast:
3	chr1:180887952..180890108-chr1:181002346..181005032,2	MCF-7	breast:
4	chr1:180896933..180898442-chr1:180909661..180911964,2	MCF-7	breast:
5	chr1:180907561..180909890-chr1:180910550..180913382,3	K562	blood:
6	chr1:180894020..180896970-chr1:180921543..180923993,2	MCF-7	breast:
7	chr1:180888347..180891443-chr1:180893391..180896382,5	K562	blood:
8	chr1:180906727..180908421-chr1:180914394..180916378,2	K562	blood:
9	chr1:180880902..180883587-chr1:180884208..180886874,3	MCF-7	breast:
10	chr1:180850757..180851768-chr1:180886019..180887077,4	MCF-7	breast:
11	chr1:180903623..180906495-chr1:180908086..180910235,2	K562	blood:
12	chr1:180902276..180903975-chr1:180910710..180913163,2	K562	blood:
13	chr1:180898990..180902817-chr1:180903024..180908375,8	MCF-7	breast:
14	chr1:180469860..180472607-chr1:180890916..180893412,2	K562	blood:
15	chr1:180903603..180906339-chr1:180906763..180908593,2	MCF-7	breast:
16	chr1:180889227..180893527-chr1:180894947..180897442,3	MCF-7	breast:
17	chr1:180858397..180859188-chr1:180886465..180887001,2	MCF-7	breast:
18	chr1:180879805..180882226-chr1:180894957..180896873,2	MCF-7	breast:
19	chr1:180893606..180898291-chr1:180898738..180903047,8	K562	blood:
20	chr1:180898990..180902817-chr1:180903024..180908375,8	MCF-7	breast:
21	chr1:180888347..180891443-chr1:180893391..180896382,5	K562	blood:
22	chr1:180895591..180897824-chr1:181056738..181059275,3	MCF-7	breast:
23	chr1:180885638..180890175-chr1:180892218..180894358,4	MCF-7	breast:
24	chr1:180902411..180904358-chr1:180905767..180907490,2	K562	blood:
25	chr1:180907255..180908886-chr1:180910363..180913028,2	MCF-7	breast:
26	chr1:180892738..180895948-chr1:181056431..181059504,3	K562	blood:
27	chr1:180906727..180909279-chr1:180913509..180916378,2	K562	blood:
28	chr1:180885638..180890175-chr1:180892218..180894358,4	MCF-7	breast:
29	chr1:180893452..180895106-chr1:180898363..180900238,2	K562	blood:
30	chr1:180484648..180485397-chr1:180889598..180890483,3	K562	blood:
31	chr1:180888923..180890978-chr1:181056565..181059087,3	K562	blood:
32	chr1:180904867..180908227-chr1:180990589..180993954,4	MCF-7	breast:
33	chr1:180875236..180876989-chr1:180891969..180894800,2	K562	blood:
34	chr1:180901585..180904153-chr1:181057174..181059444,2	K562	blood:
35	chr1:180903603..180906339-chr1:180906763..180908593,2	MCF-7	breast:
36	chr1:180865980..180867777-chr1:180893565..180896342,2	K562	blood:
37	chr1:180902411..180904358-chr1:180905767..180907490,2	K562	blood:
38	chr1:180891831..180893938-chr1:180895346..180897268,3	K562	blood:
39	chr1:180907672..180909851-chr1:180910031..180911701,2	MCF-7	breast:
40	chr1:180900719..180903154-chr1:180917426..180920329,2	MCF-7	breast:
41	chr1:180875742..180876725-chr1:180890397..180891119,2	K562	blood:
42	chr1:180901050..180903975-chr1:180910710..180912524,2	K562	blood:
43	chr1:180891831..180893938-chr1:180895346..180897268,3	K562	blood:
44	chr1:180897298..180899956-chr1:180904454..180906228,2	K562	blood:
45	chr1:180887784..180890040-chr1:180897369..180898976,2	K562	blood:
46	chr1:180893452..180895106-chr1:180898363..180900238,2	K562	blood:
47	chr1:180892623..180894701-chr1:180898056..180900567,2	MCF-7	breast:
48	chr1:180892623..180894701-chr1:180898056..180900567,2	MCF-7	breast:
49	chr1:180887789..180890423-chr1:181056301..181058398,2	K562	blood:

No data

Variant related genes	Relation type
KIAA1614	TF binding region
KIAA1614	CpG island
ENSG00000135835	chromatin interactions
ENSG00000135823	chromatin interactions
ENSG00000135847	chromatin interactions
ENSG00000153029	chromatin interactions
ENSG00000162783	chromatin interactions
ENSG00000225857	chromatin interactions

Extended variants
information (count: 935 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:935 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556881046	chr1:180886760-180886761	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs188071778	chr1:180886770-180886771	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs192830545	chr1:180886781-180886782	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565022474	chr1:180886790-180886791	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532464687	chr1:180886800-180886801	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs3761905	chr1:180886810-180886811	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs569304151	chr1:180886817-180886818	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530324006	chr1:180886833-180886834	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs373079631	chr1:180886837-180886838	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs548589616	chr1:180886842-180886843	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs113168559	chr1:180886894-180886895	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs534575119	chr1:180886903-180886904	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs183950261	chr1:180886912-180886913	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs79422534	chr1:180886944-180886945	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs371291178	chr1:180886955-180886956	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs115549411	chr1:180886957-180886958	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs369406279	chr1:180886962-180886963	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs201506771	chr1:180886990-180886991	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs376376187	chr1:180887018-180887019	Bivalent Enhancer Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200852158	chr1:180887034-180887035	Bivalent Enhancer Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377498784	chr1:180887039-180887040	Bivalent Enhancer Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200591163	chr1:180887040-180887041	Bivalent Enhancer Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542848675	chr1:180887070-180887071	Bivalent Enhancer Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532774950	chr1:180887140-180887141	Bivalent Enhancer Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76042657	chr1:180887142-180887143	Bivalent Enhancer Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540152106	chr1:180887173-180887174	Bivalent Enhancer Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375334021	chr1:180887175-180887176	Bivalent Enhancer Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566260660	chr1:180887178-180887179	Bivalent Enhancer Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115660111	chr1:180887183-180887184	Bivalent Enhancer Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373008671	chr1:180887203-180887204	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138111787	chr1:180887226-180887227	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544337189	chr1:180887240-180887241	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563038031	chr1:180887287-180887288	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530225878	chr1:180887288-180887289	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7551076	chr1:180887289-180887290	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs567159162	chr1:180887298-180887299	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13374657	chr1:180887377-180887378	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs552928002	chr1:180887378-180887379	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571218530	chr1:180887397-180887398	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74133669	chr1:180887406-180887407	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs114284556	chr1:180887420-180887421	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568980628	chr1:180887424-180887425	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536037983	chr1:180887432-180887433	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74335891	chr1:180887475-180887476	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375395556	chr1:180887477-180887478	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189117831	chr1:180887490-180887491	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558437538	chr1:180887509-180887510	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573560949	chr1:180887533-180887534	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191998632	chr1:180887538-180887539	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145235430	chr1:180887545-180887546	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	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
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Renal cell carcinoma	18765545	CNVD
Nephroblastoma	17189400	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:888 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180882400-180894600	Weak transcription	Pancreas	Pancrea
2	chr1:180882600-180894000	Weak transcription	Brain Substantia Nigra	brain
3	chr1:180882800-180887000	Weak transcription	Spleen	Spleen
4	chr1:180882800-180887200	Weak transcription	Placenta	Placenta
5	chr1:180882800-180887400	Weak transcription	Gastric	stomach
6	chr1:180882800-180888000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:180882800-180889400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:180882800-180891200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr1:180882800-180892600	Weak transcription	Esophagus	oesophagus
10	chr1:180882800-180894400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr1:180883000-180886800	Weak transcription	HSMMtube	muscle
12	chr1:180883000-180891200	Weak transcription	Fetal Brain Female	brain
13	chr1:180883000-180891600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:180883000-180892200	Weak transcription	Brain Germinal Matrix	brain
15	chr1:180883000-180894600	Weak transcription	Right Ventricle	heart
16	chr1:180883000-180894800	Weak transcription	Colonic Mucosa	Colon
17	chr1:180883200-180892200	Weak transcription	Right Atrium	heart
18	chr1:180883200-180894200	Weak transcription	Brain Angular Gyrus	brain
19	chr1:180883400-180887800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr1:180883400-180892600	Weak transcription	Brain Hippocampus Middle	brain
21	chr1:180883600-180886800	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:180883600-180886800	Weak transcription	Left Ventricle	heart
23	chr1:180883600-180887200	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr1:180883600-180887600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:180883600-180888600	Weak transcription	Colon Smooth Muscle	Colon
26	chr1:180883600-180891800	Weak transcription	HSMM	muscle
27	chr1:180883600-180892000	Weak transcription	Fetal Heart	heart
28	chr1:180883600-180892200	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr1:180883600-180894200	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr1:180883600-180894200	Weak transcription	Fetal Lung	lung
31	chr1:180883600-180894800	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr1:180883600-180895000	Weak transcription	Rectal Smooth Muscle	rectum
33	chr1:180885000-180886800	Strong transcription	Stomach Smooth Muscle	stomach
34	chr1:180885000-180887200	Strong transcription	Ovary	ovary
35	chr1:180885200-180887400	Weak transcription	K562	blood
36	chr1:180885200-180891000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr1:180885400-180887600	Strong transcription	Osteobl	bone
38	chr1:180885400-180888200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr1:180885400-180889600	Genic enhancers	Fetal Muscle Trunk	muscle
40	chr1:180885400-180891200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:180885600-180887200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr1:180885600-180887800	Strong transcription	Adipose Nuclei	Adipose
43	chr1:180885600-180887800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr1:180885600-180888200	Strong transcription	Placenta Amnion	Placenta Amnion
45	chr1:180885600-180888400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr1:180885600-180888400	Strong transcription	Aorta	Aorta
47	chr1:180885600-180889600	Strong transcription	Fetal Intestine Small	intestine
48	chr1:180885800-180887600	Strong transcription	Lung	lung
49	chr1:180885800-180887800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:180885800-180889600	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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