Variant report

Variant	nsv932825
Chromosome Location	chr8:1719042-1736355
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:570)
CpG islands
(count:1282)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:1727822-1728089	K562	blood:	n/a	n/a
2	BHLHE40	chr8:1729550-1729628	K562	blood:	n/a	n/a
3	BHLHE40	chr8:1732351-1732747	K562	blood:	n/a	n/a
4	BHLHE40	chr8:1729475-1729683	GM12878	blood:	n/a	n/a
5	BHLHE40	chr8:1726728-1727045	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:1727897-1727984	K562	blood:	n/a	n/a
7	BRCA1	chr8:1734613-1734971	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr8:1734511-1735187	HCT-116	colon:	n/a	n/a
9	CCNT2	chr8:1731827-1732163	K562	blood:	n/a	n/a
10	CEBPB	chr8:1731898-1732129	A549	lung:	n/a	n/a
11	CEBPB	chr8:1731898-1732180	IMR90	lung:	n/a	n/a
12	CEBPB	chr8:1725045-1725355	IMR90	lung:	n/a	n/a
13	CEBPB	chr8:1725040-1725374	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:1731417-1731642	H1-hESC	embryonic stem cell:	n/a	chr8:1731530-1731541
15	CEBPB	chr8:1731355-1731690	IMR90	lung:	n/a	chr8:1731530-1731541
16	CEBPB	chr8:1725043-1725375	A549	lung:	n/a	n/a
17	CEBPB	chr8:1734391-1735062	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr8:1729652-1729857	HepG2	liver:	n/a	chr8:1729788-1729799
19	CEBPB	chr8:1731387-1732146	K562	blood:	n/a	chr8:1731530-1731541
20	CEBPB	chr8:1731871-1732174	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:1731368-1731671	HepG2	liver:	n/a	chr8:1731530-1731541
22	CEBPB	chr8:1725192-1725262	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr8:1734736-1735301	IMR90	lung:	n/a	n/a
24	CHD2	chr8:1729564-1729744	GM12878	blood:	n/a	n/a
25	CHD2	chr8:1736068-1736166	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr8:1734234-1734950	Hela-S3	cervix:	n/a	n/a
27	CREB1	chr8:1727754-1728073	K562	blood:	n/a	n/a
28	CTCF	chr8:1729560-1729710	HCT-116	colon:	n/a	n/a
29	CTCF	chr8:1729489-1729721	LNCaP	prostate:	n/a	n/a
30	CTCF	chr8:1729620-1729770	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr8:1729475-1729712	GM19239	blood:	n/a	n/a
32	CTCF	chr8:1729540-1729690	HPF	lung:	n/a	n/a
33	CTCF	chr8:1729560-1729710	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr8:1729560-1729710	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr8:1729600-1729750	HVMF	connective:	n/a	n/a
36	CTCF	chr8:1727800-1727950	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr8:1729520-1729670	HCM	heart:	n/a	n/a
38	CTCF	chr8:1729872-1729924	K562	blood:	n/a	n/a
39	CTCF	chr8:1729780-1729930	GM12864	blood:	n/a	n/a
40	CTCF	chr8:1729840-1729990	GM12867	blood:	n/a	n/a
41	CTCF	chr8:1729560-1729710	AG09309	skin:	n/a	n/a
42	CTCF	chr8:1729860-1730010	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr8:1729540-1729690	GM12870	blood:	n/a	n/a
44	CTCF	chr8:1729386-1729881	K562	blood:	n/a	n/a
45	CTCF	chr8:1729481-1729870	Lung_OC	lung:	n/a	n/a
46	CTCF	chr8:1729477-1729708	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr8:1729880-1730030	HPF	lung:	n/a	n/a
48	CTCF	chr8:1729504-1729689	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:1729840-1729990	GM12872	blood:	n/a	n/a
50	CTCF	chr8:1729540-1729690	MCF-7	breast:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1725179-1725229	RPTEC	kidney:	n/a
2	chr8:1725179-1725229	RPTEC	kidney:	n/a
3	chr8:1732011-1732061	HNPCEpiC	eye:	n/a
4	chr8:1728703-1728753	PrEC	prostate:	n/a
5	chr8:1734990-1735040	T-47D	breast:	n/a
6	chr8:1719380-1719430	AG04449	skin:	fetal
7	chr8:1728703-1728753	NHBE	bronchial:	n/a
8	chr8:1725179-1725229	A549	lung:	n/a
9	chr8:1733883-1733933	HMEC	breast:	n/a
10	chr8:1729607-1729657	GM06990	blood:	n/a
11	chr8:1734990-1735040	HIPEpiC	eye:	n/a
12	chr8:1725140-1725190	AG04449	skin:	fetal
13	chr8:1731923-1731973	SK-N-MC	brain:	n/a
14	chr8:1732043-1732093	HCM	heart:	n/a
15	chr8:1732043-1732093	HRCEpiC	kidney:	n/a
16	chr8:1725119-1725169	SK-N-SH_RA	brain:	n/a
17	chr8:1725179-1725229	AG04449	skin:	fetal
18	chr8:1728777-1728827	SK-N-SH_RA	brain:	n/a
19	chr8:1731480-1731530	HRPEpiC	eye:	n/a
20	chr8:1734990-1735040	GM12878	blood:	n/a
21	chr8:1733475-1733525	Hepatocyte	liver:	n/a
22	chr8:1733369-1733419	U87	brain:	n/a
23	chr8:1725140-1725190	SKMC	muscle:	n/a
24	chr8:1731776-1731826	HCM	heart:	n/a
25	chr8:1728777-1728827	Caco-2	colon:	n/a
26	chr8:1726903-1726953	NHBE	bronchial:	n/a
27	chr8:1725140-1725190	SAEC	small airway:	n/a
28	chr8:1719290-1719340	IMR90	lung:	fetal
29	chr8:1733369-1733419	RPTEC	kidney:	n/a
30	chr8:1733475-1733525	SK-N-SH	brain:	n/a
31	chr8:1733883-1733933	Caco-2	colon:	n/a
32	chr8:1725179-1725229	PANC-1	pancreas:	n/a
33	chr8:1719543-1719593	IMR90	lung:	fetal
34	chr8:1733497-1733547	GM06990	blood:	n/a
35	chr8:1728777-1728827	AG04450	lung:	fetal
36	chr8:1733369-1733419	AG04450	lung:	fetal
37	chr8:1731776-1731826	GM06990	blood:	n/a
38	chr8:1719380-1719430	HRPEpiC	eye:	n/a
39	chr8:1733475-1733525	NT2-D1	testis:	n/a
40	chr8:1719380-1719430	GM12892	blood:	n/a
41	chr8:1732011-1732061	HUVEC	blood vessel:	n/a
42	chr8:1731923-1731973	HepG2	liver:	n/a
43	chr8:1719290-1719340	BJ	skin:	n/a
44	chr8:1733475-1733525	HIPEpiC	eye:	n/a
45	chr8:1733475-1733525	ovcar-3	ovarian:	n/a
46	chr8:1732043-1732093	GM12891	blood:	n/a
47	chr8:1725119-1725169	HEK293	kidney:	embryo
48	chr8:1728703-1728753	ProgFib	skin:	n/a
49	chr8:1732011-1732061	HEK293	kidney:	embryo
50	chr8:1725179-1725229	H1-hESC	embryonic stem cell:	embryo

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:1722780..1724453-chr8:1725815..1728009,2	K562	blood:
2	chr8:1717537..1720996-chr8:1730538..1734244,3	K562	blood:
3	chr8:1686924..1688783-chr8:1724884..1727054,2	MCF-7	breast:
4	chr8:1711365..1714898-chr8:1724612..1727757,4	MCF-7	breast:
5	chr8:1731431..1734296-chr8:1777100..1779564,2	MCF-7	breast:
6	chr8:1727131..1730202-chr8:1731838..1734952,3	K562	blood:
7	chr8:1722706..1724431-chr8:1770529..1772406,2	K562	blood:
8	chr8:1717744..1722491-chr8:1723636..1726849,4	MCF-7	breast:
9	chr8:1732905..1734705-chr8:1740621..1742810,2	K562	blood:
10	chr8:1711245..1713893-chr8:1726417..1729246,3	K562	blood:
11	chr8:1683449..1684285-chr8:1729073..1729982,8	K562	blood:
12	chr8:1710504..1712824-chr8:1729569..1731370,2	MCF-7	breast:
13	chr8:1722780..1724453-chr8:1725815..1728009,2	K562	blood:
14	chr8:1715615..1723539-chr8:1723885..1728177,9	MCF-7	breast:
15	chr8:1727131..1730202-chr8:1731838..1734952,3	K562	blood:
16	chr8:1716952..1719420-chr8:1723630..1725290,2	K562	blood:
17	chr8:1678487..1679403-chr8:1728856..1729643,2	K562	blood:
18	chr8:1710662..1713548-chr8:1734331..1736456,2	MCF-7	breast:
19	chr8:1711348..1713797-chr8:1729621..1731445,2	K562	blood:
20	chr8:1725864..1728236-chr8:1731701..1733830,2	MCF-7	breast:
21	chr8:1731117..1733181-chr8:1735872..1737982,3	K562	blood:
22	chr8:1690830..1693396-chr8:1731671..1734648,2	K562	blood:
23	chr8:1734427..1736636-chr8:1737511..1739234,2	K562	blood:
24	chr8:1715604..1719309-chr8:1719775..1722697,3	MCF-7	breast:
25	chr8:1725330..1728287-chr8:1728724..1731820,3	K562	blood:
26	chr8:1681316..1685438-chr8:1724958..1729595,5	K562	blood:
27	chr8:1725864..1728236-chr8:1731701..1733830,2	MCF-7	breast:
28	chr8:1716816..1721615-chr8:1726505..1732038,6	K562	blood:
29	chr8:1712944..1715681-chr8:1734053..1736692,2	K562	blood:
30	chr8:1716779..1719807-chr8:1720104..1723417,3	K562	blood:
31	chr8:1731117..1733181-chr8:1735872..1737982,3	K562	blood:
32	chr8:1692732..1694940-chr8:1731254..1732794,2	MCF-7	breast:
33	chr8:1730297..1733181-chr8:1733346..1737804,5	K562	blood:
34	chr8:1726532..1728287-chr8:1729917..1731820,2	K562	blood:
35	chr8:1726321..1728354-chr8:1771384..1774203,2	MCF-7	breast:
36	chr8:1683298..1684246-chr8:1728731..1730059,4	MCF-7	breast:
37	chr8:1710542..1713448-chr8:1725280..1729246,5	K562	blood:
38	chr8:1717537..1720996-chr8:1730538..1734244,3	K562	blood:
39	chr8:1726532..1728287-chr8:1729917..1731820,2	K562	blood:
40	chr8:1730297..1733181-chr8:1733346..1737804,5	K562	blood:
41	chr8:1712198..1712991-chr8:1724016..1724625,2	K562	blood:
42	chr8:1683305..1684236-chr8:1728901..1729771,3	MCF-7	breast:
43	chr8:1691178..1695166-chr8:1727484..1730315,3	MCF-7	breast:
44	chr8:1728494..1731142-chr8:1732363..1735530,3	MCF-7	breast:
45	chr8:1725330..1728287-chr8:1728724..1731820,3	K562	blood:
46	chr8:1716952..1719420-chr8:1723630..1725290,2	K562	blood:
47	chr8:1728494..1731142-chr8:1732363..1735530,3	MCF-7	breast:

No data

Variant related genes	Relation type
CLN8	TF binding region
CLN8	CpG island
ENSG00000104728	chromatin interactions
ENSG00000253982	chromatin interactions
ENSG00000182372	chromatin interactions

Extended variants
information (count: 994 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:994 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573279536	chr8:1719045-1719046	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs542253440	chr8:1719059-1719060	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs148754057	chr8:1719062-1719063	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs114189810	chr8:1719094-1719095	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs374723418	chr8:1719108-1719109	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs564362499	chr8:1719112-1719113	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs532828506	chr8:1719121-1719122	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs184346819	chr8:1719131-1719132	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs566084111	chr8:1719150-1719151	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374522261	chr8:1719175-1719176	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs543839915	chr8:1719180-1719181	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs370711548	chr8:1719181-1719182	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs557682976	chr8:1719186-1719187	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs143730802	chr8:1719221-1719222	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs147181589	chr8:1719231-1719232	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs368792081	chr8:1719232-1719233	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs374597781	chr8:1719235-1719236	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs200999640	chr8:1719236-1719237	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs536738656	chr8:1719237-1719238	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs386834129	chr8:1719266-1719267	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs148668081	chr8:1719270-1719271	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs142104002	chr8:1719273-1719274	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs34238807	chr8:1719281-1719282	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs386834137	chr8:1719286-1719287	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs104894064	chr8:1719290-1719291	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs148763945	chr8:1719304-1719305	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs386834139	chr8:1719308-1719309	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs376382403	chr8:1719310-1719311	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs150754905	chr8:1719319-1719320	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs370199508	chr8:1719332-1719333	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201670636	chr8:1719337-1719338	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs192196274	chr8:1719346-1719347	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs541840243	chr8:1719347-1719348	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs555757531	chr8:1719367-1719368	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs372268977	chr8:1719381-1719382	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs386834123	chr8:1719400-1719401	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs201327850	chr8:1719407-1719408	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs373957283	chr8:1719420-1719421	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs575820157	chr8:1719421-1719422	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs368365607	chr8:1719427-1719428	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs386834124	chr8:1719429-1719430	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs386834125	chr8:1719447-1719448	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs144015378	chr8:1719466-1719467	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs146424314	chr8:1719488-1719489	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs561448346	chr8:1719490-1719491	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs34030778	chr8:1719494-1719495	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs372313992	chr8:1719499-1719500	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs143918546	chr8:1719500-1719501	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs533351136	chr8:1719508-1719509	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs116605307	chr8:1719510-1719511	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Ovarian cancer	22355333	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Tetralogy of Fallot	22912587	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1132 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1713000-1719200	Weak transcription	Ovary	ovary
2	chr8:1713400-1719600	Weak transcription	Colon Smooth Muscle	Colon
3	chr8:1713400-1721000	Weak transcription	Psoas Muscle	Psoas
4	chr8:1713400-1727000	Weak transcription	NHDF-Ad	bronchial
5	chr8:1713400-1735800	Weak transcription	Fetal Brain Male	brain
6	chr8:1713600-1719200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr8:1713600-1719200	Weak transcription	Brain Germinal Matrix	brain
8	chr8:1713600-1719200	Weak transcription	Fetal Brain Female	brain
9	chr8:1713600-1719400	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr8:1713600-1719400	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr8:1713600-1719400	Weak transcription	Osteobl	bone
12	chr8:1713600-1721400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr8:1713600-1729600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr8:1713800-1719200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr8:1714000-1728000	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr8:1714000-1729800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr8:1714400-1729200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr8:1714800-1720000	Strong transcription	Primary T cells from cord blood	blood
19	chr8:1714800-1727000	Strong transcription	Fetal Intestine Small	intestine
20	chr8:1715200-1719600	Weak transcription	Dnd41	blood
21	chr8:1715400-1719200	Weak transcription	Thymus	Thymus
22	chr8:1715400-1726800	Strong transcription	Fetal Stomach	stomach
23	chr8:1715400-1727800	Weak transcription	Small Intestine	intestine
24	chr8:1715400-1729200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr8:1715600-1719200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr8:1715600-1719200	Weak transcription	Fetal Thymus	thymus
27	chr8:1715600-1725600	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr8:1716200-1719600	Weak transcription	GM12878-XiMat	blood
29	chr8:1716400-1726800	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr8:1716600-1719800	Genic enhancers	Primary B cells from peripheral blood	blood
31	chr8:1716600-1723000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr8:1716600-1725200	Strong transcription	Duodenum Mucosa	Duodenum
33	chr8:1716600-1727000	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr8:1716800-1721000	Strong transcription	Liver	Liver
35	chr8:1716800-1721200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr8:1716800-1722000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr8:1717000-1724600	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr8:1717000-1724600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr8:1717200-1722400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr8:1717400-1719200	Weak transcription	Colonic Mucosa	Colon
41	chr8:1717400-1719200	Weak transcription	NHLF	lung
42	chr8:1717400-1728400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr8:1717600-1719200	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr8:1717600-1719200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:1717600-1719200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr8:1717600-1719200	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr8:1717600-1719400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr8:1717600-1721000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr8:1717600-1721000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr8:1717600-1722000	Weak transcription	HSMMtube	muscle

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