Variant report

Variant	nsv1017511
Chromosome Location	chr8:1840497-1865887
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:1840485-1840774	K562	blood:	n/a	n/a
2	ATF2	chr8:1845619-1845955	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:1845258-1845710	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr8:1843208-1843523	GM12878	blood:	n/a	chr8:1843399-1843410
5	BHLHE40	chr8:1840626-1841001	K562	blood:	n/a	n/a
6	BHLHE40	chr8:1840627-1840944	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:1840631-1840990	HepG2	liver:	n/a	n/a
8	BRCA1	chr8:1840792-1840848	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:1843162-1843456	A549	lung:	n/a	chr8:1843289-1843300
10	CEBPB	chr8:1840650-1840906	K562	blood:	n/a	n/a
11	CEBPB	chr8:1843168-1843469	K562	blood:	n/a	chr8:1843289-1843300
12	CEBPB	chr8:1843202-1843426	MCF-7	breast:	n/a	chr8:1843289-1843300
13	CEBPB	chr8:1840538-1840820	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr8:1843200-1843355	HepG2	liver:	n/a	chr8:1843289-1843300
15	CEBPB	chr8:1843168-1843414	H1-hESC	embryonic stem cell:	n/a	chr8:1843289-1843300
16	CEBPB	chr8:1843136-1843472	Hela-S3	cervix:	n/a	chr8:1843289-1843300
17	CEBPB	chr8:1843045-1843547	IMR90	lung:	n/a	chr8:1843070-1843083 chr8:1843289-1843300 chr8:1843070-1843081
18	CEBPB	chr8:1843055-1843495	A549	lung:	n/a	chr8:1843070-1843083 chr8:1843289-1843300 chr8:1843070-1843081
19	CEBPB	chr8:1843116-1843481	HepG2	liver:	n/a	chr8:1843289-1843300
20	CTCF	chr8:1840598-1840863	HepG2	liver:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
21	CTCF	chr8:1840620-1840770	GM12872	blood:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
22	CTCF	chr8:1840620-1840770	WI-38	lung:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
23	CTCF	chr8:1840610-1840854	HepG2	liver:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
24	CTCF	chr8:1840656-1840881	GM12892	blood:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
25	CTCF	chr8:1840640-1840790	AG04449	skin:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
26	CTCF	chr8:1840640-1840790	Caco-2	colon:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
27	CTCF	chr8:1840629-1841036	K562	blood:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
28	CTCF	chr8:1840678-1840884	MCF-7	breast:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
29	CTCF	chr8:1843260-1843410	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr8:1840591-1840865	LNCaP	prostate:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
31	CTCF	chr8:1840201-1841282	SK-N-SH	brain:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
32	CTCF	chr8:1845700-1845850	K562	blood:	n/a	n/a
33	CTCF	chr8:1840620-1840770	HPF	lung:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
34	CTCF	chr8:1840620-1840770	GM12870	blood:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
35	CTCF	chr8:1840660-1840810	HEK293	kidney:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
36	CTCF	chr8:1840660-1840810	GM12866	blood:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
37	CTCF	chr8:1840620-1840770	AoAF	blood vessel:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
38	CTCF	chr8:1845680-1845830	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr8:1845500-1845650	AG04450	lung:	n/a	n/a
40	CTCF	chr8:1840576-1840889	K562	blood:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
41	CTCF	chr8:1845500-1845650	K562	blood:	n/a	n/a
42	CTCF	chr8:1840680-1840830	HEK293	kidney:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
43	CTCF	chr8:1845607-1845847	Gliobla	brain:	n/a	n/a
44	CTCF	chr8:1840640-1840790	HMEC	breast:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
45	CTCF	chr8:1845624-1845847	Medullo	brain:	n/a	n/a
46	CTCF	chr8:1845700-1845850	HPF	lung:	n/a	n/a
47	CTCF	chr8:1845754-1845763	NHEK	skin:	n/a	n/a
48	CTCF	chr8:1845540-1845690	HCM	heart:	n/a	n/a
49	CTCF	chr8:1845760-1845910	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr8:1840640-1840790	HepG2	liver:	n/a	chr8:1840715-1840733 chr8:1840717-1840738

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1848040-1848090	HNPCEpiC	eye:	n/a
2	chr8:1854795-1854845	HepG2	liver:	n/a
3	chr8:1854795-1854845	HCM	heart:	n/a
4	chr8:1864390-1864440	SKMC	muscle:	n/a
5	chr8:1848040-1848090	HNPCEpiC	eye:	n/a
6	chr8:1854795-1854845	HepG2	liver:	n/a
7	chr8:1854795-1854845	HCM	heart:	n/a
8	chr8:1864390-1864440	SKMC	muscle:	n/a
9	chr8:1848040-1848090	HEEpiC	esophagus:	n/a
10	chr8:1848741-1848791	HCPEpiC	choroid plexus:	n/a
11	chr8:1862499-1862549	HCF	heart:	n/a
12	chr8:1854947-1854997	T-47D	breast:	n/a
13	chr8:1854608-1854658	HCPEpiC	choroid plexus:	n/a
14	chr8:1864390-1864440	HCPEpiC	choroid plexus:	n/a
15	chr8:1857241-1857291	PANC-1	pancreas:	n/a
16	chr8:1857177-1857227	NB4	blood:	n/a
17	chr8:1861064-1861114	NHDF-neo	bronchial:	n/a
18	chr8:1847999-1848049	SKMC	muscle:	n/a
19	chr8:1860765-1860815	AG10803	skin:	n/a
20	chr8:1860765-1860815	AG09319	gingival:	n/a
21	chr8:1850925-1850975	HIPEpiC	eye:	n/a
22	chr8:1862499-1862549	HPAEpiC	pulmonary alveolar:	n/a
23	chr8:1861037-1861087	HCF	heart:	n/a
24	chr8:1845250-1845300	NHBE	bronchial:	n/a
25	chr8:1857569-1857619	Caco-2	colon:	n/a
26	chr8:1848040-1848090	A549	lung:	n/a
27	chr8:1857688-1857738	PFSK-1	brain:	n/a
28	chr8:1850864-1850914	HUVEC	blood vessel:	n/a
29	chr8:1847999-1848049	K562	blood:	n/a
30	chr8:1857839-1857889	ECC-1	luminal epithelium:	n/a
31	chr8:1845250-1845300	Hepatocyte	liver:	n/a
32	chr8:1847999-1848049	NHBE	bronchial:	n/a
33	chr8:1857212-1857262	ovcar-3	ovarian:	n/a
34	chr8:1851026-1851076	HUVEC	blood vessel:	n/a
35	chr8:1861064-1861114	GM12892	blood:	n/a
36	chr8:1850322-1850372	HCT-116	colon:	n/a
37	chr8:1860765-1860815	NHDF-neo	bronchial:	n/a
38	chr8:1857839-1857889	HMEC	breast:	n/a
39	chr8:1857177-1857227	BE2_C	brain:	n/a
40	chr8:1848741-1848791	PrEC	prostate:	n/a
41	chr8:1854947-1854997	SAEC	small airway:	n/a
42	chr8:1854795-1854845	NB4	blood:	n/a
43	chr8:1857839-1857889	IMR90	lung:	fetal
44	chr8:1862499-1862549	Hela-S3	cervix:	n/a
45	chr8:1853599-1853649	A549	lung:	n/a
46	chr8:1864390-1864440	SK-N-SH	brain:	n/a
47	chr8:1854947-1854997	BE2_C	brain:	n/a
48	chr8:1862572-1862622	ECC-1	luminal epithelium:	n/a
49	chr8:1848741-1848791	SKMC	muscle:	n/a
50	chr8:1850463-1850513	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:1840317..1841126-chr8:2027343..2028221,2	MCF-7	breast:
2	chr8:1843830..1846046-chr8:1856723..1858500,2	MCF-7	breast:
3	chr8:1849167..1851254-chr8:1973705..1975822,2	MCF-7	breast:
4	chr8:1848105..1850497-chr8:1856585..1858723,2	K562	blood:
5	chr8:1842826..1843459-chr8:1992468..1993115,2	K562	blood:
6	chr8:1843830..1846046-chr8:1856723..1858500,2	MCF-7	breast:
7	chr8:1840277..1841232-chr8:1978419..1979386,5	K562	blood:
8	chr8:1839446..1841757-chr8:1844731..1847507,2	MCF-7	breast:
9	chr8:1856064..1857841-chr8:1860067..1862495,2	K562	blood:
10	chr8:1840240..1841043-chr8:1971863..1972750,4	MCF-7	breast:
11	chr8:1845240..1845932-chr8:1971897..1973021,5	MCF-7	breast:
12	chr8:1848105..1850497-chr8:1856585..1858723,2	K562	blood:
13	chr8:1862307..1864338-chr8:1926078..1927839,2	K562	blood:
14	chr8:1840257..1840999-chr8:1978353..1979355,3	MCF-7	breast:
15	chr8:1839446..1841757-chr8:1844731..1847507,2	MCF-7	breast:
16	chr8:1845361..1846326-chr8:1971978..1972609,2	MCF-7	breast:
17	chr8:1839403..1841214-chr8:1971479..1972941,9	K562	blood:
18	chr8:1848233..1850462-chr8:1857880..1860759,2	MCF-7	breast:
19	chr8:1856064..1857841-chr8:1860067..1862495,2	K562	blood:
20	chr8:1846010..1848656-chr8:1851814..1854261,2	K562	blood:
21	chr8:1839996..1842403-chr8:1970017..1972283,2	K562	blood:
22	chr8:1845253..1846025-chr8:1978398..1979174,5	MCF-7	breast:
23	chr8:1848233..1850462-chr8:1857880..1860759,2	MCF-7	breast:

Variant related genes	Relation type
ARHGEF10	TF binding region
ARHGEF10	CpG island
ENSG00000104728	chromatin interactions

Extended variants
information (count: 1622 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:1622 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6558560	chr8:1840497-1840498	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs568046139	chr8:1840506-1840507	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs11774726	chr8:1840560-1840561	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369018175	chr8:1840565-1840566	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550598262	chr8:1840600-1840601	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs193168489	chr8:1840621-1840622	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs185297741	chr8:1840646-1840647	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs539077226	chr8:1840649-1840650	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs552766827	chr8:1840671-1840672	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs565809428	chr8:1840673-1840674	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs4242520	chr8:1840697-1840698	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs554680642	chr8:1840698-1840699	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs574734613	chr8:1840718-1840719	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs553900874	chr8:1840720-1840721	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs78371477	chr8:1840733-1840734	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs557327865	chr8:1840748-1840749	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs577480346	chr8:1840750-1840751	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs188994990	chr8:1840757-1840758	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs113018913	chr8:1840769-1840770	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs377356207	chr8:1840794-1840795	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs541936003	chr8:1840827-1840828	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs561867986	chr8:1840831-1840832	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs532161335	chr8:1840832-1840833	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs530420636	chr8:1840837-1840838	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs4875939	chr8:1840856-1840857	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs202081826	chr8:1840866-1840867	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs200989387	chr8:1840867-1840868	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs113963205	chr8:1840868-1840869	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs567321290	chr8:1840881-1840882	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs73671030	chr8:1840903-1840904	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs145659675	chr8:1840906-1840907	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs370652704	chr8:1840921-1840922	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs75895242	chr8:1840927-1840928	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs567846768	chr8:1840928-1840929	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs182087224	chr8:1840932-1840933	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs73671031	chr8:1840934-1840935	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs375424117	chr8:1840942-1840943	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs6420198	chr8:1840952-1840953	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs568584359	chr8:1840977-1840978	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs571376203	chr8:1840978-1840979	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs145399329	chr8:1841002-1841003	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557355679	chr8:1841004-1841005	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184890102	chr8:1841025-1841026	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546486807	chr8:1841042-1841043	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553713302	chr8:1841043-1841044	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566654482	chr8:1841044-1841045	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188331449	chr8:1841047-1841048	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535777898	chr8:1841054-1841055	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs149225743	chr8:1841085-1841086	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs143402036	chr8:1841088-1841089	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
Tetralogy of Fallot	22912587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1065 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1774000-1845000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr8:1802200-1845000	Weak transcription	Right Atrium	heart
3	chr8:1806000-1844000	Strong transcription	HUES48 Cell Line	embryonic stem cell
4	chr8:1808600-1848400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr8:1813000-1840800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr8:1816200-1845000	Weak transcription	Hela-S3	cervix
7	chr8:1819000-1853200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr8:1820200-1842800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr8:1822000-1844000	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr8:1822200-1844400	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr8:1822800-1858200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr8:1824400-1841000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr8:1824400-1864800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr8:1827800-1844000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
15	chr8:1828600-1858800	Weak transcription	Colonic Mucosa	Colon
16	chr8:1831400-1840800	Weak transcription	Fetal Heart	heart
17	chr8:1832000-1841600	Weak transcription	NHDF-Ad	bronchial
18	chr8:1832400-1840800	Weak transcription	Stomach Mucosa	stomach
19	chr8:1832600-1842400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr8:1833800-1844000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:1835000-1840800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr8:1835200-1844800	Weak transcription	Placenta	Placenta
23	chr8:1835200-1845000	Weak transcription	Colon Smooth Muscle	Colon
24	chr8:1835400-1840800	Weak transcription	Duodenum Mucosa	Duodenum
25	chr8:1835400-1842800	Weak transcription	HMEC	breast
26	chr8:1835600-1840800	Weak transcription	Fetal Intestine Large	intestine
27	chr8:1835600-1842600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr8:1835800-1842400	Weak transcription	A549	lung
29	chr8:1836000-1842600	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr8:1836000-1844000	Weak transcription	Fetal Intestine Small	intestine
31	chr8:1836200-1842400	Weak transcription	Left Ventricle	heart
32	chr8:1836200-1842600	Weak transcription	HSMMtube	muscle
33	chr8:1836200-1857400	Weak transcription	Esophagus	oesophagus
34	chr8:1836400-1852800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr8:1836600-1843200	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:1836800-1840600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr8:1836800-1842800	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr8:1837200-1842600	Weak transcription	Fetal Kidney	kidney
39	chr8:1837200-1842600	Weak transcription	Right Ventricle	heart
40	chr8:1837200-1844800	Weak transcription	Brain Germinal Matrix	brain
41	chr8:1837400-1840600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr8:1837400-1840800	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr8:1837400-1843600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr8:1838000-1844000	Strong transcription	H1 Cell Line	embryonic stem cell
45	chr8:1838200-1842600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:1838400-1840800	Weak transcription	Gastric	stomach
47	chr8:1838400-1842400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr8:1838400-1842600	Weak transcription	Fetal Lung	lung
49	chr8:1838600-1840800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr8:1838600-1842600	Weak transcription	Rectal Smooth Muscle	rectum

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