Variant report

Variant	nsv609527
Chromosome Location	chr8:1681733-1753497
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2832)
CpG islands
(count:3114)
Chromatin interactive
region (count:124)
LncRNA
region (count:20)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2832 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:1693302-1694253	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:1710733-1711272	K562	blood:	n/a	n/a
3	ARID3A	chr8:1698531-1698750	K562	blood:	n/a	n/a
4	ARID3A	chr8:1703564-1704299	K562	blood:	n/a	n/a
5	ARID3A	chr8:1693554-1694651	K562	blood:	n/a	n/a
6	ARID3A	chr8:1748328-1748700	K562	blood:	n/a	n/a
7	ARID3A	chr8:1707125-1707584	K562	blood:	n/a	n/a
8	ARID3A	chr8:1712466-1712804	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:1683588-1683957	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:1703700-1704244	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:1708103-1708744	K562	blood:	n/a	n/a
12	ARID3A	chr8:1690095-1690840	HepG2	liver:	n/a	n/a
13	ARID3A	chr8:1706530-1706868	K562	blood:	n/a	n/a
14	ARID3A	chr8:1700948-1701221	HepG2	liver:	n/a	n/a
15	ATF1	chr8:1708076-1708663	K562	blood:	n/a	n/a
16	ATF1	chr8:1748612-1748850	K562	blood:	n/a	n/a
17	ATF1	chr8:1693624-1694708	K562	blood:	n/a	n/a
18	ATF1	chr8:1706175-1706913	K562	blood:	n/a	n/a
19	ATF1	chr8:1727822-1728089	K562	blood:	n/a	n/a
20	ATF1	chr8:1711832-1712081	K562	blood:	n/a	n/a
21	ATF1	chr8:1703574-1704210	K562	blood:	n/a	n/a
22	ATF2	chr8:1711806-1712187	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr8:1749879-1750996	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr8:1693748-1694670	GM12878	blood:	n/a	n/a
25	ATF2	chr8:1714860-1715262	GM12878	blood:	n/a	n/a
26	ATF2	chr8:1750246-1750745	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr8:1711802-1712124	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr8:1750748-1751324	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr8:1711835-1712169	GM12878	blood:	n/a	n/a
30	ATF2	chr8:1693583-1694333	GM12878	blood:	n/a	n/a
31	ATF3	chr8:1693623-1693916	K562	blood:	n/a	n/a
32	ATF3	chr8:1712527-1712754	K562	blood:	n/a	n/a
33	ATF3	chr8:1711826-1712058	K562	blood:	n/a	n/a
34	ATF3	chr8:1711797-1712028	K562	blood:	n/a	n/a
35	ATF3	chr8:1694289-1694617	K562	blood:	n/a	n/a
36	ATF3	chr8:1703576-1704226	K562	blood:	n/a	n/a
37	ATF3	chr8:1694307-1694619	K562	blood:	n/a	n/a
38	BACH1	chr8:1711099-1711111	K562	blood:	n/a	n/a
39	BACH1	chr8:1703814-1704099	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr8:1703737-1704233	K562	blood:	n/a	n/a
41	BACH1	chr8:1694205-1694780	K562	blood:	n/a	n/a
42	BACH1	chr8:1711786-1712750	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr8:1708143-1708723	K562	blood:	n/a	n/a
44	BACH1	chr8:1697399-1697624	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr8:1753328-1753359	K562	blood:	n/a	n/a
46	BATF	chr8:1703886-1704057	GM12878	blood:	n/a	chr8:1703978-1703988 chr8:1703973-1703984
47	BATF	chr8:1694269-1694678	GM12878	blood:	n/a	n/a
48	BATF	chr8:1684606-1684963	GM12878	blood:	n/a	chr8:1684797-1684808
49	BATF	chr8:1684612-1684879	GM12878	blood:	n/a	chr8:1684797-1684808
50	BATF	chr8:1703806-1704093	GM12878	blood:	n/a	chr8:1703978-1703988 chr8:1703973-1703984

(count:3114 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1719290-1719340	CMK	blood:	n/a
2	chr8:1713012-1713062	AoSMC	blood vessel:	n/a
3	chr8:1712330-1712380	BJ	skin:	n/a
4	chr8:1719290-1719340	CMK	blood:	n/a
5	chr8:1713012-1713062	AoSMC	blood vessel:	n/a
6	chr8:1712330-1712380	BJ	skin:	n/a
7	chr8:1707330-1707380	U87	brain:	n/a
8	chr8:1711433-1711483	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:1692726-1692776	GM19239	blood:	n/a
10	chr8:1731776-1731826	K562	blood:	n/a
11	chr8:1726903-1726953	SK-N-SH_RA	brain:	n/a
12	chr8:1740065-1740115	MCF-7	breast:	n/a
13	chr8:1733883-1733933	IMR90	lung:	fetal
14	chr8:1731574-1731624	HEK293	kidney:	embryo
15	chr8:1697536-1697586	GM06990	blood:	n/a
16	chr8:1719380-1719430	ProgFib	skin:	n/a
17	chr8:1725140-1725190	HIPEpiC	eye:	n/a
18	chr8:1733475-1733525	GM19239	blood:	n/a
19	chr8:1704075-1704125	AG04450	lung:	fetal
20	chr8:1732043-1732093	SK-N-SH	brain:	n/a
21	chr8:1725119-1725169	SK-N-MC	brain:	n/a
22	chr8:1740065-1740115	NT2-D1	testis:	n/a
23	chr8:1692458-1692508	HEEpiC	esophagus:	n/a
24	chr8:1708447-1708497	PANC-1	pancreas:	n/a
25	chr8:1711046-1711096	AG09309	skin:	n/a
26	chr8:1734990-1735040	HCM	heart:	n/a
27	chr8:1704013-1704063	SKMC	muscle:	n/a
28	chr8:1728777-1728827	SKMC	muscle:	n/a
29	chr8:1737564-1737614	Caco-2	colon:	n/a
30	chr8:1733369-1733419	HL-60	blood:	n/a
31	chr8:1733475-1733525	ProgFib	skin:	n/a
32	chr8:1740059-1740109	HCM	heart:	n/a
33	chr8:1711235-1711285	HUVEC	blood vessel:	n/a
34	chr8:1717660-1717710	Hela-S3	cervix:	n/a
35	chr8:1697408-1697458	HCF	heart:	n/a
36	chr8:1692019-1692069	HEEpiC	esophagus:	n/a
37	chr8:1732043-1732093	SKMC	muscle:	n/a
38	chr8:1697459-1697509	AG04450	lung:	fetal
39	chr8:1732011-1732061	HCPEpiC	choroid plexus:	n/a
40	chr8:1712170-1712220	ProgFib	skin:	n/a
41	chr8:1704075-1704125	HNPCEpiC	eye:	n/a
42	chr8:1731574-1731624	MCF-7	breast:	n/a
43	chr8:1729607-1729657	PFSK-1	brain:	n/a
44	chr8:1712330-1712380	PANC-1	pancreas:	n/a
45	chr8:1713012-1713062	RPTEC	kidney:	n/a
46	chr8:1728703-1728753	T-47D	breast:	n/a
47	chr8:1704013-1704063	GM06990	blood:	n/a
48	chr8:1713012-1713062	MCF-7	breast:	n/a
49	chr8:1737564-1737614	K562	blood:	n/a
50	chr8:1740059-1740109	HEK293	kidney:	embryo

(count:124 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:1693010..1695707-chr8:1719687..1722075,2	MCF-7	breast:
2	chr8:1691178..1695166-chr8:1727484..1730315,3	MCF-7	breast:
3	chr8:1734427..1736636-chr8:1737511..1739234,2	K562	blood:
4	chr8:1725330..1728287-chr8:1728724..1731820,3	K562	blood:
5	chr8:1725864..1728236-chr8:1731701..1733830,2	MCF-7	breast:
6	chr8:1716952..1719420-chr8:1723630..1725290,2	K562	blood:
7	chr8:1690830..1693396-chr8:1731671..1734648,2	K562	blood:
8	chr8:1728494..1731142-chr8:1732363..1735530,3	MCF-7	breast:
9	chr8:1716816..1721615-chr8:1726505..1732038,6	K562	blood:
10	chr8:1692167..1695898-chr8:1702417..1705508,6	MCF-7	breast:
11	chr8:1715615..1723539-chr8:1723885..1728177,9	MCF-7	breast:
12	chr8:1712944..1715681-chr8:1734053..1736692,2	K562	blood:
13	chr8:1731117..1733181-chr8:1735872..1737982,3	K562	blood:
14	chr8:1711866..1713979-chr8:1739471..1742255,2	K562	blood:
15	chr8:1691117..1696538-chr8:1710667..1714961,13	MCF-7	breast:
16	chr8:1692125..1694169-chr8:1767018..1769382,2	MCF-7	breast:
17	chr8:1711245..1713893-chr8:1726417..1729246,3	K562	blood:
18	chr8:1683298..1684246-chr8:1728731..1730059,4	MCF-7	breast:
19	chr8:1692732..1694940-chr8:1731254..1732794,2	MCF-7	breast:
20	chr8:1692503..1695228-chr8:1698804..1700487,2	K562	blood:
21	chr8:1717537..1720996-chr8:1730538..1734244,3	K562	blood:
22	chr8:1693384..1695306-chr8:1757717..1760683,2	MCF-7	breast:
23	chr8:1725864..1728236-chr8:1731701..1733830,2	MCF-7	breast:
24	chr8:1726321..1728354-chr8:1771384..1774203,2	MCF-7	breast:
25	chr8:1708066..1710813-chr8:1745165..1747310,2	MCF-7	breast:
26	chr8:1683449..1684285-chr8:1729073..1729982,8	K562	blood:
27	chr8:1686398..1691493-chr8:1692732..1695929,5	MCF-7	breast:
28	chr8:1683305..1684236-chr8:1728901..1729771,3	MCF-7	breast:
29	chr8:1730297..1733181-chr8:1733346..1737804,5	K562	blood:
30	chr8:1710662..1713548-chr8:1734331..1736456,2	MCF-7	breast:
31	chr8:1726532..1728287-chr8:1729917..1731820,2	K562	blood:
32	chr8:1683305..1684236-chr8:1728901..1729771,3	MCF-7	breast:
33	chr8:1690830..1693396-chr8:1731671..1734648,2	K562	blood:
34	chr8:1732905..1734705-chr8:1740621..1742810,2	K562	blood:
35	chr8:1711111..1712724-chr8:1772703..1775383,2	MCF-7	breast:
36	chr8:1687352..1688981-chr8:1706866..1709759,2	K562	blood:
37	chr8:1732905..1734705-chr8:1740621..1742810,2	K562	blood:
38	chr8:1686924..1688783-chr8:1724884..1727054,2	MCF-7	breast:
39	chr8:1683326..1684222-chr8:1978338..1978975,3	K562	blood:
40	chr8:1687744..1690285-chr8:1712438..1714050,2	MCF-7	breast:
41	chr8:1715604..1719309-chr8:1719775..1722697,3	MCF-7	breast:
42	chr8:1730297..1733181-chr8:1733346..1737804,5	K562	blood:
43	chr8:1725330..1728287-chr8:1728724..1731820,3	K562	blood:
44	chr8:1716779..1719807-chr8:1720104..1723417,3	K562	blood:
45	chr8:1692017..1693877-chr8:1696631..1699350,2	MCF-7	breast:
46	chr8:1704279..1706282-chr8:1706404..1709103,2	MCF-7	breast:
47	chr8:1683298..1683841-chr8:1971940..1972481,2	K562	blood:
48	chr8:1745622..1748028-chr8:1770752..1773401,2	K562	blood:
49	chr8:1688805..1690612-chr8:1693113..1695827,3	K562	blood:
50	chr8:1656737..1659589-chr8:1707662..1709873,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSMD1-9	chr8:1743563-1744122	XLOC_006976
2	lnc-ERICH1-7	chr8:1712467-1712505	ENSG00000253982.1
3	lnc-ERICH1-14	chr8:1696619-1698501	l_3532_chr8:1696618-1698904_brain
4	lnc-CSMD1-9	chr8:1741068-1743334	XLOC_006976
5	lnc-CLN8-2	chr8:1703947-1704248	NONHSAT124676
6	lnc-CLN8-2	chr8:1707463-1707667	NONHSAT124676
7	lnc-CLN8-1	chr8:1748169-1748191	XLOC_006688
8	lnc-ERICH1-14	chr8:1698596-1698904	l_3532_chr8:1696618-1698904_brain
9	lnc-ERICH1-7	chr8:1706374-1708613	NONHSAT124678
10	lnc-ERICH1-7	chr8:1712467-1712500	NONHSAT124681
11	lnc-ERICH1-7	chr8:1712600-1712668	ENSG00000253982.1
12	lnc-CLN8-2	chr8:1707463-1707677	NONHSAT124677
13	lnc-ERICH1-7	chr8:1709431-1711094	NONHSAT124681
14	lnc-ERICH1-7	chr8:1710247-1711094	ENSG00000253982.1
15	lnc-CLN8-1	chr8:1748840-1749522	XLOC_006688
16	lnc-CLN8-2	chr8:1706415-1706472	NONHSAT124677
17	lnc-ERICH1-7	chr8:1709431-1711094	NONHSAT124680
18	lnc-ERICH1-7	chr8:1710156-1711094	ENSG00000253982.1
19	lnc-ERICH1-7	chr8:1712600-1712716	NONHSAT124680
20	lnc-CLN8-2	chr8:1703954-1704248	NONHSAT124677

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3674	chr8:1749299-1749320	MIMAT0018097

No data

Variant related genes	Relation type
CLN8	TF binding region
ENSG00000253982	TF binding region
CLN8	CpG island
ENSG00000253982	CpG island
ENSG00000254265	chromatin interactions
ENSG00000126351	chromatin interactions
ENSG00000182372	chromatin interactions
ENSG00000207826	chromatin interactions
ENSG00000104728	chromatin interactions
ENSG00000253982	chromatin interactions
ACVR1B	miRNA target sites
LIMD1	miRNA target sites

Extended variants
information (count: 4136 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:4136 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2972180	chr8:1681733-1681734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546425139	chr8:1681743-1681744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554663053	chr8:1681745-1681746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188921346	chr8:1681746-1681747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562963958	chr8:1681749-1681750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs193221831	chr8:1681755-1681756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141556107	chr8:1681758-1681759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559399619	chr8:1681762-1681763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575713958	chr8:1681763-1681764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13249016	chr8:1681781-1681782	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs548415951	chr8:1681785-1681786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558129866	chr8:1681797-1681798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568227066	chr8:1681801-1681802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199950778	chr8:1681831-1681832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530850558	chr8:1681836-1681837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183882455	chr8:1681838-1681839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150910033	chr8:1681864-1681865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114684485	chr8:1681872-1681873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558831584	chr8:1681876-1681877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545695671	chr8:1681890-1681891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566166533	chr8:1681893-1681894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375950181	chr8:1681901-1681902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186625468	chr8:1681959-1681960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114315785	chr8:1681966-1681967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191379372	chr8:1682016-1682017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112784268	chr8:1682024-1682025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111567830	chr8:1682046-1682047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557213806	chr8:1682058-1682059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576813218	chr8:1682078-1682079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545788060	chr8:1682086-1682087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559048772	chr8:1682095-1682096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530459297	chr8:1682105-1682106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572623131	chr8:1682149-1682150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139426845	chr8:1682204-1682205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545373703	chr8:1682242-1682243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541919493	chr8:1682243-1682244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561892090	chr8:1682277-1682278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530709479	chr8:1682283-1682284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550935575	chr8:1682285-1682286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564401950	chr8:1682335-1682336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2977191	chr8:1682338-1682339	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs115871090	chr8:1682340-1682341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565900643	chr8:1682360-1682361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184328278	chr8:1682388-1682389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552204789	chr8:1682436-1682437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548251522	chr8:1682469-1682470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564086415	chr8:1682477-1682478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537246909	chr8:1682501-1682502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189750579	chr8:1682547-1682548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs78056584	chr8:1682554-1682555	Weak transcription	n/a	n/a	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:3212 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1681400-1681800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:1681600-1684000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr8:1681800-1682600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:1682600-1682800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:1682600-1682800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:1682800-1684200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr8:1682800-1685600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:1683400-1683600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:1683400-1683800	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr8:1683400-1683800	Active TSS	Colon Smooth Muscle	Colon
11	chr8:1683400-1684000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr8:1683400-1684200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr8:1683400-1684200	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr8:1683400-1684400	Enhancers	Dnd41	blood
15	chr8:1683400-1684600	Enhancers	Fetal Intestine Small	intestine
16	chr8:1683400-1684800	Enhancers	Brain Angular Gyrus	brain
17	chr8:1683400-1686400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr8:1683600-1683800	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr8:1683600-1683800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr8:1683600-1683800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr8:1683600-1683800	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr8:1683600-1684000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr8:1683600-1684000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr8:1683600-1684000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr8:1683600-1684000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr8:1683600-1684000	Enhancers	Liver	Liver
27	chr8:1683600-1684000	Active TSS	Rectal Mucosa Donor 29	rectum
28	chr8:1683600-1684000	Enhancers	Rectal Smooth Muscle	rectum
29	chr8:1683600-1684000	Enhancers	Hela-S3	cervix
30	chr8:1683600-1684200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr8:1683600-1684200	Enhancers	Brain Hippocampus Middle	brain
32	chr8:1683600-1684200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr8:1683600-1684200	Enhancers	Brain Substantia Nigra	brain
34	chr8:1683600-1684200	Enhancers	Duodenum Mucosa	Duodenum
35	chr8:1683600-1684200	Enhancers	K562	blood
36	chr8:1683600-1684400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr8:1683600-1684600	Enhancers	Stomach Mucosa	stomach
38	chr8:1683600-1685200	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr8:1683600-1686200	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr8:1683600-1686200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr8:1683800-1684000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:1683800-1684000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
43	chr8:1683800-1684000	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr8:1683800-1684000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
45	chr8:1683800-1684000	Flanking Active TSS	Colon Smooth Muscle	Colon
46	chr8:1683800-1684000	Enhancers	Osteobl	bone
47	chr8:1683800-1684200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr8:1683800-1684200	Enhancers	Primary T cells from cord blood	blood
49	chr8:1683800-1684200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
50	chr8:1683800-1684200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood

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