Variant report

Variant	esv2755149
Chromosome Location	chr8:1689290-1755281
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2523)
CpG islands
(count:3116)
Chromatin interactive
region (count:105)
LncRNA
region (count:20)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2523 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:1703700-1704244	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:1712466-1712804	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:1708103-1708744	K562	blood:	n/a	n/a
4	ARID3A	chr8:1703564-1704299	K562	blood:	n/a	n/a
5	ARID3A	chr8:1693302-1694253	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:1693554-1694651	K562	blood:	n/a	n/a
7	ARID3A	chr8:1700948-1701221	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:1748328-1748700	K562	blood:	n/a	n/a
9	ARID3A	chr8:1707125-1707584	K562	blood:	n/a	n/a
10	ARID3A	chr8:1690095-1690840	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:1698531-1698750	K562	blood:	n/a	n/a
12	ARID3A	chr8:1706530-1706868	K562	blood:	n/a	n/a
13	ARID3A	chr8:1710733-1711272	K562	blood:	n/a	n/a
14	ATF1	chr8:1748612-1748850	K562	blood:	n/a	n/a
15	ATF1	chr8:1703574-1704210	K562	blood:	n/a	n/a
16	ATF1	chr8:1706175-1706913	K562	blood:	n/a	n/a
17	ATF1	chr8:1708076-1708663	K562	blood:	n/a	n/a
18	ATF1	chr8:1727822-1728089	K562	blood:	n/a	n/a
19	ATF1	chr8:1693624-1694708	K562	blood:	n/a	n/a
20	ATF1	chr8:1711832-1712081	K562	blood:	n/a	n/a
21	ATF2	chr8:1693583-1694333	GM12878	blood:	n/a	n/a
22	ATF2	chr8:1714860-1715262	GM12878	blood:	n/a	n/a
23	ATF2	chr8:1711806-1712187	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr8:1749879-1750996	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr8:1711835-1712169	GM12878	blood:	n/a	n/a
26	ATF2	chr8:1711802-1712124	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr8:1750246-1750745	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	chr8:1693748-1694670	GM12878	blood:	n/a	n/a
30	ATF3	chr8:1712527-1712754	K562	blood:	n/a	n/a
31	ATF3	chr8:1694289-1694617	K562	blood:	n/a	n/a
32	ATF3	chr8:1693623-1693916	K562	blood:	n/a	n/a
33	ATF3	chr8:1711797-1712028	K562	blood:	n/a	n/a
34	ATF3	chr8:1711826-1712058	K562	blood:	n/a	n/a
35	ATF3	chr8:1694307-1694619	K562	blood:	n/a	n/a
36	ATF3	chr8:1703576-1704226	K562	blood:	n/a	n/a
37	BACH1	chr8:1753328-1753359	K562	blood:	n/a	n/a
38	BACH1	chr8:1711786-1712750	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr8:1708143-1708723	K562	blood:	n/a	n/a
40	BACH1	chr8:1703814-1704099	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr8:1697399-1697624	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr8:1703737-1704233	K562	blood:	n/a	n/a
43	BACH1	chr8:1694205-1694780	K562	blood:	n/a	n/a
44	BACH1	chr8:1711099-1711111	K562	blood:	n/a	n/a
45	BATF	chr8:1693700-1694177	GM12878	blood:	n/a	n/a
46	BATF	chr8:1694269-1694678	GM12878	blood:	n/a	n/a
47	BATF	chr8:1703886-1704057	GM12878	blood:	n/a	chr8:1703978-1703988 chr8:1703973-1703984
48	BATF	chr8:1703806-1704093	GM12878	blood:	n/a	chr8:1703978-1703988 chr8:1703973-1703984
49	BCL11A	chr8:1693800-1694181	GM12878	blood:	n/a	chr8:1693810-1693819
50	BCL11A	chr8:1693806-1694271	GM12878	blood:	n/a	chr8:1693810-1693819 chr8:1694175-1694184

(count:3116 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1728777-1728827	PrEC	prostate:	n/a
2	chr8:1746360-1746410	HL-60	blood:	n/a
3	chr8:1731574-1731624	ovcar-3	ovarian:	n/a
4	chr8:1719543-1719593	HIPEpiC	eye:	n/a
5	chr8:1697536-1697586	HUVEC	blood vessel:	n/a
6	chr8:1728777-1728827	PrEC	prostate:	n/a
7	chr8:1746360-1746410	HL-60	blood:	n/a
8	chr8:1731574-1731624	ovcar-3	ovarian:	n/a
9	chr8:1719543-1719593	HIPEpiC	eye:	n/a
10	chr8:1697536-1697586	HUVEC	blood vessel:	n/a
11	chr8:1692458-1692508	BE2_C	brain:	n/a
12	chr8:1692019-1692069	NHDF-neo	bronchial:	n/a
13	chr8:1731574-1731624	HL-60	blood:	n/a
14	chr8:1719380-1719430	ovcar-3	ovarian:	n/a
15	chr8:1719380-1719430	SK-N-SH_RA	brain:	n/a
16	chr8:1697408-1697458	CMK	blood:	n/a
17	chr8:1719543-1719593	NB4	blood:	n/a
18	chr8:1733497-1733547	H1-hESC	embryonic stem cell:	embryo
19	chr8:1728777-1728827	BJ	skin:	n/a
20	chr8:1711433-1711483	MCF10A-Er-Src	breast:	n/a
21	chr8:1717660-1717710	Hela-S3	cervix:	n/a
22	chr8:1731776-1731826	CMK	blood:	n/a
23	chr8:1712170-1712220	PrEC	prostate:	n/a
24	chr8:1708447-1708497	Caco-2	colon:	n/a
25	chr8:1728703-1728753	AG04450	lung:	fetal
26	chr8:1712170-1712220	GM06990	blood:	n/a
27	chr8:1734990-1735040	PANC-1	pancreas:	n/a
28	chr8:1697408-1697458	GM12892	blood:	n/a
29	chr8:1725119-1725169	SAEC	small airway:	n/a
30	chr8:1704075-1704125	AG09319	gingival:	n/a
31	chr8:1692107-1692157	HMEC	breast:	n/a
32	chr8:1704013-1704063	HRPEpiC	eye:	n/a
33	chr8:1704075-1704125	ECC-1	luminal epithelium:	n/a
34	chr8:1708526-1708576	PFSK-1	brain:	n/a
35	chr8:1732043-1732093	GM12892	blood:	n/a
36	chr8:1708438-1708488	ovcar-3	ovarian:	n/a
37	chr8:1719543-1719593	CMK	blood:	n/a
38	chr8:1711433-1711483	AG09309	skin:	n/a
39	chr8:1732011-1732061	IMR90	lung:	fetal
40	chr8:1713012-1713062	H1-hESC	embryonic stem cell:	embryo
41	chr8:1725119-1725169	GM19239	blood:	n/a
42	chr8:1692107-1692157	PFSK-1	brain:	n/a
43	chr8:1708526-1708576	ProgFib	skin:	n/a
44	chr8:1704075-1704125	CMK	blood:	n/a
45	chr8:1711433-1711483	LNCaP	prostate:	n/a
46	chr8:1692019-1692069	HCM	heart:	n/a
47	chr8:1711046-1711096	GM12892	blood:	n/a
48	chr8:1733883-1733933	PANC-1	pancreas:	n/a
49	chr8:1726903-1726953	Hela-S3	cervix:	n/a
50	chr8:1731480-1731530	HUVEC	blood vessel:	n/a

(count:105 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:1710901..1715165-chr8:1763143..1767602,4	K562	blood:
2	chr8:1676916..1679793-chr8:1711386..1713857,2	K562	blood:
3	chr8:1690439..1692118-chr8:1706880..1708703,2	MCF-7	breast:
4	chr8:1690439..1692118-chr8:1706880..1708703,2	MCF-7	breast:
5	chr8:1715615..1723539-chr8:1723885..1728177,9	MCF-7	breast:
6	chr8:1712198..1712991-chr8:1724016..1724625,2	K562	blood:
7	chr8:1717744..1722491-chr8:1723636..1726849,4	MCF-7	breast:
8	chr8:1688805..1690612-chr8:1693113..1695827,3	K562	blood:
9	chr8:1727131..1730202-chr8:1731838..1734952,3	K562	blood:
10	chr8:1695351..1696872-chr8:1698699..1700709,2	MCF-7	breast:
11	chr8:1683243..1684210-chr8:1693916..1694440,2	K562	blood:
12	chr8:1691178..1695166-chr8:1727484..1730315,3	MCF-7	breast:
13	chr8:1702392..1708895-chr8:1709221..1714010,17	MCF-7	breast:
14	chr8:1696563..1699440-chr8:1706967..1709806,2	MCF-7	breast:
15	chr17:38219023..38219851-chr8:1710924..1711761,2	Hela-S3	cervix:
16	chr8:1726532..1728287-chr8:1729917..1731820,2	K562	blood:
17	chr8:1712944..1715681-chr8:1734053..1736692,2	K562	blood:
18	chr8:1692732..1694940-chr8:1731254..1732794,2	MCF-7	breast:
19	chr8:1726532..1728287-chr8:1729917..1731820,2	K562	blood:
20	chr8:1712944..1715681-chr8:1734053..1736692,2	K562	blood:
21	chr8:1682026..1683754-chr8:1708602..1710119,2	MCF-7	breast:
22	chr8:1692503..1695228-chr8:1698804..1700487,2	K562	blood:
23	chr8:1710542..1713448-chr8:1725280..1729246,5	K562	blood:
24	chr8:1725864..1728236-chr8:1731701..1733830,2	MCF-7	breast:
25	chr8:1693010..1695707-chr8:1719687..1722075,2	MCF-7	breast:
26	chr8:1717537..1720996-chr8:1730538..1734244,3	K562	blood:
27	chr8:1725330..1728287-chr8:1728724..1731820,3	K562	blood:
28	chr8:1693384..1695306-chr8:1757717..1760683,2	MCF-7	breast:
29	chr8:1730297..1733181-chr8:1733346..1737804,5	K562	blood:
30	chr8:1684265..1686317-chr8:1693828..1695451,2	K562	blood:
31	chr8:1692503..1695228-chr8:1698804..1700487,2	K562	blood:
32	chr8:1708066..1710813-chr8:1745165..1747310,2	MCF-7	breast:
33	chr8:1725864..1728236-chr8:1731701..1733830,2	MCF-7	breast:
34	chr8:1704279..1706282-chr8:1706404..1709103,2	MCF-7	breast:
35	chr8:1681796..1686732-chr8:1704250..1709938,6	K562	blood:
36	chr8:1656737..1659589-chr8:1707662..1709873,2	K562	blood:
37	chr8:1715604..1719309-chr8:1719775..1722697,3	MCF-7	breast:
38	chr8:1696563..1699440-chr8:1706967..1709806,2	MCF-7	breast:
39	chr8:1690830..1693396-chr8:1731671..1734648,2	K562	blood:
40	chr8:1711245..1713893-chr8:1726417..1729246,3	K562	blood:
41	chr8:1710504..1712824-chr8:1729569..1731370,2	MCF-7	breast:
42	chr8:1691178..1695166-chr8:1727484..1730315,3	MCF-7	breast:
43	chr8:1683449..1684285-chr8:1729073..1729982,8	K562	blood:
44	chr8:1727131..1730202-chr8:1731838..1734952,3	K562	blood:
45	chr8:1716952..1719420-chr8:1723630..1725290,2	K562	blood:
46	chr8:1702544..1704176-chr8:1706755..1708609,2	MCF-7	breast:
47	chr8:1716779..1719807-chr8:1720104..1723417,3	K562	blood:
48	chr8:1693361..1695232-chr8:1714605..1717570,2	MCF-7	breast:
49	chr8:1695837..1698728-chr8:1710665..1712737,2	MCF-7	breast:
50	chr8:1734427..1736636-chr8:1737511..1739234,2	K562	blood:

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

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

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
ENSG00000126351	chromatin interactions
ENSG00000104728	chromatin interactions
ENSG00000182372	chromatin interactions
ENSG00000207826	chromatin interactions
ENSG00000254265	chromatin interactions
ENSG00000253982	chromatin interactions
ACVR1B	miRNA target sites
LIMD1	miRNA target sites

Extended variants
information (count: 3701 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:3701 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs41526952	chr8:1689290-1689291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
2	rs535301493	chr8:1689304-1689305	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555507364	chr8:1689305-1689306	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs373918779	chr8:1689321-1689322	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs73672952	chr8:1689353-1689354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs574941716	chr8:1689374-1689375	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs576814953	chr8:1689377-1689378	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs2469723	chr8:1689379-1689380	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs2472071	chr8:1689382-1689383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2472072	chr8:1689413-1689414	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545938685	chr8:1689423-1689424	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs559422853	chr8:1689478-1689479	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs182405403	chr8:1689491-1689492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs548512924	chr8:1689494-1689495	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs535636370	chr8:1689497-1689498	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs73672953	chr8:1689502-1689503	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs531143231	chr8:1689510-1689511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs111744439	chr8:1689513-1689514	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs551287817	chr8:1689519-1689520	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs570510136	chr8:1689556-1689557	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs539445502	chr8:1689562-1689563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs111493673	chr8:1689575-1689576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs546580948	chr8:1689583-1689584	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs186938895	chr8:1689590-1689591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371428700	chr8:1689606-1689607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs113475308	chr8:1689607-1689608	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538906999	chr8:1689608-1689609	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs111785258	chr8:1689610-1689611	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs111484605	chr8:1689618-1689619	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs537786302	chr8:1689645-1689646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557624839	chr8:1689648-1689649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs577467735	chr8:1689652-1689653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs139443083	chr8:1689653-1689654	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559288044	chr8:1689659-1689660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190598043	chr8:1689663-1689664	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs183407999	chr8:1689696-1689697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs528716729	chr8:1689708-1689709	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs189102291	chr8:1689709-1689710	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566063882	chr8:1689733-1689734	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs544770561	chr8:1689748-1689749	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564781213	chr8:1689752-1689753	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2469722	chr8:1689791-1689792	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs547150213	chr8:1689798-1689799	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs145038889	chr8:1689812-1689813	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs377083218	chr8:1689813-1689814	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs11784247	chr8:1689819-1689820	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11779979	chr8:1689867-1689868	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs566443178	chr8:1689875-1689876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535000625	chr8:1689876-1689877	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs529011167	chr8:1689882-1689883	Weak transcription Enhancers	Chromatin interactive region	1 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:3086 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1685200-1692400	Weak transcription	Brain Substantia Nigra	brain
2	chr8:1686000-1690200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:1686800-1692400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:1688400-1690200	Enhancers	K562	blood
5	chr8:1688600-1690000	Enhancers	HepG2	liver
6	chr8:1690000-1690600	Enhancers	Liver	Liver
7	chr8:1690000-1690600	Flanking Active TSS	HepG2	liver
8	chr8:1690200-1690600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:1690200-1690600	Flanking Active TSS	K562	blood
10	chr8:1690200-1691000	ZNF genes & repeats	Primary B cells from cord blood	blood
11	chr8:1690600-1691000	Enhancers	K562	blood
12	chr8:1690600-1691200	Enhancers	HepG2	liver
13	chr8:1690600-1692400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:1691000-1692400	Weak transcription	Primary B cells from cord blood	blood
15	chr8:1691000-1693000	Weak transcription	K562	blood
16	chr8:1691200-1692800	Bivalent Enhancer	HepG2	liver
17	chr8:1691400-1691600	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
18	chr8:1691600-1693200	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr8:1691600-1693400	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr8:1691800-1692200	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr8:1692000-1694000	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr8:1692000-1694000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:1692000-1694200	Enhancers	Esophagus	oesophagus
24	chr8:1692000-1694800	Enhancers	Spleen	Spleen
25	chr8:1692200-1692400	Enhancers	H9 Cell Line	embryonic stem cell
26	chr8:1692200-1692400	Weak transcription	Right Atrium	heart
27	chr8:1692200-1693200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr8:1692200-1694800	Enhancers	Placenta	Placenta
29	chr8:1692200-1695400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr8:1692200-1695600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr8:1692200-1696200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr8:1692200-1696400	Enhancers	Primary B cells from peripheral blood	blood
33	chr8:1692400-1692600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr8:1692400-1692600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr8:1692400-1692600	Enhancers	Brain Anterior Caudate	brain
36	chr8:1692400-1692600	Enhancers	Colonic Mucosa	Colon
37	chr8:1692400-1692600	Enhancers	Right Atrium	heart
38	chr8:1692400-1692800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr8:1692400-1692800	Enhancers	Adipose Nuclei	Adipose
40	chr8:1692400-1692800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr8:1692400-1692800	Enhancers	Lung	lung
42	chr8:1692400-1692800	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr8:1692400-1693000	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr8:1692400-1693400	Enhancers	Duodenum Mucosa	Duodenum
45	chr8:1692400-1693600	Enhancers	Gastric	stomach
46	chr8:1692400-1693800	Enhancers	Primary B cells from cord blood	blood
47	chr8:1692400-1694600	Enhancers	Brain Substantia Nigra	brain
48	chr8:1692400-1694800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr8:1692400-1694800	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr8:1692400-1695000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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