Variant report

Variant	nsv539296
Chromosome Location	chr8:1563559-1684995
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	chr8:1644107-1644129	K562	blood:	n/a	n/a
2	ARID3A	chr8:1683588-1683957	HepG2	liver:	n/a	n/a
3	ATF1	chr8:1612841-1613066	K562	blood:	n/a	n/a
4	ATF1	chr8:1631106-1631363	K562	blood:	n/a	n/a
5	ATF2	chr8:1606188-1606635	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr8:1631111-1631356	K562	blood:	n/a	n/a
7	BACH1	chr8:1650236-1650243	K562	blood:	n/a	n/a
8	BACH1	chr8:1600054-1600554	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:1649454-1650069	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr8:1583024-1583221	GM12878	blood:	n/a	chr8:1583128-1583139
11	BATF	chr8:1684606-1684963	GM12878	blood:	n/a	chr8:1684797-1684808
12	BATF	chr8:1684612-1684879	GM12878	blood:	n/a	chr8:1684797-1684808
13	BCL3	chr8:1613411-1613643	GM12878	blood:	n/a	chr8:1613634-1613643
14	BHLHE40	chr8:1644069-1644250	K562	blood:	n/a	chr8:1644168-1644184 chr8:1644160-1644176
15	BHLHE40	chr8:1610754-1610850	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:1598474-1598541	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:1684761-1684921	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:1589261-1589514	K562	blood:	n/a	chr8:1589361-1589370 chr8:1589362-1589371 chr8:1589355-1589376 chr8:1589361-1589370
19	BHLHE40	chr8:1683587-1683959	K562	blood:	n/a	n/a
20	BHLHE40	chr8:1650131-1650342	K562	blood:	n/a	n/a
21	BHLHE40	chr8:1649469-1649782	K562	blood:	n/a	n/a
22	BRCA1	chr8:1649391-1649753	H1-hESC	embryonic stem cell:	n/a	n/a
23	CBX3	chr8:1649363-1649896	K562	blood:	n/a	n/a
24	CCNT2	chr8:1643955-1644221	K562	blood:	n/a	n/a
25	CCNT2	chr8:1649151-1649813	K562	blood:	n/a	n/a
26	CEBPB	chr8:1631047-1631403	HepG2	liver:	n/a	chr8:1631220-1631231
27	CEBPB	chr8:1628160-1628398	A549	lung:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
28	CEBPB	chr8:1598267-1598411	HepG2	liver:	n/a	chr8:1598339-1598350 chr8:1598339-1598348
29	CEBPB	chr8:1631078-1631329	K562	blood:	n/a	chr8:1631220-1631231
30	CEBPB	chr8:1580668-1580977	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr8:1631046-1631432	Hela-S3	cervix:	n/a	chr8:1631220-1631231
32	CEBPB	chr8:1644002-1644239	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr8:1631051-1631490	K562	blood:	n/a	chr8:1631220-1631231
34	CEBPB	chr8:1628117-1628387	Hela-S3	cervix:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
35	CEBPB	chr8:1628099-1628437	HepG2	liver:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
36	CEBPB	chr8:1600966-1601219	HepG2	liver:	n/a	chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601079-1601092 chr8:1601079-1601090 chr8:1601080-1601091 chr8:1601081-1601090
37	CEBPB	chr8:1648538-1648896	K562	blood:	n/a	chr8:1648683-1648694 chr8:1648683-1648696
38	CEBPB	chr8:1648609-1648806	HepG2	liver:	n/a	chr8:1648683-1648694 chr8:1648683-1648696
39	CEBPB	chr8:1631054-1631361	K562	blood:	n/a	chr8:1631220-1631231
40	CEBPB	chr8:1628240-1628361	H1-hESC	embryonic stem cell:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
41	CEBPB	chr8:1601039-1601179	IMR90	lung:	n/a	chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601079-1601092 chr8:1601079-1601090 chr8:1601080-1601091 chr8:1601081-1601090
42	CEBPB	chr8:1649373-1649573	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr8:1630919-1631593	HCT-116	colon:	n/a	chr8:1631220-1631231
44	CEBPB	chr8:1631004-1631475	HCT-116	colon:	n/a	chr8:1631220-1631231
45	CEBPB	chr8:1652131-1652460	A549	lung:	n/a	n/a
46	CEBPB	chr8:1652172-1652395	HepG2	liver:	n/a	n/a
47	CEBPB	chr8:1631129-1631386	IMR90	lung:	n/a	chr8:1631220-1631231
48	CEBPB	chr8:1628133-1628450	K562	blood:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
49	CEBPB	chr8:1577269-1577487	HepG2	liver:	n/a	chr8:1577393-1577404 chr8:1577393-1577406 chr8:1577395-1577406 chr8:1577393-1577406 chr8:1577395-1577404
50	CEBPB	chr8:1601046-1601180	K562	blood:	n/a	chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601079-1601092 chr8:1601079-1601090 chr8:1601080-1601091 chr8:1601081-1601090

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1651101-1651151	GM12892	blood:	n/a
2	chr8:1601314-1601364	NT2-D1	testis:	n/a
3	chr8:1649522-1649572	SKMC	muscle:	n/a
4	chr8:1616925-1616975	ECC-1	luminal epithelium:	n/a
5	chr8:1613919-1613969	ovcar-3	ovarian:	n/a
6	chr8:1623483-1623533	Caco-2	colon:	n/a
7	chr8:1596244-1596294	HMEC	breast:	n/a
8	chr8:1588899-1588949	HCT-116	colon:	n/a
9	chr8:1651101-1651151	GM12892	blood:	n/a
10	chr8:1601314-1601364	NT2-D1	testis:	n/a
11	chr8:1649522-1649572	SKMC	muscle:	n/a
12	chr8:1616925-1616975	ECC-1	luminal epithelium:	n/a
13	chr8:1613919-1613969	ovcar-3	ovarian:	n/a
14	chr8:1623483-1623533	Caco-2	colon:	n/a
15	chr8:1596244-1596294	HMEC	breast:	n/a
16	chr8:1588899-1588949	HCT-116	colon:	n/a
17	chr8:1588822-1588872	NT2-D1	testis:	n/a
18	chr8:1605546-1605596	Jurkat	blood:	n/a
19	chr8:1639892-1639942	HCF	heart:	n/a
20	chr8:1615950-1616000	AoSMC	blood vessel:	n/a
21	chr8:1617756-1617806	SKMC	muscle:	n/a
22	chr8:1588403-1588453	HNPCEpiC	eye:	n/a
23	chr8:1588899-1588949	SK-N-SH_RA	brain:	n/a
24	chr8:1624741-1624791	AG09309	skin:	n/a
25	chr8:1649868-1649918	SK-N-SH_RA	brain:	n/a
26	chr8:1579180-1579230	GM12878	blood:	n/a
27	chr8:1616450-1616500	AoSMC	blood vessel:	n/a
28	chr8:1639563-1639613	HMEC	breast:	n/a
29	chr8:1590916-1590966	HRCEpiC	kidney:	n/a
30	chr8:1581647-1581697	PANC-1	pancreas:	n/a
31	chr8:1618448-1618498	AoSMC	blood vessel:	n/a
32	chr8:1575750-1575800	U87	brain:	n/a
33	chr8:1639909-1639959	HUVEC	blood vessel:	n/a
34	chr8:1592451-1592501	NHDF-neo	bronchial:	n/a
35	chr8:1581122-1581172	GM12892	blood:	n/a
36	chr8:1616381-1616431	GM06990	blood:	n/a
37	chr8:1681514-1681564	RPTEC	kidney:	n/a
38	chr8:1626697-1626747	HAEpiC	amniotic membrane:	n/a
39	chr8:1570635-1570685	K562	blood:	n/a
40	chr8:1649758-1649808	SAEC	small airway:	n/a
41	chr8:1586825-1586875	AG04449	skin:	fetal
42	chr8:1601372-1601422	HL-60	blood:	n/a
43	chr8:1617868-1617918	AG09319	gingival:	n/a
44	chr8:1591382-1591432	ProgFib	skin:	n/a
45	chr8:1618151-1618201	HepG2	liver:	n/a
46	chr8:1592281-1592331	U87	brain:	n/a
47	chr8:1616422-1616472	NB4	blood:	n/a
48	chr8:1639563-1639613	NH-A	brain:	n/a
49	chr8:1653215-1653265	HRPEpiC	eye:	n/a
50	chr8:1651101-1651151	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:1639712..1642185-chr8:1645555..1647369,2	K562	blood:
2	chr8:1621344..1623146-chr8:1688699..1690451,2	K562	blood:
3	chr8:1681796..1686732-chr8:1704250..1709938,6	K562	blood:
4	chr8:1684817..1688387-chr8:1693951..1696420,3	K562	blood:
5	chr8:1647929..1650394-chr8:1651041..1654216,3	MCF-7	breast:
6	chr8:1648393..1649994-chr8:1655851..1658728,2	MCF-7	breast:
7	chr8:1671883..1674158-chr8:1677266..1679497,2	K562	blood:
8	chr8:1683243..1684210-chr8:1693916..1694440,2	K562	blood:
9	chr8:1683387..1685289-chr8:1686133..1688410,3	K562	blood:
10	chr8:1681316..1685438-chr8:1724958..1729595,5	K562	blood:
11	chr8:1599745..1602131-chr8:1603017..1606467,3	K562	blood:
12	chr8:1683298..1683841-chr8:1971940..1972481,2	K562	blood:
13	chr8:1683647..1684368-chr8:1711990..1712621,2	MCF-7	breast:
14	chr8:1683298..1684246-chr8:1728731..1730059,4	MCF-7	breast:
15	chr8:1578132..1580473-chr8:1601540..1604510,2	K562	blood:
16	chr8:1578132..1580473-chr8:1601540..1604510,2	K562	blood:
17	chr8:1644923..1646471-chr8:1647780..1649578,2	MCF-7	breast:
18	chr8:1683326..1684222-chr8:1978338..1978975,3	K562	blood:
19	chr8:1683305..1684236-chr8:1728901..1729771,3	MCF-7	breast:
20	chr8:1684038..1686561-chr8:1711084..1712733,2	MCF-7	breast:
21	chr8:1582447..1584354-chr8:1585808..1588032,2	K562	blood:
22	chr8:1682754..1684809-chr8:1691291..1693773,2	MCF-7	breast:
23	chr8:1649287..1651045-chr8:1651779..1654462,2	K562	blood:
24	chr8:1676916..1679793-chr8:1711386..1713857,2	K562	blood:
25	chr8:1682026..1683754-chr8:1708602..1710119,2	MCF-7	breast:
26	chr8:1647929..1650394-chr8:1651041..1654216,3	MCF-7	breast:
27	chr8:1582447..1584354-chr8:1585808..1588032,2	K562	blood:
28	chr8:1678487..1679403-chr8:1728856..1729643,2	K562	blood:
29	chr8:1684265..1686317-chr8:1693828..1695451,2	K562	blood:
30	chr8:1593850..1596302-chr8:1622198..1625044,2	K562	blood:
31	chr8:1651243..1653137-chr8:1654644..1656282,2	MCF-7	breast:
32	chr8:1648393..1649994-chr8:1655851..1658728,2	MCF-7	breast:
33	chr8:1615891..1617815-chr8:1624787..1626742,2	K562	blood:
34	chr8:1627163..1629357-chr8:1633786..1636690,2	K562	blood:
35	chr8:1683414..1685975-chr8:1702028..1704859,2	MCF-7	breast:
36	chr8:1569188..1570751-chr8:1570808..1572953,2	MCF-7	breast:
37	chr8:1683723..1685599-chr8:1688819..1690722,2	K562	blood:
38	chr8:1649287..1651045-chr8:1651779..1654462,2	K562	blood:
39	chr8:1599745..1602131-chr8:1603017..1606467,3	K562	blood:
40	chr8:1584132..1586956-chr8:1595846..1598280,3	K562	blood:
41	chr8:1639712..1642185-chr8:1645555..1647369,2	K562	blood:
42	chr1:154989909..154990782-chr8:1569714..1570480,2	MCF-7	breast:
43	chr8:1644923..1646471-chr8:1647780..1649578,2	MCF-7	breast:
44	chr8:1627163..1629357-chr8:1633786..1636690,2	K562	blood:
45	chr8:1584132..1586956-chr8:1595846..1598280,3	K562	blood:
46	chr8:1683449..1684285-chr8:1729073..1729982,8	K562	blood:
47	chr8:1644165..1646557-chr8:1648161..1651623,3	K562	blood:
48	chr8:1644165..1646557-chr8:1648161..1651623,3	K562	blood:
49	chr6:86095690..86096566-chr8:1651602..1652159,2	MCF-7	breast:
50	chr8:1651243..1653137-chr8:1654644..1656282,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERICH1-6	chr8:1568540-1568679	ENSG00000253267.1
2	lnc-ERICH1-6	chr8:1567865-1568059	ENSG00000253267.1
3	lnc-ERICH1-6	chr8:1569302-1570583	ENSG00000253267.1

Variant related genes	Relation type
DLGAP2	TF binding region
ENSG00000254265	TF binding region
ENSG00000253267	TF binding region
DLGAP2	CpG island
ENSG00000254265	CpG island
ENSG00000253267	CpG island
ENSG00000253267	chromatin interactions
ENSG00000198010	chromatin interactions
ENSG00000254265	chromatin interactions
ENSG00000182372	chromatin interactions
ENSG00000253982	chromatin interactions

Extended variants
information (count: 6876 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:6876 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541022232	chr8:1563565-1563566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112103035	chr8:1563590-1563591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201493123	chr8:1563601-1563602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543623559	chr8:1563612-1563613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13265044	chr8:1563630-1563631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180716456	chr8:1563657-1563658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563702470	chr8:1563663-1563664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs56162807	chr8:1563716-1563717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56084881	chr8:1563718-1563719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184319441	chr8:1563721-1563722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62485546	chr8:1563728-1563729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62485547	chr8:1563750-1563751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552635362	chr8:1563752-1563753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377450203	chr8:1563766-1563767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559992895	chr8:1563785-1563786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373170928	chr8:1563792-1563793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs56154011	chr8:1563822-1563823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528097542	chr8:1563825-1563826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548169015	chr8:1563854-1563855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190037570	chr8:1563869-1563870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368566453	chr8:1563882-1563883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537117936	chr8:1563885-1563886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550631711	chr8:1563888-1563889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2977207	chr8:1563904-1563905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570592216	chr8:1563906-1563907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539608756	chr8:1563909-1563910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2956960	chr8:1563910-1563911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113533424	chr8:1563916-1563917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369836064	chr8:1563938-1563939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553036029	chr8:1563945-1563946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2977208	chr8:1563952-1563953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2956961	chr8:1563961-1563962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534705076	chr8:1563975-1563976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554507215	chr8:1563995-1563996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376990955	chr8:1564002-1564003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574613346	chr8:1564005-1564006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs28505586	chr8:1564010-1564011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113004751	chr8:1564011-1564012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs28631221	chr8:1564012-1564013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543580398	chr8:1564015-1564016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145388238	chr8:1564029-1564030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs28462222	chr8:1564032-1564033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs28631538	chr8:1564038-1564039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28485616	chr8:1564044-1564045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371582682	chr8:1564053-1564054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577412444	chr8:1564061-1564062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74510901	chr8:1564065-1564066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546332371	chr8:1564071-1564072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200056474	chr8:1564081-1564082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115918490	chr8:1564136-1564137	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1562600-1564800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:1562600-1569400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:1562800-1572600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:1567800-1570200	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr8:1568000-1568400	Enhancers	Fetal Muscle Leg	muscle
6	chr8:1569400-1570000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:1569800-1570400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:1569800-1570400	Active TSS	Spleen	Spleen
9	chr8:1570000-1570400	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:1570000-1571400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:1570200-1570800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr8:1570200-1571000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr8:1570400-1571600	Weak transcription	Spleen	Spleen
14	chr8:1570400-1579800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr8:1571400-1571800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:1571600-1571800	ZNF genes & repeats	Pancreas	Pancrea
17	chr8:1571600-1571800	Enhancers	Spleen	Spleen
18	chr8:1571800-1574800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:1573200-1573400	Enhancers	Colon Smooth Muscle	Colon
20	chr8:1573400-1573800	Enhancers	Adipose Nuclei	Adipose
21	chr8:1573400-1573800	Flanking Active TSS	Colon Smooth Muscle	Colon
22	chr8:1573800-1574200	Enhancers	Colon Smooth Muscle	Colon
23	chr8:1574000-1574200	Enhancers	Fetal Muscle Leg	muscle
24	chr8:1574800-1575200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:1575000-1575200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr8:1575200-1575400	Enhancers	Spleen	Spleen
27	chr8:1575200-1599400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr8:1579800-1580000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr8:1579800-1581200	Enhancers	Fetal Brain Male	brain
30	chr8:1580000-1580800	Enhancers	Fetal Brain Female	brain
31	chr8:1580600-1581000	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr8:1580800-1581200	Active TSS	Gastric	stomach
33	chr8:1581400-1581800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr8:1593400-1594600	Weak transcription	Fetal Brain Male	brain
35	chr8:1594200-1594400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:1594400-1595000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:1595000-1595200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr8:1595800-1596800	Enhancers	Gastric	stomach
39	chr8:1596000-1596200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr8:1596800-1598000	Weak transcription	Gastric	stomach
41	chr8:1599400-1599600	Bivalent Enhancer	Brain Substantia Nigra	brain
42	chr8:1599400-1600000	Enhancers	H9 Cell Line	embryonic stem cell
43	chr8:1599400-1600200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr8:1599400-1601200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:1599600-1599800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
46	chr8:1599600-1600400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr8:1599600-1600600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
48	chr8:1599600-1601000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr8:1599600-1601600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr8:1599800-1600000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell

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