Variant report

Variant	nsv609528
Chromosome Location	chr8:1685064-1728292
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1991)
CpG islands
(count:2016)
Chromatin interactive
region (count:85)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1991 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

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	chr8:1703564-1704299	K562	blood:	n/a	n/a
3	ARID3A	chr8:1693554-1694651	K562	blood:	n/a	n/a
4	ARID3A	chr8:1698531-1698750	K562	blood:	n/a	n/a
5	ARID3A	chr8:1706530-1706868	K562	blood:	n/a	n/a
6	ARID3A	chr8:1703700-1704244	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:1710733-1711272	K562	blood:	n/a	n/a
8	ARID3A	chr8:1712466-1712804	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:1707125-1707584	K562	blood:	n/a	n/a
10	ARID3A	chr8:1708103-1708744	K562	blood:	n/a	n/a
11	ARID3A	chr8:1700948-1701221	HepG2	liver:	n/a	n/a
12	ARID3A	chr8:1690095-1690840	HepG2	liver:	n/a	n/a
13	ATF1	chr8:1693624-1694708	K562	blood:	n/a	n/a
14	ATF1	chr8:1708076-1708663	K562	blood:	n/a	n/a
15	ATF1	chr8:1711832-1712081	K562	blood:	n/a	n/a
16	ATF1	chr8:1706175-1706913	K562	blood:	n/a	n/a
17	ATF1	chr8:1703574-1704210	K562	blood:	n/a	n/a
18	ATF1	chr8:1727822-1728089	K562	blood:	n/a	n/a
19	ATF2	chr8:1711802-1712124	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr8:1711835-1712169	GM12878	blood:	n/a	n/a
21	ATF2	chr8:1693748-1694670	GM12878	blood:	n/a	n/a
22	ATF2	chr8:1714860-1715262	GM12878	blood:	n/a	n/a
23	ATF2	chr8:1693583-1694333	GM12878	blood:	n/a	n/a
24	ATF2	chr8:1711806-1712187	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr8:1693623-1693916	K562	blood:	n/a	n/a
26	ATF3	chr8:1694289-1694617	K562	blood:	n/a	n/a
27	ATF3	chr8:1711797-1712028	K562	blood:	n/a	n/a
28	ATF3	chr8:1694307-1694619	K562	blood:	n/a	n/a
29	ATF3	chr8:1703576-1704226	K562	blood:	n/a	n/a
30	ATF3	chr8:1712527-1712754	K562	blood:	n/a	n/a
31	ATF3	chr8:1711826-1712058	K562	blood:	n/a	n/a
32	BACH1	chr8:1703814-1704099	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr8:1708143-1708723	K562	blood:	n/a	n/a
34	BACH1	chr8:1694205-1694780	K562	blood:	n/a	n/a
35	BACH1	chr8:1703737-1704233	K562	blood:	n/a	n/a
36	BACH1	chr8:1711099-1711111	K562	blood:	n/a	n/a
37	BACH1	chr8:1697399-1697624	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr8:1711786-1712750	H1-hESC	embryonic stem cell:	n/a	n/a
39	BATF	chr8:1693700-1694177	GM12878	blood:	n/a	n/a
40	BATF	chr8:1703886-1704057	GM12878	blood:	n/a	chr8:1703978-1703988 chr8:1703973-1703984
41	BATF	chr8:1703806-1704093	GM12878	blood:	n/a	chr8:1703978-1703988 chr8:1703973-1703984
42	BATF	chr8:1694269-1694678	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:1693800-1694181	GM12878	blood:	n/a	chr8:1693810-1693819
44	BCL11A	chr8:1715013-1715222	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:1693806-1694271	GM12878	blood:	n/a	chr8:1693810-1693819 chr8:1694175-1694184
46	BCL3	chr8:1711088-1711547	A549	lung:	n/a	chr8:1711502-1711515 chr8:1711465-1711478 chr8:1711536-1711545
47	BCL3	chr8:1711828-1712236	A549	lung:	n/a	chr8:1712008-1712017
48	BCL3	chr8:1711834-1712485	A549	lung:	n/a	chr8:1712414-1712427 chr8:1712415-1712428 chr8:1712008-1712017
49	BCLAF1	chr8:1693796-1694653	GM12878	blood:	n/a	chr8:1693810-1693819 chr8:1694175-1694184
50	BCLAF1	chr8:1693787-1694651	GM12878	blood:	n/a	chr8:1693810-1693819 chr8:1694175-1694184

(count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1712271-1712321	CMK	blood:	n/a
2	chr8:1692726-1692776	NHDF-neo	bronchial:	n/a
3	chr8:1725140-1725190	NB4	blood:	n/a
4	chr8:1712271-1712321	CMK	blood:	n/a
5	chr8:1692726-1692776	NHDF-neo	bronchial:	n/a
6	chr8:1725140-1725190	NB4	blood:	n/a
7	chr8:1719543-1719593	HUVEC	blood vessel:	n/a
8	chr8:1719380-1719430	U87	brain:	n/a
9	chr8:1719290-1719340	HAEpiC	amniotic membrane:	n/a
10	chr8:1712170-1712220	NT2-D1	testis:	n/a
11	chr8:1692107-1692157	NH-A	brain:	n/a
12	chr8:1692726-1692776	HEEpiC	esophagus:	n/a
13	chr8:1712330-1712380	AG04450	lung:	fetal
14	chr8:1704013-1704063	HUVEC	blood vessel:	n/a
15	chr8:1697536-1697586	HepG2	liver:	n/a
16	chr8:1711046-1711096	AG04449	skin:	fetal
17	chr8:1711433-1711483	H1-hESC	embryonic stem cell:	embryo
18	chr8:1708526-1708576	NH-A	brain:	n/a
19	chr8:1711046-1711096	PFSK-1	brain:	n/a
20	chr8:1725119-1725169	HIPEpiC	eye:	n/a
21	chr8:1708447-1708497	ProgFib	skin:	n/a
22	chr8:1707330-1707380	GM12892	blood:	n/a
23	chr8:1719380-1719430	HPAEpiC	pulmonary alveolar:	n/a
24	chr8:1707330-1707380	NH-A	brain:	n/a
25	chr8:1692458-1692508	ovcar-3	ovarian:	n/a
26	chr8:1717660-1717710	GM12878	blood:	n/a
27	chr8:1704075-1704125	HIPEpiC	eye:	n/a
28	chr8:1692726-1692776	T-47D	breast:	n/a
29	chr8:1725119-1725169	HRCEpiC	kidney:	n/a
30	chr8:1707330-1707380	HEEpiC	esophagus:	n/a
31	chr8:1697536-1697586	SK-N-SH	brain:	n/a
32	chr8:1711046-1711096	SK-N-SH	brain:	n/a
33	chr8:1707330-1707380	SK-N-MC	brain:	n/a
34	chr8:1713012-1713062	HCPEpiC	choroid plexus:	n/a
35	chr8:1719290-1719340	IMR90	lung:	fetal
36	chr8:1697536-1697586	AG04450	lung:	fetal
37	chr8:1692107-1692157	A549	lung:	n/a
38	chr8:1708526-1708576	HIPEpiC	eye:	n/a
39	chr8:1692458-1692508	GM12878	blood:	n/a
40	chr8:1712271-1712321	HCPEpiC	choroid plexus:	n/a
41	chr8:1708447-1708497	PrEC	prostate:	n/a
42	chr8:1707477-1707527	HL-60	blood:	n/a
43	chr8:1707413-1707463	HEEpiC	esophagus:	n/a
44	chr8:1725179-1725229	HCT-116	colon:	n/a
45	chr8:1697459-1697509	Jurkat	blood:	n/a
46	chr8:1704075-1704125	GM12891	blood:	n/a
47	chr8:1712271-1712321	PANC-1	pancreas:	n/a
48	chr8:1717660-1717710	Hela-S3	cervix:	n/a
49	chr8:1707413-1707463	ProgFib	skin:	n/a
50	chr8:1713012-1713062	ECC-1	luminal epithelium:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:1708451..1710291-chr8:1769924..1772142,2	K562	blood:
2	chr8:1710901..1715165-chr8:1763143..1767602,4	K562	blood:
3	chr8:1684038..1686561-chr8:1711084..1712733,2	MCF-7	breast:
4	chr8:1710542..1713448-chr8:1725280..1729246,5	K562	blood:
5	chr8:1688805..1690612-chr8:1693113..1695827,3	K562	blood:
6	chr8:1683414..1685975-chr8:1702028..1704859,2	MCF-7	breast:
7	chr8:1683723..1685599-chr8:1688819..1690722,2	K562	blood:
8	chr8:1692125..1694169-chr8:1767018..1769382,2	MCF-7	breast:
9	chr8:1726321..1728354-chr8:1771384..1774203,2	MCF-7	breast:
10	chr8:1684817..1688387-chr8:1693951..1696420,3	K562	blood:
11	chr8:1692017..1693877-chr8:1696631..1699350,2	MCF-7	breast:
12	chr8:1656737..1659589-chr8:1707662..1709873,2	K562	blood:
13	chr8:1702544..1704176-chr8:1706755..1708609,2	MCF-7	breast:
14	chr8:1708066..1710813-chr8:1745165..1747310,2	MCF-7	breast:
15	chr8:1687352..1688981-chr8:1706866..1709759,2	K562	blood:
16	chr8:1681796..1686732-chr8:1704250..1709938,6	K562	blood:
17	chr8:1712944..1715681-chr8:1734053..1736692,2	K562	blood:
18	chr8:1691178..1695166-chr8:1727484..1730315,3	MCF-7	breast:
19	chr8:1716952..1719420-chr8:1723630..1725290,2	K562	blood:
20	chr8:1686924..1688783-chr8:1724884..1727054,2	MCF-7	breast:
21	chr8:1691178..1695166-chr8:1727484..1730315,3	MCF-7	breast:
22	chr8:1683243..1684210-chr8:1693916..1694440,2	K562	blood:
23	chr17:38219023..38219851-chr8:1710924..1711761,2	Hela-S3	cervix:
24	chr8:1686924..1688783-chr8:1724884..1727054,2	MCF-7	breast:
25	chr8:1692167..1695898-chr8:1702417..1705508,6	MCF-7	breast:
26	chr8:1712198..1712991-chr8:1724016..1724625,2	K562	blood:
27	chr8:1711365..1714898-chr8:1724612..1727757,4	MCF-7	breast:
28	chr8:1716952..1719420-chr8:1723630..1725290,2	K562	blood:
29	chr8:1693361..1695232-chr8:1714605..1717570,2	MCF-7	breast:
30	chr8:1722780..1724453-chr8:1725815..1728009,2	K562	blood:
31	chr8:1722706..1724431-chr8:1770529..1772406,2	K562	blood:
32	chr8:1722780..1724453-chr8:1725815..1728009,2	K562	blood:
33	chr8:1715604..1719309-chr8:1719775..1722697,3	MCF-7	breast:
34	chr8:1690830..1693396-chr8:1731671..1734648,2	K562	blood:
35	chr8:1716816..1721615-chr8:1726505..1732038,6	K562	blood:
36	chr8:1688805..1690612-chr8:1693113..1695827,3	K562	blood:
37	chr8:1726532..1728287-chr8:1729917..1731820,2	K562	blood:
38	chr8:1725330..1728287-chr8:1728724..1731820,3	K562	blood:
39	chr8:1692017..1693877-chr8:1696631..1699350,2	MCF-7	breast:
40	chr8:1695837..1698728-chr8:1710665..1712737,2	MCF-7	breast:
41	chr8:1695351..1696872-chr8:1698699..1700709,2	MCF-7	breast:
42	chr8:1691840..1698609-chr8:1701330..1706354,17	MCF-7	breast:
43	chr8:1686398..1691493-chr8:1692732..1695929,5	MCF-7	breast:
44	chr8:1717744..1722491-chr8:1723636..1726849,4	MCF-7	breast:
45	chr8:1690439..1692118-chr8:1706880..1708703,2	MCF-7	breast:
46	chr8:1692503..1695228-chr8:1698804..1700487,2	K562	blood:
47	chr8:1684817..1688387-chr8:1693951..1696420,3	K562	blood:
48	chr8:1717537..1720996-chr8:1730538..1734244,3	K562	blood:
49	chr8:1711111..1712724-chr8:1772703..1775383,2	MCF-7	breast:
50	chr8:1702392..1708895-chr8:1709221..1714010,17	MCF-7	breast:

(count:16 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 2529 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:2529 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11992719	chr8:1685064-1685065	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184870536	chr8:1685120-1685121	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs560576684	chr8:1685128-1685129	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs11992759	chr8:1685130-1685131	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs529939885	chr8:1685134-1685135	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs543192671	chr8:1685179-1685180	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs11992782	chr8:1685213-1685214	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs138691506	chr8:1685252-1685253	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs112202098	chr8:1685263-1685264	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs386720671	chr8:1685270-1685271	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs11989533	chr8:1685271-1685272	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs138536196	chr8:1685278-1685279	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs567706203	chr8:1685279-1685280	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs11992793	chr8:1685282-1685283	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs534649538	chr8:1685286-1685287	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs11992795	chr8:1685287-1685288	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs189242941	chr8:1685289-1685290	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs559129150	chr8:1685293-1685294	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs180971749	chr8:1685299-1685300	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs535018085	chr8:1685300-1685301	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs554832167	chr8:1685301-1685302	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs566410351	chr8:1685302-1685303	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs574141766	chr8:1685303-1685304	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs543406472	chr8:1685307-1685308	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs61065232	chr8:1685308-1685309	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs545551103	chr8:1685309-1685310	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs57708096	chr8:1685310-1685311	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs11989562	chr8:1685317-1685318	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs181110615	chr8:1685318-1685319	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs530676878	chr8:1685327-1685328	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs550164713	chr8:1685328-1685329	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs569923108	chr8:1685334-1685335	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539149534	chr8:1685338-1685339	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs552236942	chr8:1685340-1685341	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs565973232	chr8:1685341-1685342	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs534885924	chr8:1685343-1685344	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs554693136	chr8:1685347-1685348	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs79915082	chr8:1685348-1685349	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs60900152	chr8:1685349-1685350	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs192062132	chr8:1685350-1685351	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs545924884	chr8:1685353-1685354	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553101674	chr8:1685357-1685358	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs572929337	chr8:1685361-1685362	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs542058483	chr8:1685362-1685363	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs182947019	chr8:1685370-1685371	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs530857945	chr8:1685371-1685372	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs11990321	chr8:1685372-1685373	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs563734549	chr8:1685373-1685374	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs532390486	chr8:1685390-1685391	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs552296598	chr8:1685392-1685393	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:117)

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

Chromatin state (count:2273 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1682800-1685600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:1683400-1686400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:1683600-1685200	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr8:1683600-1686200	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr8:1683600-1686200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr8:1683800-1685200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr8:1683800-1685200	Enhancers	Primary B cells from cord blood	blood
8	chr8:1683800-1686200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:1683800-1686400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr8:1683800-1686600	Enhancers	HUVEC	blood vessel
11	chr8:1684000-1685600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr8:1684000-1685600	Weak transcription	Osteobl	bone
13	chr8:1684000-1685800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr8:1684000-1686200	Enhancers	GM12878-XiMat	blood
15	chr8:1684200-1685200	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr8:1684200-1685600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr8:1684200-1685600	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr8:1684200-1685600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr8:1684200-1685800	Weak transcription	K562	blood
20	chr8:1684200-1686000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr8:1684200-1686000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:1684200-1686000	Enhancers	Adipose Nuclei	Adipose
23	chr8:1684200-1686000	Enhancers	Fetal Thymus	thymus
24	chr8:1684200-1686400	Enhancers	NH-A	brain
25	chr8:1684400-1685600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr8:1684400-1685600	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr8:1684400-1685600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr8:1684400-1686000	Weak transcription	HSMMtube	muscle
29	chr8:1684600-1685600	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr8:1684800-1685800	Weak transcription	Left Ventricle	heart
31	chr8:1684800-1686400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:1684800-1686400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr8:1685000-1685200	Enhancers	Brain Substantia Nigra	brain
34	chr8:1685000-1685400	Weak transcription	Placenta	Placenta
35	chr8:1685000-1685600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr8:1685200-1692400	Weak transcription	Brain Substantia Nigra	brain
37	chr8:1685400-1685800	Enhancers	Fetal Muscle Leg	muscle
38	chr8:1685400-1686000	Enhancers	Placenta	Placenta
39	chr8:1685600-1685800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr8:1685600-1685800	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr8:1685600-1685800	Enhancers	HSMM	muscle
42	chr8:1685600-1686000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr8:1685600-1686000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr8:1685600-1686200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr8:1685600-1686200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr8:1685600-1686200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
47	chr8:1685600-1686200	Enhancers	Osteobl	bone
48	chr8:1685600-1686400	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr8:1685600-1686400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr8:1685600-1686400	Enhancers	Muscle Satellite Cultured Cells	--

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