Variant report

Variant	nsv609524
Chromosome Location	chr8:1594307-1643287
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	ATF1	chr8:1612841-1613066	K562	blood:	n/a	n/a
2	ATF1	chr8:1631106-1631363	K562	blood:	n/a	n/a
3	ATF2	chr8:1606188-1606635	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr8:1631111-1631356	K562	blood:	n/a	n/a
5	BACH1	chr8:1600054-1600554	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr8:1613411-1613643	GM12878	blood:	n/a	chr8:1613634-1613643
7	BHLHE40	chr8:1598474-1598541	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:1610754-1610850	GM12878	blood:	n/a	n/a
9	CEBPB	chr8:1631047-1631403	HepG2	liver:	n/a	chr8:1631220-1631231
10	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
11	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
12	CEBPB	chr8:1631004-1631475	HCT-116	colon:	n/a	chr8:1631220-1631231
13	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
14	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
15	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
16	CEBPB	chr8:1631078-1631329	K562	blood:	n/a	chr8:1631220-1631231
17	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
18	CEBPB	chr8:1600968-1601172	MCF-7	breast:	n/a	chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601079-1601092 chr8:1601079-1601090 chr8:1601080-1601091 chr8:1601081-1601090
19	CEBPB	chr8:1631046-1631432	Hela-S3	cervix:	n/a	chr8:1631220-1631231
20	CEBPB	chr8:1631051-1631490	K562	blood:	n/a	chr8:1631220-1631231
21	CEBPB	chr8:1628110-1628439	IMR90	lung:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
22	CEBPB	chr8:1631129-1631386	IMR90	lung:	n/a	chr8:1631220-1631231
23	CEBPB	chr8:1598267-1598411	HepG2	liver:	n/a	chr8:1598339-1598350 chr8:1598339-1598348
24	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
25	CEBPB	chr8:1630919-1631593	HCT-116	colon:	n/a	chr8:1631220-1631231
26	CEBPB	chr8:1631113-1631408	A549	lung:	n/a	chr8:1631220-1631231
27	CEBPB	chr8:1631054-1631361	K562	blood:	n/a	chr8:1631220-1631231
28	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
29	CHD2	chr8:1606162-1606617	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr8:1624240-1624390	GM12865	blood:	n/a	n/a
31	CTCF	chr8:1607807-1607898	Lung_OC	lung:	n/a	n/a
32	CTCF	chr8:1609079-1609141	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chr8:1611313-1611348	GM19239	blood:	n/a	n/a
34	CTCF	chr8:1616651-1616818	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:1614240-1614390	GM12872	blood:	n/a	n/a
36	CTCF	chr8:1610925-1611115	GM19239	blood:	n/a	n/a
37	CTCF	chr8:1642850-1642919	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr8:1595780-1595930	HepG2	liver:	n/a	n/a
39	CTCF	chr8:1595860-1596010	A549	lung:	n/a	n/a
40	CTCF	chr8:1616699-1616794	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr8:1616699-1616780	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:1616615-1616757	HepG2	liver:	n/a	n/a
43	CTCF	chr8:1628751-1628810	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:1627606-1627668	GM13977	blood:	n/a	n/a
45	CTCF	chr8:1627660-1627810	K562	blood:	n/a	n/a
46	CTCF	chr8:1595864-1595915	MCF-7	breast:	n/a	n/a
47	CUX1	chr8:1630984-1631321	K562	blood:	n/a	n/a
48	E2F6	chr8:1639851-1639984	K562	blood:	n/a	chr8:1639930-1639942
49	E2F6	chr8:1630296-1630411	K562	blood:	n/a	n/a
50	EP300	chr8:1628247-1628270	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1614107-1614157	ECC-1	luminal epithelium:	n/a
2	chr8:1616656-1616706	MCF-7	breast:	n/a
3	chr8:1614107-1614157	ECC-1	luminal epithelium:	n/a
4	chr8:1616656-1616706	MCF-7	breast:	n/a
5	chr8:1614053-1614103	AG10803	skin:	n/a
6	chr8:1616111-1616161	SK-N-SH	brain:	n/a
7	chr8:1642577-1642627	A549	lung:	n/a
8	chr8:1613877-1613927	BE2_C	brain:	n/a
9	chr8:1623303-1623353	T-47D	breast:	n/a
10	chr8:1624822-1624872	K562	blood:	n/a
11	chr8:1624741-1624791	HAEpiC	amniotic membrane:	n/a
12	chr8:1639573-1639623	SK-N-MC	brain:	n/a
13	chr8:1614053-1614103	HIPEpiC	eye:	n/a
14	chr8:1623303-1623353	PANC-1	pancreas:	n/a
15	chr8:1639892-1639942	HCT-116	colon:	n/a
16	chr8:1623483-1623533	PANC-1	pancreas:	n/a
17	chr8:1601314-1601364	MCF-7	breast:	n/a
18	chr8:1620928-1620978	HAEpiC	amniotic membrane:	n/a
19	chr8:1636504-1636554	GM12892	blood:	n/a
20	chr8:1642577-1642627	SK-N-MC	brain:	n/a
21	chr8:1614053-1614103	NT2-D1	testis:	n/a
22	chr8:1624818-1624868	CMK	blood:	n/a
23	chr8:1642380-1642430	ECC-1	luminal epithelium:	n/a
24	chr8:1616422-1616472	RPTEC	kidney:	n/a
25	chr8:1616925-1616975	ovcar-3	ovarian:	n/a
26	chr8:1623378-1623428	NHDF-neo	bronchial:	n/a
27	chr8:1616381-1616431	NB4	blood:	n/a
28	chr8:1624818-1624868	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:1618151-1618201	HMEC	breast:	n/a
30	chr8:1616381-1616431	MCF-7	breast:	n/a
31	chr8:1615950-1616000	SK-N-SH_RA	brain:	n/a
32	chr8:1618151-1618201	LNCaP	prostate:	n/a
33	chr8:1624822-1624872	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:1640712-1640762	LNCaP	prostate:	n/a
35	chr8:1642577-1642627	HEK293	kidney:	embryo
36	chr8:1640712-1640762	HL-60	blood:	n/a
37	chr8:1615080-1615130	T-47D	breast:	n/a
38	chr8:1626419-1626469	HCT-116	colon:	n/a
39	chr8:1639892-1639942	Hela-S3	cervix:	n/a
40	chr8:1640712-1640762	HNPCEpiC	eye:	n/a
41	chr8:1642625-1642675	AG04450	lung:	fetal
42	chr8:1601314-1601364	HCPEpiC	choroid plexus:	n/a
43	chr8:1623378-1623428	NHBE	bronchial:	n/a
44	chr8:1639573-1639623	HepG2	liver:	n/a
45	chr8:1616925-1616975	LNCaP	prostate:	n/a
46	chr8:1616622-1616672	NB4	blood:	n/a
47	chr8:1617868-1617918	SK-N-SH_RA	brain:	n/a
48	chr8:1618448-1618498	HEEpiC	esophagus:	n/a
49	chr8:1613919-1613969	GM06990	blood:	n/a
50	chr8:1623303-1623353	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:1615891..1617815-chr8:1624787..1626742,2	K562	blood:
2	chr8:1599745..1602131-chr8:1603017..1606467,3	K562	blood:
3	chr8:1584132..1586956-chr8:1595846..1598280,3	K562	blood:
4	chr8:1627163..1629357-chr8:1633786..1636690,2	K562	blood:
5	chr8:1599745..1602131-chr8:1603017..1606467,3	K562	blood:
6	chr8:1593850..1596302-chr8:1622198..1625044,2	K562	blood:
7	chr8:1627163..1629357-chr8:1633786..1636690,2	K562	blood:
8	chr8:1578132..1580473-chr8:1601540..1604510,2	K562	blood:
9	chr8:1639712..1642185-chr8:1645555..1647369,2	K562	blood:
10	chr8:1621344..1623146-chr8:1688699..1690451,2	K562	blood:

Variant related genes	Relation type
DLGAP2	TF binding region
DLGAP2	CpG island
ENSG00000198010	chromatin interactions

Extended variants
information (count: 3006 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:3006 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4557727	chr8:1594307-1594308	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574914955	chr8:1594308-1594309	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs193120685	chr8:1594320-1594321	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs184731339	chr8:1594327-1594328	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs563846311	chr8:1594330-1594331	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs188316943	chr8:1594344-1594345	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs377502610	chr8:1594348-1594349	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs191579174	chr8:1594352-1594353	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs183763694	chr8:1594353-1594354	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs73671283	chr8:1594390-1594391	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs117619057	chr8:1594395-1594396	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs2469731	chr8:1594401-1594402	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs189687803	chr8:1594416-1594417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs370376319	chr8:1594436-1594437	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs569261794	chr8:1594437-1594438	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs79925025	chr8:1594475-1594476	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2469730	chr8:1594481-1594482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs181230678	chr8:1594493-1594494	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs2469729	chr8:1594541-1594542	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs2469728	chr8:1594543-1594544	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551328212	chr8:1594547-1594548	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs570664638	chr8:1594548-1594549	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2469727	chr8:1594552-1594553	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs2472090	chr8:1594580-1594581	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs539716847	chr8:1594581-1594582	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2469726	chr8:1594594-1594595	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs186841144	chr8:1594603-1594604	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2469725	chr8:1594608-1594609	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs566453674	chr8:1594661-1594662	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566064972	chr8:1594668-1594669	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs373765890	chr8:1594675-1594676	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs139176709	chr8:1594686-1594687	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs144063247	chr8:1594693-1594694	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs190142061	chr8:1594696-1594697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs144888645	chr8:1594713-1594714	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs555155412	chr8:1594751-1594752	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs577511461	chr8:1594755-1594756	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs367649818	chr8:1594757-1594758	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs546076121	chr8:1594796-1594797	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs558956555	chr8:1594800-1594801	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs181893962	chr8:1594902-1594903	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs541396081	chr8:1594909-1594910	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs561643204	chr8:1594930-1594931	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs530585730	chr8:1594956-1594957	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs372624265	chr8:1594957-1594958	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs550504495	chr8:1594959-1594960	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs564297585	chr8:1594995-1594996	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs35844058	chr8:1594996-1594997	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs79296900	chr8:1595008-1595009	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs546895330	chr8:1595032-1595033	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1575200-1599400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:1593400-1594600	Weak transcription	Fetal Brain Male	brain
3	chr8:1594200-1594400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:1594400-1595000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:1595000-1595200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:1595800-1596800	Enhancers	Gastric	stomach
7	chr8:1596000-1596200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:1596800-1598000	Weak transcription	Gastric	stomach
9	chr8:1599400-1599600	Bivalent Enhancer	Brain Substantia Nigra	brain
10	chr8:1599400-1600000	Enhancers	H9 Cell Line	embryonic stem cell
11	chr8:1599400-1600200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:1599400-1601200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:1599600-1599800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
14	chr8:1599600-1600400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr8:1599600-1600600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
16	chr8:1599600-1601000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr8:1599600-1601600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr8:1599800-1600000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
19	chr8:1599800-1600400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr8:1599800-1600800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr8:1599800-1601200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr8:1600000-1601000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr8:1600000-1601200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
24	chr8:1600200-1600400	Enhancers	Fetal Kidney	kidney
25	chr8:1600200-1600800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr8:1600200-1601200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr8:1600400-1601000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr8:1600400-1601000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
29	chr8:1600400-1601000	Bivalent Enhancer	Fetal Kidney	kidney
30	chr8:1600400-1604800	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr8:1600800-1604800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr8:1600800-1605000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr8:1601000-1601200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr8:1601000-1603400	Weak transcription	Gastric	stomach
35	chr8:1601000-1604800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr8:1601200-1601800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:1601200-1604600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:1601800-1605600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr8:1602000-1604800	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr8:1604000-1604200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr8:1604000-1604200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr8:1604000-1604200	Enhancers	Gastric	stomach
43	chr8:1604600-1605400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:1604800-1605000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr8:1604800-1605000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr8:1604800-1605800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr8:1604800-1605800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr8:1604800-1605800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr8:1604800-1605800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr8:1604800-1605800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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