Variant report

Variant	nsv890028
Chromosome Location	chr8:5839103-5923666
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:236)
CpG islands
(count:245)
Chromatin interactive
region (count:3)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:236 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:5850953-5851324	K562	blood:	n/a	n/a
2	BHLHE40	chr8:5851096-5851152	K562	blood:	n/a	n/a
3	BHLHE40	chr8:5851125-5851150	GM12878	blood:	n/a	n/a
4	BRCA1	chr8:5875790-5876111	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr8:5848023-5848042	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr8:5850952-5851325	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr8:5923557-5923830	HepG2	liver:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
8	CEBPB	chr8:5903426-5903622	A549	lung:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
9	CEBPB	chr8:5879099-5879536	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr8:5855136-5855336	HepG2	liver:	n/a	chr8:5855245-5855256
11	CEBPB	chr8:5871244-5871593	HepG2	liver:	n/a	chr8:5871421-5871434
12	CEBPB	chr8:5917160-5917474	H1-hESC	embryonic stem cell:	n/a	chr8:5917295-5917306
13	CEBPB	chr8:5923564-5923858	IMR90	lung:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
14	CEBPB	chr8:5920888-5921158	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr8:5871254-5871589	IMR90	lung:	n/a	chr8:5871421-5871434
16	CEBPB	chr8:5850953-5851324	K562	blood:	n/a	n/a
17	CEBPB	chr8:5871257-5871567	A549	lung:	n/a	chr8:5871421-5871434
18	CEBPB	chr8:5871276-5871564	H1-hESC	embryonic stem cell:	n/a	chr8:5871421-5871434
19	CEBPB	chr8:5875401-5876188	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr8:5903392-5903683	K562	blood:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
21	CEBPB	chr8:5877716-5878268	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr8:5883252-5883353	A549	lung:	n/a	n/a
23	CEBPB	chr8:5923536-5923736	K562	blood:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
24	CEBPB	chr8:5917232-5917357	HepG2	liver:	n/a	chr8:5917295-5917306
25	CEBPB	chr8:5850585-5850618	HepG2	liver:	n/a	chr8:5850591-5850602
26	CEBPB	chr8:5923529-5923871	H1-hESC	embryonic stem cell:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
27	CEBPB	chr8:5871279-5871583	K562	blood:	n/a	chr8:5871421-5871434
28	CEBPB	chr8:5903414-5903669	HepG2	liver:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
29	CEBPZ	chr8:5850952-5851322	HepG2	liver:	n/a	n/a
30	CHD1	chr8:5917698-5917701	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr8:5877874-5878141	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr8:5863780-5863930	GM12865	blood:	n/a	n/a
33	CTCF	chr8:5917440-5917766	K562	blood:	n/a	chr8:5917622-5917643
34	CTCF	chr8:5917480-5917630	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr8:5917553-5917637	MCF-7	breast:	n/a	n/a
36	CTCF	chr8:5923540-5923690	AG04449	skin:	n/a	n/a
37	CTCF	chr8:5917500-5917650	AG04449	skin:	n/a	chr8:5917622-5917643
38	CTCF	chr8:5917543-5917628	ProgFib	skin:	n/a	n/a
39	CTCF	chr8:5917597-5917598	K562	blood:	n/a	n/a
40	CTCF	chr8:5917500-5917650	HMF	breast:	n/a	chr8:5917622-5917643
41	CTCF	chr8:5918380-5918530	HBMEC	blood vessel:	n/a	chr8:5918506-5918524 chr8:5918513-5918521
42	CTCF	chr8:5917544-5917713	LNCaP	prostate:	n/a	chr8:5917622-5917643
43	CTCF	chr8:5917580-5917730	MCF-7	breast:	n/a	chr8:5917622-5917643
44	CTCF	chr8:5923588-5923691	Lung_OC	lung:	n/a	n/a
45	CTCF	chr8:5917560-5917710	NHDF-neo	bronchial:	n/a	chr8:5917622-5917643
46	CTCF	chr8:5851121-5851325	K562	blood:	n/a	n/a
47	CTCF	chr8:5917473-5917696	H1-hESC	embryonic stem cell:	n/a	chr8:5917622-5917643
48	CTCF	chr8:5917600-5917619	K562	blood:	n/a	n/a
49	CTCF	chr8:5923582-5923671	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr8:5912626-5912695	Lung_OC	lung:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:5910061-5910111	CMK	blood:	n/a
2	chr8:5910061-5910111	CMK	blood:	n/a
3	chr8:5909945-5909995	GM12892	blood:	n/a
4	chr8:5910061-5910111	HCF	heart:	n/a
5	chr8:5909945-5909995	AG04449	skin:	fetal
6	chr8:5910061-5910111	NB4	blood:	n/a
7	chr8:5910061-5910111	K562	blood:	n/a
8	chr8:5910061-5910111	HCPEpiC	choroid plexus:	n/a
9	chr8:5902873-5902923	PANC-1	pancreas:	n/a
10	chr8:5909945-5909995	Jurkat	blood:	n/a
11	chr8:5909945-5909995	HEK293	kidney:	embryo
12	chr8:5909880-5909930	SK-N-SH_RA	brain:	n/a
13	chr8:5909880-5909930	HUVEC	blood vessel:	n/a
14	chr8:5910061-5910111	HEEpiC	esophagus:	n/a
15	chr8:5909945-5909995	PFSK-1	brain:	n/a
16	chr8:5909880-5909930	MCF10A-Er-Src	breast:	n/a
17	chr8:5909880-5909930	GM12891	blood:	n/a
18	chr8:5909945-5909995	MCF-7	breast:	n/a
19	chr8:5909945-5909995	HepG2	liver:	n/a
20	chr8:5909880-5909930	HepG2	liver:	n/a
21	chr8:5909880-5909930	AG04449	skin:	fetal
22	chr8:5909945-5909995	IMR90	lung:	fetal
23	chr8:5909880-5909930	ProgFib	skin:	n/a
24	chr8:5910061-5910111	NHDF-neo	bronchial:	n/a
25	chr8:5909880-5909930	HRCEpiC	kidney:	n/a
26	chr8:5909945-5909995	AG10803	skin:	n/a
27	chr8:5902873-5902923	HIPEpiC	eye:	n/a
28	chr8:5909880-5909930	HRPEpiC	eye:	n/a
29	chr8:5909880-5909930	AG04450	lung:	fetal
30	chr8:5909880-5909930	AG09309	skin:	n/a
31	chr8:5909880-5909930	HCM	heart:	n/a
32	chr8:5902873-5902923	GM12891	blood:	n/a
33	chr8:5909945-5909995	AG09319	gingival:	n/a
34	chr8:5909880-5909930	T-47D	breast:	n/a
35	chr8:5909945-5909995	Hela-S3	cervix:	n/a
36	chr8:5909945-5909995	HAEpiC	amniotic membrane:	n/a
37	chr8:5902873-5902923	BJ	skin:	n/a
38	chr8:5909880-5909930	H1-hESC	embryonic stem cell:	embryo
39	chr8:5902873-5902923	SAEC	small airway:	n/a
40	chr8:5909880-5909930	HRE	kidney:	n/a
41	chr8:5910061-5910111	A549	lung:	n/a
42	chr8:5902873-5902923	LNCaP	prostate:	n/a
43	chr8:5902873-5902923	MCF-7	breast:	n/a
44	chr8:5902873-5902923	AG09319	gingival:	n/a
45	chr8:5909945-5909995	Caco-2	colon:	n/a
46	chr8:5902873-5902923	NHBE	bronchial:	n/a
47	chr8:5902873-5902923	HCF	heart:	n/a
48	chr8:5909945-5909995	HCPEpiC	choroid plexus:	n/a
49	chr8:5909945-5909995	GM19239	blood:	n/a
50	chr8:5909945-5909995	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:5905980..5908043-chr8:5909546..5912210,2	K562	blood:
2	chr8:5917249..5917976-chr8:5997130..5997653,2	MCF-7	breast:
3	chr8:5905980..5908043-chr8:5909546..5912210,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-3	chr8:5916524-5916600	ENSG00000253880
2	lnc-ANGPT2-3	chr8:5923520-5923650	XLOC_006984
3	lnc-ANGPT2-3	chr8:5901875-5902047	ENSG00000253880
4	lnc-ANGPT2-3	chr8:5917266-5917339	ENSG00000253880
5	lnc-ANGPT2-4	chr8:5894123-5894292	ENSG00000253189
6	lnc-ANGPT2-3	chr8:5917266-5917339	XLOC_006984
7	lnc-ANGPT2-3	chr8:5916524-5916659	XLOC_006984
8	lnc-ANGPT2-5	chr8:5858959-5859084	XLOC_006983
9	lnc-ANGPT2-4	chr8:5893955-5893990	ENSG00000253189
10	lnc-ANGPT2-4	chr8:5894372-5894496	ENSG00000253189
11	lnc-ANGPT2-5	chr8:5860524-5860623	XLOC_006983
12	lnc-ANGPT2-3	chr8:5916281-5916302	XLOC_006984

No data

Variant related genes	Relation type
ENSG00000253189	TF binding region
ENSG00000253189	CpG island
ACVR2A	miRNA target sites
ACVR1B	miRNA target sites

Extended variants
information (count: 3397 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:3397 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2840391	chr8:5847221-5847222	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564339324	chr8:5847257-5847258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79041680	chr8:5847262-5847263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541602384	chr8:5847285-5847286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2816454	chr8:5847294-5847295	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs191921814	chr8:5847406-5847407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529096387	chr8:5847419-5847420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547272498	chr8:5847421-5847422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183930531	chr8:5847447-5847448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs890011	chr8:5847449-5847450	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs890012	chr8:5847453-5847454	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs537003622	chr8:5847477-5847478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556936621	chr8:5847495-5847496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2840392	chr8:5847514-5847515	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs116747840	chr8:5847515-5847516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74419522	chr8:5847523-5847524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs80183881	chr8:5847527-5847528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369055790	chr8:5847542-5847543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs117793168	chr8:5847543-5847544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372483731	chr8:5847551-5847552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141738063	chr8:5847562-5847563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs890013	chr8:5847571-5847572	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs7839113	chr8:5847587-5847588	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
24	rs374493507	chr8:5847595-5847596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188776836	chr8:5847600-5847601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184470677	chr8:5847807-5847808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536170492	chr8:5847810-5847811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73519906	chr8:5847852-5847853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77009210	chr8:5847862-5847863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539984690	chr8:5847867-5847868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558010674	chr8:5847907-5847908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147745493	chr8:5847939-5847940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543442130	chr8:5847952-5847953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115051686	chr8:5847982-5847983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149206890	chr8:5847986-5847987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs117640680	chr8:5847996-5847997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559556971	chr8:5848001-5848002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533017880	chr8:5848021-5848022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577373086	chr8:5848025-5848026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190104924	chr8:5848042-5848043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192946437	chr8:5848044-5848045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565974486	chr8:5848049-5848050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530605968	chr8:5848076-5848077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549064538	chr8:5848089-5848090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567292383	chr8:5848109-5848110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374672622	chr8:5848148-5848149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547785013	chr8:5848159-5848160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115724549	chr8:5848181-5848182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539694465	chr8:5848187-5848188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2703194	chr8:5858800-5858801	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:127)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	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
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Type 2 diabetes	21526130	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20688739	CNVD
Osteosarcoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5847200-5847600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr8:5847800-5848200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr8:5858800-5860000	Enhancers	Placenta Amnion	Placenta Amnion
4	chr8:5859000-5859400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr8:5860000-5860600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr8:5863000-5870200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:5865600-5866200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:5865600-5866200	Enhancers	Fetal Heart	heart
9	chr8:5865600-5866200	Enhancers	Hela-S3	cervix
10	chr8:5865800-5866200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr8:5865800-5866200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr8:5866000-5866200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:5866200-5875000	Weak transcription	Hela-S3	cervix
14	chr8:5866600-5869400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:5869400-5870400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:5870200-5870400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:5871200-5871600	Enhancers	NHEK	skin
18	chr8:5871400-5871600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:5871600-5872200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr8:5871600-5875000	Weak transcription	NHEK	skin
21	chr8:5872200-5872400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:5872400-5875000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:5872800-5874000	Enhancers	Fetal Brain Male	brain
24	chr8:5874000-5875000	Weak transcription	Fetal Brain Male	brain
25	chr8:5874400-5876800	Enhancers	Fetal Heart	heart
26	chr8:5874600-5874800	Enhancers	Aorta	Aorta
27	chr8:5874600-5876000	Enhancers	Fetal Muscle Leg	muscle
28	chr8:5874800-5875800	Weak transcription	Aorta	Aorta
29	chr8:5874800-5876000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr8:5874800-5876400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr8:5874800-5876600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr8:5874800-5876600	Enhancers	HMEC	breast
33	chr8:5875000-5875800	Enhancers	Fetal Brain Male	brain
34	chr8:5875000-5876600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:5875000-5878200	Enhancers	NHEK	skin
36	chr8:5875000-5878800	Enhancers	HUVEC	blood vessel
37	chr8:5875000-5879000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr8:5875000-5879800	Enhancers	Hela-S3	cervix
39	chr8:5875200-5875600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr8:5875200-5875600	Enhancers	NH-A	brain
41	chr8:5875200-5876200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr8:5875400-5875800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr8:5875400-5876000	Enhancers	NHDF-Ad	bronchial
44	chr8:5875600-5876000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr8:5875600-5876000	Flanking Active TSS	NH-A	brain
46	chr8:5875800-5876000	Enhancers	Aorta	Aorta
47	chr8:5875800-5876200	Enhancers	Osteobl	bone
48	chr8:5875800-5876600	Enhancers	NHLF	lung
49	chr8:5876000-5876600	Enhancers	NH-A	brain
50	chr8:5876000-5877200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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