Variant report

Variant	nsv890029
Chromosome Location	chr8:5872394-5926632
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	BRCA1	chr8:5875790-5876111	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr8:5923536-5923736	K562	blood:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
3	CEBPB	chr8:5903426-5903622	A549	lung:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
4	CEBPB	chr8:5923529-5923871	H1-hESC	embryonic stem cell:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
5	CEBPB	chr8:5923557-5923830	HepG2	liver:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
6	CEBPB	chr8:5917160-5917474	H1-hESC	embryonic stem cell:	n/a	chr8:5917295-5917306
7	CEBPB	chr8:5877716-5878268	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr8:5917232-5917357	HepG2	liver:	n/a	chr8:5917295-5917306
9	CEBPB	chr8:5883252-5883353	A549	lung:	n/a	n/a
10	CEBPB	chr8:5875401-5876188	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr8:5903414-5903669	HepG2	liver:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
12	CEBPB	chr8:5920888-5921158	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr8:5923564-5923858	IMR90	lung:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
14	CEBPB	chr8:5903392-5903683	K562	blood:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
15	CEBPB	chr8:5879099-5879536	Hela-S3	cervix:	n/a	n/a
16	CHD1	chr8:5917698-5917701	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr8:5877874-5878141	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr8:5918380-5918530	HBMEC	blood vessel:	n/a	chr8:5918506-5918524 chr8:5918513-5918521
19	CTCF	chr8:5917543-5917628	ProgFib	skin:	n/a	n/a
20	CTCF	chr8:5917440-5917766	K562	blood:	n/a	chr8:5917622-5917643
21	CTCF	chr8:5917600-5917750	MCF-7	breast:	n/a	chr8:5917622-5917643
22	CTCF	chr8:5917559-5917654	HepG2	liver:	n/a	chr8:5917622-5917643
23	CTCF	chr8:5917538-5917668	Hela-S3	cervix:	n/a	chr8:5917622-5917643
24	CTCF	chr8:5917544-5917713	LNCaP	prostate:	n/a	chr8:5917622-5917643
25	CTCF	chr8:5917580-5917730	MCF-7	breast:	n/a	chr8:5917622-5917643
26	CTCF	chr8:5917500-5917650	HBMEC	blood vessel:	n/a	chr8:5917622-5917643
27	CTCF	chr8:5917480-5917630	HL-60	blood:	n/a	n/a
28	CTCF	chr8:5917497-5917697	GM12878	blood:	n/a	chr8:5917622-5917643
29	CTCF	chr8:5917557-5917650	Lung_OC	lung:	n/a	chr8:5917622-5917643
30	CTCF	chr8:5917460-5917610	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr8:5917553-5917637	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:5912626-5912695	Lung_OC	lung:	n/a	n/a
33	CTCF	chr8:5917500-5917650	AG04449	skin:	n/a	chr8:5917622-5917643
34	CTCF	chr8:5917500-5917650	HCPEpiC	choroid plexus:	n/a	chr8:5917622-5917643
35	CTCF	chr8:5923596-5923677	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr8:5925433-5925541	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:5923540-5923690	AG04449	skin:	n/a	n/a
38	CTCF	chr8:5923588-5923691	Lung_OC	lung:	n/a	n/a
39	CTCF	chr8:5917607-5917625	GM12878	blood:	n/a	n/a
40	CTCF	chr8:5917533-5917651	MCF-7	breast:	n/a	chr8:5917622-5917643
41	CTCF	chr8:5917480-5917630	Caco-2	colon:	n/a	n/a
42	CTCF	chr8:5917600-5917750	HMEC	breast:	n/a	chr8:5917622-5917643
43	CTCF	chr8:5917500-5917650	AG10803	skin:	n/a	chr8:5917622-5917643
44	CTCF	chr8:5917500-5917650	HMF	breast:	n/a	chr8:5917622-5917643
45	CTCF	chr8:5917480-5917630	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr8:5917540-5917690	SAEC	small airway:	n/a	chr8:5917622-5917643
47	CTCF	chr8:5923540-5923690	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr8:5917480-5917630	HRE	kidney:	n/a	n/a
49	CTCF	chr8:5900840-5900990	GM12873	blood:	n/a	n/a
50	CTCF	chr8:5917480-5917630	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:5909880-5909930	GM12892	blood:	n/a
2	chr8:5909945-5909995	NB4	blood:	n/a
3	chr8:5902873-5902923	HPAEpiC	pulmonary alveolar:	n/a
4	chr8:5909880-5909930	HAEpiC	amniotic membrane:	n/a
5	chr8:5909880-5909930	HMEC	breast:	n/a
6	chr8:5902873-5902923	HCM	heart:	n/a
7	chr8:5909880-5909930	SK-N-MC	brain:	n/a
8	chr8:5909945-5909995	BE2_C	brain:	n/a
9	chr8:5902873-5902923	SK-N-MC	brain:	n/a
10	chr8:5902873-5902923	NHDF-neo	bronchial:	n/a
11	chr8:5909945-5909995	AG04450	lung:	fetal
12	chr8:5902873-5902923	HIPEpiC	eye:	n/a
13	chr8:5910061-5910111	AG09309	skin:	n/a
14	chr8:5909880-5909930	PFSK-1	brain:	n/a
15	chr8:5909880-5909930	GM06990	blood:	n/a
16	chr8:5902873-5902923	HRE	kidney:	n/a
17	chr8:5909880-5909930	GM12891	blood:	n/a
18	chr8:5910061-5910111	H1-hESC	embryonic stem cell:	embryo
19	chr8:5902873-5902923	HMEC	breast:	n/a
20	chr8:5909945-5909995	ProgFib	skin:	n/a
21	chr8:5909945-5909995	NT2-D1	testis:	n/a
22	chr8:5902873-5902923	MCF10A-Er-Src	breast:	n/a
23	chr8:5909945-5909995	PFSK-1	brain:	n/a
24	chr8:5909880-5909930	PANC-1	pancreas:	n/a
25	chr8:5909945-5909995	HRCEpiC	kidney:	n/a
26	chr8:5909945-5909995	HIPEpiC	eye:	n/a
27	chr8:5909880-5909930	Jurkat	blood:	n/a
28	chr8:5909945-5909995	HMEC	breast:	n/a
29	chr8:5910061-5910111	HNPCEpiC	eye:	n/a
30	chr8:5902873-5902923	MCF-7	breast:	n/a
31	chr8:5910061-5910111	BE2_C	brain:	n/a
32	chr8:5910061-5910111	IMR90	lung:	fetal
33	chr8:5909880-5909930	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:5909945-5909995	HCT-116	colon:	n/a
35	chr8:5902873-5902923	NT2-D1	testis:	n/a
36	chr8:5909945-5909995	HCF	heart:	n/a
37	chr8:5902873-5902923	RPTEC	kidney:	n/a
38	chr8:5909945-5909995	HL-60	blood:	n/a
39	chr8:5909880-5909930	ovcar-3	ovarian:	n/a
40	chr8:5910061-5910111	HAEpiC	amniotic membrane:	n/a
41	chr8:5902873-5902923	HNPCEpiC	eye:	n/a
42	chr8:5909945-5909995	T-47D	breast:	n/a
43	chr8:5902873-5902923	SK-N-SH	brain:	n/a
44	chr8:5910061-5910111	HPAEpiC	pulmonary alveolar:	n/a
45	chr8:5910061-5910111	Hela-S3	cervix:	n/a
46	chr8:5910061-5910111	HUVEC	blood vessel:	n/a
47	chr8:5909880-5909930	ECC-1	luminal epithelium:	n/a
48	chr8:5909880-5909930	HepG2	liver:	n/a
49	chr8:5909880-5909930	NHBE	bronchial:	n/a
50	chr8:5910061-5910111	AG04449	skin:	fetal

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

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

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

Extended variants
information (count: 2720 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:2720 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4875668	chr8:5872394-5872395	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574016651	chr8:5872397-5872398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2840423	chr8:5872407-5872408	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs184718367	chr8:5872413-5872414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532973073	chr8:5872438-5872439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545148164	chr8:5872443-5872444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563244472	chr8:5872468-5872469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189430757	chr8:5872469-5872470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145537398	chr8:5872488-5872489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566898375	chr8:5872501-5872502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529587771	chr8:5872507-5872508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547761573	chr8:5872555-5872556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569049508	chr8:5872566-5872567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs77351882	chr8:5872575-5872576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138147444	chr8:5872578-5872579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529964251	chr8:5872587-5872588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537944657	chr8:5872595-5872596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4875669	chr8:5872599-5872600	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs537526035	chr8:5872622-5872623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555826650	chr8:5872624-5872625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536713053	chr8:5872628-5872629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574081361	chr8:5872673-5872674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181801662	chr8:5872692-5872693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187404950	chr8:5872695-5872696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141716925	chr8:5872702-5872703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576634210	chr8:5872709-5872710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115080989	chr8:5872742-5872743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563465721	chr8:5872753-5872754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539210271	chr8:5872767-5872768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs80191555	chr8:5872807-5872808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs12056862	chr8:5872844-5872845	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs12056863	chr8:5872872-5872873	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528081833	chr8:5872924-5872925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189059079	chr8:5872940-5872941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75442001	chr8:5872942-5872943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs4875670	chr8:5872965-5872966	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs114157631	chr8:5873034-5873035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570240957	chr8:5873064-5873065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115195398	chr8:5873080-5873081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4875671	chr8:5873093-5873094	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs555569268	chr8:5873095-5873096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575266516	chr8:5873106-5873107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567721070	chr8:5873107-5873108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534711938	chr8:5873115-5873116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112069803	chr8:5873121-5873122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201113604	chr8:5873125-5873126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149270396	chr8:5873140-5873141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538910512	chr8:5873141-5873142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548064197	chr8:5873149-5873150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556782415	chr8:5873160-5873161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

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
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5866200-5875000	Weak transcription	Hela-S3	cervix
2	chr8:5871600-5875000	Weak transcription	NHEK	skin
3	chr8:5872200-5872400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr8:5872400-5875000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr8:5872800-5874000	Enhancers	Fetal Brain Male	brain
6	chr8:5874000-5875000	Weak transcription	Fetal Brain Male	brain
7	chr8:5874400-5876800	Enhancers	Fetal Heart	heart
8	chr8:5874600-5874800	Enhancers	Aorta	Aorta
9	chr8:5874600-5876000	Enhancers	Fetal Muscle Leg	muscle
10	chr8:5874800-5875800	Weak transcription	Aorta	Aorta
11	chr8:5874800-5876000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr8:5874800-5876400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:5874800-5876600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr8:5874800-5876600	Enhancers	HMEC	breast
15	chr8:5875000-5875800	Enhancers	Fetal Brain Male	brain
16	chr8:5875000-5876600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr8:5875000-5878200	Enhancers	NHEK	skin
18	chr8:5875000-5878800	Enhancers	HUVEC	blood vessel
19	chr8:5875000-5879000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:5875000-5879800	Enhancers	Hela-S3	cervix
21	chr8:5875200-5875600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:5875200-5875600	Enhancers	NH-A	brain
23	chr8:5875200-5876200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr8:5875400-5875800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr8:5875400-5876000	Enhancers	NHDF-Ad	bronchial
26	chr8:5875600-5876000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr8:5875600-5876000	Flanking Active TSS	NH-A	brain
28	chr8:5875800-5876000	Enhancers	Aorta	Aorta
29	chr8:5875800-5876200	Enhancers	Osteobl	bone
30	chr8:5875800-5876600	Enhancers	NHLF	lung
31	chr8:5876000-5876600	Enhancers	NH-A	brain
32	chr8:5876000-5877200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr8:5876000-5878000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:5876400-5876600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr8:5876400-5876600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:5876600-5877200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr8:5876600-5877400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:5876600-5878600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr8:5876800-5878600	Weak transcription	Fetal Heart	heart
40	chr8:5877200-5878400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:5877400-5877600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr8:5877400-5878000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr8:5878000-5878200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr8:5878000-5879000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr8:5878200-5878400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr8:5878600-5880000	Enhancers	Fetal Heart	heart
47	chr8:5879000-5879400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr8:5879000-5879600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr8:5879000-5879600	Enhancers	Brain Germinal Matrix	brain
50	chr8:5879200-5879400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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