Variant report

Variant	nsv539600
Chromosome Location	chr8:49190915-49243694
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	chr8:49231315-49231583	K562	blood:	n/a	n/a
2	ARID3A	chr8:49231260-49231612	HepG2	liver:	n/a	n/a
3	BACH1	chr8:49231426-49231446	K562	blood:	n/a	n/a
4	BATF	chr8:49198448-49198713	GM12878	blood:	n/a	n/a
5	BCL3	chr8:49196659-49196994	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:49231361-49231600	K562	blood:	n/a	n/a
7	BHLHE40	chr8:49231303-49231542	GM12878	blood:	n/a	n/a
8	CEBPB	chr8:49192104-49192326	A549	lung:	n/a	chr8:49192229-49192240 chr8:49192224-49192241 chr8:49192227-49192240 chr8:49192227-49192238
9	CEBPB	chr8:49230798-49231644	IMR90	lung:	n/a	chr8:49230825-49230837
10	CEBPB	chr8:49236856-49237085	A549	lung:	n/a	n/a
11	CEBPB	chr8:49230799-49231668	Hela-S3	cervix:	n/a	chr8:49230825-49230837
12	CEBPB	chr8:49236780-49237173	IMR90	lung:	n/a	n/a
13	CEBPB	chr8:49194117-49194421	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr8:49192155-49192346	K562	blood:	n/a	chr8:49192229-49192240 chr8:49192224-49192241 chr8:49192227-49192240 chr8:49192227-49192238
15	CEBPB	chr8:49203529-49204137	IMR90	lung:	n/a	chr8:49203660-49203671
16	CEBPB	chr8:49200236-49200618	IMR90	lung:	n/a	n/a
17	CEBPB	chr8:49194059-49194509	IMR90	lung:	n/a	n/a
18	CEBPB	chr8:49221060-49221411	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:49230975-49231227	K562	blood:	n/a	n/a
20	CEBPB	chr8:49192693-49192938	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr8:49236816-49237121	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr8:49217857-49218223	IMR90	lung:	n/a	n/a
23	CEBPB	chr8:49192073-49192360	HepG2	liver:	n/a	chr8:49192229-49192240 chr8:49192094-49192107 chr8:49192224-49192241 chr8:49192227-49192240 chr8:49192227-49192238
24	CEBPB	chr8:49228450-49228727	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:49203494-49203729	A549	lung:	n/a	chr8:49203660-49203671
26	CEBPB	chr8:49229216-49229733	IMR90	lung:	n/a	n/a
27	CEBPB	chr8:49203523-49203774	HepG2	liver:	n/a	chr8:49203660-49203671
28	CEBPB	chr8:49194137-49194357	A549	lung:	n/a	n/a
29	CEBPB	chr8:49192664-49192961	IMR90	lung:	n/a	n/a
30	CHD1	chr8:49217687-49218343	IMR90	lung:	n/a	n/a
31	CHD2	chr8:49231401-49231700	GM12878	blood:	n/a	n/a
32	CHD2	chr8:49230818-49231728	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr8:49231420-49231556	K562	blood:	n/a	n/a
34	CHD2	chr8:49231471-49231589	HepG2	liver:	n/a	n/a
35	CTCF	chr8:49231696-49231820	GM19238	blood:	n/a	n/a
36	CTCF	chr8:49231262-49231579	HepG2	liver:	n/a	chr8:49231427-49231445 chr8:49231429-49231450 chr8:49231428-49231444
37	CTCF	chr8:49231349-49231617	A549	lung:	n/a	chr8:49231427-49231445 chr8:49231429-49231450 chr8:49231428-49231444
38	CTCF	chr8:49232620-49232770	AG09319	gingival:	n/a	n/a
39	CTCF	chr8:49218060-49218210	BJ	skin:	n/a	n/a
40	CTCF	chr8:49231360-49231510	HUVEC	blood vessel:	n/a	chr8:49231427-49231445 chr8:49231429-49231450 chr8:49231428-49231444
41	CTCF	chr8:49231660-49231810	K562	blood:	n/a	n/a
42	CTCF	chr8:49233620-49233770	NHEK	skin:	n/a	chr8:49233673-49233694 chr8:49233680-49233693 chr8:49233679-49233695 chr8:49233684-49233693 chr8:49233681-49233691 chr8:49233678-49233696
43	CTCF	chr8:49231240-49231390	WI-38	lung:	n/a	n/a
44	CTCF	chr8:49232620-49232770	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr8:49233580-49233730	HepG2	liver:	n/a	chr8:49233673-49233694 chr8:49233680-49233693 chr8:49233679-49233695 chr8:49233684-49233693 chr8:49233681-49233691 chr8:49233678-49233696
46	CTCF	chr8:49233580-49233730	HUVEC	blood vessel:	n/a	chr8:49233673-49233694 chr8:49233680-49233693 chr8:49233679-49233695 chr8:49233684-49233693 chr8:49233681-49233691 chr8:49233678-49233696
47	CTCF	chr8:49231400-49231550	HL-60	blood:	n/a	chr8:49231427-49231445 chr8:49231429-49231450 chr8:49231428-49231444
48	CTCF	chr8:49218120-49218270	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr8:49233502-49233816	H1-hESC	embryonic stem cell:	n/a	chr8:49233673-49233694 chr8:49233680-49233693 chr8:49233679-49233695 chr8:49233684-49233693 chr8:49233681-49233691 chr8:49233678-49233696
50	CTCF	chr8:49231826-49231827	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:49241635-49241685	U87	brain:	n/a
2	chr8:49241737-49241787	HMEC	breast:	n/a
3	chr8:49241635-49241685	U87	brain:	n/a
4	chr8:49241737-49241787	HMEC	breast:	n/a
5	chr8:49229620-49229670	BE2_C	brain:	n/a
6	chr8:49241685-49241735	BJ	skin:	n/a
7	chr8:49241685-49241735	HEEpiC	esophagus:	n/a
8	chr8:49231190-49231240	LNCaP	prostate:	n/a
9	chr8:49195258-49195308	ovcar-3	ovarian:	n/a
10	chr8:49219660-49219710	GM12878	blood:	n/a
11	chr8:49231190-49231240	NB4	blood:	n/a
12	chr8:49241685-49241735	SAEC	small airway:	n/a
13	chr8:49241685-49241735	HepG2	liver:	n/a
14	chr8:49210718-49210768	BJ	skin:	n/a
15	chr8:49219660-49219710	SKMC	muscle:	n/a
16	chr8:49229380-49229430	MCF10A-Er-Src	breast:	n/a
17	chr8:49231559-49231609	HMEC	breast:	n/a
18	chr8:49229620-49229670	GM06990	blood:	n/a
19	chr8:49231655-49231705	HUVEC	blood vessel:	n/a
20	chr8:49231655-49231705	SAEC	small airway:	n/a
21	chr8:49219660-49219710	A549	lung:	n/a
22	chr8:49231688-49231738	AG10803	skin:	n/a
23	chr8:49231190-49231240	HRCEpiC	kidney:	n/a
24	chr8:49231786-49231836	NT2-D1	testis:	n/a
25	chr8:49241737-49241787	HEEpiC	esophagus:	n/a
26	chr8:49231786-49231836	HUVEC	blood vessel:	n/a
27	chr8:49235737-49235787	Caco-2	colon:	n/a
28	chr8:49241737-49241787	GM06990	blood:	n/a
29	chr8:49231559-49231609	RPTEC	kidney:	n/a
30	chr8:49231655-49231705	GM12891	blood:	n/a
31	chr8:49241635-49241685	HCPEpiC	choroid plexus:	n/a
32	chr8:49231559-49231609	HAEpiC	amniotic membrane:	n/a
33	chr8:49241685-49241735	ovcar-3	ovarian:	n/a
34	chr8:49210718-49210768	NT2-D1	testis:	n/a
35	chr8:49235737-49235787	PANC-1	pancreas:	n/a
36	chr8:49231688-49231738	HepG2	liver:	n/a
37	chr8:49195258-49195308	SK-N-MC	brain:	n/a
38	chr8:49229620-49229670	HRPEpiC	eye:	n/a
39	chr8:49229620-49229670	AG04449	skin:	fetal
40	chr8:49195258-49195308	Hela-S3	cervix:	n/a
41	chr8:49231786-49231836	NHDF-neo	bronchial:	n/a
42	chr8:49195258-49195308	GM06990	blood:	n/a
43	chr8:49195258-49195308	GM19239	blood:	n/a
44	chr8:49229380-49229430	ProgFib	skin:	n/a
45	chr8:49219660-49219710	Jurkat	blood:	n/a
46	chr8:49219660-49219710	HCF	heart:	n/a
47	chr8:49231655-49231705	HEK293	kidney:	embryo
48	chr8:49231655-49231705	HRCEpiC	kidney:	n/a
49	chr8:49219660-49219710	PrEC	prostate:	n/a
50	chr8:49231655-49231705	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:49084383..49085325-chr8:49233271..49234265,2	K562	blood:
2	chr8:49231421..49235901-chr8:49831866..49835382,4	MCF-7	breast:
3	chr8:49233686..49235659-chr8:49424325..49425913,2	MCF-7	breast:
4	chr8:49231010..49232106-chr8:49667714..49668868,4	MCF-7	breast:
5	chr8:49233283..49233917-chr8:49838000..49838703,2	MCF-7	breast:
6	chr8:49236947..49237860-chr8:49837763..49838543,2	MCF-7	breast:
7	chr8:49231036..49231653-chr8:49839118..49840050,2	MCF-7	breast:
8	chr8:49101995..49104424-chr8:49230662..49232530,2	MCF-7	breast:
9	chr8:49231059..49231908-chr8:49838295..49838841,2	K562	blood:
10	chr8:49230639..49234892-chr8:49832465..49836593,5	MCF-7	breast:
11	chr8:49235083..49235906-chr8:49837806..49838740,2	MCF-7	breast:
12	chr8:49231028..49232049-chr8:49837754..49838644,8	MCF-7	breast:
13	chr8:49229484..49233078-chr8:49318380..49320785,3	MCF-7	breast:
14	chr8:49231670..49234533-chr8:49280162..49283024,2	MCF-7	breast:
15	chr8:49238452..49240367-chr8:49240866..49242918,2	MCF-7	breast:
16	chr8:49183187..49183854-chr8:49233346..49234106,2	MCF-7	breast:
17	chr8:49232603..49233354-chr8:49837851..49838387,2	MCF-7	breast:
18	chr8:49238452..49240367-chr8:49240866..49242918,2	MCF-7	breast:
19	chr8:49231222..49233241-chr8:49427300..49430063,3	MCF-7	breast:
20	chr15:100568889..100569389-chr8:49235711..49236467,2	MCF-7	breast:
21	chr8:49227294..49228250-chr8:49837799..49838312,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKDC-3	chr8:49206586-49207254	NONHSAT126474
2	lnc-PRKDC-1	chr8:49222196-49222442	NONHSAT126476
3	lnc-PRKDC-1	chr8:49222196-49222460	XLOC_007079
4	lnc-PRKDC-1	chr8:49221830-49221939	NONHSAT126476
5	lnc-PRKDC-1	chr8:49221910-49221939	XLOC_007079

Variant related genes	Relation type
RNU6-295P	TF binding region
ENSG00000253654	TF binding region
RNU6-295P	CpG island
ENSG00000253654	CpG island
ENSG00000253140	chromatin interactions
ENSG00000019549	chromatin interactions

Extended variants
information (count: 1821 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1821 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139095147	chr8:49190973-49190974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs6997499	chr8:49190984-49190985	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs562611984	chr8:49191073-49191074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531421656	chr8:49191098-49191099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572857994	chr8:49191099-49191100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539904506	chr8:49191136-49191137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369339867	chr8:49191138-49191139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181356986	chr8:49191153-49191154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs74451002	chr8:49191234-49191235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544145873	chr8:49191243-49191244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562629935	chr8:49191260-49191261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112533000	chr8:49191266-49191267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541661663	chr8:49191333-49191334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372570323	chr8:49191370-49191371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145032486	chr8:49191381-49191382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552689008	chr8:49191420-49191421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186385690	chr8:49191537-49191538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559998878	chr8:49191538-49191539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531735905	chr8:49191574-49191575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543982431	chr8:49191661-49191662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34782609	chr8:49191664-49191665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527240845	chr8:49191689-49191690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189760722	chr8:49191719-49191720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568672228	chr8:49191764-49191765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182055649	chr8:49191772-49191773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149108339	chr8:49191794-49191795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186446158	chr8:49191799-49191800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533676302	chr8:49191805-49191806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558222225	chr8:49191861-49191862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs377311440	chr8:49191874-49191875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368964578	chr8:49191878-49191879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543809617	chr8:49191932-49191933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556085292	chr8:49191933-49191934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570516441	chr8:49191954-49191955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146219154	chr8:49191957-49191958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190860433	chr8:49191972-49191973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76948763	chr8:49192004-49192005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs4484725	chr8:49192019-49192020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7832830	chr8:49192096-49192097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546358242	chr8:49192109-49192110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560056291	chr8:49192131-49192132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564566261	chr8:49192165-49192166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531790811	chr8:49192247-49192248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549913773	chr8:49192300-49192301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs202234279	chr8:49192364-49192365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115016642	chr8:49192365-49192366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34701134	chr8:49192366-49192367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568404416	chr8:49192372-49192373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369937869	chr8:49192373-49192374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs386412684	chr8:49192375-49192376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
22q11 deletion syndrome	20357662	CNVD

Chromatin state (count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49183000-49201400	Weak transcription	Fetal Intestine Small	intestine
2	chr8:49186600-49192000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:49186800-49192000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr8:49186800-49192000	Weak transcription	HMEC	breast
5	chr8:49186800-49192000	Weak transcription	NHEK	skin
6	chr8:49186800-49192200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:49186800-49199400	Weak transcription	Right Atrium	heart
8	chr8:49187000-49192000	Weak transcription	HUVEC	blood vessel
9	chr8:49187000-49192200	Weak transcription	Osteobl	bone
10	chr8:49187000-49192400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr8:49187200-49191000	Weak transcription	NHDF-Ad	bronchial
12	chr8:49187200-49191400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr8:49187200-49192000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr8:49187200-49192200	Weak transcription	NH-A	brain
15	chr8:49187200-49192400	Weak transcription	NHLF	lung
16	chr8:49187200-49198000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:49187800-49194400	Weak transcription	Fetal Stomach	stomach
18	chr8:49188800-49192200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr8:49189200-49194400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:49190800-49197000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr8:49191000-49192600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr8:49191000-49195200	Enhancers	NHDF-Ad	bronchial
23	chr8:49191200-49197200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:49191400-49193000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr8:49192000-49193400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr8:49192000-49194800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:49192000-49194800	Enhancers	NHEK	skin
28	chr8:49192000-49195000	Enhancers	Muscle Satellite Cultured Cells	--
29	chr8:49192000-49195200	Enhancers	HMEC	breast
30	chr8:49192000-49195200	Enhancers	HUVEC	blood vessel
31	chr8:49192200-49192800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr8:49192200-49193000	Enhancers	NH-A	brain
33	chr8:49192200-49193200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr8:49192200-49193200	Enhancers	Osteobl	bone
35	chr8:49192200-49194400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr8:49192400-49193000	Enhancers	Placenta Amnion	Placenta Amnion
37	chr8:49192400-49197000	Enhancers	NHLF	lung
38	chr8:49192600-49193200	Enhancers	HSMM	muscle
39	chr8:49192800-49193200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr8:49193000-49193400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr8:49193000-49194000	Weak transcription	NH-A	brain
42	chr8:49193200-49194200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr8:49193200-49194400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:49193200-49196400	Weak transcription	Osteobl	bone
45	chr8:49193400-49194800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr8:49193400-49196200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr8:49194000-49194400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:49194000-49195000	Enhancers	Fetal Lung	lung
49	chr8:49194000-49195000	Enhancers	NH-A	brain
50	chr8:49194200-49194600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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