Variant report

Variant	nsv6362
Chromosome Location	chr8:119554736-119599269
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:314)
CpG islands
(count:366)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:119575980-119576542	GM12878	blood:	n/a	n/a
2	BATF	chr8:119576054-119576428	GM12878	blood:	n/a	n/a
3	BATF	chr8:119589681-119589990	GM12878	blood:	n/a	n/a
4	BATF	chr8:119589703-119590043	GM12878	blood:	n/a	n/a
5	BCL11A	chr8:119566177-119566360	GM12878	blood:	n/a	n/a
6	BCL11A	chr8:119576068-119576701	GM12878	blood:	n/a	n/a
7	BCL11A	chr8:119576030-119576753	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:119567570-119567812	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCLAF1	chr8:119576016-119576692	GM12878	blood:	n/a	n/a
10	BCLAF1	chr8:119576030-119576911	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:119578382-119578938	GM12878	blood:	n/a	n/a
12	BHLHE40	chr8:119589915-119590053	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:119577202-119578085	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:119576021-119576964	GM12878	blood:	n/a	n/a
15	BRCA1	chr8:119558962-119559075	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr8:119560466-119560795	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr8:119577596-119577664	GM12878	blood:	n/a	n/a
18	CEBPB	chr8:119558845-119559181	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr8:119587011-119587336	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr8:119561174-119561285	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:119560746-119561255	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr8:119586995-119587332	IMR90	lung:	n/a	n/a
23	CEBPB	chr8:119558840-119559175	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:119567991-119568243	IMR90	lung:	n/a	chr8:119568100-119568111
25	CEBPB	chr8:119596186-119596326	IMR90	lung:	n/a	chr8:119596251-119596264
26	CEBPB	chr8:119561074-119561271	HepG2	liver:	n/a	n/a
27	CHD1	chr8:119578974-119579049	GM12878	blood:	n/a	n/a
28	CHD1	chr8:119575880-119578744	GM12878	blood:	n/a	n/a
29	CHD2	chr8:119558913-119559131	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr8:119561064-119561260	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr8:119580570-119580640	GM12878	blood:	n/a	n/a
32	CHD2	chr8:119578277-119578306	GM12878	blood:	n/a	n/a
33	CHD2	chr8:119575369-119577874	GM12878	blood:	n/a	n/a
34	CTCF	chr8:119582300-119582450	HepG2	liver:	n/a	chr8:119582404-119582425
35	CTCF	chr8:119577560-119577710	GM12864	blood:	n/a	chr8:119577693-119577702
36	CTCF	chr8:119577980-119578130	GM12871	blood:	n/a	n/a
37	CTCF	chr8:119573802-119573882	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr8:119598704-119598807	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr8:119577582-119577781	GM12878	blood:	n/a	chr8:119577693-119577702
40	CTCF	chr8:119577600-119577750	GM12868	blood:	n/a	chr8:119577693-119577702
41	CTCF	chr8:119560871-119560969	MCF-7	breast:	n/a	n/a
42	CUX1	chr8:119575602-119575796	GM12878	blood:	n/a	n/a
43	CUX1	chr8:119576029-119577854	GM12878	blood:	n/a	chr8:119576807-119576816 chr8:119576801-119576815
44	CUX1	chr8:119578203-119578714	GM12878	blood:	n/a	n/a
45	E2F4	chr8:119575772-119575843	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr8:119598071-119598154	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr8:119576772-119577211	GM12878	blood:	n/a	n/a
48	EBF1	chr8:119577010-119577347	GM12878	blood:	n/a	n/a
49	EBF1	chr8:119576429-119576733	GM12878	blood:	n/a	n/a
50	EBF1	chr8:119566190-119566347	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:119558921-119558971	NT2-D1	testis:	n/a
2	chr8:119558921-119558971	NHDF-neo	bronchial:	n/a
3	chr8:119561032-119561082	ECC-1	luminal epithelium:	n/a
4	chr8:119561032-119561082	RPTEC	kidney:	n/a
5	chr8:119586905-119586955	GM12891	blood:	n/a
6	chr8:119560948-119560998	HCPEpiC	choroid plexus:	n/a
7	chr8:119558921-119558971	HCM	heart:	n/a
8	chr8:119586905-119586955	HEEpiC	esophagus:	n/a
9	chr8:119558921-119558971	AG04449	skin:	fetal
10	chr8:119560948-119560998	GM12891	blood:	n/a
11	chr8:119586905-119586955	SK-N-SH_RA	brain:	n/a
12	chr8:119558921-119558971	NHBE	bronchial:	n/a
13	chr8:119560948-119560998	K562	blood:	n/a
14	chr8:119567541-119567591	SK-N-MC	brain:	n/a
15	chr8:119567541-119567591	Caco-2	colon:	n/a
16	chr8:119561032-119561082	HCPEpiC	choroid plexus:	n/a
17	chr8:119567541-119567591	HCPEpiC	choroid plexus:	n/a
18	chr8:119558921-119558971	SK-N-SH	brain:	n/a
19	chr8:119561032-119561082	GM06990	blood:	n/a
20	chr8:119558921-119558971	HAEpiC	amniotic membrane:	n/a
21	chr8:119567541-119567591	HIPEpiC	eye:	n/a
22	chr8:119561032-119561082	AG10803	skin:	n/a
23	chr8:119560948-119560998	Hela-S3	cervix:	n/a
24	chr8:119567541-119567591	HRCEpiC	kidney:	n/a
25	chr8:119586905-119586955	ProgFib	skin:	n/a
26	chr8:119576599-119576649	CMK	blood:	n/a
27	chr8:119558921-119558971	BE2_C	brain:	n/a
28	chr8:119576599-119576649	HNPCEpiC	eye:	n/a
29	chr8:119561032-119561082	PFSK-1	brain:	n/a
30	chr8:119586905-119586955	SK-N-SH	brain:	n/a
31	chr8:119560948-119560998	Caco-2	colon:	n/a
32	chr8:119558921-119558971	ProgFib	skin:	n/a
33	chr8:119586905-119586955	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:119576599-119576649	SK-N-SH	brain:	n/a
35	chr8:119558921-119558971	HUVEC	blood vessel:	n/a
36	chr8:119561032-119561082	MCF-7	breast:	n/a
37	chr8:119561032-119561082	NHBE	bronchial:	n/a
38	chr8:119561032-119561082	HRE	kidney:	n/a
39	chr8:119561032-119561082	K562	blood:	n/a
40	chr8:119567541-119567591	ECC-1	luminal epithelium:	n/a
41	chr8:119560948-119560998	HRCEpiC	kidney:	n/a
42	chr8:119567541-119567591	MCF-7	breast:	n/a
43	chr8:119561032-119561082	HCM	heart:	n/a
44	chr8:119576599-119576649	AG09319	gingival:	n/a
45	chr8:119558921-119558971	HEK293	kidney:	embryo
46	chr8:119567541-119567591	HRPEpiC	eye:	n/a
47	chr8:119586905-119586955	GM06990	blood:	n/a
48	chr8:119567541-119567591	PFSK-1	brain:	n/a
49	chr8:119576599-119576649	ECC-1	luminal epithelium:	n/a
50	chr8:119576599-119576649	Hepatocyte	liver:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:119593350..119595391-chr8:119606701..119608716,2	MCF-7	breast:
2	chr17:41399379..41402179-chr8:119586621..119589601,3	K562	blood:
3	chr20:49410939..49411525-chr8:119599245..119599765,2	MCF-7	breast:
4	chr17:41398945..41402179-chr8:119586621..119589621,3	K562	blood:
5	chr8:119568051..119569877-chr8:119570145..119573095,2	MCF-7	breast:
6	chr8:119572899..119575048-chr8:119586649..119588943,2	MCF-7	breast:
7	chr17:41465859..41468087-chr8:119586601..119588121,2	MCF-7	breast:
8	chr8:119568051..119569877-chr8:119570145..119573095,2	MCF-7	breast:
9	chr17:41380614..41382191-chr8:119586621..119588121,2	K562	blood:
10	chr8:119572899..119575048-chr8:119586649..119588943,2	MCF-7	breast:
11	chr2:48510170..48510784-chr8:119556555..119557269,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNFRSF11B-4	chr8:119573406-119576339	NONHSAT128411

No data

Variant related genes	Relation type
SAMD12	TF binding region
SAMD12	CpG island
ENSG00000124243	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000236383	chromatin interactions

Extended variants
information (count: 1723 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:1723 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144339973	chr8:119554744-119554745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs71505417	chr8:119554764-119554765	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs7826003	chr8:119554765-119554766	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs574891895	chr8:119554781-119554782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377645556	chr8:119554797-119554798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7825771	chr8:119554802-119554803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs557446152	chr8:119554805-119554806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12678125	chr8:119554845-119554846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs537863200	chr8:119554852-119554853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79320236	chr8:119554892-119554893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564321792	chr8:119554913-119554914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573239247	chr8:119554943-119554944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576536245	chr8:119554946-119554947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141628302	chr8:119555063-119555064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372732029	chr8:119555067-119555068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561998084	chr8:119555104-119555105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528890937	chr8:119555122-119555123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550271874	chr8:119555130-119555131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562631138	chr8:119555146-119555147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146224927	chr8:119555148-119555149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555639836	chr8:119555154-119555155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs61459669	chr8:119555198-119555199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180828882	chr8:119555225-119555226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565205470	chr8:119555229-119555230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574477520	chr8:119555230-119555231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549309836	chr8:119555234-119555235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534061386	chr8:119555261-119555262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567535282	chr8:119555272-119555273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543200394	chr8:119555291-119555292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557049587	chr8:119555292-119555293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10111755	chr8:119555360-119555361	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs78886443	chr8:119555390-119555391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139074703	chr8:119555391-119555392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs386729175	chr8:119555414-119555415	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs573103402	chr8:119555416-119555417	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs373019105	chr8:119555444-119555445	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs540386320	chr8:119555450-119555451	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs562059582	chr8:119555487-119555488	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs574221630	chr8:119555490-119555491	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs73708724	chr8:119555500-119555501	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs559716039	chr8:119555521-119555522	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs562336641	chr8:119555542-119555543	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs372408347	chr8:119555592-119555593	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs566870628	chr8:119555616-119555617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376298170	chr8:119555632-119555633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560251520	chr8:119555634-119555635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562451063	chr8:119555637-119555638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549174479	chr8:119555671-119555672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs56123443	chr8:119555766-119555767	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs60086839	chr8:119555826-119555827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:144)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119550600-119558800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr8:119550800-119558200	Weak transcription	Left Ventricle	heart
3	chr8:119551000-119555400	Weak transcription	GM12878-XiMat	blood
4	chr8:119554000-119560200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:119555000-119555200	Enhancers	HSMMtube	muscle
6	chr8:119555000-119555400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr8:119555000-119555400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:119555400-119555600	ZNF genes & repeats	GM12878-XiMat	blood
9	chr8:119555400-119558400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr8:119555400-119558400	Weak transcription	Aorta	Aorta
11	chr8:119555600-119560600	Weak transcription	GM12878-XiMat	blood
12	chr8:119556200-119556800	Enhancers	NHDF-Ad	bronchial
13	chr8:119556200-119557400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:119556400-119557200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr8:119556400-119557200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr8:119556600-119556800	Enhancers	NHLF	lung
17	chr8:119556600-119558400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr8:119556600-119560800	Enhancers	Fetal Heart	heart
19	chr8:119556800-119557000	Enhancers	Osteobl	bone
20	chr8:119556800-119557400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:119556800-119558400	Weak transcription	NHDF-Ad	bronchial
22	chr8:119556800-119559000	Weak transcription	Brain Angular Gyrus	brain
23	chr8:119557000-119557200	Enhancers	Fetal Lung	lung
24	chr8:119557000-119559800	Enhancers	Fetal Brain Male	brain
25	chr8:119557200-119557400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr8:119557200-119558200	Weak transcription	Fetal Lung	lung
27	chr8:119557200-119558200	Weak transcription	Osteobl	bone
28	chr8:119557200-119558400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr8:119557200-119558400	Weak transcription	NHLF	lung
30	chr8:119557200-119558600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr8:119557400-119557800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr8:119557400-119558400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr8:119557400-119558400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:119557800-119560800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr8:119558200-119558400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:119558200-119558800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr8:119558200-119558800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:119558200-119558800	Enhancers	Left Ventricle	heart
39	chr8:119558200-119559200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr8:119558200-119559200	Enhancers	HMEC	breast
41	chr8:119558200-119559400	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr8:119558200-119559600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr8:119558200-119559600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr8:119558200-119559600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr8:119558200-119559600	Enhancers	Fetal Brain Female	brain
46	chr8:119558200-119559600	Enhancers	Fetal Lung	lung
47	chr8:119558200-119559600	Enhancers	NHEK	skin
48	chr8:119558200-119559800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr8:119558200-119559800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr8:119558200-119559800	Enhancers	Fetal Muscle Leg	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links