Variant report

Variant	nsv886695
Chromosome Location	chr6:140878731-141041329
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:952)
CpG islands
(count:122)
Chromatin interactive
region (count:26)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:952 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:140905921-140905975	K562	blood:	n/a	n/a
2	ATF1	chr6:140893405-140893685	K562	blood:	n/a	n/a
3	ATF1	chr6:141032327-141032490	K562	blood:	n/a	n/a
4	ATF2	chr6:140907528-140908482	GM12878	blood:	n/a	n/a
5	ATF2	chr6:140893204-140893707	GM12878	blood:	n/a	n/a
6	ATF2	chr6:140962459-140962964	GM12878	blood:	n/a	n/a
7	ATF2	chr6:140907544-140908522	GM12878	blood:	n/a	n/a
8	BACH1	chr6:140931711-140931747	K562	blood:	n/a	n/a
9	BATF	chr6:140907543-140908374	GM12878	blood:	n/a	n/a
10	BATF	chr6:140999274-140999525	GM12878	blood:	n/a	n/a
11	BATF	chr6:140962571-140962917	GM12878	blood:	n/a	n/a
12	BATF	chr6:140893208-140893582	GM12878	blood:	n/a	chr6:140893374-140893385
13	BATF	chr6:140962532-140962960	GM12878	blood:	n/a	n/a
14	BATF	chr6:140957343-140957787	GM12878	blood:	n/a	n/a
15	BATF	chr6:140907813-140908309	GM12878	blood:	n/a	n/a
16	BCL11A	chr6:140907600-140908344	GM12878	blood:	n/a	n/a
17	BCL11A	chr6:140957373-140957725	GM12878	blood:	n/a	n/a
18	BCL11A	chr6:140962597-140962976	GM12878	blood:	n/a	n/a
19	BCL11A	chr6:140962665-140962965	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:140907738-140908243	GM12878	blood:	n/a	n/a
21	BCL3	chr6:140907733-140908269	GM12878	blood:	n/a	n/a
22	BCL3	chr6:140923817-140924135	GM12878	blood:	n/a	n/a
23	BCL3	chr6:140907648-140908396	GM12878	blood:	n/a	n/a
24	BCLAF1	chr6:140907860-140908292	GM12878	blood:	n/a	n/a
25	BCLAF1	chr6:140907489-140908402	GM12878	blood:	n/a	n/a
26	BCLAF1	chr6:140957284-140957740	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:140962545-140962966	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:141032530-141032747	GM12878	blood:	n/a	n/a
29	CBX3	chr6:140948115-140948497	K562	blood:	n/a	n/a
30	CCNT2	chr6:141006502-141006618	K562	blood:	n/a	n/a
31	CEBPB	chr6:140905206-140905380	HepG2	liver:	n/a	chr6:140905237-140905248
32	CEBPB	chr6:140944593-140944912	A549	lung:	n/a	chr6:140944736-140944747
33	CEBPB	chr6:140950718-140951059	HepG2	liver:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
34	CEBPB	chr6:140950735-140950999	A549	lung:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
35	CEBPB	chr6:140950874-140950971	Hela-S3	cervix:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
36	CEBPB	chr6:140944554-140945005	IMR90	lung:	n/a	chr6:140944736-140944747
37	CEBPB	chr6:140950761-140951042	K562	blood:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
38	CEBPB	chr6:140950786-140950984	H1-hESC	embryonic stem cell:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
39	CEBPB	chr6:140893190-140893832	GM12878	blood:	n/a	n/a
40	CEBPB	chr6:140992588-140992943	HepG2	liver:	n/a	chr6:140992865-140992876
41	CEBPB	chr6:140944568-140944937	Hela-S3	cervix:	n/a	chr6:140944736-140944747
42	CEBPB	chr6:140950521-140950534	K562	blood:	n/a	n/a
43	CEBPB	chr6:141019569-141019573	K562	blood:	n/a	n/a
44	CEBPB	chr6:141006378-141006630	IMR90	lung:	n/a	n/a
45	CEBPB	chr6:140926256-140926456	HepG2	liver:	n/a	chr6:140926351-140926362 chr6:140926350-140926363
46	CEBPB	chr6:140933530-140933696	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:140907389-140908537	GM12878	blood:	n/a	n/a
48	CEBPB	chr6:141023864-141024001	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:140911779-140912094	IMR90	lung:	n/a	chr6:140911918-140911929 chr6:140911918-140911931 chr6:140911917-140911934 chr6:140911918-140911931 chr6:140911918-140911929 chr6:140911918-140911931
50	CEBPB	chr6:140893279-140893621	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:140957775-140957825	ovcar-3	ovarian:	n/a
2	chr6:140923112-140923162	CMK	blood:	n/a
3	chr6:140923112-140923162	HCF	heart:	n/a
4	chr6:140923112-140923162	AG09319	gingival:	n/a
5	chr6:140923112-140923162	BE2_C	brain:	n/a
6	chr6:140957775-140957825	SKMC	muscle:	n/a
7	chr6:140923112-140923162	ECC-1	luminal epithelium:	n/a
8	chr6:140957775-140957825	Jurkat	blood:	n/a
9	chr6:140923112-140923162	HAEpiC	amniotic membrane:	n/a
10	chr6:140923112-140923162	ProgFib	skin:	n/a
11	chr6:140923112-140923162	HCPEpiC	choroid plexus:	n/a
12	chr6:140923112-140923162	NT2-D1	testis:	n/a
13	chr6:140957775-140957825	MCF10A-Er-Src	breast:	n/a
14	chr6:140923112-140923162	GM12892	blood:	n/a
15	chr6:140957775-140957825	ProgFib	skin:	n/a
16	chr6:140923112-140923162	LNCaP	prostate:	n/a
17	chr6:140923112-140923162	Caco-2	colon:	n/a
18	chr6:140957775-140957825	IMR90	lung:	fetal
19	chr6:140923112-140923162	HCM	heart:	n/a
20	chr6:140923112-140923162	NHDF-neo	bronchial:	n/a
21	chr6:140923112-140923162	SK-N-SH	brain:	n/a
22	chr6:140957775-140957825	SK-N-SH	brain:	n/a
23	chr6:140923112-140923162	HRCEpiC	kidney:	n/a
24	chr6:140957775-140957825	ECC-1	luminal epithelium:	n/a
25	chr6:140957775-140957825	NHDF-neo	bronchial:	n/a
26	chr6:140923112-140923162	SK-N-MC	brain:	n/a
27	chr6:140957775-140957825	HRE	kidney:	n/a
28	chr6:140923112-140923162	AG10803	skin:	n/a
29	chr6:140957775-140957825	HAEpiC	amniotic membrane:	n/a
30	chr6:140957775-140957825	RPTEC	kidney:	n/a
31	chr6:140957775-140957825	NH-A	brain:	n/a
32	chr6:140923112-140923162	HepG2	liver:	n/a
33	chr6:140923112-140923162	NB4	blood:	n/a
34	chr6:140957775-140957825	PFSK-1	brain:	n/a
35	chr6:140923112-140923162	HNPCEpiC	eye:	n/a
36	chr6:140923112-140923162	K562	blood:	n/a
37	chr6:140923112-140923162	NHBE	bronchial:	n/a
38	chr6:140957775-140957825	AG09319	gingival:	n/a
39	chr6:140923112-140923162	HMEC	breast:	n/a
40	chr6:140923112-140923162	AoSMC	blood vessel:	n/a
41	chr6:140957775-140957825	NT2-D1	testis:	n/a
42	chr6:140957775-140957825	AG10803	skin:	n/a
43	chr6:140957775-140957825	GM12878	blood:	n/a
44	chr6:140923112-140923162	HIPEpiC	eye:	n/a
45	chr6:140923112-140923162	U87	brain:	n/a
46	chr6:140923112-140923162	Hela-S3	cervix:	n/a
47	chr6:140957775-140957825	AG09309	skin:	n/a
48	chr6:140923112-140923162	AG09309	skin:	n/a
49	chr6:140957775-140957825	HRCEpiC	kidney:	n/a
50	chr6:140923112-140923162	HRPEpiC	eye:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:140905860..140907615-chr6:140923172..140925767,2	K562	blood:
2	chr6:140781738..140784199-chr6:140901701..140903255,2	MCF-7	breast:
3	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
4	chr6:140905427..140908857-chr6:140910975..140913769,3	K562	blood:
5	chr6:140874402..140877217-chr6:140878375..140880350,3	K562	blood:
6	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
7	chr6:140919169..140921783-chr6:140922844..140925130,2	MCF-7	breast:
8	chr6:140919169..140921783-chr6:140922844..140925130,2	MCF-7	breast:
9	chr6:140919683..140922477-chr6:140922951..140925065,2	K562	blood:
10	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
11	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
12	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
13	chr6:141041326..141043698-chr6:141051751..141054060,2	K562	blood:
14	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
15	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:
16	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
17	chr6:140905427..140908857-chr6:140910975..140913769,3	K562	blood:
18	chr6:140912649..140915188-chr6:140915453..140918177,2	K562	blood:
19	chr6:140905860..140907615-chr6:140923172..140925767,2	K562	blood:
20	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
21	chr6:140912649..140915188-chr6:140915453..140918177,2	K562	blood:
22	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
23	chr6:140919683..140922477-chr6:140922951..140925065,2	K562	blood:
24	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:
25	chr6:139691177..139693399-chr6:140971784..140974474,2	MCF-7	breast:
26	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HECA-10	chr6:140928455-140928491	l_3279_chr6:140928454-140973185_placenta
2	lnc-HECA-10	chr6:140972927-140973185	l_3279_chr6:140928454-140973185_placenta

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4465	chr6:141004992-141005013	MIMAT0018992

No data

Variant related genes	Relation type
ENSG00000221336	TF binding region
MIR4465	TF binding region
ENSG00000221336	CpG island
MIR4465	CpG island

Extended variants
information (count: 4623 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4623 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533287035	chr6:140881242-140881243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs544798565	chr6:140881243-140881244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185070066	chr6:140881248-140881249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572285882	chr6:140881281-140881282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542581612	chr6:140881301-140881302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112540624	chr6:140881330-140881331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531226254	chr6:140881334-140881335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138945697	chr6:140881346-140881347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142682595	chr6:140881378-140881379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186835625	chr6:140881379-140881380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372362520	chr6:140881433-140881434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs80327293	chr6:140881464-140881465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533006079	chr6:140881480-140881481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11961093	chr6:140881575-140881576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530725539	chr6:140881596-140881597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548002117	chr6:140881624-140881625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566311598	chr6:140881643-140881644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192128340	chr6:140881666-140881667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530398596	chr6:140881669-140881670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548616654	chr6:140881736-140881737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569993657	chr6:140881749-140881750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184244070	chr6:140881773-140881774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188856747	chr6:140881777-140881778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535337660	chr6:140881803-140881804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182531693	chr6:140881818-140881819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200999156	chr6:140881826-140881827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs35653405	chr6:140881835-140881836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534823941	chr6:140881841-140881842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185520186	chr6:140881849-140881850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569263092	chr6:140881850-140881851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs36050152	chr6:140881859-140881860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572166628	chr6:140881907-140881908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs137962585	chr6:140881967-140881968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189656024	chr6:140881974-140881975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149482243	chr6:140881986-140881987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143984183	chr6:140881999-140882000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368377621	chr6:140882056-140882057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9495764	chr6:140882108-140882109	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs564915460	chr6:140882116-140882117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375679621	chr6:140882128-140882129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557753542	chr6:140882137-140882138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532230189	chr6:140882174-140882175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1414832	chr6:140882229-140882230	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs185747696	chr6:140882277-140882278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532909364	chr6:140882339-140882340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530240129	chr6:140882441-140882442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148555261	chr6:140882444-140882445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs9484404	chr6:140882498-140882499	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs190116119	chr6:140882519-140882520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs36092968	chr6:140882541-140882542	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140881200-140881800	Enhancers	HSMM	muscle
2	chr6:140881800-140883800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:140883200-140883400	Enhancers	Duodenum Smooth Muscle	Duodenum
4	chr6:140883800-140887600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:140885400-140887000	Weak transcription	NHDF-Ad	bronchial
6	chr6:140886400-140886800	Enhancers	HSMMtube	muscle
7	chr6:140886600-140886800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr6:140886600-140887600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr6:140886800-140887000	Enhancers	Duodenum Smooth Muscle	Duodenum
10	chr6:140886800-140887200	Weak transcription	HSMMtube	muscle
11	chr6:140887000-140887400	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr6:140887000-140888200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr6:140887000-140888800	Enhancers	Adipose Nuclei	Adipose
14	chr6:140887000-140888800	Enhancers	NHDF-Ad	bronchial
15	chr6:140887000-140889000	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr6:140887000-140889000	Enhancers	Fetal Heart	heart
17	chr6:140887000-140889000	Enhancers	HUVEC	blood vessel
18	chr6:140887000-140889200	Enhancers	Osteobl	bone
19	chr6:140887000-140889400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr6:140887200-140888200	Enhancers	HSMMtube	muscle
21	chr6:140887400-140887800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr6:140887400-140888000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr6:140887400-140888200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr6:140887400-140889000	Enhancers	Muscle Satellite Cultured Cells	--
25	chr6:140887400-140889000	Enhancers	Rectal Smooth Muscle	rectum
26	chr6:140887400-140889200	Enhancers	Hela-S3	cervix
27	chr6:140887400-140889200	Enhancers	HSMM	muscle
28	chr6:140887600-140888400	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr6:140887600-140888400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:140887600-140888400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr6:140887600-140888400	Enhancers	HMEC	breast
32	chr6:140887600-140888800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr6:140887600-140888800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr6:140887600-140888800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:140887600-140888800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr6:140887600-140888800	Enhancers	Colon Smooth Muscle	Colon
37	chr6:140887600-140888800	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr6:140887600-140888800	Enhancers	NH-A	brain
39	chr6:140887600-140888800	Enhancers	NHLF	lung
40	chr6:140887800-140888800	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr6:140888000-140888400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr6:140888000-140888400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr6:140888000-140888400	Enhancers	Fetal Kidney	kidney
44	chr6:140888000-140888400	Enhancers	Placenta Amnion	Placenta Amnion
45	chr6:140888000-140888400	Enhancers	K562	blood
46	chr6:140888000-140888400	Enhancers	NHEK	skin
47	chr6:140888000-140888800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr6:140888000-140888800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:140888200-140888600	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr6:140888200-140888600	Flanking Active TSS	HSMMtube	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links