Variant report

Variant	nsv603240
Chromosome Location	chr6:58296648-58654742
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:769)
CpG islands
(count:245)
Chromatin interactive
region (count:2)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:769 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:58312840-58313086	GM12878	blood:	n/a	n/a
2	BATF	chr6:58312874-58313181	GM12878	blood:	n/a	chr6:58313100-58313108
3	BATF	chr6:58312874-58313176	GM12878	blood:	n/a	chr6:58313100-58313108
4	BATF	chr6:58326544-58326859	GM12878	blood:	n/a	n/a
5	BCL11A	chr6:58312939-58313153	GM12878	blood:	n/a	chr6:58313103-58313112
6	BCL11A	chr6:58312858-58313167	GM12878	blood:	n/a	chr6:58313103-58313112
7	BCLAF1	chr6:58312816-58313161	GM12878	blood:	n/a	chr6:58313103-58313112
8	BHLHE40	chr6:58312965-58313069	GM12878	blood:	n/a	n/a
9	CEBPB	chr6:58441968-58442111	HepG2	liver:	n/a	chr6:58442072-58442083 chr6:58442073-58442084
10	CEBPB	chr6:58524736-58524936	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr6:58302675-58303028	K562	blood:	n/a	n/a
12	CEBPB	chr6:58576509-58576728	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:58506303-58506382	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:58357831-58357857	HepG2	liver:	n/a	chr6:58357833-58357844 chr6:58357834-58357845
15	CEBPB	chr6:58385936-58386118	IMR90	lung:	n/a	n/a
16	CEBPB	chr6:58524581-58524685	IMR90	lung:	n/a	n/a
17	CEBPB	chr6:58334093-58334264	HepG2	liver:	n/a	chr6:58334239-58334250 chr6:58334239-58334248 chr6:58334237-58334250 chr6:58334239-58334248 chr6:58334239-58334248 chr6:58334237-58334250 chr6:58334239-58334250 chr6:58334239-58334248 chr6:58334237-58334250 chr6:58334237-58334248
18	CEBPD	chr6:58300940-58301286	K562	blood:	n/a	n/a
19	CEBPD	chr6:58302568-58303070	K562	blood:	n/a	n/a
20	CHD2	chr6:58312973-58313106	GM12878	blood:	n/a	n/a
21	CHD2	chr6:58364578-58364789	K562	blood:	n/a	n/a
22	CTCF	chr6:58507900-58508050	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr6:58507800-58507950	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr6:58297009-58297115	GM19238	blood:	n/a	n/a
25	CTCF	chr6:58329820-58329970	RPTEC	kidney:	n/a	n/a
26	CTCF	chr6:58418289-58418467	MCF-7	breast:	n/a	n/a
27	CTCF	chr6:58329840-58329990	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr6:58507900-58508050	HMF	breast:	n/a	n/a
29	CTCF	chr6:58376711-58376785	ProgFib	skin:	n/a	n/a
30	CTCF	chr6:58296940-58297090	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr6:58296940-58297090	GM12878	blood:	n/a	n/a
32	CTCF	chr6:58329880-58330030	GM12872	blood:	n/a	n/a
33	CTCF	chr6:58508323-58508332	GM10248	blood:	n/a	n/a
34	CTCF	chr6:58329760-58329910	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr6:58508102-58508211	GM13976	blood:	n/a	chr6:58508122-58508143 chr6:58508127-58508145
36	CTCF	chr6:58296907-58297108	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:58374296-58374396	GM13977	blood:	n/a	n/a
38	CTCF	chr6:58329862-58329947	A549	lung:	n/a	n/a
39	CTCF	chr6:58329803-58329986	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr6:58296920-58297070	HMF	breast:	n/a	n/a
41	CTCF	chr6:58418286-58418458	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr6:58296936-58297133	MCF-7	breast:	n/a	n/a
43	CTCF	chr6:58296900-58297050	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr6:58296920-58297070	SAEC	small airway:	n/a	n/a
45	CTCF	chr6:58296920-58297070	HepG2	liver:	n/a	n/a
46	CTCF	chr6:58296720-58296870	AG04450	lung:	n/a	n/a
47	CTCF	chr6:58374248-58374349	GM20000	blood:	n/a	n/a
48	CTCF	chr6:58329800-58329950	AG09319	gingival:	n/a	n/a
49	CTCF	chr6:58374338-58374408	Lung_OC	lung:	n/a	n/a
50	CTCF	chr6:58329820-58329970	GM12873	blood:	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	chr6:58584053-58584103	RPTEC	kidney:	n/a
2	chr6:58584053-58584103	RPTEC	kidney:	n/a
3	chr6:58399599-58399649	LNCaP	prostate:	n/a
4	chr6:58399599-58399649	SK-N-SH	brain:	n/a
5	chr6:58584053-58584103	ovcar-3	ovarian:	n/a
6	chr6:58399664-58399714	HRCEpiC	kidney:	n/a
7	chr6:58399664-58399714	Hela-S3	cervix:	n/a
8	chr6:58584053-58584103	AG09309	skin:	n/a
9	chr6:58399599-58399649	BJ	skin:	n/a
10	chr6:58584053-58584103	NH-A	brain:	n/a
11	chr6:58399793-58399843	NHDF-neo	bronchial:	n/a
12	chr6:58399793-58399843	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:58584053-58584103	MCF-7	breast:	n/a
14	chr6:58584053-58584103	SK-N-SH_RA	brain:	n/a
15	chr6:58399793-58399843	ECC-1	luminal epithelium:	n/a
16	chr6:58399599-58399649	HCF	heart:	n/a
17	chr6:58399599-58399649	HUVEC	blood vessel:	n/a
18	chr6:58399664-58399714	HRE	kidney:	n/a
19	chr6:58399793-58399843	RPTEC	kidney:	n/a
20	chr6:58584053-58584103	NHDF-neo	bronchial:	n/a
21	chr6:58584053-58584103	PFSK-1	brain:	n/a
22	chr6:58399664-58399714	AG04449	skin:	fetal
23	chr6:58399599-58399649	HCT-116	colon:	n/a
24	chr6:58399664-58399714	CMK	blood:	n/a
25	chr6:58399793-58399843	PANC-1	pancreas:	n/a
26	chr6:58399793-58399843	HL-60	blood:	n/a
27	chr6:58399793-58399843	HCM	heart:	n/a
28	chr6:58399599-58399649	IMR90	lung:	fetal
29	chr6:58399793-58399843	ovcar-3	ovarian:	n/a
30	chr6:58399664-58399714	A549	lung:	n/a
31	chr6:58399664-58399714	GM12891	blood:	n/a
32	chr6:58399599-58399649	Hepatocyte	liver:	n/a
33	chr6:58399599-58399649	HEK293	kidney:	embryo
34	chr6:58584053-58584103	GM12891	blood:	n/a
35	chr6:58399664-58399714	K562	blood:	n/a
36	chr6:58399793-58399843	SK-N-SH	brain:	n/a
37	chr6:58584053-58584103	U87	brain:	n/a
38	chr6:58399599-58399649	AG09319	gingival:	n/a
39	chr6:58584053-58584103	HPAEpiC	pulmonary alveolar:	n/a
40	chr6:58399664-58399714	NB4	blood:	n/a
41	chr6:58584053-58584103	SK-N-MC	brain:	n/a
42	chr6:58399793-58399843	HUVEC	blood vessel:	n/a
43	chr6:58399599-58399649	HIPEpiC	eye:	n/a
44	chr6:58399664-58399714	ovcar-3	ovarian:	n/a
45	chr6:58399599-58399649	NH-A	brain:	n/a
46	chr6:58399793-58399843	HCPEpiC	choroid plexus:	n/a
47	chr6:58399793-58399843	Hela-S3	cervix:	n/a
48	chr6:58399599-58399649	SK-N-SH_RA	brain:	n/a
49	chr6:58584053-58584103	Jurkat	blood:	n/a
50	chr6:58399793-58399843	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:58293670..58295896-chr6:58296442..58298545,2	K562	blood:
2	chr6:58293670..58295896-chr6:58296442..58300027,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAG2-7	chr6:58488888-58489027	ENSG00000223633.2
2	lnc-BAG2-7	chr6:58488888-58489027	ENSG00000223633.1
3	lnc-BAG2-7	chr6:58513504-58513860	ENSG00000223633.2
4	lnc-BAG2-6	chr6:58297873-58297934	ENSG00000225096
5	lnc-BAG2-6	chr6:58298372-58298496	ENSG00000225096
6	lnc-RAB23-19	chr6:58397998-58399412	NONHSAT113321

No data

Variant related genes	Relation type
GAPDHP15	TF binding region
ENSG00000223633	TF binding region
ENSG00000216687	TF binding region
RBBP4P4	TF binding region
GAPDHP15	CpG island
ENSG00000223633	CpG island
ENSG00000216687	CpG island
RBBP4P4	CpG island
ENSG00000214563	chromatin interactions

Extended variants
information (count: 2154 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2154 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12663198	chr6:58296648-58296649	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536128605	chr6:58296654-58296655	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs35784219	chr6:58296706-58296707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs78425854	chr6:58296714-58296715	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs557408746	chr6:58296734-58296735	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs569229302	chr6:58296740-58296741	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs539401051	chr6:58296762-58296763	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs558192726	chr6:58296763-58296764	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs72882908	chr6:58296777-58296778	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs139812554	chr6:58296795-58296796	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs553181355	chr6:58296905-58296906	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs574586443	chr6:58296924-58296925	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs143205518	chr6:58296929-58296930	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs2179127	chr6:58296951-58296952	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs527814883	chr6:58296973-58296974	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs563389329	chr6:58297000-58297001	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs530843668	chr6:58297015-58297016	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs545361696	chr6:58297057-58297058	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs2142655	chr6:58297068-58297069	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs6933522	chr6:58297082-58297083	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs540851553	chr6:58297093-58297094	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs565828636	chr6:58297124-58297125	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs528154170	chr6:58297137-58297138	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs60444898	chr6:58297166-58297167	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs150328850	chr6:58297209-58297210	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs145794656	chr6:58297225-58297226	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551154769	chr6:58297228-58297229	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2142656	chr6:58297248-58297249	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs494546	chr6:58297266-58297267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs540140808	chr6:58297318-58297319	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs563202043	chr6:58297376-58297377	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs558154182	chr6:58297386-58297387	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs201796857	chr6:58297391-58297392	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs566899691	chr6:58297408-58297409	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs143805919	chr6:58297431-58297432	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs532882746	chr6:58297516-58297517	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368751189	chr6:58297517-58297518	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs185991956	chr6:58297542-58297543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562562528	chr6:58297589-58297590	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs60326108	chr6:58297626-58297627	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs535256094	chr6:58297706-58297707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs35593703	chr6:58297762-58297763	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557137683	chr6:58297773-58297774	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs575423796	chr6:58297792-58297793	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs545721564	chr6:58297836-58297837	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs563725758	chr6:58297930-58297931	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs572543360	chr6:58297938-58297939	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs190015783	chr6:58297991-58297992	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs374660891	chr6:58298033-58298034	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs561578361	chr6:58298043-58298044	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	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
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58288400-58301000	Weak transcription	Ovary	ovary
2	chr6:58293000-58309600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr6:58301000-58301200	ZNF genes & repeats	Ovary	ovary
4	chr6:58301200-58301600	Active TSS	K562	blood
5	chr6:58301200-58310800	Weak transcription	Ovary	ovary
6	chr6:58301600-58302400	Weak transcription	K562	blood
7	chr6:58302200-58303200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:58302400-58302600	Enhancers	K562	blood
9	chr6:58302400-58303200	Enhancers	NHDF-Ad	bronchial
10	chr6:58302600-58303200	Enhancers	HSMM	muscle
11	chr6:58302600-58303400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:58303200-58309000	Weak transcription	HSMM	muscle
13	chr6:58307400-58307600	Weak transcription	Fetal Muscle Leg	muscle
14	chr6:58307600-58307800	Enhancers	HSMMtube	muscle
15	chr6:58307600-58308400	Enhancers	Fetal Muscle Leg	muscle
16	chr6:58307800-58309600	Weak transcription	HSMMtube	muscle
17	chr6:58308400-58310400	Weak transcription	Fetal Muscle Leg	muscle
18	chr6:58309000-58313000	Enhancers	HSMM	muscle
19	chr6:58309600-58310200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr6:58309600-58310800	Enhancers	NHDF-Ad	bronchial
21	chr6:58309600-58311000	Enhancers	Muscle Satellite Cultured Cells	--
22	chr6:58309600-58311000	Enhancers	Fetal Heart	heart
23	chr6:58309600-58313000	Enhancers	HSMMtube	muscle
24	chr6:58309800-58310600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr6:58310200-58311800	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr6:58310400-58311200	Enhancers	Fetal Muscle Leg	muscle
27	chr6:58310800-58311000	Enhancers	Ovary	ovary
28	chr6:58311000-58312000	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr6:58311000-58312200	Weak transcription	Ovary	ovary
30	chr6:58311200-58312200	Weak transcription	Fetal Muscle Leg	muscle
31	chr6:58311800-58312000	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr6:58312000-58312200	Enhancers	Muscle Satellite Cultured Cells	--
33	chr6:58312000-58313000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr6:58312000-58313000	Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr6:58312200-58312400	Enhancers	Fetal Muscle Leg	muscle
36	chr6:58312200-58312400	Enhancers	Ovary	ovary
37	chr6:58312200-58312600	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr6:58312600-58313000	Enhancers	Muscle Satellite Cultured Cells	--
39	chr6:58313000-58313200	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr6:58313000-58314800	Weak transcription	HSMM	muscle
41	chr6:58313200-58317800	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr6:58314800-58315200	Enhancers	HSMM	muscle
43	chr6:58315200-58316200	Weak transcription	HSMM	muscle
44	chr6:58316200-58317200	Enhancers	HSMM	muscle
45	chr6:58317800-58318200	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr6:58318200-58318400	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr6:58321000-58321200	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr6:58334000-58334800	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr6:58334400-58335000	Enhancers	Ovary	ovary
50	chr6:58334800-58340000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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