Variant report

Variant	nsv885887
Chromosome Location	chr6:53961784-54046264
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	chr6:53962447-53962872	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:54000571-54001192	HepG2	liver:	n/a	n/a
3	BACH1	chr6:53968321-53968664	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:53968331-53968637	K562	blood:	n/a	n/a
5	BHLHE40	chr6:53972403-53972554	HepG2	liver:	n/a	chr6:53972454-53972463 chr6:53972454-53972463 chr6:53972455-53972464 chr6:53972448-53972469
6	BHLHE40	chr6:53962611-53962857	HepG2	liver:	n/a	n/a
7	CEBPB	chr6:54000830-54001154	MCF-7	breast:	n/a	chr6:54001140-54001152
8	CEBPB	chr6:54021521-54021860	IMR90	lung:	n/a	chr6:54021669-54021680
9	CEBPB	chr6:54021570-54021811	H1-hESC	embryonic stem cell:	n/a	chr6:54021669-54021680
10	CEBPB	chr6:54000781-54001160	Hela-S3	cervix:	n/a	chr6:54001140-54001152
11	CEBPB	chr6:53999730-54000040	IMR90	lung:	n/a	chr6:53999861-53999874 chr6:53999861-53999874 chr6:53999863-53999874 chr6:53999863-53999874 chr6:53999861-53999872
12	CEBPB	chr6:53999774-54000050	HepG2	liver:	n/a	chr6:53999861-53999874 chr6:53999861-53999874 chr6:53999863-53999874 chr6:53999863-53999874 chr6:53999861-53999872
13	CEBPB	chr6:54013296-54013543	HepG2	liver:	n/a	chr6:54013402-54013413
14	CEBPB	chr6:54000822-54001146	A549	lung:	n/a	n/a
15	CEBPB	chr6:54000793-54001084	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr6:54000745-54001162	MCF-7	breast:	n/a	chr6:54001140-54001152
17	CEBPB	chr6:54000729-54001186	A549	lung:	n/a	chr6:54001140-54001152
18	CEBPB	chr6:54021522-54021851	Hela-S3	cervix:	n/a	chr6:54021669-54021680
19	CEBPB	chr6:54000889-54001075	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:54035385-54035738	HepG2	liver:	n/a	chr6:54035563-54035574
21	CEBPB	chr6:54008035-54008201	HepG2	liver:	n/a	chr6:54008071-54008082
22	CEBPB	chr6:54021570-54021851	A549	lung:	n/a	chr6:54021669-54021680
23	CEBPB	chr6:53962546-53962803	Hela-S3	cervix:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
24	CEBPB	chr6:54021630-54021782	K562	blood:	n/a	chr6:54021669-54021680
25	CEBPB	chr6:54021515-54021861	HepG2	liver:	n/a	chr6:54021669-54021680
26	CEBPB	chr6:53984491-53984712	HepG2	liver:	n/a	chr6:53984572-53984583
27	CEBPB	chr6:54000686-54001217	HCT-116	colon:	n/a	chr6:54001140-54001152
28	CEBPB	chr6:53962593-53962858	HepG2	liver:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
29	CEBPB	chr6:53962398-53962934	HepG2	liver:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
30	CEBPB	chr6:53962549-53962950	HepG2	liver:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
31	CEBPB	chr6:53962505-53962816	A549	lung:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
32	CEBPB	chr6:53962535-53962901	HepG2	liver:	n/a	chr6:53962727-53962738 chr6:53962716-53962727
33	CEBPB	chr6:54000759-54001219	ECC-1	luminal epithelium:	n/a	chr6:54001140-54001152
34	CEBPB	chr6:54037561-54037646	IMR90	lung:	n/a	n/a
35	CEBPB	chr6:54000804-54001144	HepG2	liver:	n/a	n/a
36	CEBPD	chr6:53962610-53962878	HepG2	liver:	n/a	chr6:53962728-53962739
37	CEBPZ	chr6:54032136-54032174	HepG2	liver:	n/a	n/a
38	CTCF	chr6:54038675-54038721	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr6:54002340-54002490	GM12869	blood:	n/a	n/a
40	CTCF	chr6:53994580-53994730	HepG2	liver:	n/a	chr6:53994600-53994609 chr6:53994600-53994613
41	CTCF	chr6:54008783-54008849	Fibrobl	skin:	n/a	n/a
42	CTCF	chr6:54040949-54041016	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr6:53975180-53975247	Lung_OC	lung:	n/a	n/a
44	CUX1	chr6:53965712-53965730	GM12878	blood:	n/a	n/a
45	E2F4	chr6:53988468-53988758	MCF10A-Er-Src	breast:	n/a	n/a
46	EGR1	chr6:53996022-53996460	ECC-1	luminal epithelium:	n/a	n/a
47	ELF1	chr6:54000790-54001065	HepG2	liver:	n/a	n/a
48	ELK1	chr6:53967800-53967839	K562	blood:	n/a	n/a
49	EP300	chr6:53962594-53962837	HepG2	liver:	n/a	n/a
50	EP300	chr6:54000682-54001135	HepG2	liver:	n/a	chr6:54000911-54000920

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:54001868-54001918	IMR90	lung:	fetal
2	chr6:54001665-54001715	HCPEpiC	choroid plexus:	n/a
3	chr6:54001868-54001918	H1-hESC	embryonic stem cell:	embryo
4	chr6:54001868-54001918	SK-N-SH_RA	brain:	n/a
5	chr6:54001665-54001715	HEEpiC	esophagus:	n/a
6	chr6:54001868-54001918	GM12878	blood:	n/a
7	chr6:54001868-54001918	NHBE	bronchial:	n/a
8	chr6:54001665-54001715	NT2-D1	testis:	n/a
9	chr6:54001895-54001945	GM12891	blood:	n/a
10	chr6:54001665-54001715	AoSMC	blood vessel:	n/a
11	chr6:54001665-54001715	SAEC	small airway:	n/a
12	chr6:54001895-54001945	NT2-D1	testis:	n/a
13	chr6:54001895-54001945	IMR90	lung:	fetal
14	chr6:54001868-54001918	T-47D	breast:	n/a
15	chr6:54001895-54001945	NHBE	bronchial:	n/a
16	chr6:54001868-54001918	HepG2	liver:	n/a
17	chr6:54001895-54001945	HAEpiC	amniotic membrane:	n/a
18	chr6:54001895-54001945	AG04450	lung:	fetal
19	chr6:54001895-54001945	PFSK-1	brain:	n/a
20	chr6:54001895-54001945	HEK293	kidney:	embryo
21	chr6:54001895-54001945	GM12892	blood:	n/a
22	chr6:54001895-54001945	PANC-1	pancreas:	n/a
23	chr6:54001665-54001715	RPTEC	kidney:	n/a
24	chr6:54001895-54001945	HNPCEpiC	eye:	n/a
25	chr6:54001895-54001945	BJ	skin:	n/a
26	chr6:54001868-54001918	HCT-116	colon:	n/a
27	chr6:54001665-54001715	AG09319	gingival:	n/a
28	chr6:54001895-54001945	HIPEpiC	eye:	n/a
29	chr6:54001895-54001945	HPAEpiC	pulmonary alveolar:	n/a
30	chr6:54001895-54001945	AG09319	gingival:	n/a
31	chr6:54001868-54001918	Hela-S3	cervix:	n/a
32	chr6:54001895-54001945	NH-A	brain:	n/a
33	chr6:54001868-54001918	AG04450	lung:	fetal
34	chr6:54001665-54001715	ProgFib	skin:	n/a
35	chr6:54001665-54001715	AG09309	skin:	n/a
36	chr6:54001895-54001945	NHDF-neo	bronchial:	n/a
37	chr6:54001868-54001918	HEK293	kidney:	embryo
38	chr6:54001665-54001715	HCM	heart:	n/a
39	chr6:54001895-54001945	AG04449	skin:	fetal
40	chr6:54001868-54001918	HAEpiC	amniotic membrane:	n/a
41	chr6:54001665-54001715	SK-N-MC	brain:	n/a
42	chr6:54001895-54001945	SK-N-SH	brain:	n/a
43	chr6:54001665-54001715	NHBE	bronchial:	n/a
44	chr6:54001895-54001945	ProgFib	skin:	n/a
45	chr6:54001868-54001918	HRCEpiC	kidney:	n/a
46	chr6:54001868-54001918	HIPEpiC	eye:	n/a
47	chr6:54001895-54001945	CMK	blood:	n/a
48	chr6:54001665-54001715	SK-N-SH	brain:	n/a
49	chr6:54001895-54001945	HepG2	liver:	n/a
50	chr6:54001868-54001918	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:53990110..53992835-chr6:54232926..54235323,2	K562	blood:
2	chr6:53992281..53994885-chr6:54000066..54003038,2	MCF-7	breast:
3	chr6:53992281..53994885-chr6:54000066..54003038,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC1-9	chr6:53973667-53973851	NONHSAT113221
2	lnc-LRRC1-8	chr6:53967721-53970422	ucscGeneNc_uc003pce_2
3	lnc-LRRC1-9	chr6:53979728-53979909	NONHSAT113221
4	lnc-LRRC1-8	chr6:53967721-53970052	NONHSAT113215
5	lnc-LRRC1-9	chr6:53975371-53975476	NONHSAT113221
6	lnc-LRRC1-8	chr6:53967547-53967621	ucscGeneNc_uc003pce_2
7	lnc-LRRC1-8	chr6:53967547-53967621	NONHSAT113215
8	lnc-LRRC1-9	chr6:53971647-53971816	NONHSAT113221

Variant related genes	Relation type
MLIP	TF binding region
MLIP	CpG island
ENSG00000228231	chromatin interactions

Extended variants
information (count: 3116 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3116 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs685893	chr6:53961784-53961785	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369268917	chr6:53961804-53961805	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs527352801	chr6:53961852-53961853	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs547516636	chr6:53961934-53961935	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs373504313	chr6:53961960-53961961	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs532932011	chr6:53962033-53962034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549555527	chr6:53962089-53962090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573116848	chr6:53962216-53962217	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs182047257	chr6:53962241-53962242	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs9474735	chr6:53962250-53962251	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs555106508	chr6:53962258-53962259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370070435	chr6:53962266-53962267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373495277	chr6:53962326-53962327	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs533986217	chr6:53962350-53962351	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs141229023	chr6:53962412-53962413	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs186129259	chr6:53962415-53962416	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs546175751	chr6:53962430-53962431	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs556313138	chr6:53962465-53962466	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs191374451	chr6:53962499-53962500	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs542180025	chr6:53962516-53962517	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs562215871	chr6:53962518-53962519	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs150747793	chr6:53962542-53962543	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs76928941	chr6:53962546-53962547	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs137870316	chr6:53962570-53962571	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs532910530	chr6:53962572-53962573	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs183125870	chr6:53962601-53962602	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs188361709	chr6:53962676-53962677	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs115714423	chr6:53962696-53962697	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs548870227	chr6:53962712-53962713	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs567805029	chr6:53962713-53962714	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs192025777	chr6:53962742-53962743	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs534502537	chr6:53962776-53962777	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs557579426	chr6:53962821-53962822	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs377480207	chr6:53962851-53962852	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs370807190	chr6:53962855-53962856	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs149463780	chr6:53962861-53962862	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs536794747	chr6:53962896-53962897	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs1280942	chr6:53962918-53962919	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs576360688	chr6:53962927-53962928	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs485026	chr6:53962938-53962939	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs377649894	chr6:53962946-53962947	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs71546129	chr6:53962947-53962948	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs200758320	chr6:53962948-53962949	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs59359046	chr6:53962949-53962950	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs1280943	chr6:53962950-53962951	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs561710668	chr6:53962952-53962953	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs4549620	chr6:53962969-53962970	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs183070417	chr6:53962999-53963000	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs386701268	chr6:53963008-53963009	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs556639176	chr6:53963057-53963058	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	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
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	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
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:53945000-53970800	Weak transcription	Right Atrium	heart
2	chr6:53959400-53975800	Weak transcription	Fetal Muscle Leg	muscle
3	chr6:53959800-53967000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr6:53960000-53965400	Weak transcription	Fetal Heart	heart
5	chr6:53960200-53964200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr6:53960600-53962600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr6:53960600-53963600	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr6:53961000-53964400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr6:53961000-53966800	Weak transcription	Fetal Brain Male	brain
10	chr6:53961400-53967400	Weak transcription	Fetal Brain Female	brain
11	chr6:53961600-53965400	Weak transcription	Left Ventricle	heart
12	chr6:53961600-53966800	Weak transcription	Psoas Muscle	Psoas
13	chr6:53961600-53966800	Weak transcription	Right Ventricle	heart
14	chr6:53962400-53963800	Enhancers	HepG2	liver
15	chr6:53962600-53963800	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr6:53962800-53964200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:53963800-53965400	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr6:53964200-53964400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
19	chr6:53964200-53964600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr6:53964400-53964600	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr6:53964400-53965000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr6:53964600-53964800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr6:53964600-53965200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr6:53964800-53965000	Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr6:53965000-53965200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr6:53965000-53966600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr6:53965200-53965400	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr6:53965200-53965600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:53965400-53965600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr6:53965400-53965800	Enhancers	Left Ventricle	heart
31	chr6:53965400-53966200	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr6:53965400-53968400	Enhancers	Fetal Heart	heart
33	chr6:53965600-53965800	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr6:53965600-53966000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:53965800-53968200	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr6:53965800-53974200	Weak transcription	Left Ventricle	heart
37	chr6:53966000-53967800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:53966200-53966600	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr6:53966600-53966800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr6:53966600-53972800	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr6:53966800-53967600	Enhancers	Fetal Brain Male	brain
42	chr6:53966800-53967600	Enhancers	Right Ventricle	heart
43	chr6:53966800-53968800	Enhancers	Psoas Muscle	Psoas
44	chr6:53967000-53967600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:53967000-53973200	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr6:53967200-53967600	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr6:53967200-53976200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr6:53967400-53968000	Enhancers	Fetal Brain Female	brain
49	chr6:53967600-53967800	Weak transcription	Fetal Brain Male	brain
50	chr6:53967600-53975800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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