Variant report

Variant	nsv1048577
Chromosome Location	chr15:76868215-76895763
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:65)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:65 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr15:76867574-76868256	GM12878	blood:	n/a	n/a
2	BATF	chr15:76868780-76869125	GM12878	blood:	n/a	n/a
3	BATF	chr15:76867553-76868299	GM12878	blood:	n/a	n/a
4	CEBPB	chr15:76869014-76869478	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr15:76869227-76869506	HepG2	liver:	n/a	n/a
6	CEBPB	chr15:76867534-76868241	GM12878	blood:	n/a	n/a
7	CHD2	chr15:76869098-76869401	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr15:76881400-76881550	HEK293	kidney:	n/a	n/a
9	CTCF	chr15:76881480-76881630	HEEpiC	esophagus:	n/a	n/a
10	CTCF	chr15:76881380-76881530	NHEK	skin:	n/a	n/a
11	CTCF	chr15:76881508-76881622	Pancreas_OC	pancreas:	n/a	n/a
12	CTCF	chr15:76869020-76869170	AG10803	skin:	n/a	n/a
13	CTCF	chr15:76882560-76882710	NHEK	skin:	n/a	n/a
14	CTCF	chr15:76881453-76881628	MCF-7	breast:	n/a	n/a
15	CTCF	chr15:76881480-76881630	MCF-7	breast:	n/a	n/a
16	CTCF	chr15:76881300-76881450	NHEK	skin:	n/a	n/a
17	CTCF	chr15:76869047-76869085	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr15:76869022-76869108	Gliobla	brain:	n/a	n/a
19	CTCF	chr15:76881480-76881630	HepG2	liver:	n/a	n/a
20	CTCF	chr15:76881460-76881610	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr15:76881520-76881670	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr15:76881440-76881590	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr15:76881400-76881550	Caco-2	colon:	n/a	n/a
24	CTCF	chr15:76881511-76881568	MCF-7	breast:	n/a	n/a
25	EBF1	chr15:76868806-76869204	GM12878	blood:	n/a	n/a
26	EBF1	chr15:76868902-76869184	GM12878	blood:	n/a	n/a
27	EP300	chr15:76869124-76869557	HepG2	liver:	n/a	n/a
28	FOXA1	chr15:76869134-76869542	HepG2	liver:	n/a	n/a
29	FOXA2	chr15:76869083-76869415	HepG2	liver:	n/a	n/a
30	GATA3	chr15:76883261-76883422	SH-SY5Y	brain:	n/a	n/a
31	HNF4A	chr15:76869226-76869499	HepG2	liver:	n/a	n/a
32	HNF4G	chr15:76869228-76869538	HepG2	liver:	n/a	n/a
33	IKZF1	chr15:76868890-76869081	GM12878	blood:	n/a	n/a
34	MAX	chr15:76869230-76869513	Hela-S3	cervix:	n/a	n/a
35	MAX	chr15:76872719-76872775	NB4	blood:	n/a	chr15:76872722-76872732 chr15:76872738-76872748
36	MAZ	chr15:76869256-76869453	Hela-S3	cervix:	n/a	n/a
37	MAZ	chr15:76869060-76869066	GM12878	blood:	n/a	n/a
38	MTA3	chr15:76867427-76868243	GM12878	blood:	n/a	n/a
39	MYC	chr15:76881873-76881952	H1-hESC	embryonic stem cell:	n/a	n/a
40	NFIC	chr15:76868939-76869620	ECC-1	luminal epithelium:	n/a	n/a
41	NFIC	chr15:76869108-76869530	HepG2	liver:	n/a	n/a
42	NFIC	chr15:76867503-76868285	GM12878	blood:	n/a	n/a
43	NFIC	chr15:76869060-76869678	ECC-1	luminal epithelium:	n/a	n/a
44	NFIC	chr15:76867309-76868397	GM12878	blood:	n/a	n/a
45	NR2F2	chr15:76869025-76869526	MCF-7	breast:	n/a	n/a
46	POLR2A	chr15:76884234-76884374	MCF-7	breast:	n/a	n/a
47	POLR2A	chr15:76881790-76881791	MCF-7	breast:	n/a	n/a
48	POLR2A	chr15:76872099-76872252	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr15:76881795-76881944	MCF-7	breast:	n/a	n/a
50	POLR2A	chr15:76870310-76870387	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76868964-76869014	HPAEpiC	pulmonary alveolar:	n/a
2	chr15:76868964-76869014	BE2_C	brain:	n/a
3	chr15:76868964-76869014	AG09319	gingival:	n/a
4	chr15:76868964-76869014	SKMC	muscle:	n/a
5	chr15:76868964-76869014	SK-N-SH	brain:	n/a
6	chr15:76868964-76869014	PrEC	prostate:	n/a
7	chr15:76868964-76869014	HCPEpiC	choroid plexus:	n/a
8	chr15:76868964-76869014	LNCaP	prostate:	n/a
9	chr15:76868964-76869014	HMEC	breast:	n/a
10	chr15:76868964-76869014	GM19239	blood:	n/a
11	chr15:76868964-76869014	H1-hESC	embryonic stem cell:	embryo
12	chr15:76868964-76869014	MCF10A-Er-Src	breast:	n/a
13	chr15:76868964-76869014	BJ	skin:	n/a
14	chr15:76868964-76869014	NHBE	bronchial:	n/a
15	chr15:76868964-76869014	SAEC	small airway:	n/a
16	chr15:76868964-76869014	HNPCEpiC	eye:	n/a
17	chr15:76868964-76869014	HUVEC	blood vessel:	n/a
18	chr15:76868964-76869014	U87	brain:	n/a
19	chr15:76868964-76869014	Hepatocyte	liver:	n/a
20	chr15:76868964-76869014	HepG2	liver:	n/a
21	chr15:76868964-76869014	AG10803	skin:	n/a
22	chr15:76868964-76869014	Hela-S3	cervix:	n/a
23	chr15:76868964-76869014	HEEpiC	esophagus:	n/a
24	chr15:76868964-76869014	HL-60	blood:	n/a
25	chr15:76868964-76869014	ProgFib	skin:	n/a
26	chr15:76868964-76869014	HCM	heart:	n/a
27	chr15:76868964-76869014	ECC-1	luminal epithelium:	n/a
28	chr15:76868964-76869014	NB4	blood:	n/a
29	chr15:76868964-76869014	A549	lung:	n/a
30	chr15:76868964-76869014	SK-N-MC	brain:	n/a
31	chr15:76868964-76869014	GM06990	blood:	n/a
32	chr15:76868964-76869014	IMR90	lung:	fetal
33	chr15:76868964-76869014	AG04449	skin:	fetal
34	chr15:76868964-76869014	SK-N-SH_RA	brain:	n/a
35	chr15:76868964-76869014	GM12878	blood:	n/a
36	chr15:76868964-76869014	HRPEpiC	eye:	n/a
37	chr15:76868964-76869014	HRE	kidney:	n/a
38	chr15:76868964-76869014	NH-A	brain:	n/a
39	chr15:76868964-76869014	HCF	heart:	n/a
40	chr15:76868964-76869014	HIPEpiC	eye:	n/a
41	chr15:76868964-76869014	Jurkat	blood:	n/a
42	chr15:76868964-76869014	PANC-1	pancreas:	n/a
43	chr15:76868964-76869014	Caco-2	colon:	n/a
44	chr15:76868964-76869014	HRCEpiC	kidney:	n/a
45	chr15:76868964-76869014	K562	blood:	n/a
46	chr15:76868964-76869014	ovcar-3	ovarian:	n/a
47	chr15:76868964-76869014	AoSMC	blood vessel:	n/a
48	chr15:76868964-76869014	HCT-116	colon:	n/a
49	chr15:76868964-76869014	MCF-7	breast:	n/a
50	chr15:76868964-76869014	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:76877558..76879609-chr15:76881319..76882907,2	K562	blood:
2	chr15:76855877..76857707-chr15:76866696..76869240,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3713	chr15:76878988-76879007	MIMAT0018164

No data

Variant related genes	Relation type
SCAPER	TF binding region
MIR3713	TF binding region
SCAPER	CpG island
MIR3713	CpG island
ENSG00000266449	chromatin interactions

Extended variants
information (count: 929 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:929 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183086170	chr15:76868230-76868231	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs187853074	chr15:76868281-76868282	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs577148302	chr15:76868304-76868305	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs570183707	chr15:76868320-76868321	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs191707302	chr15:76868321-76868322	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs140445469	chr15:76868375-76868376	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs114887945	chr15:76868416-76868417	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs57682236	chr15:76868478-76868479	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs563556090	chr15:76868539-76868540	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs377367535	chr15:76868591-76868592	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs574966704	chr15:76868608-76868609	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs545468699	chr15:76868614-76868615	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs2459360	chr15:76868664-76868665	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs528078168	chr15:76868674-76868675	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs188183929	chr15:76868704-76868705	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs117228051	chr15:76868719-76868720	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs144410071	chr15:76868768-76868769	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs547273246	chr15:76868799-76868800	Enhancers Weak transcription Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs554591000	chr15:76868804-76868805	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs550764269	chr15:76868812-76868813	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs569098376	chr15:76868813-76868814	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs539672339	chr15:76868916-76868917	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs552625998	chr15:76868933-76868934	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs62030411	chr15:76868964-76868965	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs116743933	chr15:76868991-76868992	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs553101096	chr15:76869025-76869026	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs147811899	chr15:76869044-76869045	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs79851567	chr15:76869057-76869058	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs368893205	chr15:76869058-76869059	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs398070702	chr15:76869065-76869066	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs371180401	chr15:76869123-76869124	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs141344270	chr15:76869156-76869157	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs192800519	chr15:76869158-76869159	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs142656613	chr15:76869161-76869162	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs112912502	chr15:76869209-76869210	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs564203323	chr15:76869210-76869211	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs184435510	chr15:76869218-76869219	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs79890594	chr15:76869222-76869223	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs80083592	chr15:76869223-76869224	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs151016233	chr15:76869241-76869242	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs2404739	chr15:76869372-76869373	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs529174355	chr15:76869394-76869395	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs550874525	chr15:76869400-76869401	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs562807373	chr15:76869415-76869416	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs140437618	chr15:76869458-76869459	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs559234065	chr15:76869459-76869460	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs186634383	chr15:76869460-76869461	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs75468747	chr15:76869486-76869487	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs74368852	chr15:76869511-76869512	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs150413228	chr15:76869524-76869525	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:229 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76846000-76869000	Weak transcription	Left Ventricle	heart
2	chr15:76846000-76869000	Weak transcription	Pancreas	Pancrea
3	chr15:76846200-76868800	Weak transcription	Fetal Intestine Small	intestine
4	chr15:76850200-76868400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr15:76857000-76868800	Weak transcription	Liver	Liver
6	chr15:76858600-76869000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr15:76860000-76868400	Weak transcription	Esophagus	oesophagus
8	chr15:76861600-76869200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr15:76861800-76869000	Weak transcription	Colonic Mucosa	Colon
10	chr15:76861800-76869000	Weak transcription	Placenta	Placenta
11	chr15:76862600-76868800	Weak transcription	Adipose Nuclei	Adipose
12	chr15:76862600-76869000	Weak transcription	Right Ventricle	heart
13	chr15:76862600-76872000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr15:76863000-76869000	Weak transcription	Fetal Muscle Leg	muscle
15	chr15:76863400-76868600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr15:76865000-76868800	Weak transcription	Osteobl	bone
17	chr15:76865000-76869000	Weak transcription	Gastric	stomach
18	chr15:76865000-76869000	Weak transcription	Psoas Muscle	Psoas
19	chr15:76865200-76868800	Weak transcription	Primary T cells from cord blood	blood
20	chr15:76865200-76868800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr15:76865200-76869000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr15:76865200-76869000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr15:76865200-76869200	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr15:76865200-76869200	Weak transcription	Fetal Stomach	stomach
25	chr15:76865400-76868400	Weak transcription	Ovary	ovary
26	chr15:76865400-76869000	Weak transcription	Fetal Lung	lung
27	chr15:76865600-76869000	Weak transcription	Brain Substantia Nigra	brain
28	chr15:76865600-76869000	Weak transcription	A549	lung
29	chr15:76865600-76869000	Weak transcription	HepG2	liver
30	chr15:76865600-76869400	Weak transcription	Brain Hippocampus Middle	brain
31	chr15:76867000-76868400	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr15:76867000-76868400	Enhancers	Primary B cells from peripheral blood	blood
33	chr15:76867400-76868800	Enhancers	Fetal Heart	heart
34	chr15:76867600-76868800	Weak transcription	Small Intestine	intestine
35	chr15:76867600-76868800	Enhancers	Hela-S3	cervix
36	chr15:76867800-76868400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr15:76868000-76868800	Active TSS	Duodenum Mucosa	Duodenum
38	chr15:76868000-76869000	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr15:76868000-76869600	ZNF genes & repeats	GM12878-XiMat	blood
40	chr15:76868200-76868400	Enhancers	Right Atrium	heart
41	chr15:76868200-76868800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr15:76868200-76870000	Weak transcription	Primary B cells from cord blood	blood
43	chr15:76868400-76868800	Weak transcription	Right Atrium	heart
44	chr15:76868400-76869000	Weak transcription	Primary B cells from peripheral blood	blood
45	chr15:76868400-76869800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr15:76868400-76870800	Enhancers	Esophagus	oesophagus
47	chr15:76868400-76871000	Enhancers	Ovary	ovary
48	chr15:76868600-76870800	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr15:76868800-76869000	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr15:76868800-76869000	Enhancers	Stomach Smooth Muscle	stomach

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