Variant report

Variant	nsv116
Chromosome Location	chr15:76880628-76914288
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:47)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:47 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr15:76907137-76907384	GM12878	blood:	n/a	n/a
2	BATF	chr15:76907151-76907359	GM12878	blood:	n/a	n/a
3	CEBPB	chr15:76908855-76909056	HepG2	liver:	n/a	chr15:76908970-76908981
4	CTCF	chr15:76882560-76882710	NHEK	skin:	n/a	n/a
5	CTCF	chr15:76900780-76900838	MCF-7	breast:	n/a	n/a
6	CTCF	chr15:76881400-76881550	HEK293	kidney:	n/a	n/a
7	CTCF	chr15:76881511-76881568	MCF-7	breast:	n/a	n/a
8	CTCF	chr15:76881508-76881622	Pancreas_OC	pancreas:	n/a	n/a
9	CTCF	chr15:76881440-76881590	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr15:76881400-76881550	Caco-2	colon:	n/a	n/a
11	CTCF	chr15:76881380-76881530	NHEK	skin:	n/a	n/a
12	CTCF	chr15:76881480-76881630	MCF-7	breast:	n/a	n/a
13	CTCF	chr15:76900782-76900839	MCF-7	breast:	n/a	n/a
14	CTCF	chr15:76881453-76881628	MCF-7	breast:	n/a	n/a
15	CTCF	chr15:76881300-76881450	NHEK	skin:	n/a	n/a
16	CTCF	chr15:76881480-76881630	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr15:76900797-76900818	MCF-7	breast:	n/a	n/a
18	CTCF	chr15:76900763-76900839	MCF-7	breast:	n/a	n/a
19	CTCF	chr15:76881460-76881610	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr15:76881480-76881630	HepG2	liver:	n/a	n/a
21	CTCF	chr15:76881520-76881670	WERI-Rb-1	eye:	n/a	n/a
22	E2F4	chr15:76908851-76909148	MCF10A-Er-Src	breast:	n/a	chr15:76909112-76909121
23	FOXA2	chr15:76900721-76901342	A549	lung:	n/a	n/a
24	GATA3	chr15:76883261-76883422	SH-SY5Y	brain:	n/a	n/a
25	JUN	chr15:76908819-76909010	HepG2	liver:	n/a	chr15:76908879-76908892
26	MAFK	chr15:76909554-76909754	HepG2	liver:	n/a	chr15:76909671-76909686
27	MAFK	chr15:76909563-76909816	HepG2	liver:	n/a	chr15:76909671-76909686
28	MYC	chr15:76881873-76881952	H1-hESC	embryonic stem cell:	n/a	n/a
29	NFIC	chr15:76906959-76907386	GM12878	blood:	n/a	n/a
30	POLR2A	chr15:76884234-76884374	MCF-7	breast:	n/a	n/a
31	POLR2A	chr15:76895856-76895943	ProgFib	skin:	n/a	n/a
32	POLR2A	chr15:76910508-76910585	A549	lung:	n/a	n/a
33	POLR2A	chr15:76910505-76910585	MCF-7	breast:	n/a	n/a
34	POLR2A	chr15:76912273-76912366	Gliobla	brain:	n/a	n/a
35	POLR2A	chr15:76912273-76912390	A549	lung:	n/a	n/a
36	POLR2A	chr15:76910040-76910053	Gliobla	brain:	n/a	n/a
37	POLR2A	chr15:76912277-76912357	MCF-7	breast:	n/a	n/a
38	POLR2A	chr15:76881795-76881944	MCF-7	breast:	n/a	n/a
39	POLR2A	chr15:76908606-76908747	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr15:76908057-76908119	MCF-7	breast:	n/a	n/a
41	POLR2A	chr15:76910502-76910503	A549	lung:	n/a	n/a
42	POLR2A	chr15:76881790-76881791	MCF-7	breast:	n/a	n/a
43	RAD21	chr15:76881428-76881536	HepG2	liver:	n/a	n/a
44	RAD21	chr15:76881379-76881726	H1-hESC	embryonic stem cell:	n/a	n/a
45	RUNX3	chr15:76907146-76907395	GM12878	blood:	n/a	n/a
46	STAT3	chr15:76912527-76912591	MCF10A-Er-Src	breast:	n/a	n/a
47	STAT3	chr15:76906407-76906633	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76901065-76901115	MCF10A-Er-Src	breast:	n/a
2	chr15:76901065-76901115	NT2-D1	testis:	n/a
3	chr15:76901065-76901115	GM12878	blood:	n/a
4	chr15:76901065-76901115	HNPCEpiC	eye:	n/a
5	chr15:76901065-76901115	K562	blood:	n/a
6	chr15:76901065-76901115	BJ	skin:	n/a
7	chr15:76901065-76901115	HMEC	breast:	n/a
8	chr15:76901065-76901115	ProgFib	skin:	n/a
9	chr15:76901065-76901115	HCPEpiC	choroid plexus:	n/a
10	chr15:76901065-76901115	AG04450	lung:	fetal
11	chr15:76901065-76901115	HIPEpiC	eye:	n/a
12	chr15:76901065-76901115	HCM	heart:	n/a
13	chr15:76901065-76901115	LNCaP	prostate:	n/a
14	chr15:76901065-76901115	Hela-S3	cervix:	n/a
15	chr15:76901065-76901115	U87	brain:	n/a
16	chr15:76901065-76901115	HRPEpiC	eye:	n/a
17	chr15:76901065-76901115	GM12892	blood:	n/a
18	chr15:76901065-76901115	GM19239	blood:	n/a
19	chr15:76901065-76901115	HUVEC	blood vessel:	n/a
20	chr15:76901065-76901115	NHBE	bronchial:	n/a
21	chr15:76901065-76901115	HepG2	liver:	n/a
22	chr15:76901065-76901115	HRE	kidney:	n/a
23	chr15:76901065-76901115	MCF-7	breast:	n/a
24	chr15:76901065-76901115	SAEC	small airway:	n/a
25	chr15:76901065-76901115	GM12891	blood:	n/a
26	chr15:76901065-76901115	SKMC	muscle:	n/a
27	chr15:76901065-76901115	H1-hESC	embryonic stem cell:	embryo
28	chr15:76901065-76901115	CMK	blood:	n/a
29	chr15:76901065-76901115	AG10803	skin:	n/a
30	chr15:76901065-76901115	HCT-116	colon:	n/a
31	chr15:76901065-76901115	SK-N-SH	brain:	n/a
32	chr15:76901065-76901115	T-47D	breast:	n/a
33	chr15:76901065-76901115	BE2_C	brain:	n/a
34	chr15:76901065-76901115	SK-N-MC	brain:	n/a
35	chr15:76901065-76901115	NB4	blood:	n/a
36	chr15:76901065-76901115	NH-A	brain:	n/a
37	chr15:76901065-76901115	HAEpiC	amniotic membrane:	n/a
38	chr15:76901065-76901115	AG09319	gingival:	n/a
39	chr15:76901065-76901115	Jurkat	blood:	n/a
40	chr15:76901065-76901115	AG09309	skin:	n/a
41	chr15:76901065-76901115	PFSK-1	brain:	n/a
42	chr15:76901065-76901115	PrEC	prostate:	n/a
43	chr15:76901065-76901115	RPTEC	kidney:	n/a
44	chr15:76901065-76901115	SK-N-SH_RA	brain:	n/a
45	chr15:76901065-76901115	AG04449	skin:	fetal
46	chr15:76901065-76901115	HCF	heart:	n/a
47	chr15:76901065-76901115	Caco-2	colon:	n/a
48	chr15:76901065-76901115	PANC-1	pancreas:	n/a
49	chr15:76901065-76901115	IMR90	lung:	fetal
50	chr15:76901065-76901115	ECC-1	luminal epithelium:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:76877558..76879609-chr15:76881319..76882907,2	K562	blood:

No data

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

Extended variants
information (count: 1198 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1198 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536690452	chr15:76880651-76880652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555197195	chr15:76880691-76880692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370606102	chr15:76880710-76880711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181526982	chr15:76880741-76880742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186269992	chr15:76880757-76880758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565359856	chr15:76880764-76880765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577052319	chr15:76880814-76880815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540711017	chr15:76880862-76880863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573184324	chr15:76880863-76880864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147955621	chr15:76880884-76880885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547882077	chr15:76880891-76880892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs367900512	chr15:76880900-76880901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs4886818	chr15:76880939-76880940	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs530732919	chr15:76880985-76880986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552471051	chr15:76881000-76881001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112614522	chr15:76881021-76881022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141805791	chr15:76881047-76881048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369121365	chr15:76881117-76881118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11072603	chr15:76881138-76881139	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs374626110	chr15:76881145-76881146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566181137	chr15:76881153-76881154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181110291	chr15:76881155-76881156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147115950	chr15:76881157-76881158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570301160	chr15:76881174-76881175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186555469	chr15:76881230-76881231	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367662453	chr15:76881252-76881253	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35507437	chr15:76881276-76881277	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559237855	chr15:76881284-76881285	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147971231	chr15:76881298-76881299	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372914169	chr15:76881300-76881301	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541275817	chr15:76881335-76881336	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs574305567	chr15:76881336-76881337	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs12101910	chr15:76881338-76881339	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs376134717	chr15:76881354-76881355	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs34497250	chr15:76881377-76881378	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574207423	chr15:76881400-76881401	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs540957522	chr15:76881418-76881419	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs541778001	chr15:76881430-76881431	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs563112839	chr15:76881459-76881460	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs530559137	chr15:76881482-76881483	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs140730118	chr15:76881488-76881489	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528247230	chr15:76881494-76881495	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs369580433	chr15:76881505-76881506	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546825636	chr15:76881528-76881529	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs190659889	chr15:76881538-76881539	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs113998171	chr15:76881599-76881600	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs548692172	chr15:76881614-76881615	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs150108432	chr15:76881735-76881736	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs12908421	chr15:76881794-76881795	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs558822983	chr15:76881805-76881806	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76869400-76881200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr15:76870400-76881200	Weak transcription	Lung	lung
3	chr15:76871000-76883600	Weak transcription	Ovary	ovary
4	chr15:76874200-76881600	Weak transcription	Esophagus	oesophagus
5	chr15:76875600-76881600	Weak transcription	Primary B cells from cord blood	blood
6	chr15:76876000-76883600	Weak transcription	Aorta	Aorta
7	chr15:76877400-76883400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr15:76878000-76881600	Weak transcription	Left Ventricle	heart
9	chr15:76878200-76884200	Weak transcription	Right Ventricle	heart
10	chr15:76878600-76881200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:76878800-76884800	Weak transcription	Primary T cells from cord blood	blood
12	chr15:76879200-76881200	Weak transcription	Fetal Stomach	stomach
13	chr15:76879400-76881600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr15:76879400-76881600	Weak transcription	Primary B cells from peripheral blood	blood
15	chr15:76879400-76883400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr15:76879600-76881200	Weak transcription	Thymus	Thymus
17	chr15:76879600-76881400	Weak transcription	Stomach Smooth Muscle	stomach
18	chr15:76879600-76881600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr15:76879600-76883400	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr15:76879800-76881800	Weak transcription	Liver	Liver
21	chr15:76879800-76881800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr15:76879800-76885600	Weak transcription	Pancreas	Pancrea
23	chr15:76880200-76883200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr15:76880400-76883200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr15:76880400-76883200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr15:76880400-76883600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr15:76880600-76883200	Weak transcription	Fetal Muscle Trunk	muscle
28	chr15:76880600-76883400	Weak transcription	Fetal Muscle Leg	muscle
29	chr15:76881000-76881600	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr15:76881000-76881600	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr15:76881200-76881400	Enhancers	Duodenum Mucosa	Duodenum
32	chr15:76881200-76881800	Enhancers	Fetal Intestine Small	intestine
33	chr15:76881200-76882000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr15:76881200-76882000	ZNF genes & repeats	Lung	lung
35	chr15:76881200-76882400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr15:76881200-76882400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr15:76881200-76882400	Enhancers	Fetal Intestine Large	intestine
38	chr15:76881200-76882400	Strong transcription	Fetal Stomach	stomach
39	chr15:76881200-76882600	Strong transcription	Thymus	Thymus
40	chr15:76881400-76881600	Flanking Active TSS	Duodenum Mucosa	Duodenum
41	chr15:76881400-76881800	Active TSS	Colonic Mucosa	Colon
42	chr15:76881400-76882000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr15:76881400-76882200	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr15:76881400-76882400	Strong transcription	Stomach Smooth Muscle	stomach
45	chr15:76881400-76882400	Enhancers	NHEK	skin
46	chr15:76881600-76881800	Enhancers	Duodenum Mucosa	Duodenum
47	chr15:76881600-76882000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr15:76881600-76882000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
49	chr15:76881600-76882000	Enhancers	Left Ventricle	heart
50	chr15:76881600-76882000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum

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