Variant report

Variant	nsv827340
Chromosome Location	chr15:56298487-56302591
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:35)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:35 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:56301135-56301199	K562	blood:	n/a	n/a
2	BHLHE40	chr15:56298674-56298896	HepG2	liver:	n/a	n/a
3	CEBPB	chr15:56298629-56298817	K562	blood:	n/a	chr15:56298720-56298731
4	CEBPB	chr15:56298546-56298903	A549	lung:	n/a	chr15:56298720-56298731
5	CEBPB	chr15:56298565-56298884	K562	blood:	n/a	chr15:56298720-56298731
6	CEBPB	chr15:56298541-56298913	IMR90	lung:	n/a	chr15:56298720-56298731
7	CEBPB	chr15:56298655-56298882	Hela-S3	cervix:	n/a	chr15:56298720-56298731
8	CEBPB	chr15:56298629-56298888	HepG2	liver:	n/a	chr15:56298720-56298731
9	FOS	chr15:56298675-56298872	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr15:56301883-56302056	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr15:56298651-56298896	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr15:56298657-56298997	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr15:56298673-56298895	MCF10A-Er-Src	breast:	n/a	n/a
14	MYC	chr15:56298626-56298904	MCF10A-Er-Src	breast:	n/a	n/a
15	MYC	chr15:56298613-56298913	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr15:56299206-56299648	H1-neurons	neurons:	n/a	n/a
17	POLR2A	chr15:56299304-56299519	H1-neurons	neurons:	n/a	n/a
18	POLR2A	chr15:56301765-56301766	MCF10A-Er-Src	breast:	n/a	n/a
19	POLR2A	chr15:56299484-56299596	GM12878	blood:	n/a	n/a
20	POLR2A	chr15:56299343-56299555	A549	lung:	n/a	n/a
21	POLR2A	chr15:56298494-56298612	ProgFib	skin:	n/a	n/a
22	POLR2A	chr15:56299473-56299597	GM12878	blood:	n/a	n/a
23	RCOR1	chr15:56299241-56299408	K562	blood:	n/a	n/a
24	RCOR1	chr15:56301373-56301612	K562	blood:	n/a	n/a
25	REST	chr15:56299486-56299608	PANC-1	pancreas:	n/a	n/a
26	SETDB1	chr15:56298496-56298815	U2OS	brain:	n/a	n/a
27	STAT3	chr15:56298632-56298917	MCF10A-Er-Src	breast:	n/a	n/a
28	STAT3	chr15:56298665-56298905	MCF10A-Er-Src	breast:	n/a	n/a
29	STAT3	chr15:56299834-56299850	MCF10A-Er-Src	breast:	n/a	n/a
30	STAT3	chr15:56298681-56298913	MCF10A-Er-Src	breast:	n/a	n/a
31	STAT3	chr15:56298665-56298896	MCF10A-Er-Src	breast:	n/a	n/a
32	TAF1	chr15:56299481-56299609	HepG2	liver:	n/a	n/a
33	TEAD4	chr15:56301233-56301558	K562	blood:	n/a	n/a
34	USF1	chr15:56298693-56298814	HepG2	liver:	n/a	chr15:56298768-56298779
35	USF1	chr15:56298675-56298835	HepG2	liver:	n/a	chr15:56298768-56298779

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56299380-56299430	AoSMC	blood vessel:	n/a
2	chr15:56299380-56299430	HCT-116	colon:	n/a
3	chr15:56299380-56299430	HL-60	blood:	n/a
4	chr15:56299380-56299430	HEK293	kidney:	embryo
5	chr15:56299380-56299430	SKMC	muscle:	n/a
6	chr15:56299380-56299430	ProgFib	skin:	n/a
7	chr15:56299380-56299430	GM19239	blood:	n/a
8	chr15:56299380-56299430	HepG2	liver:	n/a
9	chr15:56299380-56299430	RPTEC	kidney:	n/a
10	chr15:56299380-56299430	HMEC	breast:	n/a
11	chr15:56299380-56299430	PrEC	prostate:	n/a
12	chr15:56299380-56299430	Caco-2	colon:	n/a
13	chr15:56299380-56299430	ovcar-3	ovarian:	n/a
14	chr15:56299380-56299430	NHDF-neo	bronchial:	n/a
15	chr15:56299380-56299430	GM12892	blood:	n/a
16	chr15:56299380-56299430	HNPCEpiC	eye:	n/a
17	chr15:56299380-56299430	ECC-1	luminal epithelium:	n/a
18	chr15:56299380-56299430	GM12891	blood:	n/a
19	chr15:56299380-56299430	HCF	heart:	n/a
20	chr15:56299380-56299430	NT2-D1	testis:	n/a
21	chr15:56299380-56299430	GM06990	blood:	n/a
22	chr15:56299380-56299430	HCM	heart:	n/a
23	chr15:56299380-56299430	PFSK-1	brain:	n/a
24	chr15:56299380-56299430	HRE	kidney:	n/a
25	chr15:56299380-56299430	BE2_C	brain:	n/a
26	chr15:56299380-56299430	SAEC	small airway:	n/a
27	chr15:56299380-56299430	HIPEpiC	eye:	n/a
28	chr15:56299380-56299430	CMK	blood:	n/a
29	chr15:56299380-56299430	HEEpiC	esophagus:	n/a
30	chr15:56299380-56299430	PANC-1	pancreas:	n/a
31	chr15:56299380-56299430	AG04449	skin:	fetal
32	chr15:56299380-56299430	BJ	skin:	n/a
33	chr15:56299380-56299430	SK-N-SH	brain:	n/a
34	chr15:56299380-56299430	HRCEpiC	kidney:	n/a
35	chr15:56299380-56299430	K562	blood:	n/a
36	chr15:56299380-56299430	MCF10A-Er-Src	breast:	n/a
37	chr15:56299380-56299430	SK-N-SH_RA	brain:	n/a
38	chr15:56299380-56299430	NH-A	brain:	n/a
39	chr15:56299380-56299430	HUVEC	blood vessel:	n/a
40	chr15:56299380-56299430	IMR90	lung:	fetal
41	chr15:56299380-56299430	Hepatocyte	liver:	n/a
42	chr15:56299380-56299430	T-47D	breast:	n/a
43	chr15:56299380-56299430	AG09309	skin:	n/a
44	chr15:56299380-56299430	Jurkat	blood:	n/a
45	chr15:56299380-56299430	NHBE	bronchial:	n/a
46	chr15:56299380-56299430	LNCaP	prostate:	n/a
47	chr15:56299380-56299430	U87	brain:	n/a
48	chr15:56299380-56299430	HAEpiC	amniotic membrane:	n/a
49	chr15:56299380-56299430	MCF-7	breast:	n/a
50	chr15:56299380-56299430	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:56284954..56286880-chr15:56299616..56301777,2	K562	blood:
2	chr15:56284455..56287261-chr15:56299264..56302045,2	MCF-7	breast:

No data

Variant related genes	Relation type
CNOT6LP1	TF binding region
CNOT6LP1	CpG island
ENSG00000069869	chromatin interactions

Extended variants
information (count: 130 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:130 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111633367	chr15:56298507-56298508	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs201837887	chr15:56298524-56298525	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566824272	chr15:56298576-56298577	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548134212	chr15:56298616-56298617	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113646661	chr15:56298637-56298638	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143683874	chr15:56298664-56298665	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550636574	chr15:56298680-56298681	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs151065397	chr15:56298721-56298722	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141331463	chr15:56298739-56298740	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547180879	chr15:56298741-56298742	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567004674	chr15:56298748-56298749	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536167262	chr15:56298819-56298820	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs555367740	chr15:56298839-56298840	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs558857119	chr15:56299006-56299007	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575297601	chr15:56299037-56299038	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs145120251	chr15:56299057-56299058	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376835805	chr15:56299080-56299081	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540016437	chr15:56299119-56299120	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189370980	chr15:56299121-56299122	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573827925	chr15:56299131-56299132	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182210564	chr15:56299147-56299148	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75760999	chr15:56299198-56299199	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569897944	chr15:56299213-56299214	Active TSS Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530807571	chr15:56299218-56299219	Active TSS Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs62046379	chr15:56299233-56299234	Active TSS Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs564383350	chr15:56299252-56299253	Active TSS Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs28571735	chr15:56299271-56299272	Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs367942930	chr15:56299310-56299311	Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs546849307	chr15:56299311-56299312	Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs62046380	chr15:56299364-56299365	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs138977625	chr15:56299393-56299394	Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs7176495	chr15:56299411-56299412	Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs140708650	chr15:56299416-56299417	Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs569618302	chr15:56299417-56299418	Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs537833184	chr15:56299419-56299420	Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs557799741	chr15:56299423-56299424	Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs571209218	chr15:56299441-56299442	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs566176909	chr15:56299444-56299445	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs533911324	chr15:56299445-56299446	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs553617077	chr15:56299454-56299455	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs573755970	chr15:56299455-56299456	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs187247328	chr15:56299462-56299463	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs191621651	chr15:56299480-56299481	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570223471	chr15:56299483-56299484	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs556028111	chr15:56299490-56299491	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575939570	chr15:56299522-56299523	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs544153979	chr15:56299538-56299539	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs564526121	chr15:56299542-56299543	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs533234494	chr15:56299634-56299635	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs576404191	chr15:56299677-56299678	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	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
Colorectal cancer	16774939	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
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56292400-56298800	Weak transcription	A549	lung
2	chr15:56295000-56298600	Weak transcription	HMEC	breast
3	chr15:56295000-56298800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr15:56295000-56298800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr15:56295000-56299000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr15:56296800-56299000	Weak transcription	K562	blood
7	chr15:56298200-56298800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr15:56298200-56298800	Enhancers	Placenta	Placenta
9	chr15:56298400-56298800	Enhancers	NHEK	skin
10	chr15:56298400-56299600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr15:56298400-56300000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr15:56298600-56298800	Enhancers	HMEC	breast
13	chr15:56298600-56299800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr15:56298600-56299800	Active TSS	Muscle Satellite Cultured Cells	--
15	chr15:56298600-56299800	Active TSS	Brain Inferior Temporal Lobe	brain
16	chr15:56298600-56300000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr15:56298800-56299000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr15:56298800-56299200	Flanking Active TSS	A549	lung
19	chr15:56298800-56299200	Flanking Active TSS	HMEC	breast
20	chr15:56298800-56299200	Flanking Active TSS	NHEK	skin
21	chr15:56298800-56299400	Active TSS	Aorta	Aorta
22	chr15:56298800-56299400	Active TSS	Brain Hippocampus Middle	brain
23	chr15:56298800-56299800	Active TSS	Breast Myoepithelial Primary Cells	Breast
24	chr15:56298800-56299800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr15:56298800-56299800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr15:56298800-56299800	Active TSS	Duodenum Mucosa	Duodenum
27	chr15:56298800-56299800	Active TSS	Placenta	Placenta
28	chr15:56298800-56299800	Active TSS	Ovary	ovary
29	chr15:56298800-56299800	Active TSS	HSMM	muscle
30	chr15:56298800-56299800	Active TSS	HSMMtube	muscle
31	chr15:56298800-56299800	Active TSS	HUVEC	blood vessel
32	chr15:56298800-56299800	Active TSS	Osteobl	bone
33	chr15:56298800-56300000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
34	chr15:56298800-56300000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr15:56298800-56300000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr15:56298800-56300000	Active TSS	Stomach Smooth Muscle	stomach
37	chr15:56298800-56300000	Active TSS	NHDF-Ad	bronchial
38	chr15:56298800-56300000	Active TSS	NHLF	lung
39	chr15:56299000-56299200	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr15:56299000-56299400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr15:56299000-56299400	Active TSS	Esophagus	oesophagus
42	chr15:56299000-56299600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
43	chr15:56299000-56299600	Enhancers	K562	blood
44	chr15:56299000-56299800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr15:56299000-56299800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr15:56299000-56299800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr15:56299000-56299800	Active TSS	Adipose Nuclei	Adipose
48	chr15:56299000-56299800	Active TSS	Brain Anterior Caudate	brain
49	chr15:56299000-56299800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr15:56299000-56299800	Active TSS	Fetal Brain Female	brain

The 2.0 version of rSNPBase

Variant report

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