Variant report

Variant	nsv976915
Chromosome Location	chr15:31898697-31986377
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:494)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:494 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:31931274-31931549	HepG2	liver:	n/a	n/a
2	BATF	chr15:31942586-31942812	GM12878	blood:	n/a	n/a
3	BCL11A	chr15:31942588-31942835	GM12878	blood:	n/a	n/a
4	BRCA1	chr15:31897757-31899408	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr15:31931264-31931579	IMR90	lung:	n/a	chr15:31931452-31931463
6	CEBPB	chr15:31899930-31900147	HepG2	liver:	n/a	n/a
7	CEBPB	chr15:31931325-31931534	K562	blood:	n/a	chr15:31931452-31931463
8	CEBPB	chr15:31931265-31931648	A549	lung:	n/a	chr15:31931452-31931463
9	CEBPB	chr15:31931202-31931649	Hela-S3	cervix:	n/a	chr15:31931452-31931463
10	CEBPB	chr15:31931269-31931505	HepG2	liver:	n/a	chr15:31931452-31931463
11	CEBPB	chr15:31899887-31900221	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr15:31898181-31898720	MCF-7	breast:	n/a	n/a
13	CEBPB	chr15:31931263-31931553	MCF-7	breast:	n/a	chr15:31931452-31931463
14	CEBPB	chr15:31908180-31908480	HepG2	liver:	n/a	chr15:31908327-31908338
15	CEBPB	chr15:31908263-31908457	K562	blood:	n/a	chr15:31908327-31908338
16	CEBPB	chr15:31901506-31901800	IMR90	lung:	n/a	n/a
17	CEBPB	chr15:31931278-31931622	H1-hESC	embryonic stem cell:	n/a	chr15:31931452-31931463
18	CEBPB	chr15:31931263-31931645	HepG2	liver:	n/a	chr15:31931452-31931463
19	CEBPB	chr15:31931268-31931680	A549	lung:	n/a	chr15:31931452-31931463
20	CEBPB	chr15:31897659-31899611	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr15:31972095-31972264	HepG2	liver:	n/a	n/a
22	CEBPB	chr15:31897767-31898924	A549	lung:	n/a	n/a
23	CEBPB	chr15:31931279-31931549	MCF-7	breast:	n/a	chr15:31931452-31931463
24	CEBPB	chr15:31901523-31901788	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr15:31899883-31900229	IMR90	lung:	n/a	n/a
26	CEBPB	chr15:31897770-31899026	IMR90	lung:	n/a	n/a
27	CEBPB	chr15:31931269-31931571	HepG2	liver:	n/a	chr15:31931452-31931463
28	CEBPB	chr15:31897668-31899067	A549	lung:	n/a	n/a
29	CEBPB	chr15:31931258-31931592	HepG2	liver:	n/a	chr15:31931452-31931463
30	CEBPB	chr15:31931277-31931549	A549	lung:	n/a	chr15:31931452-31931463
31	CEBPD	chr15:31931258-31931526	HepG2	liver:	n/a	n/a
32	CHD2	chr15:31901627-31901782	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr15:31945020-31945170	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr15:31942640-31942790	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr15:31942600-31942750	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr15:31942640-31942790	HAc	cerebellar:	n/a	n/a
37	CTCF	chr15:31942558-31942827	HepG2	liver:	n/a	n/a
38	CTCF	chr15:31942630-31942800	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr15:31941920-31942070	AG04449	skin:	n/a	n/a
40	CTCF	chr15:31942582-31942893	A549	lung:	n/a	n/a
41	CTCF	chr15:31941800-31941950	BJ	skin:	n/a	n/a
42	CTCF	chr15:31942627-31942806	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr15:31941970-31941984	GM10248	blood:	n/a	n/a
44	CTCF	chr15:31942600-31942750	Caco-2	colon:	n/a	n/a
45	CTCF	chr15:31942500-31942848	GM10248	blood:	n/a	n/a
46	CTCF	chr15:31942532-31942827	GM10266	blood:	n/a	n/a
47	CTCF	chr15:31940089-31940154	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:31942517-31942856	GM19240	blood:	n/a	n/a
49	CTCF	chr15:31942554-31942850	GM12878	blood:	n/a	n/a
50	CTCF	chr15:31942385-31942448	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31948075-31948125	HCPEpiC	choroid plexus:	n/a
2	chr15:31948632-31948682	MCF-7	breast:	n/a
3	chr15:31948075-31948125	AG04450	lung:	fetal
4	chr15:31948075-31948125	HIPEpiC	eye:	n/a
5	chr15:31948075-31948125	SKMC	muscle:	n/a
6	chr15:31948632-31948682	PrEC	prostate:	n/a
7	chr15:31948075-31948125	AoSMC	blood vessel:	n/a
8	chr15:31948075-31948125	AG09309	skin:	n/a
9	chr15:31948632-31948682	HCF	heart:	n/a
10	chr15:31948075-31948125	HRPEpiC	eye:	n/a
11	chr15:31948632-31948682	HepG2	liver:	n/a
12	chr15:31948632-31948682	HRE	kidney:	n/a
13	chr15:31948075-31948125	U87	brain:	n/a
14	chr15:31948075-31948125	HCM	heart:	n/a
15	chr15:31948632-31948682	AG04449	skin:	fetal
16	chr15:31948632-31948682	AoSMC	blood vessel:	n/a
17	chr15:31948075-31948125	NH-A	brain:	n/a
18	chr15:31948632-31948682	RPTEC	kidney:	n/a
19	chr15:31948632-31948682	AG09319	gingival:	n/a
20	chr15:31948632-31948682	PANC-1	pancreas:	n/a
21	chr15:31948632-31948682	HCPEpiC	choroid plexus:	n/a
22	chr15:31948632-31948682	HL-60	blood:	n/a
23	chr15:31948632-31948682	HUVEC	blood vessel:	n/a
24	chr15:31948075-31948125	Hela-S3	cervix:	n/a
25	chr15:31948075-31948125	SK-N-SH_RA	brain:	n/a
26	chr15:31948075-31948125	AG09319	gingival:	n/a
27	chr15:31948075-31948125	PANC-1	pancreas:	n/a
28	chr15:31948632-31948682	GM12891	blood:	n/a
29	chr15:31948075-31948125	NT2-D1	testis:	n/a
30	chr15:31948632-31948682	HCM	heart:	n/a
31	chr15:31948075-31948125	NHBE	bronchial:	n/a
32	chr15:31948632-31948682	SK-N-SH_RA	brain:	n/a
33	chr15:31948075-31948125	PFSK-1	brain:	n/a
34	chr15:31948075-31948125	HCF	heart:	n/a
35	chr15:31948075-31948125	CMK	blood:	n/a
36	chr15:31948632-31948682	NHBE	bronchial:	n/a
37	chr15:31948632-31948682	ECC-1	luminal epithelium:	n/a
38	chr15:31948075-31948125	GM19239	blood:	n/a
39	chr15:31948632-31948682	PFSK-1	brain:	n/a
40	chr15:31948632-31948682	SK-N-MC	brain:	n/a
41	chr15:31948075-31948125	MCF-7	breast:	n/a
42	chr15:31948632-31948682	HCT-116	colon:	n/a
43	chr15:31948632-31948682	SAEC	small airway:	n/a
44	chr15:31948632-31948682	BE2_C	brain:	n/a
45	chr15:31948075-31948125	HCT-116	colon:	n/a
46	chr15:31948075-31948125	SK-N-SH	brain:	n/a
47	chr15:31948075-31948125	SAEC	small airway:	n/a
48	chr15:31948075-31948125	NB4	blood:	n/a
49	chr15:31948632-31948682	U87	brain:	n/a
50	chr15:31948075-31948125	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:31860388..31862871-chr15:31898549..31900652,2	MCF-7	breast:
2	chr1:149222127..149223797-chr15:31897038..31899511,2	MCF-7	breast:

No data

Variant related genes	Relation type
OTUD7A	TF binding region
OTUD7A	CpG island

Extended variants
information (count: 3276 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:3276 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373087602	chr15:31898700-31898701	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs574449932	chr15:31898744-31898745	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs112200927	chr15:31898800-31898801	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs1459199	chr15:31898809-31898810	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs563407613	chr15:31898830-31898831	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs578184797	chr15:31898840-31898841	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs532414306	chr15:31898884-31898885	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs545810742	chr15:31898913-31898914	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs189392474	chr15:31898955-31898956	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs528339670	chr15:31899102-31899103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148172590	chr15:31899103-31899104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141112096	chr15:31899117-31899118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181435780	chr15:31899169-31899170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185870681	chr15:31899178-31899179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369501549	chr15:31899189-31899190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574651774	chr15:31899244-31899245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188377264	chr15:31899245-31899246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559034780	chr15:31899296-31899297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566219428	chr15:31899325-31899326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146732127	chr15:31899338-31899339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79184559	chr15:31899375-31899376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574613428	chr15:31899388-31899389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201195730	chr15:31899442-31899443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372964150	chr15:31899454-31899455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543537749	chr15:31899469-31899470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557307029	chr15:31899470-31899471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375910115	chr15:31899499-31899500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577205978	chr15:31899516-31899517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139284213	chr15:31899557-31899558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528830846	chr15:31899598-31899599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551080876	chr15:31899699-31899700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541791184	chr15:31899718-31899719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369680844	chr15:31899728-31899729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537643604	chr15:31899759-31899760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368245968	chr15:31899832-31899833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542068935	chr15:31899840-31899841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1542453	chr15:31899862-31899863	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs34026459	chr15:31899901-31899902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143105010	chr15:31899912-31899913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7177470	chr15:31899930-31899931	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs564105886	chr15:31899957-31899958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181259215	chr15:31899984-31899985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532793688	chr15:31900113-31900114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs376451235	chr15:31900161-31900162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200060589	chr15:31900217-31900218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7176725	chr15:31900227-31900228	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs370961594	chr15:31900228-31900229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186526877	chr15:31900245-31900246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200858028	chr15:31900247-31900248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1813397	chr15:31900308-31900309	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pancreatic cancer	17952125	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Renal cell carcinoma	21215367	CNVD
Schizophrenia	23813976	CNVD
Autism	21865298	CNVD
Cancer	21215367	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31877800-31900800	Weak transcription	Pancreas	Pancrea
2	chr15:31896800-31898800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr15:31897000-31899400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr15:31897000-31899600	Enhancers	Ovary	ovary
5	chr15:31897000-31899600	Enhancers	Placenta Amnion	Placenta Amnion
6	chr15:31897200-31901400	Weak transcription	Right Atrium	heart
7	chr15:31897400-31898800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr15:31897400-31899400	Enhancers	Brain Anterior Caudate	brain
9	chr15:31897400-31899600	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr15:31897400-31899600	Enhancers	NHLF	lung
11	chr15:31897400-31899600	Enhancers	Osteobl	bone
12	chr15:31897400-31902000	Enhancers	Brain Substantia Nigra	brain
13	chr15:31897400-31902400	Enhancers	Brain Hippocampus Middle	brain
14	chr15:31897600-31899000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr15:31897600-31899600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr15:31897600-31899600	Enhancers	NHDF-Ad	bronchial
17	chr15:31897600-31900000	Enhancers	Brain Cingulate Gyrus	brain
18	chr15:31897600-31901400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr15:31897600-31901800	Weak transcription	Gastric	stomach
20	chr15:31897800-31898800	Enhancers	Fetal Stomach	stomach
21	chr15:31897800-31899000	Enhancers	Muscle Satellite Cultured Cells	--
22	chr15:31897800-31899600	Enhancers	NHEK	skin
23	chr15:31897800-31901400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr15:31897800-31901600	Weak transcription	Spleen	Spleen
25	chr15:31898000-31898800	Flanking Active TSS	A549	lung
26	chr15:31898000-31899000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr15:31898000-31899000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr15:31898000-31899400	Enhancers	NH-A	brain
29	chr15:31898000-31900200	Enhancers	Stomach Smooth Muscle	stomach
30	chr15:31898000-31900800	Enhancers	Brain Angular Gyrus	brain
31	chr15:31898000-31901200	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr15:31898200-31899400	Weak transcription	Placenta	Placenta
33	chr15:31898200-31900600	Weak transcription	Esophagus	oesophagus
34	chr15:31898200-31901200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr15:31898200-31901400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr15:31898400-31900000	Enhancers	Hela-S3	cervix
37	chr15:31898400-31902000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr15:31898600-31900600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr15:31898600-31901000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr15:31898600-31901600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr15:31898800-31899200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr15:31898800-31899200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr15:31898800-31899400	Weak transcription	Fetal Stomach	stomach
44	chr15:31898800-31900200	Enhancers	A549	lung
45	chr15:31899000-31899800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr15:31899200-31899400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr15:31899200-31899600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr15:31899400-31899600	Enhancers	Placenta	Placenta
49	chr15:31899400-31899600	Enhancers	Fetal Stomach	stomach
50	chr15:31899400-31901200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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