Variant report

Variant	nsv4735
Chromosome Location	chr5:15916346-15961432
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:170)
CpG islands
(count:1159)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:170 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr5:15937148-15937153	HepG2	liver:	n/a	n/a
2	CEBPB	chr5:15946134-15946447	IMR90	lung:	n/a	chr5:15946279-15946292 chr5:15946279-15946292
3	CEBPB	chr5:15926707-15927038	IMR90	lung:	n/a	chr5:15926917-15926925
4	CHD2	chr5:15937005-15937074	K562	blood:	n/a	n/a
5	CTCF	chr5:15941340-15941490	HCFaa	heart:	n/a	n/a
6	CTCF	chr5:15948560-15948710	AoAF	blood vessel:	n/a	n/a
7	CTCF	chr5:15948440-15948590	HCM	heart:	n/a	n/a
8	CTCF	chr5:15948540-15948690	NHDF-neo	bronchial:	n/a	n/a
9	CTCF	chr5:15941362-15941604	MCF-7	breast:	n/a	chr5:15941494-15941503
10	CTCF	chr5:15927340-15927490	NHLF	lung:	n/a	n/a
11	CTCF	chr5:15948540-15948690	HUVEC	blood vessel:	n/a	n/a
12	CTCF	chr5:15941406-15941508	MCF-7	breast:	n/a	chr5:15941494-15941503
13	CTCF	chr5:15945054-15945108	GM10248	blood:	n/a	n/a
14	CTCF	chr5:15935312-15935409	MCF-7	breast:	n/a	n/a
15	CTCF	chr5:15920110-15920123	GM20000	blood:	n/a	n/a
16	CTCF	chr5:15948480-15948630	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr5:15941375-15941582	MCF-7	breast:	n/a	chr5:15941494-15941503
18	CTCF	chr5:15948540-15948664	LNCaP	prostate:	n/a	n/a
19	CTCF	chr5:15948580-15948730	HA-sp	spinal cord:	n/a	n/a
20	CTCF	chr5:15948500-15948650	AG10803	skin:	n/a	n/a
21	CTCF	chr5:15948400-15948550	NHDF-neo	bronchial:	n/a	n/a
22	CTCF	chr5:15948460-15948610	HMF	breast:	n/a	n/a
23	CTCF	chr5:15948586-15948619	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr5:15941460-15941610	HRPEpiC	eye:	n/a	chr5:15941494-15941503
25	CTCF	chr5:15948480-15948630	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr5:15948500-15948650	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr5:15941440-15941590	BE2_C	brain:	n/a	chr5:15941494-15941503
28	CTCF	chr5:15952120-15952270	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:15948440-15948590	AG04450	lung:	n/a	n/a
30	CTCF	chr5:15936840-15936990	GM12867	blood:	n/a	n/a
31	CTCF	chr5:15948540-15948690	AG09319	gingival:	n/a	n/a
32	CTCF	chr5:15948572-15948611	LNCaP	prostate:	n/a	n/a
33	CTCF	chr5:15948421-15948747	IMR90	lung:	n/a	n/a
34	CTCF	chr5:15948540-15948690	HVMF	connective:	n/a	n/a
35	CTCF	chr5:15941480-15941630	HEK293	kidney:	n/a	chr5:15941494-15941503
36	CTCF	chr5:15921400-15921461	GM20000	blood:	n/a	n/a
37	CTCF	chr5:15941295-15941752	MCF-7	breast:	n/a	chr5:15941494-15941503
38	CTCF	chr5:15948460-15948610	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr5:15955480-15955630	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr5:15941420-15941570	HBMEC	blood vessel:	n/a	chr5:15941494-15941503
41	CTCF	chr5:15941420-15941570	MCF-7	breast:	n/a	chr5:15941494-15941503
42	CTCF	chr5:15948500-15948650	AG04449	skin:	n/a	n/a
43	CTCF	chr5:15941389-15941549	MCF-7	breast:	n/a	chr5:15941494-15941503
44	CTCF	chr5:15941400-15941550	BE2_C	brain:	n/a	chr5:15941494-15941503
45	CTCF	chr5:15948618-15948636	Lung_OC	lung:	n/a	n/a
46	CTCF	chr5:15941320-15941470	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:15928920-15929070	Caco-2	colon:	n/a	n/a
48	CTCF	chr5:15941400-15941550	HepG2	liver:	n/a	chr5:15941494-15941503
49	CTCF	chr5:15948480-15948630	AG04450	lung:	n/a	n/a
50	CTCF	chr5:15948460-15948610	HPF	lung:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:15928366-15928416	IMR90	lung:	fetal
2	chr5:15925265-15925315	NHDF-neo	bronchial:	n/a
3	chr5:15936768-15936818	HCM	heart:	n/a
4	chr5:15935380-15935430	NH-A	brain:	n/a
5	chr5:15936768-15936818	AG09319	gingival:	n/a
6	chr5:15927655-15927705	SK-N-SH_RA	brain:	n/a
7	chr5:15937169-15937219	HEEpiC	esophagus:	n/a
8	chr5:15936768-15936818	H1-hESC	embryonic stem cell:	embryo
9	chr5:15932416-15932466	SKMC	muscle:	n/a
10	chr5:15935879-15935929	NT2-D1	testis:	n/a
11	chr5:15928366-15928416	AG10803	skin:	n/a
12	chr5:15930438-15930488	HRE	kidney:	n/a
13	chr5:15935380-15935430	NHBE	bronchial:	n/a
14	chr5:15935380-15935430	PFSK-1	brain:	n/a
15	chr5:15935879-15935929	HUVEC	blood vessel:	n/a
16	chr5:15935380-15935430	Hela-S3	cervix:	n/a
17	chr5:15927655-15927705	RPTEC	kidney:	n/a
18	chr5:15932416-15932466	NHBE	bronchial:	n/a
19	chr5:15927655-15927705	SK-N-SH	brain:	n/a
20	chr5:15930438-15930488	NT2-D1	testis:	n/a
21	chr5:15936642-15936692	BE2_C	brain:	n/a
22	chr5:15925265-15925315	HCT-116	colon:	n/a
23	chr5:15935380-15935430	U87	brain:	n/a
24	chr5:15935380-15935430	HRCEpiC	kidney:	n/a
25	chr5:15928114-15928164	A549	lung:	n/a
26	chr5:15928366-15928416	Caco-2	colon:	n/a
27	chr5:15939534-15939584	SK-N-SH	brain:	n/a
28	chr5:15935380-15935430	HepG2	liver:	n/a
29	chr5:15918940-15918990	GM19239	blood:	n/a
30	chr5:15928114-15928164	GM06990	blood:	n/a
31	chr5:15928114-15928164	PANC-1	pancreas:	n/a
32	chr5:15925265-15925315	ovcar-3	ovarian:	n/a
33	chr5:15928114-15928164	HUVEC	blood vessel:	n/a
34	chr5:15932416-15932466	HL-60	blood:	n/a
35	chr5:15928366-15928416	Hela-S3	cervix:	n/a
36	chr5:15939534-15939584	Hepatocyte	liver:	n/a
37	chr5:15930438-15930488	ovcar-3	ovarian:	n/a
38	chr5:15936768-15936818	HEEpiC	esophagus:	n/a
39	chr5:15918940-15918990	CMK	blood:	n/a
40	chr5:15928114-15928164	GM19239	blood:	n/a
41	chr5:15927184-15927234	SKMC	muscle:	n/a
42	chr5:15939534-15939584	HepG2	liver:	n/a
43	chr5:15939534-15939584	MCF10A-Er-Src	breast:	n/a
44	chr5:15928366-15928416	NB4	blood:	n/a
45	chr5:15927184-15927234	HCPEpiC	choroid plexus:	n/a
46	chr5:15928089-15928139	T-47D	breast:	n/a
47	chr5:15936768-15936818	MCF-7	breast:	n/a
48	chr5:15936768-15936818	GM12878	blood:	n/a
49	chr5:15935879-15935929	RPTEC	kidney:	n/a
50	chr5:15937169-15937219	Jurkat	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:15941095..15942002-chr5:15995664..15996228,2	MCF-7	breast:
2	chr5:15940925..15941957-chr5:15995066..15996242,6	MCF-7	breast:
3	chr5:15926786..15928687-chr5:15937563..15939757,2	K562	blood:
4	chr5:15926786..15928687-chr5:15937563..15939757,2	K562	blood:
5	chr5:15946299..15948949-chr5:15949742..15951432,2	MCF-7	breast:
6	chr5:15946299..15948949-chr5:15949742..15951432,2	MCF-7	breast:
7	chr5:15933771..15936627-chr5:15939185..15940965,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-887-5p	chr5:15935300-15935320	MIMAT0026720
hsa-miR-887-3p	chr5:15935338-15935359	MIMAT0004951

No data

Variant related genes	Relation type
MIR887	TF binding region
MIR887	CpG island
ENSG00000216077	chromatin interactions
MTHFD1L	Mature miRNA region

Extended variants
information (count: 1724 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1724 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567758526	chr5:15916355-15916356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs528521288	chr5:15916363-15916364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs70938034	chr5:15916479-15916480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72354935	chr5:15916480-15916481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557546090	chr5:15916488-15916489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576249377	chr5:15916492-15916493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140557158	chr5:15916499-15916500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150163604	chr5:15916506-15916507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187061807	chr5:15916511-15916512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575087257	chr5:15916536-15916537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542126284	chr5:15916554-15916555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs532777165	chr5:15916556-15916557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138664891	chr5:15916568-15916569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547034601	chr5:15916570-15916571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs13154254	chr5:15916577-15916578	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs564231797	chr5:15916609-15916610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148909301	chr5:15916640-15916641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs76274652	chr5:15916700-15916701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143528181	chr5:15916745-15916746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539346666	chr5:15916783-15916784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189457574	chr5:15916807-15916808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554980474	chr5:15916821-15916822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371937471	chr5:15916822-15916823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569963728	chr5:15916830-15916831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565992778	chr5:15916834-15916835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539057286	chr5:15916847-15916848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76132332	chr5:15916958-15916959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs569676467	chr5:15917049-15917050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537093865	chr5:15917065-15917066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555518813	chr5:15917122-15917123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138115699	chr5:15917146-15917147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs180715498	chr5:15917221-15917222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143517809	chr5:15917224-15917225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558580186	chr5:15917256-15917257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185042931	chr5:15917330-15917331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572739523	chr5:15917355-15917356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190285792	chr5:15917381-15917382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs116367971	chr5:15917384-15917385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147176487	chr5:15917399-15917400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs73062501	chr5:15917409-15917410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561879451	chr5:15917410-15917411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6869037	chr5:15917429-15917430	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs182451966	chr5:15917470-15917471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4410637	chr5:15917483-15917484	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs376295089	chr5:15917510-15917511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79378543	chr5:15917525-15917526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368547448	chr5:15917609-15917610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569640652	chr5:15917612-15917613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373317187	chr5:15917696-15917697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541446212	chr5:15917712-15917713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:627 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:15913200-15918400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:15913200-15918600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr5:15913800-15936000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr5:15914000-15918400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr5:15914000-15918600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr5:15914000-15918600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr5:15914000-15926800	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr5:15914000-15940000	Weak transcription	Colon Smooth Muscle	Colon
9	chr5:15914600-15928200	Weak transcription	Fetal Brain Male	brain
10	chr5:15915000-15919200	Enhancers	Fetal Heart	heart
11	chr5:15915000-15928000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr5:15915200-15916600	Enhancers	Ovary	ovary
13	chr5:15915600-15917600	Weak transcription	Left Ventricle	heart
14	chr5:15915600-15918600	Weak transcription	Fetal Lung	lung
15	chr5:15915600-15918600	Weak transcription	Fetal Stomach	stomach
16	chr5:15915600-15918600	Weak transcription	Small Intestine	intestine
17	chr5:15915800-15916400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr5:15915800-15916600	Enhancers	Right Ventricle	heart
19	chr5:15916400-15918400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr5:15916600-15918600	Weak transcription	Ovary	ovary
21	chr5:15916600-15924800	Weak transcription	Right Ventricle	heart
22	chr5:15917600-15917800	Enhancers	Left Ventricle	heart
23	chr5:15917800-15918600	Weak transcription	Left Ventricle	heart
24	chr5:15918400-15919200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr5:15918400-15920000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr5:15918400-15920000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr5:15918600-15918800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr5:15918600-15919000	Enhancers	H9 Cell Line	embryonic stem cell
29	chr5:15918600-15919000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr5:15918600-15919000	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr5:15918600-15919000	Enhancers	Brain Angular Gyrus	brain
32	chr5:15918600-15919000	Enhancers	Brain Anterior Caudate	brain
33	chr5:15918600-15919000	Enhancers	Brain Cingulate Gyrus	brain
34	chr5:15918600-15919000	Enhancers	Brain Hippocampus Middle	brain
35	chr5:15918600-15919000	Enhancers	Brain Substantia Nigra	brain
36	chr5:15918600-15919000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr5:15918600-15919000	Enhancers	Left Ventricle	heart
38	chr5:15918600-15919000	Enhancers	Ovary	ovary
39	chr5:15918600-15919400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr5:15918600-15919600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr5:15918600-15920000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr5:15918600-15920200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr5:15918600-15920200	Enhancers	Fetal Lung	lung
44	chr5:15918600-15920400	Enhancers	Fetal Stomach	stomach
45	chr5:15918800-15919000	Enhancers	Small Intestine	intestine
46	chr5:15918800-15919200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr5:15918800-15919400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr5:15918800-15919400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:15918800-15919600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr5:15918800-15919600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links