Variant report

Variant	nsv881445
Chromosome Location	chr5:14917813-14960920
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:689)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:14926035-14926446	GM12878	blood:	n/a	n/a
2	ATF2	chr5:14925974-14926493	GM12878	blood:	n/a	n/a
3	BATF	chr5:14926045-14926372	GM12878	blood:	n/a	n/a
4	BATF	chr5:14925992-14926450	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:14926067-14926394	GM12878	blood:	n/a	n/a
6	BDP1	chr5:14946657-14947074	Hela-S3	cervix:	n/a	n/a
7	BHLHE40	chr5:14959568-14959781	HepG2	liver:	n/a	n/a
8	BRCA1	chr5:14944555-14945635	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr5:14959305-14960017	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr5:14946828-14947318	HCT-116	colon:	n/a	n/a
11	CCNT2	chr5:14922574-14922771	K562	blood:	n/a	n/a
12	CEBPB	chr5:14924545-14924796	IMR90	lung:	n/a	chr5:14924661-14924672
13	CEBPB	chr5:14960467-14960708	HepG2	liver:	n/a	chr5:14960573-14960584
14	CEBPB	chr5:14947469-14947671	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:14960543-14960606	IMR90	lung:	n/a	chr5:14960573-14960584
16	CEBPB	chr5:14929978-14930220	IMR90	lung:	n/a	n/a
17	CEBPB	chr5:14960420-14960769	Hela-S3	cervix:	n/a	chr5:14960573-14960584
18	CEBPB	chr5:14958327-14958719	A549	lung:	n/a	n/a
19	CEBPB	chr5:14945202-14945295	A549	lung:	n/a	n/a
20	CEBPB	chr5:14923180-14923357	HepG2	liver:	n/a	chr5:14923237-14923248
21	CEBPB	chr5:14958341-14958569	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:14958217-14960214	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr5:14958329-14958645	A549	lung:	n/a	n/a
24	CEBPB	chr5:14924624-14924847	Hela-S3	cervix:	n/a	chr5:14924661-14924672
25	CEBPB	chr5:14923169-14923369	IMR90	lung:	n/a	chr5:14923237-14923248
26	CEBPB	chr5:14925980-14926410	IMR90	lung:	n/a	n/a
27	CEBPB	chr5:14958360-14958629	IMR90	lung:	n/a	n/a
28	CEBPB	chr5:14923206-14923348	K562	blood:	n/a	chr5:14923237-14923248
29	CEBPB	chr5:14924615-14924815	HepG2	liver:	n/a	chr5:14924661-14924672
30	CEBPB	chr5:14946918-14947641	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:14958279-14958702	MCF-7	breast:	n/a	n/a
32	CEBPB	chr5:14923152-14923388	Hela-S3	cervix:	n/a	chr5:14923237-14923248
33	CEBPB	chr5:14930125-14930203	HepG2	liver:	n/a	n/a
34	CEBPB	chr5:14944975-14945941	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:14924580-14924767	H1-hESC	embryonic stem cell:	n/a	chr5:14924661-14924672
36	CEBPD	chr5:14919123-14919790	K562	blood:	n/a	n/a
37	CHD2	chr5:14959220-14960136	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr5:14947118-14947121	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr5:14958389-14958664	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr5:14926263-14926326	GM12878	blood:	n/a	n/a
41	CHD2	chr5:14945132-14945553	Hela-S3	cervix:	n/a	n/a
42	CREB1	chr5:14925955-14926566	GM12878	blood:	n/a	n/a
43	CTCF	chr5:14957660-14957810	GM12865	blood:	n/a	chr5:14957730-14957746 chr5:14957731-14957752 chr5:14957733-14957740 chr5:14957729-14957747
44	CTCF	chr5:14947360-14947510	GM12872	blood:	n/a	n/a
45	CTCF	chr5:14947120-14947270	WI-38	lung:	n/a	chr5:14947122-14947140 chr5:14947124-14947145
46	CTCF	chr5:14947040-14947190	GM12878	blood:	n/a	chr5:14947122-14947140 chr5:14947124-14947145
47	CTCF	chr5:14926300-14926450	HMF	breast:	n/a	n/a
48	CTCF	chr5:14957620-14957770	GM12875	blood:	n/a	chr5:14957730-14957746 chr5:14957731-14957752 chr5:14957733-14957740 chr5:14957729-14957747
49	CTCF	chr5:14957640-14957790	HCT-116	colon:	n/a	chr5:14957730-14957746 chr5:14957731-14957752 chr5:14957733-14957740 chr5:14957729-14957747
50	CTCF	chr5:14947060-14947210	HCT-116	colon:	n/a	chr5:14947122-14947140 chr5:14947124-14947145

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:14926200-14926250	NT2-D1	testis:	n/a
2	chr5:14957124-14957174	LNCaP	prostate:	n/a
3	chr5:14957124-14957174	ECC-1	luminal epithelium:	n/a
4	chr5:14957124-14957174	HAEpiC	amniotic membrane:	n/a
5	chr5:14957124-14957174	HRCEpiC	kidney:	n/a
6	chr5:14926200-14926250	HIPEpiC	eye:	n/a
7	chr5:14957124-14957174	HPAEpiC	pulmonary alveolar:	n/a
8	chr5:14926200-14926250	NHBE	bronchial:	n/a
9	chr5:14926200-14926250	MCF-7	breast:	n/a
10	chr5:14957124-14957174	HNPCEpiC	eye:	n/a
11	chr5:14926200-14926250	HCF	heart:	n/a
12	chr5:14957124-14957174	HRPEpiC	eye:	n/a
13	chr5:14926200-14926250	NB4	blood:	n/a
14	chr5:14957124-14957174	Hepatocyte	liver:	n/a
15	chr5:14957124-14957174	HMEC	breast:	n/a
16	chr5:14926200-14926250	AG09319	gingival:	n/a
17	chr5:14957124-14957174	GM12891	blood:	n/a
18	chr5:14926200-14926250	GM06990	blood:	n/a
19	chr5:14926200-14926250	LNCaP	prostate:	n/a
20	chr5:14957124-14957174	NT2-D1	testis:	n/a
21	chr5:14926200-14926250	GM12892	blood:	n/a
22	chr5:14926200-14926250	K562	blood:	n/a
23	chr5:14926200-14926250	SK-N-MC	brain:	n/a
24	chr5:14926200-14926250	SKMC	muscle:	n/a
25	chr5:14926200-14926250	HRE	kidney:	n/a
26	chr5:14957124-14957174	NHBE	bronchial:	n/a
27	chr5:14926200-14926250	SK-N-SH_RA	brain:	n/a
28	chr5:14926200-14926250	Hepatocyte	liver:	n/a
29	chr5:14926200-14926250	AG04450	lung:	fetal
30	chr5:14957124-14957174	NHDF-neo	bronchial:	n/a
31	chr5:14926200-14926250	Caco-2	colon:	n/a
32	chr5:14957124-14957174	T-47D	breast:	n/a
33	chr5:14926200-14926250	HEK293	kidney:	embryo
34	chr5:14926200-14926250	HCPEpiC	choroid plexus:	n/a
35	chr5:14926200-14926250	PANC-1	pancreas:	n/a
36	chr5:14957124-14957174	HUVEC	blood vessel:	n/a
37	chr5:14926200-14926250	HCM	heart:	n/a
38	chr5:14926200-14926250	AG10803	skin:	n/a
39	chr5:14926200-14926250	PFSK-1	brain:	n/a
40	chr5:14926200-14926250	ECC-1	luminal epithelium:	n/a
41	chr5:14926200-14926250	Jurkat	blood:	n/a
42	chr5:14926200-14926250	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:14926200-14926250	SAEC	small airway:	n/a
44	chr5:14957124-14957174	SK-N-SH_RA	brain:	n/a
45	chr5:14926200-14926250	MCF10A-Er-Src	breast:	n/a
46	chr5:14926200-14926250	HepG2	liver:	n/a
47	chr5:14926200-14926250	HRCEpiC	kidney:	n/a
48	chr5:14926200-14926250	U87	brain:	n/a
49	chr5:14926200-14926250	HNPCEpiC	eye:	n/a
50	chr5:14926200-14926250	GM12891	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:14869954..14872343-chr5:14960382..14962303,2	MCF-7	breast:
2	chr5:14664017..14666090-chr5:14925708..14927348,2	MCF-7	breast:
3	chr5:14871785..14872721-chr5:14946511..14947536,3	MCF-7	breast:
4	chr5:14937263..14940130-chr5:14945612..14948261,3	K562	blood:
5	chr5:14946624..14947805-chr5:15003290..15004336,15	MCF-7	breast:
6	chr5:14938562..14940130-chr5:14945918..14948261,2	K562	blood:
7	chr5:14686822..14687524-chr5:14944560..14945527,2	MCF-7	breast:
8	chr5:14947263..14949591-chr5:14957146..14961444,5	MCF-7	breast:
9	chr5:14946879..14947508-chr5:15013777..15014301,2	MCF-7	breast:
10	chr5:14727240..14728065-chr5:14946815..14947417,2	MCF-7	breast:
11	chr5:14727214..14727733-chr5:14946754..14947623,2	MCF-7	breast:
12	chr5:14663571..14666270-chr5:14954053..14956449,2	MCF-7	breast:
13	chr5:14946629..14947384-chr5:15003311..15004216,3	K562	blood:
14	chr5:14946729..14947608-chr5:15003318..15004150,4	MCF-7	breast:
15	chr5:14853860..14855427-chr5:14933232..14934776,2	MCF-7	breast:
16	chr5:14937263..14940130-chr5:14945612..14948261,3	K562	blood:
17	chr5:14938562..14940130-chr5:14945918..14948261,2	K562	blood:

No data

Variant related genes	Relation type
SEPHS2P1	TF binding region
SEPHS2P1	CpG island
ENSG00000154124	chromatin interactions
ENSG00000154122	chromatin interactions
ENSG00000261360	chromatin interactions
ENSG00000272057	chromatin interactions
ENSG00000250247	chromatin interactions

Extended variants
information (count: 1683 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1683 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs966987	chr5:14917813-14917814	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147367665	chr5:14917820-14917821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373462230	chr5:14917821-14917822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559698105	chr5:14917824-14917825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533128729	chr5:14917830-14917831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545247301	chr5:14917869-14917870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192792754	chr5:14917875-14917876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79316741	chr5:14917878-14917879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550290466	chr5:14917879-14917880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568360192	chr5:14917955-14917956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149916702	chr5:14917994-14917995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184743383	chr5:14918002-14918003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs16903737	chr5:14918024-14918025	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs566047474	chr5:14918027-14918028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552439298	chr5:14918042-14918043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs16903738	chr5:14918047-14918048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs78935123	chr5:14918053-14918054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7729085	chr5:14918158-14918159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77494352	chr5:14918166-14918167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536736436	chr5:14918204-14918205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192024397	chr5:14918218-14918219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570825849	chr5:14918226-14918227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184200346	chr5:14918242-14918243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs16903739	chr5:14918264-14918265	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs553279366	chr5:14918273-14918274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73066932	chr5:14918294-14918295	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs74514367	chr5:14918359-14918360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113786872	chr5:14918408-14918409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs377226423	chr5:14918409-14918410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543506537	chr5:14918478-14918479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562221115	chr5:14918509-14918510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529215587	chr5:14918515-14918516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547407815	chr5:14918527-14918528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188949603	chr5:14918540-14918541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370576629	chr5:14918543-14918544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568420546	chr5:14918559-14918560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533428764	chr5:14918560-14918561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551695950	chr5:14918614-14918615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs193044670	chr5:14918631-14918632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537651319	chr5:14918636-14918637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555137706	chr5:14918656-14918657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567379120	chr5:14918662-14918663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534738664	chr5:14918684-14918685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535933739	chr5:14918707-14918708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577754803	chr5:14918750-14918751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs80006022	chr5:14918751-14918752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78720410	chr5:14918764-14918765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557219066	chr5:14918852-14918853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575306187	chr5:14918865-14918866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542822162	chr5:14918951-14918952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
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
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
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Gastric cancer	17229543	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14912000-14919200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr5:14914400-14919000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:14914400-14919000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr5:14914800-14918800	Enhancers	HMEC	breast
5	chr5:14914800-14922600	Weak transcription	Spleen	Spleen
6	chr5:14915800-14918000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr5:14915800-14920000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr5:14916000-14925400	Weak transcription	HSMM	muscle
9	chr5:14916200-14918600	Enhancers	Osteobl	bone
10	chr5:14916400-14922600	Weak transcription	Left Ventricle	heart
11	chr5:14916600-14929200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr5:14917200-14918400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr5:14917200-14918800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr5:14917400-14918200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr5:14917400-14918200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr5:14917400-14918400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr5:14917400-14918600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr5:14917400-14918800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr5:14917400-14919000	Enhancers	NHDF-Ad	bronchial
20	chr5:14917600-14918000	Enhancers	Fetal Muscle Leg	muscle
21	chr5:14917600-14918400	Enhancers	Muscle Satellite Cultured Cells	--
22	chr5:14917600-14918800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr5:14917800-14918200	Enhancers	Fetal Stomach	stomach
24	chr5:14918000-14918200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:14918400-14919800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr5:14918400-14920000	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr5:14918600-14919800	Weak transcription	Osteobl	bone
28	chr5:14918600-14924800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr5:14918800-14920000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr5:14918800-14920200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:14918800-14925200	Weak transcription	HMEC	breast
32	chr5:14919000-14925200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:14919000-14926000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr5:14919200-14925400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr5:14919800-14920000	Enhancers	Placenta	Placenta
36	chr5:14919800-14920800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr5:14919800-14921000	Enhancers	Osteobl	bone
38	chr5:14920000-14920600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr5:14920000-14921000	Enhancers	Muscle Satellite Cultured Cells	--
40	chr5:14920000-14921600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr5:14920000-14926200	Weak transcription	Placenta	Placenta
42	chr5:14920200-14921200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr5:14920400-14920600	Enhancers	NHLF	lung
44	chr5:14920400-14920800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr5:14920600-14925400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr5:14920800-14921600	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr5:14920800-14922600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr5:14920800-14925400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr5:14921000-14924800	Weak transcription	Osteobl	bone
50	chr5:14921000-14925000	Weak transcription	Muscle Satellite Cultured Cells	--

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