Variant report

Variant	esv19164
Chromosome Location	chr5:17342748-17357008
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:17343703-17344196	GM12878	blood:	n/a	n/a
2	BATF	chr5:17354193-17354509	GM12878	blood:	n/a	n/a
3	BATF	chr5:17343760-17344168	GM12878	blood:	n/a	chr5:17343996-17344007
4	BATF	chr5:17343783-17344161	GM12878	blood:	n/a	chr5:17343996-17344007
5	BATF	chr5:17353871-17354044	GM12878	blood:	n/a	n/a
6	BATF	chr5:17354195-17354502	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:17352535-17352691	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr5:17346827-17346867	GM12878	blood:	n/a	n/a
9	BHLHE40	chr5:17343829-17344187	GM12878	blood:	n/a	n/a
10	BRCA1	chr5:17343823-17344125	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr5:17346874-17347274	Hela-S3	cervix:	n/a	chr5:17346935-17346946
12	CEBPB	chr5:17349354-17349424	A549	lung:	n/a	n/a
13	CEBPB	chr5:17356262-17356263	A549	lung:	n/a	n/a
14	CEBPB	chr5:17353388-17353588	A549	lung:	n/a	n/a
15	CEBPB	chr5:17343818-17344196	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:17346866-17347310	IMR90	lung:	n/a	chr5:17346935-17346946
17	CEBPB	chr5:17356136-17356434	IMR90	lung:	n/a	n/a
18	CHD2	chr5:17356242-17356330	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr5:17343791-17344150	GM12878	blood:	n/a	n/a
20	CHD2	chr5:17343847-17344213	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr5:17347620-17347770	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr5:17343840-17343990	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr5:17347480-17347630	MCF-7	breast:	n/a	n/a
24	CTCF	chr5:17347280-17347430	AG09309	skin:	n/a	n/a
25	CTCF	chr5:17347620-17347770	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr5:17347717-17347771	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr5:17345198-17345240	LNCaP	prostate:	n/a	n/a
28	CTCF	chr5:17347560-17347710	GM12873	blood:	n/a	n/a
29	CTCF	chr5:17347582-17347773	K562	blood:	n/a	n/a
30	CTCF	chr5:17347460-17347610	NB4	blood:	n/a	n/a
31	CTCF	chr5:17347620-17347770	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr5:17347600-17347750	GM12874	blood:	n/a	n/a
33	CTCF	chr5:17347580-17347730	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr5:17347460-17347610	A549	lung:	n/a	n/a
35	CTCF	chr5:17347580-17347730	A549	lung:	n/a	n/a
36	EBF1	chr5:17354246-17354448	GM12878	blood:	n/a	n/a
37	EBF1	chr5:17343794-17344241	GM12878	blood:	n/a	chr5:17344013-17344022 chr5:17344011-17344024 chr5:17344013-17344022 chr5:17344012-17344022 chr5:17344011-17344022
38	EBF1	chr5:17355821-17355957	GM12878	blood:	n/a	chr5:17355858-17355869
39	EBF1	chr5:17354257-17354470	GM12878	blood:	n/a	n/a
40	EBF1	chr5:17343762-17344231	GM12878	blood:	n/a	chr5:17344013-17344022 chr5:17344011-17344024 chr5:17344013-17344022 chr5:17344012-17344022 chr5:17344011-17344022
41	EBF1	chr5:17343722-17344231	GM12878	blood:	n/a	chr5:17344013-17344022 chr5:17344011-17344024 chr5:17344013-17344022 chr5:17344012-17344022 chr5:17344011-17344022
42	EP300	chr5:17352504-17352852	H1-hESC	embryonic stem cell:	n/a	n/a
43	EP300	chr5:17343844-17344165	GM12878	blood:	n/a	chr5:17344000-17344009 chr5:17343980-17343990
44	EP300	chr5:17343630-17344521	A549	lung:	n/a	chr5:17344000-17344009 chr5:17343980-17343990
45	EP300	chr5:17343817-17344155	GM12878	blood:	n/a	chr5:17344000-17344009 chr5:17343980-17343990
46	EP300	chr5:17343850-17344128	GM12878	blood:	n/a	chr5:17344000-17344009 chr5:17343980-17343990
47	EP300	chr5:17343602-17344519	A549	lung:	n/a	chr5:17344000-17344009 chr5:17343980-17343990
48	EP300	chr5:17343783-17344175	Hela-S3	cervix:	n/a	chr5:17344000-17344009 chr5:17343980-17343990
49	FOS	chr5:17356035-17356437	MCF10A-Er-Src	breast:	n/a	chr5:17356250-17356261 chr5:17356172-17356183
50	FOS	chr5:17346925-17347120	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17354521-17354571	HepG2	liver:	n/a
2	chr5:17354674-17354724	ovcar-3	ovarian:	n/a
3	chr5:17351261-17351311	Caco-2	colon:	n/a
4	chr5:17352463-17352513	Caco-2	colon:	n/a
5	chr5:17354504-17354554	HCT-116	colon:	n/a
6	chr5:17351261-17351311	U87	brain:	n/a
7	chr5:17354674-17354724	GM06990	blood:	n/a
8	chr5:17354674-17354724	AG04449	skin:	fetal
9	chr5:17354521-17354571	HCM	heart:	n/a
10	chr5:17351261-17351311	HAEpiC	amniotic membrane:	n/a
11	chr5:17354521-17354571	SKMC	muscle:	n/a
12	chr5:17354674-17354724	Caco-2	colon:	n/a
13	chr5:17352463-17352513	HPAEpiC	pulmonary alveolar:	n/a
14	chr5:17351261-17351311	AoSMC	blood vessel:	n/a
15	chr5:17354521-17354571	NB4	blood:	n/a
16	chr5:17354504-17354554	NHBE	bronchial:	n/a
17	chr5:17354504-17354554	GM12878	blood:	n/a
18	chr5:17354674-17354724	Hela-S3	cervix:	n/a
19	chr5:17354674-17354724	RPTEC	kidney:	n/a
20	chr5:17354504-17354554	K562	blood:	n/a
21	chr5:17354504-17354554	A549	lung:	n/a
22	chr5:17354521-17354571	HCPEpiC	choroid plexus:	n/a
23	chr5:17354674-17354724	PrEC	prostate:	n/a
24	chr5:17354521-17354571	NHBE	bronchial:	n/a
25	chr5:17354504-17354554	GM06990	blood:	n/a
26	chr5:17351261-17351311	HPAEpiC	pulmonary alveolar:	n/a
27	chr5:17354674-17354724	HPAEpiC	pulmonary alveolar:	n/a
28	chr5:17352463-17352513	SK-N-MC	brain:	n/a
29	chr5:17351261-17351311	A549	lung:	n/a
30	chr5:17354521-17354571	GM06990	blood:	n/a
31	chr5:17354674-17354724	SK-N-SH_RA	brain:	n/a
32	chr5:17354674-17354724	AG09319	gingival:	n/a
33	chr5:17351261-17351311	GM06990	blood:	n/a
34	chr5:17354674-17354724	AG10803	skin:	n/a
35	chr5:17354504-17354554	SKMC	muscle:	n/a
36	chr5:17354521-17354571	PFSK-1	brain:	n/a
37	chr5:17351261-17351311	HEEpiC	esophagus:	n/a
38	chr5:17352463-17352513	HIPEpiC	eye:	n/a
39	chr5:17354504-17354554	MCF-7	breast:	n/a
40	chr5:17354521-17354571	IMR90	lung:	fetal
41	chr5:17351261-17351311	GM12892	blood:	n/a
42	chr5:17352463-17352513	H1-hESC	embryonic stem cell:	embryo
43	chr5:17352463-17352513	HRE	kidney:	n/a
44	chr5:17354674-17354724	PANC-1	pancreas:	n/a
45	chr5:17354521-17354571	GM12878	blood:	n/a
46	chr5:17352463-17352513	SAEC	small airway:	n/a
47	chr5:17352463-17352513	NH-A	brain:	n/a
48	chr5:17354504-17354554	HRE	kidney:	n/a
49	chr5:17354674-17354724	ProgFib	skin:	n/a
50	chr5:17351261-17351311	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:17348620..17350126-chr5:17350951..17353449,2	MCF-7	breast:
2	chr11:61734609..61735212-chr5:17354143..17355140,3	Hela-S3	cervix:
3	chr5:17348620..17350126-chr5:17350951..17353449,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-1	chr5:17354243-17355008	ENSG00000248223
2	lnc-BASP1-10	chr5:17345725-17346064	NONHSAT100625
3	lnc-BASP1-1	chr5:17354019-17354119	ENSG00000248223

Variant related genes	Relation type
FTH1P10	TF binding region
ENSG00000248223	TF binding region
RN7SKP133	TF binding region
FTH1P10	CpG island
ENSG00000248223	CpG island
RN7SKP133	CpG island
ENSG00000167996	chromatin interactions

Extended variants
information (count: 589 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551118767	chr5:17342761-17342762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375464997	chr5:17342774-17342775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189099355	chr5:17342778-17342779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535568272	chr5:17342807-17342808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6861876	chr5:17342819-17342820	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs147924925	chr5:17342825-17342826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536513398	chr5:17342835-17342836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4702206	chr5:17342848-17342849	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs145416484	chr5:17342863-17342864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181578421	chr5:17342866-17342867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534882204	chr5:17342902-17342903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11362240	chr5:17342903-17342904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10066708	chr5:17342959-17342960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186546651	chr5:17342984-17342985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190724866	chr5:17342985-17342986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6862515	chr5:17342987-17342988	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs574709168	chr5:17343009-17343010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150378831	chr5:17343015-17343016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554022748	chr5:17343021-17343022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181965129	chr5:17343029-17343030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559034731	chr5:17343048-17343049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577515769	chr5:17343062-17343063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373064266	chr5:17343063-17343064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577445634	chr5:17343064-17343065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186219950	chr5:17343075-17343076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376915664	chr5:17343097-17343098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs66941382	chr5:17343112-17343113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs59192453	chr5:17343117-17343118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530583444	chr5:17343183-17343184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544337524	chr5:17343202-17343203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs6862610	chr5:17343229-17343230	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs529891999	chr5:17343301-17343302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546862193	chr5:17343409-17343410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs112984487	chr5:17343464-17343465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72346349	chr5:17343483-17343484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs58247236	chr5:17343497-17343498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189753944	chr5:17343557-17343558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2652648	chr5:17343559-17343560	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs182836831	chr5:17343568-17343569	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs569179309	chr5:17343616-17343617	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556655102	chr5:17343627-17343628	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs372601151	chr5:17343629-17343630	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs537915662	chr5:17343685-17343686	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs554627745	chr5:17343798-17343799	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs568245556	chr5:17343820-17343821	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs185660077	chr5:17343850-17343851	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs141110989	chr5:17343873-17343874	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs144814285	chr5:17343951-17343952	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs116087552	chr5:17343973-17343974	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs138641622	chr5:17343993-17343994	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	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
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	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
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	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
Melanoma	22183965	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17339400-17343800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:17340000-17343600	Enhancers	A549	lung
3	chr5:17340600-17343000	Enhancers	Hela-S3	cervix
4	chr5:17340800-17343800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr5:17341200-17343600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr5:17341200-17343800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr5:17341400-17343600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr5:17341400-17343600	Weak transcription	Stomach Mucosa	stomach
9	chr5:17341400-17343600	Weak transcription	HUVEC	blood vessel
10	chr5:17341400-17343600	Weak transcription	Osteobl	bone
11	chr5:17341800-17343800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr5:17342000-17343600	Weak transcription	Aorta	Aorta
13	chr5:17342000-17343800	Weak transcription	Fetal Lung	lung
14	chr5:17343000-17343400	Weak transcription	Hela-S3	cervix
15	chr5:17343400-17343800	Enhancers	Hela-S3	cervix
16	chr5:17343400-17344000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:17343400-17344400	Enhancers	Primary B cells from peripheral blood	blood
18	chr5:17343600-17344000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr5:17343600-17344000	Flanking Active TSS	GM12878-XiMat	blood
20	chr5:17343600-17344000	Enhancers	NHDF-Ad	bronchial
21	chr5:17343600-17344200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:17343600-17344200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr5:17343600-17344200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr5:17343600-17344200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr5:17343600-17344200	Enhancers	Ovary	ovary
26	chr5:17343600-17344200	Enhancers	HMEC	breast
27	chr5:17343600-17344200	Enhancers	NHEK	skin
28	chr5:17343600-17344200	Enhancers	NHLF	lung
29	chr5:17343600-17344400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr5:17343600-17344400	Enhancers	Stomach Mucosa	stomach
31	chr5:17343600-17344400	Flanking Active TSS	A549	lung
32	chr5:17343600-17344400	Enhancers	HUVEC	blood vessel
33	chr5:17343600-17344400	Enhancers	Osteobl	bone
34	chr5:17343600-17344800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr5:17343800-17344000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr5:17343800-17344000	Enhancers	Aorta	Aorta
37	chr5:17343800-17344200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr5:17343800-17344200	Enhancers	H9 Cell Line	embryonic stem cell
39	chr5:17343800-17344200	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr5:17343800-17344200	Enhancers	Fetal Lung	lung
41	chr5:17343800-17344200	Enhancers	Gastric	stomach
42	chr5:17343800-17344200	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr5:17343800-17344200	Enhancers	NH-A	brain
44	chr5:17343800-17344400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr5:17343800-17344400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr5:17343800-17344400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr5:17343800-17344400	Enhancers	Placenta	Placenta
48	chr5:17343800-17344400	Flanking Active TSS	Hela-S3	cervix
49	chr5:17343800-17344800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr5:17344000-17344200	Enhancers	HSMMtube	muscle

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