Variant report

Variant	nsv470992
Chromosome Location	chr5:17638846-17739449
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	BACH1	chr5:17680992-17681026	K562	blood:	n/a	n/a
2	BCL3	chr5:17694847-17695529	A549	lung:	n/a	chr5:17695250-17695259
3	BRCA1	chr5:17694481-17695921	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr5:17691746-17692676	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr5:17679984-17680257	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:17679832-17680634	Hela-S3	cervix:	n/a	chr5:17680161-17680172
7	CEBPB	chr5:17679962-17680276	A549	lung:	n/a	chr5:17680161-17680172
8	CEBPB	chr5:17727071-17727684	Hela-S3	cervix:	n/a	chr5:17727253-17727266 chr5:17727329-17727342
9	CEBPB	chr5:17729684-17729956	IMR90	lung:	n/a	chr5:17729818-17729829 chr5:17729820-17729829 chr5:17729820-17729829 chr5:17729818-17729831 chr5:17729820-17729829 chr5:17729818-17729831
10	CEBPB	chr5:17729679-17730005	A549	lung:	n/a	chr5:17729818-17729829 chr5:17729820-17729829 chr5:17729820-17729829 chr5:17729818-17729831 chr5:17729820-17729829 chr5:17729818-17729831
11	CEBPB	chr5:17691305-17691412	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr5:17667008-17667264	A549	lung:	n/a	n/a
13	CEBPB	chr5:17729587-17730068	A549	lung:	n/a	chr5:17729818-17729829 chr5:17729820-17729829 chr5:17729820-17729829 chr5:17729818-17729831 chr5:17729820-17729829 chr5:17729818-17729831
14	CEBPB	chr5:17676779-17677058	HepG2	liver:	n/a	chr5:17676912-17676923
15	CEBPB	chr5:17679987-17680283	HepG2	liver:	n/a	chr5:17680161-17680172
16	CEBPB	chr5:17729677-17729966	K562	blood:	n/a	chr5:17729818-17729829 chr5:17729820-17729829 chr5:17729820-17729829 chr5:17729818-17729831 chr5:17729820-17729829 chr5:17729818-17729831
17	CEBPB	chr5:17679981-17680265	ECC-1	luminal epithelium:	n/a	chr5:17680161-17680172
18	CEBPB	chr5:17679822-17680468	A549	lung:	n/a	chr5:17680161-17680172
19	CEBPB	chr5:17691832-17692471	Hela-S3	cervix:	n/a	chr5:17692053-17692070
20	CEBPB	chr5:17679986-17680295	A549	lung:	n/a	chr5:17680161-17680172
21	CEBPB	chr5:17680006-17680300	IMR90	lung:	n/a	chr5:17680161-17680172
22	CEBPB	chr5:17667048-17667244	IMR90	lung:	n/a	n/a
23	CEBPB	chr5:17680008-17680237	ECC-1	luminal epithelium:	n/a	chr5:17680161-17680172
24	CEBPB	chr5:17676882-17676947	K562	blood:	n/a	chr5:17676912-17676923
25	CEBPB	chr5:17694461-17695782	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:17729711-17729983	Hela-S3	cervix:	n/a	chr5:17729818-17729829 chr5:17729820-17729829 chr5:17729820-17729829 chr5:17729818-17729831 chr5:17729820-17729829 chr5:17729818-17729831
27	CEBPB	chr5:17713504-17713704	HepG2	liver:	n/a	n/a
28	CEBPB	chr5:17694817-17695648	A549	lung:	n/a	n/a
29	CEBPB	chr5:17729636-17730012	HepG2	liver:	n/a	chr5:17729818-17729829 chr5:17729820-17729829 chr5:17729820-17729829 chr5:17729818-17729831 chr5:17729820-17729829 chr5:17729818-17729831
30	CEBPB	chr5:17694987-17695485	MCF-7	breast:	n/a	n/a
31	CEBPB	chr5:17679965-17680281	MCF-7	breast:	n/a	chr5:17680161-17680172
32	CEBPB	chr5:17695079-17695387	A549	lung:	n/a	n/a
33	CEBPB	chr5:17676818-17677046	A549	lung:	n/a	chr5:17676912-17676923
34	CEBPB	chr5:17729734-17729939	H1-hESC	embryonic stem cell:	n/a	chr5:17729818-17729829 chr5:17729820-17729829 chr5:17729820-17729829 chr5:17729818-17729831 chr5:17729820-17729829 chr5:17729818-17729831
35	CEBPB	chr5:17676850-17677041	IMR90	lung:	n/a	chr5:17676912-17676923
36	CEBPB	chr5:17694967-17695479	A549	lung:	n/a	n/a
37	CEBPB	chr5:17694967-17695397	MCF-7	breast:	n/a	n/a
38	CEBPB	chr5:17729720-17730107	MCF-7	breast:	n/a	chr5:17729818-17729829 chr5:17729820-17729829 chr5:17729820-17729829 chr5:17729818-17729831 chr5:17729820-17729829 chr5:17729818-17729831
39	CHD2	chr5:17694498-17695438	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr5:17679972-17680355	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr5:17655460-17655610	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:17670540-17670690	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr5:17670517-17670622	A549	lung:	n/a	n/a
44	CTCF	chr5:17688800-17688950	GM06990	blood:	n/a	n/a
45	CTCF	chr5:17655481-17655573	K562	blood:	n/a	n/a
46	CTCF	chr5:17670539-17670602	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:17649458-17649537	ProgFib	skin:	n/a	n/a
48	CTCF	chr5:17670340-17670590	HEK293	kidney:	n/a	n/a
49	CTCF	chr5:17670503-17670697	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr5:17670460-17670610	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17664567-17664617	GM06990	blood:	n/a
2	chr5:17664567-17664617	AG04449	skin:	fetal
3	chr5:17664567-17664617	NB4	blood:	n/a
4	chr5:17655356-17655406	SK-N-SH	brain:	n/a
5	chr5:17670475-17670525	BJ	skin:	n/a
6	chr5:17656637-17656687	GM12892	blood:	n/a
7	chr5:17670475-17670525	A549	lung:	n/a
8	chr5:17670475-17670525	IMR90	lung:	fetal
9	chr5:17656637-17656687	NHBE	bronchial:	n/a
10	chr5:17670442-17670492	AG09309	skin:	n/a
11	chr5:17670475-17670525	HNPCEpiC	eye:	n/a
12	chr5:17664567-17664617	CMK	blood:	n/a
13	chr5:17655356-17655406	HAEpiC	amniotic membrane:	n/a
14	chr5:17670475-17670525	GM12878	blood:	n/a
15	chr5:17655356-17655406	AG04449	skin:	fetal
16	chr5:17656637-17656687	HIPEpiC	eye:	n/a
17	chr5:17656637-17656687	HL-60	blood:	n/a
18	chr5:17670442-17670492	HMEC	breast:	n/a
19	chr5:17656637-17656687	IMR90	lung:	fetal
20	chr5:17654594-17654644	HL-60	blood:	n/a
21	chr5:17664567-17664617	HCPEpiC	choroid plexus:	n/a
22	chr5:17655356-17655406	BE2_C	brain:	n/a
23	chr5:17654594-17654644	Hepatocyte	liver:	n/a
24	chr5:17656637-17656687	SK-N-SH_RA	brain:	n/a
25	chr5:17670475-17670525	GM12891	blood:	n/a
26	chr5:17656637-17656687	GM19239	blood:	n/a
27	chr5:17664567-17664617	HPAEpiC	pulmonary alveolar:	n/a
28	chr5:17656637-17656687	NH-A	brain:	n/a
29	chr5:17656637-17656687	ovcar-3	ovarian:	n/a
30	chr5:17670475-17670525	HIPEpiC	eye:	n/a
31	chr5:17670475-17670525	CMK	blood:	n/a
32	chr5:17654594-17654644	H1-hESC	embryonic stem cell:	embryo
33	chr5:17655356-17655406	SK-N-SH_RA	brain:	n/a
34	chr5:17654594-17654644	NHDF-neo	bronchial:	n/a
35	chr5:17655356-17655406	GM19239	blood:	n/a
36	chr5:17656637-17656687	AG09319	gingival:	n/a
37	chr5:17670475-17670525	AG04450	lung:	fetal
38	chr5:17670475-17670525	HCT-116	colon:	n/a
39	chr5:17655356-17655406	HRE	kidney:	n/a
40	chr5:17670442-17670492	GM12892	blood:	n/a
41	chr5:17654594-17654644	K562	blood:	n/a
42	chr5:17664567-17664617	HMEC	breast:	n/a
43	chr5:17670475-17670525	HCM	heart:	n/a
44	chr5:17655356-17655406	A549	lung:	n/a
45	chr5:17670475-17670525	AG09309	skin:	n/a
46	chr5:17664567-17664617	HRE	kidney:	n/a
47	chr5:17656637-17656687	LNCaP	prostate:	n/a
48	chr5:17664567-17664617	HNPCEpiC	eye:	n/a
49	chr5:17654594-17654644	NB4	blood:	n/a
50	chr5:17654594-17654644	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:17693367..17696364-chr5:17702400..17704641,2	MCF-7	breast:
2	chr5:17702899..17705763-chr5:17710587..17714118,3	MCF-7	breast:
3	chr5:17693367..17696364-chr5:17702400..17704641,2	MCF-7	breast:
4	chr5:17719378..17721402-chr5:17724190..17726007,2	MCF-7	breast:
5	chr5:17644806..17646667-chr5:17648582..17651312,2	MCF-7	breast:
6	chr5:17217433..17219821-chr5:17690448..17693197,3	MCF-7	breast:
7	chr5:17632983..17635813-chr5:17637711..17640599,2	K562	blood:
8	chr5:17737382..17739045-chr5:17741320..17743486,2	K562	blood:
9	chr5:17719378..17721402-chr5:17724190..17726007,2	MCF-7	breast:
10	chr5:17702899..17705763-chr5:17710587..17714118,3	MCF-7	breast:
11	chr5:17216395..17218536-chr5:17655025..17657774,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-7	chr5:17684693-17684796	NONHSAT100665
2	lnc-MYO10-19	chr5:17654482-17654752	NONHSAT100661
3	lnc-BASP1-7	chr5:17684693-17684796	ENSG00000249937
4	lnc-MYO10-17	chr5:17643071-17643337	NONHSAT100659

Variant related genes	Relation type
ENSG00000250715	TF binding region
ENSG00000248337	TF binding region
ENSG00000248160	TF binding region
ENSG00000249937	TF binding region
ENSG00000248542	TF binding region
ENSG00000248471	TF binding region
ENSG00000269466	TF binding region
ENSG00000250715	CpG island
ENSG00000248337	CpG island
ENSG00000248160	CpG island
ENSG00000249937	CpG island
ENSG00000248542	CpG island
ENSG00000248471	CpG island
ENSG00000269466	CpG island
ENSG00000248542	chromatin interactions
ENSG00000250782	chromatin interactions
ENSG00000176788	chromatin interactions
ENSG00000215196	chromatin interactions

Extended variants
information (count: 1857 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1857 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6894435	chr5:17638847-17638848	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537187457	chr5:17638855-17638856	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557192013	chr5:17638886-17638887	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs4599573	chr5:17639011-17639012	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs111843046	chr5:17639016-17639017	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs552962265	chr5:17639030-17639031	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs73061086	chr5:17639050-17639051	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs112360028	chr5:17639064-17639065	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200946580	chr5:17639091-17639092	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs530909342	chr5:17639092-17639093	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs34528895	chr5:17639156-17639157	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs566535159	chr5:17639171-17639172	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs184251852	chr5:17639238-17639239	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs34688480	chr5:17639239-17639240	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs561054684	chr5:17639270-17639271	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535968369	chr5:17639277-17639278	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs547195082	chr5:17639278-17639279	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs111639521	chr5:17639302-17639303	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146024490	chr5:17639308-17639309	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs1514851	chr5:17639309-17639310	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs571313664	chr5:17639312-17639313	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs75406603	chr5:17639314-17639315	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs557055315	chr5:17639323-17639324	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567389722	chr5:17639352-17639353	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs188582566	chr5:17639372-17639373	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs553165391	chr5:17639373-17639374	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs573042819	chr5:17639387-17639388	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs113289800	chr5:17639472-17639473	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558431547	chr5:17639488-17639489	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs72742672	chr5:17639501-17639502	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs72742673	chr5:17639505-17639506	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192286252	chr5:17639538-17639539	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs537679380	chr5:17639603-17639604	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs185235395	chr5:17639642-17639643	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs561019800	chr5:17639659-17639660	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs72494145	chr5:17639665-17639666	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs55816751	chr5:17639675-17639676	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540455433	chr5:17639686-17639687	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs75098513	chr5:17639697-17639698	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs559061987	chr5:17639703-17639704	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201700640	chr5:17639727-17639728	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs560779313	chr5:17639744-17639745	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs372451542	chr5:17639748-17639749	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs369514194	chr5:17639749-17639750	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs371889408	chr5:17639750-17639751	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532693672	chr5:17639767-17639768	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376843280	chr5:17639784-17639785	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs367723113	chr5:17639786-17639787	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs552792082	chr5:17639823-17639824	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs139944170	chr5:17639828-17639829	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17639200-17640000	Enhancers	Liver	Liver
2	chr5:17652200-17652400	Enhancers	HSMM	muscle
3	chr5:17662200-17662800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:17662800-17663000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:17662800-17663400	Enhancers	Fetal Muscle Trunk	muscle
6	chr5:17663000-17669200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr5:17664200-17664800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr5:17664200-17665400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr5:17664200-17665600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr5:17664200-17665800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:17664400-17664800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr5:17664400-17664800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr5:17664400-17665000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr5:17664400-17665000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr5:17664400-17665800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr5:17664600-17664800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:17664800-17665800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr5:17665600-17668000	Enhancers	Primary B cells from cord blood	blood
19	chr5:17666000-17668000	Enhancers	Primary B cells from peripheral blood	blood
20	chr5:17670400-17670800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr5:17678800-17680000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr5:17678800-17680000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr5:17678800-17680800	Enhancers	HMEC	breast
24	chr5:17678800-17681400	Enhancers	Hela-S3	cervix
25	chr5:17679000-17680600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:17679200-17680800	Enhancers	A549	lung
27	chr5:17679600-17680000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr5:17679600-17680600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:17679800-17680200	Enhancers	NHEK	skin
30	chr5:17681400-17684400	Weak transcription	Hela-S3	cervix
31	chr5:17682800-17683000	Enhancers	Ovary	ovary
32	chr5:17683000-17684400	Weak transcription	Ovary	ovary
33	chr5:17684400-17684800	Flanking Active TSS	Ovary	ovary
34	chr5:17684400-17685200	Active TSS	Hela-S3	cervix
35	chr5:17684800-17685200	Enhancers	Ovary	ovary
36	chr5:17690200-17690800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:17690200-17690800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr5:17690200-17691600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr5:17691400-17697000	Enhancers	Hela-S3	cervix
40	chr5:17692000-17692200	Enhancers	HMEC	breast
41	chr5:17692200-17692400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr5:17692200-17692600	Enhancers	Placenta	Placenta
43	chr5:17692600-17694200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr5:17694200-17696400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr5:17694200-17696600	Enhancers	NHEK	skin
46	chr5:17694400-17696600	Enhancers	HMEC	breast
47	chr5:17694600-17695000	Enhancers	A549	lung
48	chr5:17694600-17696400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr5:17695000-17695800	Flanking Active TSS	A549	lung
50	chr5:17695400-17696000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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