Variant report

Variant	nsv514309
Chromosome Location	chr5:68821588-68854548
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:125)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:125 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:68823022-68823295	K562	blood:	n/a	n/a
2	CEBPB	chr5:68823213-68823538	A549	lung:	n/a	n/a
3	CEBPB	chr5:68823197-68823519	K562	blood:	n/a	n/a
4	CEBPB	chr5:68823245-68823491	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr5:68834723-68834923	HepG2	liver:	n/a	n/a
6	CEBPB	chr5:68823171-68823667	MCF-7	breast:	n/a	n/a
7	CEBPB	chr5:68823244-68823535	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:68823192-68823535	K562	blood:	n/a	n/a
9	CEBPB	chr5:68823233-68823538	IMR90	lung:	n/a	n/a
10	CEBPB	chr5:68823188-68823480	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr5:68834691-68834785	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:68821436-68821696	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr5:68823181-68823660	MCF-7	breast:	n/a	n/a
14	CTCF	chr5:68838421-68838427	GM20000	blood:	n/a	n/a
15	CTCF	chr5:68833702-68833774	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr5:68833553-68833648	GM10266	blood:	n/a	n/a
17	CTCF	chr5:68833712-68833842	LNCaP	prostate:	n/a	n/a
18	CTCF	chr5:68838439-68838481	GM20000	blood:	n/a	n/a
19	CTCF	chr5:68833712-68833856	Pancreas_OC	pancreas:	n/a	n/a
20	CTCF	chr5:68833676-68833858	LNCaP	prostate:	n/a	n/a
21	EP300	chr5:68823857-68824255	T-47D	breast:	n/a	n/a
22	EP300	chr5:68823661-68824329	ECC-1	luminal epithelium:	n/a	n/a
23	EP300	chr5:68823783-68824405	MCF-7	breast:	n/a	n/a
24	EP300	chr5:68823743-68824277	T-47D	breast:	n/a	n/a
25	ESR1	chr5:68823882-68824194	T-47D	breast:	n/a	n/a
26	FOSL2	chr5:68854022-68854510	HepG2	liver:	n/a	n/a
27	FOSL2	chr5:68853021-68853476	HepG2	liver:	n/a	n/a
28	FOSL2	chr5:68834556-68834951	HepG2	liver:	n/a	n/a
29	FOSL2	chr5:68853016-68853504	HepG2	liver:	n/a	n/a
30	FOXA1	chr5:68852945-68853686	HepG2	liver:	n/a	n/a
31	FOXA1	chr5:68834450-68834935	HepG2	liver:	n/a	n/a
32	FOXA1	chr5:68840155-68840694	HepG2	liver:	n/a	n/a
33	FOXA1	chr5:68823841-68824216	T-47D	breast:	n/a	n/a
34	FOXA1	chr5:68852246-68852676	HepG2	liver:	n/a	n/a
35	FOXA1	chr5:68842830-68843191	HepG2	liver:	n/a	chr5:68842988-68843000
36	FOXA1	chr5:68823961-68824238	T-47D	breast:	n/a	n/a
37	FOXA2	chr5:68853042-68853441	A549	lung:	n/a	n/a
38	GATA3	chr5:68823895-68824315	MCF-7	breast:	n/a	n/a
39	GATA3	chr5:68823786-68824375	T-47D	breast:	n/a	n/a
40	GATA3	chr5:68823494-68824389	MCF-7	breast:	n/a	n/a
41	GATA3	chr5:68823165-68824674	MCF-7	breast:	n/a	chr5:68824609-68824617
42	GATA3	chr5:68826314-68827044	MCF-7	breast:	n/a	n/a
43	GATA3	chr5:68823243-68823716	T-47D	breast:	n/a	n/a
44	GATA3	chr5:68823130-68824494	MCF-7	breast:	n/a	n/a
45	GATA3	chr5:68823097-68824374	T-47D	breast:	n/a	n/a
46	GATA3	chr5:68826308-68826876	MCF-7	breast:	n/a	n/a
47	HDAC2	chr5:68823703-68824324	MCF-7	breast:	n/a	n/a
48	HDAC2	chr5:68823793-68824366	MCF-7	breast:	n/a	n/a
49	JUND	chr5:68853139-68853405	HepG2	liver:	n/a	n/a
50	JUND	chr5:68853176-68853401	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:68852996-68853046	ProgFib	skin:	n/a
2	chr5:68852996-68853046	AG09319	gingival:	n/a
3	chr5:68852996-68853046	CMK	blood:	n/a
4	chr5:68852996-68853046	Hela-S3	cervix:	n/a
5	chr5:68852996-68853046	ECC-1	luminal epithelium:	n/a
6	chr5:68852996-68853046	BJ	skin:	n/a
7	chr5:68852996-68853046	K562	blood:	n/a
8	chr5:68852996-68853046	PrEC	prostate:	n/a
9	chr5:68852996-68853046	HCPEpiC	choroid plexus:	n/a
10	chr5:68852996-68853046	ovcar-3	ovarian:	n/a
11	chr5:68852996-68853046	HEK293	kidney:	embryo
12	chr5:68852996-68853046	A549	lung:	n/a
13	chr5:68852996-68853046	MCF-7	breast:	n/a
14	chr5:68852996-68853046	GM12878	blood:	n/a
15	chr5:68852996-68853046	HepG2	liver:	n/a
16	chr5:68852996-68853046	AG10803	skin:	n/a
17	chr5:68852996-68853046	NH-A	brain:	n/a
18	chr5:68852996-68853046	HRE	kidney:	n/a
19	chr5:68852996-68853046	NHBE	bronchial:	n/a
20	chr5:68852996-68853046	SK-N-MC	brain:	n/a
21	chr5:68852996-68853046	AG04450	lung:	fetal
22	chr5:68852996-68853046	IMR90	lung:	fetal
23	chr5:68852996-68853046	U87	brain:	n/a
24	chr5:68852996-68853046	H1-hESC	embryonic stem cell:	embryo
25	chr5:68852996-68853046	HUVEC	blood vessel:	n/a
26	chr5:68852996-68853046	NB4	blood:	n/a
27	chr5:68852996-68853046	T-47D	breast:	n/a
28	chr5:68852996-68853046	HCM	heart:	n/a
29	chr5:68852996-68853046	HCF	heart:	n/a
30	chr5:68852996-68853046	RPTEC	kidney:	n/a
31	chr5:68852996-68853046	HPAEpiC	pulmonary alveolar:	n/a
32	chr5:68852996-68853046	HNPCEpiC	eye:	n/a
33	chr5:68852996-68853046	Jurkat	blood:	n/a
34	chr5:68852996-68853046	LNCaP	prostate:	n/a
35	chr5:68852996-68853046	AG04449	skin:	fetal
36	chr5:68852996-68853046	Caco-2	colon:	n/a
37	chr5:68852996-68853046	GM12891	blood:	n/a
38	chr5:68852996-68853046	HIPEpiC	eye:	n/a
39	chr5:68852996-68853046	HCT-116	colon:	n/a
40	chr5:68852996-68853046	PFSK-1	brain:	n/a
41	chr5:68852996-68853046	SK-N-SH	brain:	n/a
42	chr5:68852996-68853046	AG09309	skin:	n/a
43	chr5:68852996-68853046	GM12892	blood:	n/a
44	chr5:68852996-68853046	Hepatocyte	liver:	n/a
45	chr5:68852996-68853046	HL-60	blood:	n/a
46	chr5:68852996-68853046	BE2_C	brain:	n/a
47	chr5:68852996-68853046	HRPEpiC	eye:	n/a
48	chr5:68852996-68853046	SK-N-SH_RA	brain:	n/a
49	chr5:68852996-68853046	PANC-1	pancreas:	n/a
50	chr5:68852996-68853046	HMEC	breast:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:68711082..68712894-chr5:68825364..68828331,2	MCF-7	breast:
2	chr5:68813539..68815320-chr5:68820921..68822712,2	MCF-7	breast:
3	chr5:68811437..68815245-chr5:68822688..68826346,4	MCF-7	breast:
4	chr5:68786843..68790127-chr5:68821932..68828319,7	MCF-7	breast:
5	chr5:68820102..68821620-chr5:68821807..68823888,2	MCF-7	breast:
6	chr5:68820102..68821620-chr5:68821807..68823888,2	MCF-7	breast:
7	chr5:68787211..68792044-chr5:68819088..68825852,9	MCF-7	breast:
8	chr5:68791729..68794377-chr5:68827769..68829901,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000238740	TF binding region
OCLN	TF binding region
GTF2H2C	TF binding region
RNU6-724P	TF binding region
ENSG00000238740	CpG island
OCLN	CpG island
GTF2H2C	CpG island
RNU6-724P	CpG island
ENSG00000152939	chromatin interactions
ENSG00000197822	chromatin interactions

Extended variants
information (count: 511 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527694370	chr5:68821682-68821683	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs77394936	chr5:68821705-68821706	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs573023238	chr5:68821749-68821750	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs73772569	chr5:68821753-68821754	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs532259650	chr5:68821754-68821755	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369683287	chr5:68821800-68821801	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550390807	chr5:68821900-68821901	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs540284874	chr5:68822029-68822030	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs181724632	chr5:68822032-68822033	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs186282334	chr5:68822092-68822093	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs373584818	chr5:68822203-68822204	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189938693	chr5:68822218-68822219	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs148552999	chr5:68822225-68822226	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533802311	chr5:68822226-68822227	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558551889	chr5:68822349-68822350	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs141706396	chr5:68822381-68822382	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs34754039	chr5:68822382-68822383	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs58056210	chr5:68822401-68822402	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs115444195	chr5:68822402-68822403	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs538515461	chr5:68822408-68822409	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs142931888	chr5:68822442-68822443	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574966493	chr5:68822451-68822452	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186264893	chr5:68822459-68822460	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs143229176	chr5:68822493-68822494	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544569626	chr5:68822505-68822506	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554264031	chr5:68822514-68822515	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs146441694	chr5:68822544-68822545	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs377045871	chr5:68822570-68822571	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs545828270	chr5:68822643-68822644	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs191556842	chr5:68822646-68822647	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs183061422	chr5:68822653-68822654	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs78811453	chr5:68822698-68822699	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs559725773	chr5:68822712-68822713	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs527347933	chr5:68822714-68822715	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs548049240	chr5:68822715-68822716	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs560206151	chr5:68822731-68822732	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371409699	chr5:68822746-68822747	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs111564927	chr5:68822787-68822788	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs185197737	chr5:68822822-68822823	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs531226063	chr5:68822827-68822828	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs373744018	chr5:68822830-68822831	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs549147209	chr5:68822831-68822832	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs552228080	chr5:68822833-68822834	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542703192	chr5:68822870-68822871	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs570457067	chr5:68822875-68822876	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs370626118	chr5:68822948-68822949	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs189889341	chr5:68823034-68823035	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs143311759	chr5:68823035-68823036	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs568613262	chr5:68823036-68823037	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs536062452	chr5:68823066-68823067	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	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
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pseudo-TORCH syndrome	20727516	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68790200-68824600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:68799000-68823200	Weak transcription	Placenta	Placenta
3	chr5:68799400-68821800	Weak transcription	Fetal Stomach	stomach
4	chr5:68805600-68821600	Weak transcription	Lung	lung
5	chr5:68805600-68823400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr5:68805600-68826200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr5:68805600-68826600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr5:68806000-68824200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr5:68806400-68826400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr5:68807000-68821600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:68810400-68821600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr5:68810400-68821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr5:68810400-68823600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr5:68814000-68823400	Weak transcription	Fetal Lung	lung
15	chr5:68814400-68823600	Weak transcription	Small Intestine	intestine
16	chr5:68814600-68822000	Weak transcription	Fetal Kidney	kidney
17	chr5:68815400-68826600	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr5:68815800-68831000	Weak transcription	HepG2	liver
19	chr5:68816000-68821600	Weak transcription	Liver	Liver
20	chr5:68816000-68821600	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr5:68816800-68822600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:68817000-68821600	Weak transcription	Pancreas	Pancrea
23	chr5:68817200-68827200	Weak transcription	GM12878-XiMat	blood
24	chr5:68817400-68823400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr5:68817400-68823400	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr5:68817600-68821600	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr5:68818000-68821600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr5:68818000-68821600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:68818000-68821600	Weak transcription	Duodenum Mucosa	Duodenum
30	chr5:68818000-68823000	Weak transcription	Stomach Mucosa	stomach
31	chr5:68819000-68821600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr5:68819800-68824600	Genic enhancers	Fetal Intestine Small	intestine
33	chr5:68820600-68822200	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr5:68820600-68823000	Genic enhancers	Fetal Intestine Large	intestine
35	chr5:68821400-68821800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr5:68821400-68822600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
37	chr5:68821400-68822800	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr5:68821600-68821800	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr5:68821600-68822000	Enhancers	Duodenum Mucosa	Duodenum
40	chr5:68821600-68822200	Strong transcription	Lung	lung
41	chr5:68821600-68822400	Strong transcription	H1 Cell Line	embryonic stem cell
42	chr5:68821600-68822400	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr5:68821600-68822400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr5:68821600-68822800	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr5:68821600-68822800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr5:68821600-68822800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr5:68821600-68822800	Strong transcription	Liver	Liver
48	chr5:68821600-68823200	Genic enhancers	Pancreas	Pancrea
49	chr5:68821800-68822000	Genic enhancers	Sigmoid Colon	Sigmoid Colon
50	chr5:68821800-68822400	Strong transcription	Fetal Stomach	stomach

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