Variant report

Variant	nsv968189
Chromosome Location	chr5:68829015-68919282
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:763)
CpG islands
(count:613)
Chromatin interactive
region (count:1)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:763 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:68855731-68856077	GM12878	blood:	n/a	n/a
2	BATF	chr5:68857142-68857346	GM12878	blood:	n/a	n/a
3	BATF	chr5:68856265-68856477	GM12878	blood:	n/a	n/a
4	BATF	chr5:68856954-68857395	GM12878	blood:	n/a	n/a
5	BATF	chr5:68897780-68898118	GM12878	blood:	n/a	n/a
6	BATF	chr5:68855769-68856236	GM12878	blood:	n/a	n/a
7	BATF	chr5:68897794-68898185	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:68897742-68898263	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:68857029-68857406	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:68897862-68898148	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:68855639-68856223	GM12878	blood:	n/a	chr5:68855979-68855988
12	BCL11A	chr5:68855749-68856242	GM12878	blood:	n/a	chr5:68855979-68855988
13	BCLAF1	chr5:68855724-68856111	K562	blood:	n/a	chr5:68855979-68855988
14	BCLAF1	chr5:68855724-68856135	GM12878	blood:	n/a	chr5:68855979-68855988
15	BCLAF1	chr5:68855732-68856164	GM12878	blood:	n/a	chr5:68855979-68855988
16	BCLAF1	chr5:68855724-68856116	K562	blood:	n/a	chr5:68855979-68855988
17	BHLHE40	chr5:68855820-68856132	HepG2	liver:	n/a	chr5:68855927-68855943 chr5:68855911-68855927
18	BRCA1	chr5:68855848-68856045	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr5:68855601-68856119	K562	blood:	n/a	n/a
20	CBX3	chr5:68855493-68856354	K562	blood:	n/a	n/a
21	CEBPB	chr5:68855845-68856045	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr5:68834691-68834785	HepG2	liver:	n/a	n/a
23	CEBPB	chr5:68834723-68834923	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:68857055-68857464	K562	blood:	n/a	n/a
25	CEBPB	chr5:68857201-68857397	K562	blood:	n/a	n/a
26	CEBPD	chr5:68911591-68912003	K562	blood:	n/a	n/a
27	CEBPD	chr5:68855760-68856284	K562	blood:	n/a	n/a
28	CHD2	chr5:68855853-68856047	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr5:68855844-68855949	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr5:68855923-68856048	GM12878	blood:	n/a	n/a
31	CREB1	chr5:68855831-68856118	A549	lung:	n/a	n/a
32	CTCF	chr5:68870845-68870938	Medullo	brain:	n/a	n/a
33	CTCF	chr5:68855616-68856209	A549	lung:	n/a	n/a
34	CTCF	chr5:68855838-68856031	T-47D	breast:	n/a	n/a
35	CTCF	chr5:68870569-68870638	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr5:68855720-68855870	BJ	skin:	n/a	n/a
37	CTCF	chr5:68833712-68833842	LNCaP	prostate:	n/a	n/a
38	CTCF	chr5:68855980-68856130	BJ	skin:	n/a	n/a
39	CTCF	chr5:68855783-68856107	GM10266	blood:	n/a	n/a
40	CTCF	chr5:68855980-68856130	Caco-2	colon:	n/a	n/a
41	CTCF	chr5:68855720-68855870	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr5:68890437-68890536	LNCaP	prostate:	n/a	n/a
43	CTCF	chr5:68855980-68856130	GM12872	blood:	n/a	n/a
44	CTCF	chr5:68914414-68914605	K562	blood:	n/a	n/a
45	CTCF	chr5:68855720-68855870	AG04450	lung:	n/a	n/a
46	CTCF	chr5:68855692-68856174	A549	lung:	n/a	n/a
47	CTCF	chr5:68855853-68855972	GM19240	blood:	n/a	n/a
48	CTCF	chr5:68855720-68855870	HMF	breast:	n/a	n/a
49	CTCF	chr5:68855740-68855890	BE2_C	brain:	n/a	n/a
50	CTCF	chr5:68856000-68856150	GM12867	blood:	n/a	n/a

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:68852996-68853046	GM12891	blood:	n/a
2	chr5:68852996-68853046	BJ	skin:	n/a
3	chr5:68857760-68857810	H1-hESC	embryonic stem cell:	embryo
4	chr5:68852996-68853046	GM12891	blood:	n/a
5	chr5:68852996-68853046	BJ	skin:	n/a
6	chr5:68857760-68857810	H1-hESC	embryonic stem cell:	embryo
7	chr5:68857760-68857810	SK-N-MC	brain:	n/a
8	chr5:68855810-68855860	GM19239	blood:	n/a
9	chr5:68868293-68868343	GM12878	blood:	n/a
10	chr5:68868293-68868343	HCPEpiC	choroid plexus:	n/a
11	chr5:68856065-68856115	RPTEC	kidney:	n/a
12	chr5:68856062-68856112	ovcar-3	ovarian:	n/a
13	chr5:68852996-68853046	A549	lung:	n/a
14	chr5:68856062-68856112	IMR90	lung:	fetal
15	chr5:68856062-68856112	Hela-S3	cervix:	n/a
16	chr5:68855873-68855923	HAEpiC	amniotic membrane:	n/a
17	chr5:68852996-68853046	HCF	heart:	n/a
18	chr5:68857760-68857810	PFSK-1	brain:	n/a
19	chr5:68855873-68855923	HIPEpiC	eye:	n/a
20	chr5:68852996-68853046	NH-A	brain:	n/a
21	chr5:68857760-68857810	MCF-7	breast:	n/a
22	chr5:68855873-68855923	SAEC	small airway:	n/a
23	chr5:68852996-68853046	Hepatocyte	liver:	n/a
24	chr5:68856062-68856112	HCPEpiC	choroid plexus:	n/a
25	chr5:68852996-68853046	HIPEpiC	eye:	n/a
26	chr5:68856062-68856112	NB4	blood:	n/a
27	chr5:68856077-68856127	HRCEpiC	kidney:	n/a
28	chr5:68868293-68868343	MCF-7	breast:	n/a
29	chr5:68855873-68855923	Hepatocyte	liver:	n/a
30	chr5:68855873-68855923	AG04450	lung:	fetal
31	chr5:68855873-68855923	AoSMC	blood vessel:	n/a
32	chr5:68856077-68856127	GM12891	blood:	n/a
33	chr5:68857760-68857810	CMK	blood:	n/a
34	chr5:68855560-68855610	HCM	heart:	n/a
35	chr5:68856077-68856127	NHBE	bronchial:	n/a
36	chr5:68856077-68856127	AG04450	lung:	fetal
37	chr5:68859882-68859932	NT2-D1	testis:	n/a
38	chr5:68856065-68856115	GM12891	blood:	n/a
39	chr5:68855560-68855610	NH-A	brain:	n/a
40	chr5:68855810-68855860	HPAEpiC	pulmonary alveolar:	n/a
41	chr5:68855560-68855610	K562	blood:	n/a
42	chr5:68855873-68855923	SK-N-SH	brain:	n/a
43	chr5:68852996-68853046	HEK293	kidney:	embryo
44	chr5:68859882-68859932	AG04450	lung:	fetal
45	chr5:68859882-68859932	HRPEpiC	eye:	n/a
46	chr5:68852996-68853046	AG04450	lung:	fetal
47	chr5:68855810-68855860	ovcar-3	ovarian:	n/a
48	chr5:68855873-68855923	AG09319	gingival:	n/a
49	chr5:68859882-68859932	H1-hESC	embryonic stem cell:	embryo
50	chr5:68855560-68855610	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:68791729..68794377-chr5:68827769..68829901,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCLN-1	chr5:68860927-68860960	NONHSAT101929
2	lnc-GTF2H2C-2	chr5:68915841-68915892	NONHSAT101932
3	lnc-GTF2H2C-2	chr5:68914140-68914221	NONHSAT101932
4	lnc-GTF2H2C-1	chr5:68890071-68890550	NONHSAT101931
5	lnc-GTF2H2C-2	chr5:68914878-68915107	NONHSAT101932
6	lnc-OCLN-1	chr5:68858500-68858597	NONHSAT101929
7	lnc-GTF2H2C-1	chr5:68889300-68889532	NONHSAT101931
8	lnc-OCLN-1	chr5:68856086-68856428	NONHSAT101929

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GTF2H2D	hsa-miR-30a-5p	chr5:68888221-68888242

Variant related genes	Relation type
GTF2H2C	TF binding region
RNU6-724P	TF binding region
ENSG00000238740	TF binding region
OCLN	TF binding region
ENSG00000248477	TF binding region
GTF2H2C	CpG island
RNU6-724P	CpG island
ENSG00000238740	CpG island
OCLN	CpG island
ENSG00000248477	CpG island

Extended variants
information (count: 635 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:635 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35267603	chr5:68829049-68829050	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs146120447	chr5:68829079-68829080	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577458469	chr5:68829083-68829084	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536568771	chr5:68829095-68829096	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532803011	chr5:68829106-68829107	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548101305	chr5:68829131-68829132	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs6859722	chr5:68829207-68829208	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562804045	chr5:68829242-68829243	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs193224838	chr5:68829247-68829248	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185562603	chr5:68829290-68829291	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs386688894	chr5:68829315-68829316	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561253538	chr5:68829316-68829317	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528355219	chr5:68829318-68829319	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546417104	chr5:68829319-68829320	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571107388	chr5:68829335-68829336	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534971001	chr5:68829336-68829337	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532133970	chr5:68829407-68829408	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550653918	chr5:68829408-68829409	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568830752	chr5:68829410-68829411	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs28612873	chr5:68829420-68829421	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs547859464	chr5:68829435-68829436	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77368551	chr5:68829459-68829460	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201460217	chr5:68829492-68829493	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140147362	chr5:68829507-68829508	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577272248	chr5:68829512-68829513	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559237516	chr5:68829565-68829566	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577526370	chr5:68829604-68829605	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538009777	chr5:68829610-68829611	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556642073	chr5:68829621-68829622	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574805439	chr5:68829626-68829627	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113659836	chr5:68829653-68829654	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560092846	chr5:68829655-68829656	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190208323	chr5:68829662-68829663	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540145768	chr5:68829686-68829687	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181757545	chr5:68829703-68829704	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562757437	chr5:68829752-68829753	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532195362	chr5:68829767-68829768	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530077993	chr5:68829776-68829777	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562635063	chr5:68829778-68829779	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529731003	chr5:68829797-68829798	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548212469	chr5:68829871-68829872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375698604	chr5:68830020-68830021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs256914	chr5:68830037-68830038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs560474393	chr5:68830051-68830052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369518478	chr5:68830551-68830552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372766137	chr5:68830632-68830633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201673353	chr5:68830633-68830634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377673456	chr5:68830663-68830664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369504788	chr5:68830680-68830681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574905779	chr5:68830755-68830756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
Autism	21865298	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Obesity	21131291	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68815800-68831000	Weak transcription	HepG2	liver
2	chr5:68821800-68830800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr5:68822400-68829400	Weak transcription	Fetal Stomach	stomach
4	chr5:68823600-68829200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr5:68824000-68830600	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr5:68824000-68855400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr5:68824200-68829600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:68824400-68832400	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr5:68826600-68830600	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr5:68827200-68829200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr5:68827200-68831000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr5:68827600-68829200	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr5:68827600-68829600	Strong transcription	Fetal Intestine Small	intestine
14	chr5:68827600-68830200	Weak transcription	GM12878-XiMat	blood
15	chr5:68827600-68830800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:68827800-68830200	Weak transcription	Brain Anterior Caudate	brain
17	chr5:68828000-68829600	Strong transcription	Liver	Liver
18	chr5:68828200-68829200	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr5:68828200-68830800	Weak transcription	Gastric	stomach
20	chr5:68828200-68840800	Weak transcription	Pancreas	Pancrea
21	chr5:68828800-68829800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:68829000-68829400	Enhancers	Fetal Intestine Large	intestine
23	chr5:68829000-68829800	Enhancers	Stomach Mucosa	stomach
24	chr5:68829200-68829400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr5:68829200-68829400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr5:68829200-68829400	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr5:68829200-68829400	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr5:68829400-68829600	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr5:68829600-68831200	Weak transcription	Liver	Liver
30	chr5:68829600-68855400	Weak transcription	Fetal Intestine Small	intestine
31	chr5:68829800-68832000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:68840800-68841000	Enhancers	Pancreas	Pancrea
33	chr5:68840800-68841000	Enhancers	HepG2	liver
34	chr5:68841000-68841200	Weak transcription	Pancreas	Pancrea
35	chr5:68841000-68855200	Weak transcription	HepG2	liver
36	chr5:68844400-68855400	Weak transcription	Fetal Intestine Large	intestine
37	chr5:68845800-68855600	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr5:68855000-68855200	Enhancers	Dnd41	blood
39	chr5:68855000-68855600	Enhancers	Primary T cells fromperipheralblood	blood
40	chr5:68855200-68855400	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr5:68855200-68855400	Enhancers	Adipose Nuclei	Adipose
42	chr5:68855200-68855400	Enhancers	Liver	Liver
43	chr5:68855200-68855400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr5:68855200-68855400	Enhancers	HepG2	liver
45	chr5:68855200-68855400	Enhancers	HUVEC	blood vessel
46	chr5:68855200-68855600	Enhancers	Right Atrium	heart
47	chr5:68855200-68855600	Flanking Active TSS	Dnd41	blood
48	chr5:68855200-68855800	Enhancers	Fetal Brain Male	brain
49	chr5:68855200-68856800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr5:68855200-68857000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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