Variant report

Variant	nsv4790
Chromosome Location	chr5:35090745-35123632
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:149)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:149 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:35116040-35116365	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:35119785-35119867	K562	blood:	n/a	n/a
3	ARID3A	chr5:35095590-35095868	HepG2	liver:	n/a	n/a
4	ATF2	chr5:35117975-35118417	GM12878	blood:	n/a	n/a
5	BATF	chr5:35118026-35118361	GM12878	blood:	n/a	n/a
6	BATF	chr5:35118040-35118362	GM12878	blood:	n/a	n/a
7	BATF	chr5:35098340-35098686	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:35118107-35118332	GM12878	blood:	n/a	chr5:35118237-35118246 chr5:35118236-35118245
9	BCL11A	chr5:35118093-35118352	GM12878	blood:	n/a	chr5:35118237-35118246 chr5:35118236-35118245
10	CEBPB	chr5:35101372-35101662	A549	lung:	n/a	chr5:35101407-35101416 chr5:35101405-35101416 chr5:35101406-35101417 chr5:35101405-35101418
11	CEBPB	chr5:35098424-35098745	HepG2	liver:	n/a	chr5:35098620-35098631 chr5:35098620-35098633 chr5:35098578-35098589
12	CEBPB	chr5:35101274-35101783	HepG2	liver:	n/a	chr5:35101407-35101416 chr5:35101405-35101416 chr5:35101406-35101417 chr5:35101405-35101418
13	CEBPB	chr5:35101255-35101525	K562	blood:	n/a	chr5:35101407-35101416 chr5:35101405-35101416 chr5:35101406-35101417 chr5:35101405-35101418
14	CEBPB	chr5:35116049-35116347	HepG2	liver:	n/a	chr5:35116198-35116211
15	CTCF	chr5:35118900-35119050	Caco-2	colon:	n/a	n/a
16	CTCF	chr5:35104745-35104973	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr5:35104840-35104990	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr5:35104840-35104990	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr5:35104820-35104970	MCF-7	breast:	n/a	n/a
20	CTCF	chr5:35104833-35104889	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr5:35104760-35104910	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr5:35104760-35104910	Caco-2	colon:	n/a	n/a
23	CTCF	chr5:35104760-35104910	HEK293	kidney:	n/a	n/a
24	CTCF	chr5:35104840-35104990	HepG2	liver:	n/a	n/a
25	CTCF	chr5:35105120-35105211	MCF-7	breast:	n/a	n/a
26	CTCF	chr5:35104814-35104948	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:35104852-35104937	HepG2	liver:	n/a	n/a
28	CTCF	chr5:35104900-35104976	LNCaP	prostate:	n/a	n/a
29	CTCF	chr5:35102580-35102730	GM12866	blood:	n/a	n/a
30	CTCF	chr5:35119460-35119610	GM12869	blood:	n/a	n/a
31	CTCF	chr5:35104794-35104921	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:35104796-35104936	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:35118937-35119074	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr5:35118820-35118970	GM06990	blood:	n/a	n/a
35	CTCF	chr5:35091260-35091410	NHEK	skin:	n/a	n/a
36	CTCF	chr5:35105130-35105202	MCF-7	breast:	n/a	n/a
37	CTCF	chr5:35104799-35104971	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:35113512-35113581	GM10248	blood:	n/a	n/a
39	CTCF	chr5:35104822-35104933	MCF-7	breast:	n/a	n/a
40	E2F6	chr5:35118783-35119269	H1-hESC	embryonic stem cell:	n/a	n/a
41	E2F6	chr5:35112308-35112968	H1-hESC	embryonic stem cell:	n/a	n/a
42	E2F6	chr5:35112497-35112843	H1-hESC	embryonic stem cell:	n/a	n/a
43	EP300	chr5:35119355-35119720	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr5:35119400-35119751	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr5:35115923-35116452	HepG2	liver:	n/a	chr5:35116097-35116111 chr5:35116330-35116339
46	EP300	chr5:35119116-35120411	SK-N-SH	brain:	n/a	n/a
47	FOS	chr5:35118073-35118455	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr5:35119330-35119561	MCF10A-Er-Src	breast:	n/a	chr5:35119394-35119406 chr5:35119397-35119408 chr5:35119395-35119405 chr5:35119395-35119405
49	FOS	chr5:35098418-35098672	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr5:35118064-35118576	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:35092023-35092073	HMEC	breast:	n/a
2	chr5:35092023-35092073	HRCEpiC	kidney:	n/a
3	chr5:35092023-35092073	HNPCEpiC	eye:	n/a
4	chr5:35092023-35092073	BE2_C	brain:	n/a
5	chr5:35092023-35092073	IMR90	lung:	fetal
6	chr5:35092023-35092073	Hepatocyte	liver:	n/a
7	chr5:35092023-35092073	PFSK-1	brain:	n/a
8	chr5:35092023-35092073	AG09309	skin:	n/a
9	chr5:35092023-35092073	U87	brain:	n/a
10	chr5:35092023-35092073	NT2-D1	testis:	n/a
11	chr5:35092023-35092073	AG04449	skin:	fetal
12	chr5:35092023-35092073	AoSMC	blood vessel:	n/a
13	chr5:35092023-35092073	HAEpiC	amniotic membrane:	n/a
14	chr5:35092023-35092073	NHDF-neo	bronchial:	n/a
15	chr5:35092023-35092073	HUVEC	blood vessel:	n/a
16	chr5:35092023-35092073	SK-N-MC	brain:	n/a
17	chr5:35092023-35092073	HL-60	blood:	n/a
18	chr5:35092023-35092073	BJ	skin:	n/a
19	chr5:35092023-35092073	AG09319	gingival:	n/a
20	chr5:35092023-35092073	GM19239	blood:	n/a
21	chr5:35092023-35092073	HEEpiC	esophagus:	n/a
22	chr5:35092023-35092073	SAEC	small airway:	n/a
23	chr5:35092023-35092073	LNCaP	prostate:	n/a
24	chr5:35092023-35092073	HRE	kidney:	n/a
25	chr5:35092023-35092073	HCT-116	colon:	n/a
26	chr5:35092023-35092073	PrEC	prostate:	n/a
27	chr5:35092023-35092073	ProgFib	skin:	n/a
28	chr5:35092023-35092073	HEK293	kidney:	embryo
29	chr5:35092023-35092073	HCM	heart:	n/a
30	chr5:35092023-35092073	NHBE	bronchial:	n/a
31	chr5:35092023-35092073	MCF10A-Er-Src	breast:	n/a
32	chr5:35092023-35092073	CMK	blood:	n/a
33	chr5:35092023-35092073	GM12878	blood:	n/a
34	chr5:35092023-35092073	AG04450	lung:	fetal
35	chr5:35092023-35092073	GM12892	blood:	n/a
36	chr5:35092023-35092073	MCF-7	breast:	n/a
37	chr5:35092023-35092073	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:35092023-35092073	T-47D	breast:	n/a
39	chr5:35092023-35092073	Hela-S3	cervix:	n/a
40	chr5:35092023-35092073	ovcar-3	ovarian:	n/a
41	chr5:35092023-35092073	Caco-2	colon:	n/a
42	chr5:35092023-35092073	GM12891	blood:	n/a
43	chr5:35092023-35092073	HCF	heart:	n/a
44	chr5:35092023-35092073	HepG2	liver:	n/a
45	chr5:35092023-35092073	SKMC	muscle:	n/a
46	chr5:35092023-35092073	SK-N-SH_RA	brain:	n/a
47	chr5:35092023-35092073	RPTEC	kidney:	n/a
48	chr5:35092023-35092073	A549	lung:	n/a
49	chr5:35092023-35092073	AG10803	skin:	n/a
50	chr5:35092023-35092073	PANC-1	pancreas:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:35119161..35121862-chr5:35122776..35125240,2	MCF-7	breast:
2	chr5:35119161..35121862-chr5:35122776..35125240,2	MCF-7	breast:
3	chr5:35091355..35093791-chr5:35095839..35097534,2	K562	blood:
4	chr5:35093395..35095961-chr5:35096148..35098601,3	MCF-7	breast:
5	chr5:35091355..35093791-chr5:35095839..35097534,2	K562	blood:
6	chr5:35113747..35115676-chr5:35118323..35120483,2	K562	blood:
7	chr5:35118263..35120993-chr5:35135116..35136770,2	MCF-7	breast:
8	chr5:35093395..35095961-chr5:35096148..35098601,3	MCF-7	breast:
9	chr5:35121930..35123865-chr5:35177997..35180572,2	MCF-7	breast:
10	chr5:35101633..35104632-chr8:30579234..30581391,2	MCF-7	breast:
11	chr5:35121026..35123400-chr5:35145194..35147687,3	MCF-7	breast:
12	chr5:35113747..35115676-chr5:35118323..35120483,2	K562	blood:

No data

Variant related genes	Relation type
PRLR	TF binding region
PRLR	CpG island
ENSG00000113494	chromatin interactions

Extended variants
information (count: 1252 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1252 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181639277	chr5:35090746-35090747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558774755	chr5:35090747-35090748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552532329	chr5:35090749-35090750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572398012	chr5:35090751-35090752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541337538	chr5:35090785-35090786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185919592	chr5:35090827-35090828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536688037	chr5:35090835-35090836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs13175770	chr5:35090862-35090863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370814231	chr5:35090863-35090864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535303983	chr5:35090869-35090870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532542521	chr5:35090886-35090887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554800498	chr5:35090910-35090911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs40530	chr5:35090943-35090944	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs559596594	chr5:35090952-35090953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs71615844	chr5:35090975-35090976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571286125	chr5:35090991-35090992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150235769	chr5:35091014-35091015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554940537	chr5:35091017-35091018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs367951961	chr5:35091029-35091030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370294841	chr5:35091064-35091065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537035364	chr5:35091066-35091067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183342666	chr5:35091074-35091075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12153103	chr5:35091076-35091077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537601173	chr5:35091088-35091089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6875116	chr5:35091089-35091090	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs539201328	chr5:35091092-35091093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558687783	chr5:35091135-35091136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572310767	chr5:35091150-35091151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557095863	chr5:35091165-35091166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113880870	chr5:35091203-35091204	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373315914	chr5:35091204-35091205	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115387261	chr5:35091259-35091260	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543794296	chr5:35091284-35091285	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs563571892	chr5:35091288-35091289	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs199706792	chr5:35091289-35091290	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs577225145	chr5:35091322-35091323	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs546321356	chr5:35091340-35091341	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs559560234	chr5:35091342-35091343	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs535249764	chr5:35091437-35091438	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376617891	chr5:35091541-35091542	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371182450	chr5:35091543-35091544	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116803811	chr5:35091578-35091579	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548438520	chr5:35091606-35091607	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs16871725	chr5:35091622-35091623	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs530759879	chr5:35091643-35091644	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550542204	chr5:35091671-35091672	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573953288	chr5:35091691-35091692	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570363744	chr5:35091710-35091711	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539100945	chr5:35091742-35091743	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116170341	chr5:35091785-35091786	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Thoracic aortic aneurysm	21092924	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
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Breast cancer	21364760	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:195 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35061600-35096000	Weak transcription	Gastric	stomach
2	chr5:35062600-35091600	Weak transcription	Colonic Mucosa	Colon
3	chr5:35064200-35091600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr5:35066400-35094600	Weak transcription	HepG2	liver
5	chr5:35080200-35093000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:35083600-35091600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr5:35083600-35094600	Weak transcription	Pancreas	Pancrea
8	chr5:35085400-35091400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr5:35088800-35114000	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr5:35089600-35091600	Weak transcription	Placenta	Placenta
11	chr5:35089800-35093000	Weak transcription	Fetal Intestine Large	intestine
12	chr5:35089800-35113800	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr5:35090000-35091400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr5:35090000-35091600	Weak transcription	NHDF-Ad	bronchial
15	chr5:35090000-35091800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr5:35090200-35091200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr5:35090200-35091400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr5:35090200-35091600	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr5:35090200-35091600	Weak transcription	Stomach Mucosa	stomach
20	chr5:35090200-35094600	Weak transcription	Liver	Liver
21	chr5:35090400-35091200	Weak transcription	Fetal Intestine Small	intestine
22	chr5:35090600-35091800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr5:35091200-35092000	Enhancers	H9 Cell Line	embryonic stem cell
24	chr5:35091200-35093400	Strong transcription	Fetal Intestine Small	intestine
25	chr5:35091400-35091600	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr5:35091400-35091800	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr5:35091600-35092000	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr5:35091600-35092000	Enhancers	Colonic Mucosa	Colon
29	chr5:35091600-35092000	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr5:35091600-35092000	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr5:35091600-35092200	Enhancers	Lung	lung
32	chr5:35091600-35092600	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr5:35091600-35092600	Enhancers	NHDF-Ad	bronchial
34	chr5:35091600-35092800	Strong transcription	Placenta	Placenta
35	chr5:35091600-35093000	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr5:35091600-35096600	Enhancers	Stomach Mucosa	stomach
37	chr5:35091800-35092400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr5:35091800-35092800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr5:35091800-35093200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr5:35092000-35092600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr5:35092000-35093000	Weak transcription	Colonic Mucosa	Colon
42	chr5:35092000-35093000	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr5:35092000-35093400	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr5:35092600-35096000	Weak transcription	NHDF-Ad	bronchial
45	chr5:35092800-35096200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr5:35092800-35100800	Weak transcription	Placenta	Placenta
47	chr5:35093000-35093400	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr5:35093000-35093600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr5:35093000-35093800	Enhancers	Colonic Mucosa	Colon
50	chr5:35093000-35093800	Enhancers	Fetal Intestine Large	intestine

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