Variant report

Variant	nsv882189
Chromosome Location	chr5:74356857-74478078
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	ARID3A	chr5:74391290-74391528	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:74463323-74463328	HepG2	liver:	n/a	n/a
3	ATF2	chr5:74382845-74383273	GM12878	blood:	n/a	n/a
4	ATF3	chr5:74391161-74391637	HCT-116	colon:	n/a	n/a
5	BATF	chr5:74382894-74383194	GM12878	blood:	n/a	chr5:74383066-74383077
6	BATF	chr5:74382934-74383265	GM12878	blood:	n/a	chr5:74383066-74383077
7	BCL11A	chr5:74382987-74383167	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:74382912-74383310	GM12878	blood:	n/a	n/a
9	BCL3	chr5:74382964-74383215	GM12878	blood:	n/a	n/a
10	BCL3	chr5:74442051-74442314	GM12878	blood:	n/a	n/a
11	BCL3	chr5:74382922-74383260	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:74361423-74361553	HepG2	liver:	n/a	n/a
13	BRCA1	chr5:74409126-74409996	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr5:74387620-74387635	GM12878	blood:	n/a	n/a
15	BRCA1	chr5:74407638-74408236	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr5:74391238-74391645	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr5:74457355-74457583	K562	blood:	n/a	n/a
18	CBX3	chr5:74463153-74463586	HCT-116	colon:	n/a	n/a
19	CEBPB	chr5:74367799-74368137	Hela-S3	cervix:	n/a	chr5:74367892-74367905
20	CEBPB	chr5:74391164-74391761	HCT-116	colon:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
21	CEBPB	chr5:74391211-74391662	HCT-116	colon:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
22	CEBPB	chr5:74371109-74371401	HepG2	liver:	n/a	chr5:74371222-74371235 chr5:74371224-74371233 chr5:74371222-74371233 chr5:74371224-74371233 chr5:74371224-74371233 chr5:74371224-74371233 chr5:74371222-74371235 chr5:74371224-74371235
23	CEBPB	chr5:74356648-74356887	IMR90	lung:	n/a	chr5:74356752-74356763
24	CEBPB	chr5:74454985-74455100	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr5:74384227-74385305	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:74466982-74467091	K562	blood:	n/a	chr5:74467037-74467048
27	CEBPB	chr5:74454948-74455035	A549	lung:	n/a	n/a
28	CEBPB	chr5:74391282-74391485	HepG2	liver:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
29	CEBPB	chr5:74441751-74441886	HepG2	liver:	n/a	chr5:74441789-74441800 chr5:74441789-74441802 chr5:74441789-74441802 chr5:74441790-74441801
30	CEBPB	chr5:74391225-74391610	MCF-7	breast:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
31	CEBPB	chr5:74391206-74391531	IMR90	lung:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
32	CEBPB	chr5:74391179-74391555	HepG2	liver:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
33	CEBPB	chr5:74371123-74371342	K562	blood:	n/a	chr5:74371222-74371235 chr5:74371224-74371233 chr5:74371222-74371233 chr5:74371224-74371233 chr5:74371224-74371233 chr5:74371224-74371233 chr5:74371222-74371235 chr5:74371224-74371235
34	CEBPB	chr5:74391206-74391548	A549	lung:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
35	CEBPB	chr5:74412703-74413006	HepG2	liver:	n/a	n/a
36	CEBPB	chr5:74371141-74371351	A549	lung:	n/a	chr5:74371222-74371235 chr5:74371224-74371233 chr5:74371222-74371233 chr5:74371224-74371233 chr5:74371224-74371233 chr5:74371224-74371233 chr5:74371222-74371235 chr5:74371224-74371235
37	CEBPB	chr5:74391178-74391557	A549	lung:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
38	CEBPB	chr5:74391183-74391610	MCF-7	breast:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
39	CEBPB	chr5:74466954-74467123	HepG2	liver:	n/a	chr5:74467037-74467048
40	CEBPB	chr5:74454858-74455117	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:74367208-74367539	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr5:74409046-74409977	Hela-S3	cervix:	n/a	chr5:74409548-74409560
43	CEBPB	chr5:74391238-74391506	K562	blood:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
44	CEBPB	chr5:74391150-74392563	Hela-S3	cervix:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
45	CEBPB	chr5:74356651-74356897	HepG2	liver:	n/a	chr5:74356752-74356763
46	CEBPB	chr5:74391261-74391509	ECC-1	luminal epithelium:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
47	CEBPB	chr5:74391237-74391488	HepG2	liver:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
48	CEBPB	chr5:74391213-74391613	A549	lung:	n/a	chr5:74391339-74391350 chr5:74391362-74391373
49	CEBPB	chr5:74407444-74408246	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr5:74407682-74408091	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74438852-74438902	AG04449	skin:	fetal
2	chr5:74438852-74438902	SAEC	small airway:	n/a
3	chr5:74438852-74438902	A549	lung:	n/a
4	chr5:74438852-74438902	GM06990	blood:	n/a
5	chr5:74438852-74438902	HEEpiC	esophagus:	n/a
6	chr5:74438852-74438902	GM12891	blood:	n/a
7	chr5:74438852-74438902	CMK	blood:	n/a
8	chr5:74438852-74438902	PrEC	prostate:	n/a
9	chr5:74438852-74438902	ProgFib	skin:	n/a
10	chr5:74438852-74438902	HIPEpiC	eye:	n/a
11	chr5:74438852-74438902	AG04450	lung:	fetal
12	chr5:74438852-74438902	HRCEpiC	kidney:	n/a
13	chr5:74438852-74438902	PFSK-1	brain:	n/a
14	chr5:74438852-74438902	ECC-1	luminal epithelium:	n/a
15	chr5:74438852-74438902	AG09309	skin:	n/a
16	chr5:74438852-74438902	NT2-D1	testis:	n/a
17	chr5:74438852-74438902	HCT-116	colon:	n/a
18	chr5:74438852-74438902	HEK293	kidney:	embryo
19	chr5:74438852-74438902	SK-N-MC	brain:	n/a
20	chr5:74438852-74438902	HepG2	liver:	n/a
21	chr5:74438852-74438902	HRE	kidney:	n/a
22	chr5:74438852-74438902	LNCaP	prostate:	n/a
23	chr5:74438852-74438902	T-47D	breast:	n/a
24	chr5:74438852-74438902	IMR90	lung:	fetal
25	chr5:74438852-74438902	Jurkat	blood:	n/a
26	chr5:74438852-74438902	HCF	heart:	n/a
27	chr5:74438852-74438902	NHBE	bronchial:	n/a
28	chr5:74438852-74438902	NHDF-neo	bronchial:	n/a
29	chr5:74438852-74438902	Caco-2	colon:	n/a
30	chr5:74438852-74438902	HPAEpiC	pulmonary alveolar:	n/a
31	chr5:74438852-74438902	SK-N-SH	brain:	n/a
32	chr5:74438852-74438902	HMEC	breast:	n/a
33	chr5:74438852-74438902	GM12892	blood:	n/a
34	chr5:74438852-74438902	SK-N-SH_RA	brain:	n/a
35	chr5:74438852-74438902	K562	blood:	n/a
36	chr5:74438852-74438902	SKMC	muscle:	n/a
37	chr5:74438852-74438902	ovcar-3	ovarian:	n/a
38	chr5:74438852-74438902	AG09319	gingival:	n/a
39	chr5:74438852-74438902	HL-60	blood:	n/a
40	chr5:74438852-74438902	U87	brain:	n/a
41	chr5:74438852-74438902	NB4	blood:	n/a
42	chr5:74438852-74438902	HUVEC	blood vessel:	n/a
43	chr5:74438852-74438902	HRPEpiC	eye:	n/a
44	chr5:74438852-74438902	GM19239	blood:	n/a
45	chr5:74438852-74438902	H1-hESC	embryonic stem cell:	embryo
46	chr5:74438852-74438902	HNPCEpiC	eye:	n/a
47	chr5:74438852-74438902	Hela-S3	cervix:	n/a
48	chr5:74438852-74438902	HCPEpiC	choroid plexus:	n/a
49	chr5:74438852-74438902	HAEpiC	amniotic membrane:	n/a
50	chr5:74438852-74438902	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:74398898..74401626-chr5:74404084..74405845,2	K562	blood:
2	chr5:74439700..74441214-chr5:76362795..76365262,2	K562	blood:
3	chr5:74409705..74412287-chr5:74414282..74416485,2	K562	blood:
4	chr5:74398898..74401626-chr5:74404084..74405845,2	K562	blood:
5	chr5:74379971..74382375-chr5:74387089..74390026,2	K562	blood:
6	chr5:74379971..74382375-chr5:74387089..74390026,2	K562	blood:
7	chr5:74459995..74462741-chr5:74463456..74465776,2	K562	blood:
8	chr5:74348653..74349615-chr5:74462874..74463564,2	MCF-7	breast:
9	chr5:74409705..74412287-chr5:74414282..74416485,2	K562	blood:
10	chr5:74349068..74351249-chr5:74356524..74358401,2	MCF-7	breast:

Variant related genes	Relation type
ANKRD31	TF binding region
ANKRD31	CpG island
ENSG00000145700	chromatin interactions
ENSG00000250889	chromatin interactions

Extended variants
information (count: 3613 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3613 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7700965	chr5:74356857-74356858	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182580470	chr5:74356906-74356907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544058955	chr5:74356907-74356908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149070256	chr5:74356912-74356913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376914922	chr5:74356991-74356992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186572244	chr5:74357006-74357007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs61688563	chr5:74357094-74357095	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs574778244	chr5:74357138-74357139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs80276240	chr5:74357157-74357158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191423917	chr5:74357216-74357217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566414259	chr5:74357220-74357221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144633069	chr5:74357244-74357245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551843758	chr5:74357268-74357269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568657283	chr5:74357358-74357359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183630869	chr5:74357375-74357376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111723275	chr5:74357376-74357377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574561522	chr5:74357395-74357396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141492894	chr5:74357461-74357462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs10214239	chr5:74357475-74357476	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs188566000	chr5:74357574-74357575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146279412	chr5:74357577-74357578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562951342	chr5:74357582-74357583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192406673	chr5:74357610-74357611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372391314	chr5:74357715-74357716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532375959	chr5:74357741-74357742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183404985	chr5:74357754-74357755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186531530	chr5:74357763-74357764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113362417	chr5:74357767-74357768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191364020	chr5:74357794-74357795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184554439	chr5:74357807-74357808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370175752	chr5:74357832-74357833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189874640	chr5:74357847-74357848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568595891	chr5:74357856-74357857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552656771	chr5:74357879-74357880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548000648	chr5:74357933-74357934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568207820	chr5:74357949-74357950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs59992948	chr5:74357966-74357967	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs150572506	chr5:74358007-74358008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570788190	chr5:74358038-74358039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539830389	chr5:74358119-74358120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556565482	chr5:74358124-74358125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112991630	chr5:74358127-74358128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571671117	chr5:74358148-74358149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192780015	chr5:74358174-74358175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs115967238	chr5:74358255-74358256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145456079	chr5:74358306-74358307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564416884	chr5:74358341-74358342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533479744	chr5:74358417-74358418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185262110	chr5:74358513-74358514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140731097	chr5:74358526-74358527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Thoracic aortic aneurysm	21092924	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
Spinal muscular atrophy	21762474	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
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	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74350200-74357200	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr5:74350400-74360000	Enhancers	Fetal Thymus	thymus
3	chr5:74350600-74357400	Enhancers	Primary T cells fromperipheralblood	blood
4	chr5:74350800-74357200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr5:74350800-74357400	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr5:74350800-74359600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr5:74350800-74367600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:74351000-74357000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
9	chr5:74352600-74357000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr5:74352600-74357200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr5:74355600-74359000	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr5:74355600-74359400	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr5:74355600-74359600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr5:74355600-74360400	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr5:74355800-74359800	Enhancers	Primary T cells from cord blood	blood
16	chr5:74355800-74360200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr5:74356200-74359800	Enhancers	Thymus	Thymus
18	chr5:74356400-74358200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr5:74357000-74358200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr5:74357400-74357800	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr5:74357400-74358600	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr5:74357800-74360000	Enhancers	Primary T cells fromperipheralblood	blood
23	chr5:74358200-74358400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr5:74358200-74359600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
25	chr5:74358600-74360200	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr5:74359000-74359200	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr5:74359000-74359600	Enhancers	GM12878-XiMat	blood
28	chr5:74359000-74359800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr5:74359400-74362200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr5:74359600-74360200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr5:74359800-74360200	Weak transcription	Primary T cells from cord blood	blood
32	chr5:74359800-74360200	Weak transcription	Thymus	Thymus
33	chr5:74359800-74360400	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr5:74360000-74361400	Weak transcription	Fetal Thymus	thymus
35	chr5:74360200-74360400	Enhancers	Primary T cells from cord blood	blood
36	chr5:74360200-74360400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr5:74360200-74360400	Enhancers	Thymus	Thymus
38	chr5:74360200-74361600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr5:74360200-74362000	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr5:74360400-74361400	Weak transcription	Primary T cells from cord blood	blood
41	chr5:74360400-74361600	Weak transcription	Thymus	Thymus
42	chr5:74360400-74362200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr5:74360400-74363000	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr5:74361400-74363600	Enhancers	Fetal Thymus	thymus
45	chr5:74361400-74363800	Enhancers	Primary T cells from cord blood	blood
46	chr5:74361600-74362600	Enhancers	Thymus	Thymus
47	chr5:74361600-74363600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr5:74362000-74362400	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr5:74362200-74363000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr5:74362600-74363000	Weak transcription	Thymus	Thymus

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