Variant report

Variant	nsv882206
Chromosome Location	chr5:75676658-75746813
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1220)
CpG islands
(count:978)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:75698128-75698510	K562	blood:	n/a	n/a
2	ARID3A	chr5:75699736-75700579	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:75698892-75699267	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:75735110-75735253	HepG2	liver:	n/a	n/a
5	ATF1	chr5:75702435-75702701	K562	blood:	n/a	n/a
6	ATF1	chr5:75698352-75699185	K562	blood:	n/a	n/a
7	ATF2	chr5:75699475-75699882	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr5:75698195-75699207	GM12878	blood:	n/a	n/a
9	ATF2	chr5:75698174-75699090	GM12878	blood:	n/a	n/a
10	BACH1	chr5:75698288-75700186	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:75698603-75699053	K562	blood:	n/a	n/a
12	BATF	chr5:75698364-75698949	GM12878	blood:	n/a	n/a
13	BATF	chr5:75698367-75698715	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:75698654-75698981	GM12878	blood:	n/a	chr5:75698791-75698800
15	BCL11A	chr5:75698357-75698629	GM12878	blood:	n/a	chr5:75698498-75698507
16	BCL11A	chr5:75698502-75698790	GM12878	blood:	n/a	n/a
17	BCL3	chr5:75721723-75722088	GM12878	blood:	n/a	n/a
18	BCLAF1	chr5:75698544-75699379	GM12878	blood:	n/a	chr5:75699121-75699134 chr5:75698791-75698800 chr5:75699281-75699294
19	BCLAF1	chr5:75698503-75699265	GM12878	blood:	n/a	chr5:75699121-75699134 chr5:75698791-75698800
20	BCLAF1	chr5:75700010-75700706	GM12878	blood:	n/a	n/a
21	BCLAF1	chr5:75700120-75700869	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:75699749-75700619	HepG2	liver:	n/a	n/a
23	BHLHE40	chr5:75697972-75699258	K562	blood:	n/a	chr5:75698929-75698945 chr5:75698937-75698953
24	BHLHE40	chr5:75698232-75699237	GM12878	blood:	n/a	chr5:75698929-75698945 chr5:75698937-75698953
25	BHLHE40	chr5:75701026-75701229	GM12878	blood:	n/a	n/a
26	BHLHE40	chr5:75710505-75710723	K562	blood:	n/a	chr5:75710537-75710550 chr5:75710539-75710548 chr5:75710539-75710548 chr5:75710533-75710554 chr5:75710538-75710547
27	BHLHE40	chr5:75699774-75700994	K562	blood:	n/a	n/a
28	BHLHE40	chr5:75699762-75700724	GM12878	blood:	n/a	n/a
29	BRCA1	chr5:75699806-75699942	HepG2	liver:	n/a	n/a
30	BRCA1	chr5:75699625-75699856	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr5:75698994-75699134	HepG2	liver:	n/a	n/a
32	CBX3	chr5:75697937-75699229	K562	blood:	n/a	n/a
33	CBX3	chr5:75699995-75700767	K562	blood:	n/a	n/a
34	CCNT2	chr5:75702406-75702614	K562	blood:	n/a	n/a
35	CCNT2	chr5:75698149-75699533	K562	blood:	n/a	chr5:75698222-75698242 chr5:75698568-75698588
36	CEBPB	chr5:75677550-75677741	K562	blood:	n/a	n/a
37	CEBPB	chr5:75732894-75733005	HepG2	liver:	n/a	chr5:75732932-75732943
38	CEBPB	chr5:75699668-75699790	K562	blood:	n/a	n/a
39	CEBPB	chr5:75699983-75700513	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:75698779-75699069	HepG2	liver:	n/a	n/a
41	CEBPB	chr5:75685676-75686030	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:75681495-75681716	K562	blood:	n/a	chr5:75681622-75681633
43	CEBPB	chr5:75698191-75699037	GM12878	blood:	n/a	n/a
44	CEBPB	chr5:75687446-75687753	K562	blood:	n/a	chr5:75687589-75687600 chr5:75687589-75687602 chr5:75687590-75687601 chr5:75687721-75687734 chr5:75687589-75687602
45	CEBPB	chr5:75681473-75681756	HepG2	liver:	n/a	chr5:75681622-75681633
46	CEBPB	chr5:75724246-75724362	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr5:75700102-75700476	K562	blood:	n/a	n/a
48	CEBPB	chr5:75687520-75687760	HepG2	liver:	n/a	chr5:75687589-75687600 chr5:75687589-75687602 chr5:75687590-75687601 chr5:75687721-75687734 chr5:75687589-75687602
49	CEBPB	chr5:75717991-75718198	HepG2	liver:	n/a	n/a
50	CEBPB	chr5:75737410-75737599	K562	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75698343-75698393	K562	blood:	n/a
2	chr5:75701065-75701115	HCPEpiC	choroid plexus:	n/a
3	chr5:75698343-75698393	K562	blood:	n/a
4	chr5:75701065-75701115	HCPEpiC	choroid plexus:	n/a
5	chr5:75703329-75703379	HIPEpiC	eye:	n/a
6	chr5:75698732-75698782	Jurkat	blood:	n/a
7	chr5:75696047-75696097	Jurkat	blood:	n/a
8	chr5:75696047-75696097	HAEpiC	amniotic membrane:	n/a
9	chr5:75698824-75698874	HUVEC	blood vessel:	n/a
10	chr5:75698732-75698782	HepG2	liver:	n/a
11	chr5:75698824-75698874	BE2_C	brain:	n/a
12	chr5:75698461-75698511	IMR90	lung:	fetal
13	chr5:75698824-75698874	AG09309	skin:	n/a
14	chr5:75701460-75701510	SKMC	muscle:	n/a
15	chr5:75699748-75699798	CMK	blood:	n/a
16	chr5:75703329-75703379	AG04450	lung:	fetal
17	chr5:75698461-75698511	HCPEpiC	choroid plexus:	n/a
18	chr5:75699748-75699798	HNPCEpiC	eye:	n/a
19	chr5:75722317-75722367	HUVEC	blood vessel:	n/a
20	chr5:75698309-75698359	U87	brain:	n/a
21	chr5:75701065-75701115	SK-N-SH	brain:	n/a
22	chr5:75703329-75703379	HCT-116	colon:	n/a
23	chr5:75698824-75698874	NHDF-neo	bronchial:	n/a
24	chr5:75698508-75698558	AG10803	skin:	n/a
25	chr5:75698343-75698393	Hepatocyte	liver:	n/a
26	chr5:75722317-75722367	Caco-2	colon:	n/a
27	chr5:75696047-75696097	SK-N-MC	brain:	n/a
28	chr5:75737331-75737381	ECC-1	luminal epithelium:	n/a
29	chr5:75699284-75699334	HEEpiC	esophagus:	n/a
30	chr5:75698732-75698782	SAEC	small airway:	n/a
31	chr5:75699865-75699915	ovcar-3	ovarian:	n/a
32	chr5:75699748-75699798	K562	blood:	n/a
33	chr5:75740907-75740957	HIPEpiC	eye:	n/a
34	chr5:75701065-75701115	Hela-S3	cervix:	n/a
35	chr5:75740907-75740957	HRPEpiC	eye:	n/a
36	chr5:75699748-75699798	AG10803	skin:	n/a
37	chr5:75698343-75698393	AG10803	skin:	n/a
38	chr5:75698824-75698874	ProgFib	skin:	n/a
39	chr5:75698309-75698359	HNPCEpiC	eye:	n/a
40	chr5:75722317-75722367	A549	lung:	n/a
41	chr5:75698508-75698558	NHBE	bronchial:	n/a
42	chr5:75699865-75699915	NHBE	bronchial:	n/a
43	chr5:75722317-75722367	BJ	skin:	n/a
44	chr5:75699865-75699915	H1-hESC	embryonic stem cell:	embryo
45	chr5:75696047-75696097	HNPCEpiC	eye:	n/a
46	chr5:75737331-75737381	BJ	skin:	n/a
47	chr5:75698824-75698874	NT2-D1	testis:	n/a
48	chr5:75703329-75703379	HEEpiC	esophagus:	n/a
49	chr5:75696047-75696097	ovcar-3	ovarian:	n/a
50	chr5:75699284-75699334	A549	lung:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:75676600..75679486-chr5:75697591..75699159,2	K562	blood:
2	chr5:75670460..75672196-chr5:75679866..75681597,2	MCF-7	breast:
3	chr5:75661178..75661769-chr5:75698453..75699020,2	K562	blood:
4	chr5:75685103..75687444-chr5:75693897..75695814,2	K562	blood:
5	chr5:75700203..75702691-chr5:75717869..75720332,2	MCF-7	breast:
6	chr5:75682196..75684123-chr5:75696956..75698621,2	MCF-7	breast:
7	chr5:75685103..75687444-chr5:75693897..75695814,2	K562	blood:
8	chr5:75699529..75700200-chr5:75878922..75879530,2	K562	blood:
9	chr5:75691045..75693619-chr5:75698895..75701468,2	K562	blood:
10	chr5:75697502..75699104-chr5:75703353..75706054,2	K562	blood:
11	chr5:75706305..75708595-chr5:75709828..75711425,2	K562	blood:
12	chr5:75669499..75672050-chr5:75695299..75697873,2	MCF-7	breast:
13	chr5:75697576..75700443-chr5:75733295..75734866,2	K562	blood:
14	chr5:75682196..75684123-chr5:75696956..75698621,2	MCF-7	breast:
15	chr5:75697668..75699734-chr5:75720568..75722803,2	K562	blood:
16	chr5:75717306..75720750-chr5:75722224..75725340,4	K562	blood:
17	chr5:75676963..75680213-chr5:75697591..75700759,3	K562	blood:
18	chr5:75706305..75708595-chr5:75709828..75711425,2	K562	blood:
19	chr5:75679957..75682870-chr5:75683054..75686603,3	K562	blood:
20	chr5:75673917..75676615-chr5:75683010..75685997,3	K562	blood:
21	chr12:4393097..4393597-chr5:75728895..75729427,2	NB4	blood:
22	chr5:75717306..75720750-chr5:75722224..75725340,4	K562	blood:
23	chr5:75694312..75697795-chr5:75697903..75700396,3	K562	blood:
24	chr5:75679957..75682870-chr5:75683054..75686603,3	K562	blood:

No data

Variant related genes	Relation type
IQGAP2	TF binding region
IQGAP2	CpG island
ENSG00000145703	chromatin interactions

Extended variants
information (count: 2443 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2443 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1811340	chr5:75676658-75676659	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150489570	chr5:75676668-75676669	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532487134	chr5:75676703-75676704	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs552598403	chr5:75676726-75676727	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569158934	chr5:75676748-75676749	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs182688547	chr5:75676770-75676771	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs187108448	chr5:75676793-75676794	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs112518133	chr5:75676824-75676825	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200198851	chr5:75676863-75676864	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs144031225	chr5:75676897-75676898	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs190116235	chr5:75676916-75676917	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs572934983	chr5:75676975-75676976	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538365964	chr5:75677007-75677008	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs558576945	chr5:75677055-75677056	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182758424	chr5:75677093-75677094	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs543787974	chr5:75677149-75677150	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs560876178	chr5:75677152-75677153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs187374617	chr5:75677164-75677165	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs540074859	chr5:75677214-75677215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560096276	chr5:75677215-75677216	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs532285286	chr5:75677232-75677233	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs201054526	chr5:75677234-75677235	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs552410355	chr5:75677235-75677236	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572768918	chr5:75677334-75677335	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs192204978	chr5:75677337-75677338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs544888008	chr5:75677352-75677353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564864075	chr5:75677361-75677362	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs534488380	chr5:75677378-75677379	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs11959751	chr5:75677395-75677396	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs185640681	chr5:75677407-75677408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs541966736	chr5:75677434-75677435	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs188950983	chr5:75677438-75677439	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs539997001	chr5:75677490-75677491	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs530930588	chr5:75677518-75677519	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs568911563	chr5:75677577-75677578	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs201964126	chr5:75677588-75677589	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs28489639	chr5:75677636-75677637	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs147297074	chr5:75677647-75677648	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs112558046	chr5:75677663-75677664	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs574051207	chr5:75677670-75677671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113294774	chr5:75677831-75677832	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs554004448	chr5:75677832-75677833	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs112191614	chr5:75677837-75677838	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs80185295	chr5:75677884-75677885	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537433647	chr5:75677894-75677895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs530502874	chr5:75677979-75677980	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs79660415	chr5:75678028-75678029	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs890709	chr5:75678067-75678068	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs542284822	chr5:75678079-75678080	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs144476224	chr5:75678101-75678102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
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	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1754 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75669000-75676800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr5:75669000-75682400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr5:75674000-75677400	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr5:75674200-75677200	Enhancers	Primary hematopoietic stem cells	blood
5	chr5:75674200-75677200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr5:75674600-75677000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
7	chr5:75675000-75676800	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr5:75675000-75677000	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr5:75675400-75677600	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr5:75675400-75678400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:75675400-75685800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr5:75675600-75676800	Enhancers	Duodenum Mucosa	Duodenum
13	chr5:75675600-75679000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr5:75675800-75678000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr5:75675800-75678800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr5:75675800-75679000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr5:75675800-75679000	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr5:75675800-75679000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr5:75675800-75679000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr5:75676000-75676800	Flanking Active TSS	HepG2	liver
21	chr5:75676000-75677000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:75676000-75677200	Enhancers	K562	blood
23	chr5:75676000-75679000	Weak transcription	Primary T cells from cord blood	blood
24	chr5:75676200-75676800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr5:75676200-75676800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr5:75676200-75677000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr5:75676200-75677000	Enhancers	Liver	Liver
28	chr5:75676200-75677400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr5:75676200-75679800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:75676400-75676800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr5:75676400-75676800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr5:75676400-75676800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:75676400-75677000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr5:75676400-75677600	Enhancers	Placenta	Placenta
35	chr5:75676400-75678200	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr5:75676400-75679800	Weak transcription	Fetal Thymus	thymus
37	chr5:75676400-75679800	Weak transcription	Pancreas	Pancrea
38	chr5:75676600-75676800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr5:75676600-75677000	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr5:75676600-75679800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr5:75676800-75677200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr5:75676800-75678200	Enhancers	HepG2	liver
43	chr5:75676800-75678400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr5:75676800-75679800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr5:75676800-75680000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr5:75676800-75680200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr5:75676800-75681600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr5:75676800-75681800	Weak transcription	Duodenum Mucosa	Duodenum
49	chr5:75677000-75678000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr5:75677000-75679800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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