Variant report

Variant	rs2617447
Chromosome Location	chr5:96267655-96267656
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:43)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:43 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RELA	chr5:96267211-96267767	GM12878	blood:	n/a	n/a
2	CHD1	chr5:96267264-96273025	GM12878	blood:	n/a	n/a
3	POLR2A	chr5:96267041-96268025	GM12878	blood:	n/a	n/a
4	TAF1	chr5:96267295-96267730	GM12878	blood:	n/a	n/a
5	BCL3	chr5:96267263-96267671	GM12878	blood:	n/a	n/a
6	POLR2A	chr5:96267158-96273083	GM12878	blood:	n/a	n/a
7	FOXM1	chr5:96267082-96267749	GM12878	blood:	n/a	n/a
8	POLR2A	chr5:96267251-96268072	GM12892	blood:	n/a	n/a
9	POLR2A	chr5:96267228-96267759	GM12891	blood:	n/a	n/a
10	NFIC	chr5:96266924-96269107	GM12878	blood:	n/a	n/a
11	CEBPB	chr5:96266972-96268131	GM12878	blood:	n/a	n/a
12	MTA3	chr5:96267180-96268478	GM12878	blood:	n/a	n/a
13	POLR2A	chr5:96267357-96267908	GM12891	blood:	n/a	n/a
14	POLR2A	chr5:96267177-96268091	GM12892	blood:	n/a	n/a
15	RELA	chr5:96267243-96267685	GM19099	blood:	n/a	n/a
16	PML	chr5:96266960-96273172	GM12878	blood:	n/a	n/a
17	TBP	chr5:96267306-96267656	K562	blood:	n/a	n/a
18	POLR2A	chr5:96266983-96268053	GM12878	blood:	n/a	n/a
19	TBL1XR1	chr5:96267548-96267727	K562	blood:	n/a	n/a
20	TBP	chr5:96267257-96268993	GM12878	blood:	n/a	n/a
21	POLR2A	chr5:96267068-96267847	GM12892	blood:	n/a	n/a
22	POLR2A	chr5:96267301-96267943	GM12878	blood:	n/a	n/a
23	POLR2A	chr5:96267385-96267724	GM12891	blood:	n/a	n/a
24	RELA	chr5:96267182-96268014	GM12891	blood:	n/a	n/a
25	EBF1	chr5:96267217-96267955	GM12878	blood:	n/a	n/a
26	GATA1	chr5:96267043-96269474	K562	blood:	n/a	chr5:96268501-96268511 chr5:96268719-96268740
27	PML	chr5:96267345-96267676	GM12878	blood:	n/a	n/a
28	MTA3	chr5:96267156-96268091	GM12878	blood:	n/a	n/a
29	POLR2A	chr5:96267275-96267660	GM12892	blood:	n/a	n/a
30	TBL1XR1	chr5:96267319-96268092	GM12878	blood:	n/a	n/a
31	MYC	chr5:96267311-96267739	NB4	blood:	n/a	n/a
32	ARID3A	chr5:96267508-96267811	K562	blood:	n/a	n/a
33	RUNX3	chr5:96267235-96267710	GM12878	blood:	n/a	n/a
34	ATF2	chr5:96267025-96267755	GM12878	blood:	n/a	n/a
35	POLR2A	chr5:96267218-96268373	GM12891	blood:	n/a	n/a
36	CUX1	chr5:96267307-96267834	GM12878	blood:	n/a	n/a
37	POLR2A	chr5:96267329-96267748	GM12891	blood:	n/a	n/a
38	RCOR1	chr5:96267189-96268305	GM12878	blood:	n/a	n/a
39	BCLAF1	chr5:96267187-96268004	GM12878	blood:	n/a	n/a
40	ATF2	chr5:96266952-96267661	GM12878	blood:	n/a	n/a
41	RCOR1	chr5:96267258-96267822	K562	blood:	n/a	n/a
42	RUNX3	chr5:96267053-96268098	GM12878	blood:	n/a	n/a
43	EP300	chr5:96267313-96268066	GM12878	blood:	n/a	chr5:96268042-96268056

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:96267069..96273023-chr5:96293959..96302488,9	K562	blood:
2	chr5:96210071..96212183-chr5:96265050..96268256,3	K562	blood:
3	chr5:96260085..96262647-chr5:96266778..96268827,2	K562	blood:
4	chr5:96212164..96213676-chr5:96267339..96268943,2	MCF-7	breast:
5	chr5:96141925..96145850-chr5:96265867..96272606,9	K562	blood:

No data

Variant related genes	Relation type
LNPEP	TF binding region
ENSG00000200884	Chromatin interaction
ENSG00000164307	Chromatin interaction
ENSG00000113441	Chromatin interaction
ENSG00000164308	Chromatin interaction

Extended variants
information (count: 116 )
Associated
traits (count: 19 )

rSNPs within LD-proxies of this variant (count:108)

rs_ID	r²[population]
rs10038651	0.86[EUR][1000 genomes]
rs10044354	0.88[CEU][hapmap];0.86[EUR][1000 genomes]
rs10051637	0.88[CEU][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10058476	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10077945	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10434709	0.84[CEU][hapmap]
rs1046395	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1046396	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10476696	0.86[EUR][1000 genomes]
rs11135484	0.84[CEU][hapmap]
rs1216566	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1216567	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1216571	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1230358	0.82[JPT][hapmap]
rs12516666	0.85[CEU][hapmap]
rs13167902	0.84[CEU][hapmap]
rs13170029	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13358339	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1363907	0.96[CEU][hapmap];0.82[CHB][hapmap];0.94[JPT][hapmap];0.87[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1363908	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1363974	0.88[CEU][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1363976	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1423357	0.89[CEU][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1423566	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1477364	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1544777	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1559355	0.85[CEU][hapmap]
rs1820148	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1974871	0.88[CEU][hapmap];0.81[YRI][hapmap]
rs2161548	0.88[CEU][hapmap];0.86[EUR][1000 genomes]
rs2247650	0.81[CEU][hapmap]
rs2278018	0.85[CEU][hapmap]
rs2278019	0.84[CEU][hapmap]
rs2351010	0.88[CEU][hapmap];0.87[EUR][1000 genomes]
rs2351011	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2432141	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2432142	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs251339	0.81[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs251340	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs251341	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs251343	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2548224	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2548226	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2548516	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2548529	0.89[CHB][hapmap]
rs2548530	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2548532	0.96[CEU][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2549778	0.82[JPT][hapmap]
rs2549783	1.00[CEU][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2549784	0.83[YRI][hapmap]
rs2549794	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2617435	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2617439	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs27289	0.84[EUR][1000 genomes]
rs27290	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs27293	0.84[EUR][1000 genomes]
rs27295	0.84[EUR][1000 genomes]
rs27300	0.88[CEU][hapmap];0.80[EUR][1000 genomes]
rs27306	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.89[EUR][1000 genomes]
rs27307	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes]
rs27436	0.84[CEU][hapmap];0.84[EUR][1000 genomes]
rs2762	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs27659	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs27660	0.89[EUR][1000 genomes]
rs27711	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.89[EUR][1000 genomes]
rs27712	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs27993	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.89[EUR][1000 genomes]
rs2859491	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2910686	0.86[CEU][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2910687	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2910788	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2910789	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2910793	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2927608	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2927609	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3734015	0.85[CEU][hapmap]
rs3797796	0.96[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.92[YRI][hapmap];0.84[EUR][1000 genomes]
rs38029	0.89[EUR][1000 genomes]
rs38031	0.89[EUR][1000 genomes]
rs38032	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs38033	0.88[CEU][hapmap];0.87[EUR][1000 genomes]
rs38034	0.84[CEU][hapmap];0.87[EUR][1000 genomes]
rs38038	0.84[EUR][1000 genomes]
rs38039	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs38042	0.81[CEU][hapmap]
rs38043	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs38044	0.84[EUR][1000 genomes]
rs3849749	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3909451	0.88[CEU][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs39602	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs4360063	0.88[CEU][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4869313	0.80[EUR][1000 genomes]
rs4869314	0.85[CEU][hapmap]
rs55770741	0.83[EUR][1000 genomes]
rs6556942	0.96[CEU][hapmap];0.83[JPT][hapmap];0.88[YRI][hapmap];0.83[EUR][1000 genomes]
rs6859168	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6871162	0.88[CEU][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6873866	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs6887500	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs716848	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7703341	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7716222	0.88[CEU][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7719705	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7726445	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7731592	0.89[CEU][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7733312	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9127	0.91[CEU][hapmap]
rs9314181	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv948703	chr5:96078309-96368839	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv1027472	chr5:96081592-96337550	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv1028741	chr5:96082401-96372165	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv949058	chr5:96082433-96390619	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv598963	chr5:96084776-96363407	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
8	nsv531967	chr5:96127842-96302702	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:19)

SNP	Gene	Cis/trans	Tissue	Source
rs2617447	ERAP2	cis	Stomach	GTEx
rs2617447	LNPEP	cis	Esophagus Muscularis	GTEx
rs2617447	ERAP2	cis	Esophagus Muscularis	GTEx
rs2617447	LRAP	cis	normal skin	skin_eQTL
rs2617447	LRAP	Cis_1M	lymphoblastoid	RTeQTL
rs2617447	ERAP2	cis	Whole Blood	GTEx
rs2617447	ERAP2	cis	Adipose Subcutaneous	GTEx
rs2617447	ERAP2	cis	lung	GTEx
rs2617447	LRAP	cis	lesional skin	skin_eQTL
rs2617447	AC008865.1	cis	Artery Tibial	GTEx
rs2617447	ERAP2	cis	Muscle Skeletal	GTEx
rs2617447	ERAP2	cis	Nerve Tibial	GTEx
rs2617447	ERAP2	cis	Thyroid	GTEx
rs2617447	ERAP2	cis	Esophagus Mucosa	GTEx
rs2617447	LRAP	cis	uninvolved skin	skin_eQTL
rs2617447	ERAP2	cis	Heart Left Ventricle	GTEx
rs2617447	ERAP2	cis	Artery Tibial	GTEx
rs2617447	ERAP2	cis	Artery Aorta	GTEx
rs2617447	ERAP2	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96221600-96269200	Weak transcription	Fetal Brain Male	brain
2	chr5:96222000-96268600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:96229600-96269600	Weak transcription	Aorta	Aorta
4	chr5:96229800-96270000	Weak transcription	Esophagus	oesophagus
5	chr5:96237400-96269200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:96239800-96268000	Weak transcription	Colonic Mucosa	Colon
7	chr5:96242200-96268000	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr5:96246000-96268200	Weak transcription	Fetal Intestine Small	intestine
9	chr5:96246000-96270200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:96249600-96267800	Weak transcription	Fetal Intestine Large	intestine
11	chr5:96249800-96270000	Weak transcription	Lung	lung
12	chr5:96254000-96268600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr5:96257400-96269600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:96260200-96267800	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr5:96260200-96268200	Weak transcription	HMEC	breast
16	chr5:96260200-96269000	Weak transcription	Fetal Stomach	stomach
17	chr5:96260200-96269400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr5:96260400-96268200	Weak transcription	NHEK	skin
19	chr5:96260600-96268600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr5:96264000-96268000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr5:96264000-96268200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr5:96264000-96269200	Enhancers	Fetal Heart	heart
23	chr5:96264200-96268000	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr5:96264200-96268000	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr5:96264400-96267800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr5:96264400-96269000	Weak transcription	Fetal Brain Female	brain
27	chr5:96264600-96268200	Enhancers	Primary T cells fromperipheralblood	blood
28	chr5:96264800-96267800	Enhancers	Primary T cells from cord blood	blood
29	chr5:96265000-96268600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr5:96265000-96270000	Weak transcription	Pancreas	Pancrea
31	chr5:96265400-96270000	Weak transcription	Left Ventricle	heart
32	chr5:96265800-96267800	Enhancers	Dnd41	blood
33	chr5:96265800-96268200	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr5:96265800-96268200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr5:96266000-96268200	Enhancers	Fetal Thymus	thymus
36	chr5:96266000-96269400	Enhancers	Placenta	Placenta
37	chr5:96266000-96269400	Weak transcription	Right Ventricle	heart
38	chr5:96266200-96268800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr5:96266200-96269000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr5:96266400-96267800	Enhancers	Duodenum Mucosa	Duodenum
41	chr5:96266400-96267800	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr5:96266400-96268200	Enhancers	Brain Angular Gyrus	brain
43	chr5:96266400-96268200	Weak transcription	Hela-S3	cervix
44	chr5:96266400-96268400	Enhancers	Gastric	stomach
45	chr5:96266400-96268600	Enhancers	Primary B cells from peripheral blood	blood
46	chr5:96266600-96269200	Weak transcription	Brain Cingulate Gyrus	brain
47	chr5:96266800-96267800	Weak transcription	Brain Germinal Matrix	brain
48	chr5:96266800-96268200	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr5:96266800-96268200	Enhancers	K562	blood
50	chr5:96267000-96267800	Enhancers	Primary hematopoietic stem cells short term culture	blood

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