Variant report

Variant	rs13167902
Chromosome Location	chr5:96222020-96222021
allele	A/C/G
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	IRF4	chr5:96221575-96222058	GM12878	blood:	n/a	n/a
2	SPI1	chr5:96221664-96222122	HL-60	blood:	n/a	chr5:96221930-96221943 chr5:96221932-96221941 chr5:96221931-96221944
3	NFIC	chr5:96220784-96222305	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:96221465-96222053	GM12878	blood:	n/a	chr5:96221931-96221940
5	PAX5	chr5:96221459-96222022	GM12878	blood:	n/a	chr5:96221931-96221940
6	TBL1XR1	chr5:96221494-96222031	GM12878	blood:	n/a	n/a
7	MEF2A	chr5:96221530-96222128	GM12878	blood:	n/a	n/a
8	SPI1	chr5:96221545-96222198	GM12891	blood:	n/a	chr5:96221930-96221943 chr5:96221932-96221941 chr5:96221931-96221944
9	MAZ	chr5:96221624-96222104	GM12878	blood:	n/a	n/a
10	ATF2	chr5:96221343-96222204	GM12878	blood:	n/a	n/a
11	RCOR1	chr5:96221697-96222122	GM12878	blood:	n/a	n/a
12	CHD1	chr5:96221545-96222241	GM12878	blood:	n/a	n/a
13	SPI1	chr5:96221549-96222164	GM12891	blood:	n/a	chr5:96221930-96221943 chr5:96221932-96221941 chr5:96221931-96221944
14	TEAD4	chr5:96221497-96222037	K562	blood:	n/a	n/a
15	ZNF143	chr5:96221525-96222050	GM12878	blood:	n/a	n/a
16	RUNX3	chr5:96221469-96222197	GM12878	blood:	n/a	n/a
17	SPI1	chr5:96221751-96222086	GM12878	blood:	n/a	chr5:96221930-96221943 chr5:96221932-96221941 chr5:96221931-96221944
18	POU2F2	chr5:96221464-96222049	GM12878	blood:	n/a	n/a
19	SPI1	chr5:96221723-96222038	K562	blood:	n/a	chr5:96221930-96221943 chr5:96221932-96221941 chr5:96221931-96221944
20	SPI1	chr5:96221719-96222151	HL-60	blood:	n/a	chr5:96221930-96221943 chr5:96221932-96221941 chr5:96221931-96221944
21	SP1	chr5:96221576-96222092	GM12878	blood:	n/a	chr5:96221986-96221993
22	SPI1	chr5:96221640-96222099	GM12878	blood:	n/a	chr5:96221930-96221943 chr5:96221932-96221941 chr5:96221931-96221944
23	ZNF384	chr5:96221496-96222033	GM12878	blood:	n/a	n/a
24	ELF1	chr5:96221718-96222030	K562	blood:	n/a	chr5:96221932-96221943 chr5:96221931-96221942
25	RUNX3	chr5:96221553-96222094	GM12878	blood:	n/a	n/a
26	STAT3	chr5:96221346-96222056	GM12878	blood:	n/a	n/a
27	IRF1	chr5:96221734-96222097	K562	blood:	n/a	chr5:96221929-96221938 chr5:96221931-96221951
28	EGR1	chr5:96221740-96222023	K562	blood:	n/a	chr5:96221931-96221940
29	SPI1	chr5:96221777-96222025	K562	blood:	n/a	chr5:96221930-96221943 chr5:96221932-96221941 chr5:96221931-96221944
30	EP300	chr5:96221419-96222174	GM12878	blood:	n/a	chr5:96221932-96221941
31	BCL3	chr5:96221504-96222093	GM12878	blood:	n/a	chr5:96221931-96221940
32	REST	chr5:96221712-96222051	Hela-S3	cervix:	n/a	n/a
33	MXI1	chr5:96221206-96222107	GM12878	blood:	n/a	n/a
34	CREB1	chr5:96221343-96222034	GM12878	blood:	n/a	n/a
35	EP300	chr5:96221547-96222173	GM12878	blood:	n/a	chr5:96221932-96221941
36	SPI1	chr5:96221235-96222342	GM12878	blood:	n/a	chr5:96221930-96221943 chr5:96221932-96221941 chr5:96221931-96221944
37	NFATC1	chr5:96221501-96222188	GM12878	blood:	n/a	n/a
38	YY1	chr5:96221682-96222029	GM12878	blood:	n/a	n/a
39	NFATC1	chr5:96221357-96222122	GM12878	blood:	n/a	n/a
40	BCLAF1	chr5:96221475-96222097	GM12878	blood:	n/a	chr5:96221931-96221940
41	IRF4	chr5:96221421-96222138	GM12878	blood:	n/a	n/a
42	FOXM1	chr5:96221497-96222167	GM12878	blood:	n/a	n/a
43	CUX1	chr5:96221325-96222050	GM12878	blood:	n/a	n/a
44	MAX	chr5:96221498-96222049	GM12878	blood:	n/a	n/a
45	SMC3	chr5:96221566-96222237	GM12878	blood:	n/a	n/a
46	FOXM1	chr5:96221490-96222159	GM12878	blood:	n/a	n/a
47	MTA3	chr5:96221257-96222110	GM12878	blood:	n/a	n/a
48	EP300	chr5:96221479-96222345	GM12878	blood:	n/a	chr5:96222302-96222316 chr5:96221932-96221941
49	PML	chr5:96221204-96222212	GM12878	blood:	n/a	n/a
50	EBF1	chr5:96221507-96222112	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:96219913..96223749-chr5:96224783..96226806,3	MCF-7	breast:
2	chr5:96215750..96217350-chr5:96220796..96223621,2	K562	blood:

Variant related genes	Relation type
ERAP2	TF binding region
ENSG00000164308	Chromatin interaction

Extended variants
information (count: 117 )
Associated
traits (count: 20 )

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

rs_ID	r²[population]
rs10058476	0.85[CEU][hapmap]
rs10069361	0.81[CEU][hapmap];0.81[TSI][hapmap]
rs10071975	0.81[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap]
rs1019503	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs10434708	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10434709	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1056893	0.90[CHB][hapmap];0.81[CHD][hapmap];0.90[JPT][hapmap];0.80[TSI][hapmap];0.89[YRI][hapmap]
rs11135482	1.00[ASW][hapmap];0.95[CHB][hapmap];0.86[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap]
rs11135483	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11135484	0.94[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[CHD][hapmap];0.86[GIH][hapmap];0.95[JPT][hapmap];0.95[LWK][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11750025	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1216565	0.90[CHB][hapmap];0.90[JPT][hapmap];0.82[YRI][hapmap]
rs12189125	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12516666	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12653964	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12654015	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12655858	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12716486	0.81[CEU][hapmap];0.85[CHB][hapmap];0.95[JPT][hapmap]
rs13189819	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1363907	0.89[CEU][hapmap]
rs1423357	0.82[YRI][hapmap]
rs1477364	0.85[CEU][hapmap]
rs1544777	0.85[CEU][hapmap]
rs1559354	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1559355	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1559357	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs187265	0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap]
rs1974871	0.96[CEU][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap];0.86[GIH][hapmap];0.95[JPT][hapmap];1.00[TSI][hapmap]
rs1981846	0.95[CHB][hapmap];0.85[JPT][hapmap];0.80[TSI][hapmap]
rs2042385	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs2113050	0.87[CEU][hapmap];0.88[JPT][hapmap]
rs2113189	0.91[YRI][hapmap]
rs2161657	0.90[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.81[TSI][hapmap]
rs2161658	0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap]
rs2247650	0.89[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap];0.81[EUR][1000 genomes]
rs2255546	0.85[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.81[TSI][hapmap];0.89[YRI][hapmap]
rs2255633	0.85[CHB][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap]
rs2255634	0.85[CHB][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap]
rs2255637	0.85[CHB][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap]
rs2278018	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2278019	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2287988	0.90[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.81[TSI][hapmap];0.89[YRI][hapmap]
rs248215	0.81[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap]
rs251339	0.89[CEU][hapmap]
rs251344	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs2548523	0.89[CHB][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap]
rs2548524	0.85[CHB][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap]
rs2548527	0.90[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.81[TSI][hapmap]
rs2548529	0.85[CEU][hapmap]
rs2548530	0.85[CEU][hapmap]
rs2548532	0.81[CEU][hapmap]
rs2548533	0.90[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.81[TSI][hapmap];0.89[YRI][hapmap]
rs2548536	0.90[CHB][hapmap];0.90[JPT][hapmap];0.91[YRI][hapmap]
rs2548537	0.81[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.93[YRI][hapmap]
rs2548538	0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap]
rs2548539	0.90[CHB][hapmap];0.90[JPT][hapmap];0.88[YRI][hapmap]
rs2548540	0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap]
rs2549781	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs2549782	0.85[CHB][hapmap];0.90[JPT][hapmap];0.81[TSI][hapmap];0.89[YRI][hapmap]
rs2549783	0.85[CEU][hapmap]
rs2549784	0.84[CEU][hapmap]
rs2549785	0.90[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.80[TSI][hapmap];0.89[YRI][hapmap]
rs2549790	0.80[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap];0.89[YRI][hapmap]
rs2549791	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs2549794	0.85[CEU][hapmap]
rs2549795	0.90[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.81[TSI][hapmap];0.89[YRI][hapmap]
rs2549796	0.90[CHB][hapmap];0.81[CHD][hapmap];0.90[JPT][hapmap];0.81[TSI][hapmap]
rs2549797	0.90[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.81[TSI][hapmap];0.89[YRI][hapmap]
rs2617447	0.84[CEU][hapmap]
rs27294	0.81[CEU][hapmap]
rs27296	0.81[CEU][hapmap]
rs27306	0.85[CEU][hapmap]
rs27307	0.85[CEU][hapmap]
rs27397	0.81[CEU][hapmap];0.85[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.81[TSI][hapmap]
rs27436	0.81[CEU][hapmap]
rs27613	0.81[CEU][hapmap];0.81[TSI][hapmap]
rs27711	0.85[CEU][hapmap]
rs27712	0.85[CEU][hapmap]
rs27747	0.81[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap]
rs27993	0.85[CEU][hapmap]
rs2910686	0.82[CHB][hapmap];0.84[JPT][hapmap];0.84[YRI][hapmap]
rs2910787	0.81[CEU][hapmap];0.81[TSI][hapmap]
rs2927609	0.84[CEU][hapmap]
rs3734015	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3797796	0.81[CEU][hapmap]
rs38032	0.81[CEU][hapmap]
rs38035	0.81[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap]
rs38036	0.81[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap]
rs38040	0.81[CEU][hapmap];0.81[TSI][hapmap]
rs38041	0.81[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap]
rs38042	0.89[CEU][hapmap];0.90[JPT][hapmap]
rs3849749	0.85[CEU][hapmap]
rs3849750	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs4869311	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4869312	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4869313	0.87[EUR][1000 genomes]
rs4869314	1.00[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.80[YRI][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4869315	0.84[ASW][hapmap];0.96[YRI][hapmap]
rs55770741	0.83[EUR][1000 genomes]
rs56197090	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6556942	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs6868302	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7700332	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs7713127	0.81[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap]
rs7719705	0.89[CEU][hapmap]
rs7721944	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7736466	0.81[CEU][hapmap];0.85[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.81[TSI][hapmap]
rs9127	0.96[CEU][hapmap];0.93[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 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	nsv432756	chr5:96113844-96234644	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
9	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:20)

SNP	Gene	Cis/trans	Tissue	Source
rs13167902	ERAP2	cis	lymphoblastoid	seeQTL
rs13167902	ERAP2	cis	Whole Blood	GTEx
rs13167902	ERAP2	cis	Nerve Tibial	GTEx
rs13167902	ERAP2	cis	Stomach	GTEx
rs13167902	ERAP2	cis	Adipose Subcutaneous	GTEx
rs13167902	LRAP	cis	uninvolved skin	skin_eQTL
rs13167902	ERAP2	cis	Heart Left Ventricle	GTEx
rs13167902	ERAP2	cis	Artery Aorta	GTEx
rs13167902	ERAP2	cis	Muscle Skeletal	GTEx
rs13167902	LRAP	cis	multi-tissue	Pritchard
rs13167902	AC008865.1	cis	Artery Tibial	GTEx
rs13167902	ERAP2	cis	Esophagus Muscularis	GTEx
rs13167902	ERAP2	cis	lung	GTEx
rs13167902	ERAP2	cis	lymphoblastoid	GTEx
rs13167902	ERAP2	cis	Thyroid	GTEx
rs13167902	ERAP2	cis	Esophagus Mucosa	GTEx
rs13167902	ERAP2	cis	Skin Sun Exposed Lower leg	GTEx
rs13167902	LRAP	cis	lesional skin	skin_eQTL
rs13167902	LRAP	cis	normal skin	skin_eQTL
rs13167902	ERAP2	cis	Artery Tibial	GTEx

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96212600-96232000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr5:96213000-96239000	Weak transcription	Pancreas	Pancrea
3	chr5:96213200-96225200	Weak transcription	Ovary	ovary
4	chr5:96213200-96229200	Weak transcription	Aorta	Aorta
5	chr5:96213400-96223600	Weak transcription	Fetal Kidney	kidney
6	chr5:96213400-96237800	Weak transcription	Brain Substantia Nigra	brain
7	chr5:96213400-96243800	Weak transcription	HepG2	liver
8	chr5:96213400-96247000	Weak transcription	Fetal Lung	lung
9	chr5:96215400-96222400	Genic enhancers	Fetal Thymus	thymus
10	chr5:96217200-96222600	Genic enhancers	Primary B cells from peripheral blood	blood
11	chr5:96217400-96229200	Weak transcription	Colonic Mucosa	Colon
12	chr5:96217600-96228800	Weak transcription	HSMM	muscle
13	chr5:96217600-96241600	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr5:96217600-96250000	Weak transcription	Fetal Muscle Trunk	muscle
15	chr5:96217800-96224600	Weak transcription	Rectal Smooth Muscle	rectum
16	chr5:96217800-96225200	Weak transcription	Gastric	stomach
17	chr5:96217800-96228800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr5:96217800-96229200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr5:96217800-96229200	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr5:96217800-96237800	Weak transcription	NHDF-Ad	bronchial
21	chr5:96218000-96222600	Genic enhancers	Primary T cells fromperipheralblood	blood
22	chr5:96218000-96222600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
23	chr5:96218000-96222600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr5:96218000-96225200	Weak transcription	Spleen	Spleen
25	chr5:96218000-96229000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:96218000-96229000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr5:96218000-96229200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:96218000-96237000	Weak transcription	NHLF	lung
29	chr5:96218000-96264600	Weak transcription	Right Ventricle	heart
30	chr5:96218200-96222200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr5:96218200-96228600	Weak transcription	NH-A	brain
32	chr5:96218200-96228800	Weak transcription	NHEK	skin
33	chr5:96218200-96231400	Weak transcription	Colon Smooth Muscle	Colon
34	chr5:96218200-96232000	Weak transcription	Brain Anterior Caudate	brain
35	chr5:96218200-96237000	Weak transcription	Hela-S3	cervix
36	chr5:96218400-96224600	Weak transcription	Fetal Heart	heart
37	chr5:96218600-96259600	Weak transcription	HMEC	breast
38	chr5:96218800-96228600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr5:96219000-96222200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr5:96219000-96222600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr5:96220000-96222400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr5:96220200-96222400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr5:96220400-96222400	Strong transcription	Rectal Mucosa Donor 31	rectum
44	chr5:96220400-96222600	Strong transcription	Adipose Nuclei	Adipose
45	chr5:96220400-96228600	Weak transcription	Fetal Muscle Leg	muscle
46	chr5:96220600-96222200	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
47	chr5:96220600-96222400	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
48	chr5:96220600-96222600	Genic enhancers	Primary hematopoietic stem cells	blood
49	chr5:96220800-96222200	Weak transcription	Liver	Liver
50	chr5:96221000-96224000	Weak transcription	Duodenum Smooth Muscle	Duodenum

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