Variant report

Variant	rs11038403
Chromosome Location	chr11:45359713-45359714
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:45354038..45357345-chr11:45359255..45361825,3	K562	blood:

Extended variants
information (count: 116 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:115)

rs_ID	r²[population]
rs10160472	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10160502	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10160694	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10160834	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10501315	0.82[EUR][1000 genomes]
rs10838454	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10838455	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10838479	0.82[EUR][1000 genomes]
rs11038404	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11038405	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11038406	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11038409	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11038411	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11038417	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11038420	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11038423	0.93[EUR][1000 genomes]
rs11038424	0.93[EUR][1000 genomes]
rs11038426	0.93[EUR][1000 genomes]
rs11038427	0.93[EUR][1000 genomes]
rs11038429	0.90[EUR][1000 genomes]
rs11038431	0.87[EUR][1000 genomes]
rs11038432	0.87[EUR][1000 genomes]
rs11038433	0.87[EUR][1000 genomes]
rs11038434	0.85[EUR][1000 genomes]
rs11038435	0.85[EUR][1000 genomes]
rs11038437	0.85[EUR][1000 genomes]
rs11038442	0.85[EUR][1000 genomes]
rs11038443	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs11038444	0.85[EUR][1000 genomes]
rs11038450	0.84[EUR][1000 genomes]
rs11038451	0.84[EUR][1000 genomes]
rs11038455	0.84[EUR][1000 genomes]
rs11038456	0.84[EUR][1000 genomes]
rs11038457	0.84[EUR][1000 genomes]
rs11038458	0.84[EUR][1000 genomes]
rs11038459	0.82[EUR][1000 genomes]
rs11038461	0.81[EUR][1000 genomes]
rs11038462	0.84[EUR][1000 genomes]
rs11038465	0.84[EUR][1000 genomes]
rs11038466	0.84[EUR][1000 genomes]
rs11038467	0.84[EUR][1000 genomes]
rs11038469	0.84[EUR][1000 genomes]
rs11038471	0.82[EUR][1000 genomes]
rs11038472	0.81[EUR][1000 genomes]
rs11038473	0.84[EUR][1000 genomes]
rs11038474	0.84[EUR][1000 genomes]
rs11038475	0.84[EUR][1000 genomes]
rs11038477	0.84[EUR][1000 genomes]
rs11038479	0.84[EUR][1000 genomes]
rs11038481	0.84[EUR][1000 genomes]
rs11038482	0.84[EUR][1000 genomes]
rs11038483	0.82[EUR][1000 genomes]
rs11038485	0.81[EUR][1000 genomes]
rs11038486	0.82[EUR][1000 genomes]
rs11038487	0.82[EUR][1000 genomes]
rs11038492	0.82[EUR][1000 genomes]
rs11038493	0.82[EUR][1000 genomes]
rs11038494	0.82[EUR][1000 genomes]
rs11038495	0.82[EUR][1000 genomes]
rs11038496	0.82[EUR][1000 genomes]
rs11038497	0.82[EUR][1000 genomes]
rs11038498	0.82[EUR][1000 genomes]
rs11038522	1.00[CEU][hapmap]
rs1107209	1.00[CEU][hapmap]
rs11599949	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11599993	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11601006	0.93[EUR][1000 genomes]
rs11601410	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11604510	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12278000	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12360696	1.00[CEU][hapmap]
rs12361372	0.84[EUR][1000 genomes]
rs12363740	0.81[EUR][1000 genomes]
rs12364278	0.84[EUR][1000 genomes]
rs12364661	0.84[EUR][1000 genomes]
rs12365374	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12365430	0.84[EUR][1000 genomes]
rs12365455	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12365467	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12365982	0.82[EUR][1000 genomes]
rs1488668	0.82[EUR][1000 genomes]
rs1488669	0.82[EUR][1000 genomes]
rs1488670	0.82[EUR][1000 genomes]
rs17723819	0.84[EUR][1000 genomes]
rs17724032	0.82[EUR][1000 genomes]
rs17724086	0.82[EUR][1000 genomes]
rs17785901	0.82[EUR][1000 genomes]
rs17786039	1.00[CEU][hapmap]
rs1844150	0.84[EUR][1000 genomes]
rs2044877	0.92[EUR][1000 genomes]
rs56684421	0.84[AFR][1000 genomes]
rs72897413	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72897414	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72897422	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72897428	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72897458	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72897475	0.87[EUR][1000 genomes]
rs72899480	0.85[EUR][1000 genomes]
rs72899488	0.84[EUR][1000 genomes]
rs72901403	0.84[EUR][1000 genomes]
rs72901422	0.84[EUR][1000 genomes]
rs72901426	0.84[EUR][1000 genomes]
rs72901447	0.84[EUR][1000 genomes]
rs72901450	0.84[EUR][1000 genomes]
rs72901459	0.84[EUR][1000 genomes]
rs72901500	0.84[EUR][1000 genomes]
rs72903035	0.84[EUR][1000 genomes]
rs72903086	0.84[EUR][1000 genomes]
rs72903094	0.84[EUR][1000 genomes]
rs72905021	0.82[EUR][1000 genomes]
rs72905025	0.82[EUR][1000 genomes]
rs72905092	0.82[EUR][1000 genomes]
rs72905093	0.82[EUR][1000 genomes]
rs72906922	0.82[EUR][1000 genomes]
rs971897	0.84[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530619	chr11:45294176-45553928	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45355200-45361000	Weak transcription	Fetal Kidney	kidney
2	chr11:45355600-45361200	Weak transcription	Fetal Stomach	stomach
3	chr11:45356200-45360600	Weak transcription	Fetal Brain Male	brain
4	chr11:45356400-45361000	Weak transcription	Fetal Brain Female	brain
5	chr11:45357400-45361400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr11:45358400-45361200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr11:45359200-45359800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr11:45359400-45359800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:45359400-45359800	Enhancers	NHEK	skin
10	chr11:45359400-45360000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr11:45359400-45360000	Enhancers	HMEC	breast
12	chr11:45359400-45362200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr11:45359600-45359800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr11:45359600-45359800	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr11:45359600-45360800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links