Variant report

Variant	rs11101512
Chromosome Location	chr10:50023350-50023351
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:50021873..50024313-chr10:50091806..50093411,2	MCF-7	breast:
2	chr10:50016415..50019036-chr10:50020234..50023570,4	MCF-7	breast:
3	chr10:50012510..50015290-chr10:50020965..50023375,3	MCF-7	breast:
4	chr10:50022212..50024156-chr10:50029662..50031442,2	MCF-7	breast:
5	chr10:50012639..50013621-chr10:50022857..50023759,3	MCF-7	breast:
6	chr10:50021104..50023943-chr10:50032685..50035174,2	MCF-7	breast:
7	chr10:50009310..50017840-chr10:50018505..50026491,17	MCF-7	breast:

Variant related genes	Relation type
ENSG00000128815	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10857653	0.86[ASN][1000 genomes]
rs11101515	0.83[ASN][1000 genomes]
rs11101516	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11101518	1.00[CEU][hapmap];0.92[CHB][hapmap];0.88[JPT][hapmap];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11101519	1.00[CEU][hapmap];0.92[CHB][hapmap];0.89[JPT][hapmap];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11101520	1.00[CEU][hapmap];0.92[CHB][hapmap];0.88[JPT][hapmap];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11101521	1.00[CEU][hapmap];0.92[CHB][hapmap];0.88[JPT][hapmap];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11101522	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11101524	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11101525	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11101526	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11101527	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11101528	1.00[CEU][hapmap];0.92[CHB][hapmap];0.89[JPT][hapmap];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12246033	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12247830	1.00[CEU][hapmap];0.92[CHB][hapmap];0.88[JPT][hapmap];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12247839	1.00[CEU][hapmap];0.92[CHB][hapmap];0.89[JPT][hapmap];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12248218	0.92[CHB][hapmap];0.88[JPT][hapmap];0.82[ASN][1000 genomes]
rs12249974	1.00[CEU][hapmap];0.92[CHB][hapmap];0.89[JPT][hapmap];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12251517	1.00[CEU][hapmap];0.88[CHB][hapmap];0.86[JPT][hapmap];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12260555	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12261146	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12264889	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12268007	1.00[CEU][hapmap];0.92[CHB][hapmap];0.88[JPT][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12268803	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17699445	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17699451	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17836512	0.83[CHB][hapmap];0.88[JPT][hapmap]
rs2377655	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2928402	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2928403	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3750864	0.83[CHB][hapmap];0.88[JPT][hapmap]
rs41283275	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs45520233	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4596990	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61838883	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61838884	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61838885	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6537578	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6537579	1.00[CEU][hapmap];0.92[CHB][hapmap];0.88[JPT][hapmap];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7918931	0.85[CHB][hapmap];0.89[JPT][hapmap];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831865	chr10:49994254-50164239	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50005200-50026800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr10:50009600-50028000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr10:50013200-50023800	Strong transcription	GM12878-XiMat	blood
4	chr10:50013600-50028200	Strong transcription	Primary B cells from peripheral blood	blood
5	chr10:50013600-50061000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr10:50014200-50030000	Weak transcription	Right Atrium	heart
7	chr10:50015200-50063400	Strong transcription	Primary B cells from cord blood	blood
8	chr10:50015600-50029800	Weak transcription	Gastric	stomach
9	chr10:50016200-50063000	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr10:50016200-50063000	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr10:50016600-50062400	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr10:50017600-50023600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr10:50019400-50029000	Weak transcription	Primary T cells from cord blood	blood
14	chr10:50020000-50052000	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr10:50021200-50027800	Weak transcription	Fetal Thymus	thymus
16	chr10:50022200-50025200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr10:50022400-50025200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:50022600-50025200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr10:50022600-50040400	Weak transcription	Lung	lung
20	chr10:50022800-50023400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr10:50022800-50023400	Enhancers	NHEK	skin
22	chr10:50022800-50025200	Weak transcription	Spleen	Spleen
23	chr10:50023000-50025000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr10:50023200-50023400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr10:50023200-50025000	Weak transcription	Primary hematopoietic stem cells	blood
26	chr10:50023200-50025000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links