Variant report

Variant	rs10844113
Chromosome Location	chr12:32230474-32230475
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:32228668..32231442-chr12:32233018..32235183,2	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10771906	0.85[ASN][1000 genomes]
rs10771907	0.88[ASN][1000 genomes]
rs10771908	0.86[ASN][1000 genomes]
rs10771910	0.86[ASN][1000 genomes]
rs10771911	0.88[ASN][1000 genomes]
rs10771912	0.88[ASN][1000 genomes]
rs10771913	0.88[ASN][1000 genomes]
rs10844106	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10844107	0.82[CHB][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs10844108	1.00[CEU][hapmap];0.82[JPT][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10844109	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10844111	0.85[ASN][1000 genomes]
rs10844112	0.85[ASN][1000 genomes]
rs10844114	0.88[ASN][1000 genomes]
rs10844115	0.88[ASN][1000 genomes]
rs10844116	0.88[ASN][1000 genomes]
rs10844133	0.84[GIH][hapmap]
rs11051767	0.91[ASN][1000 genomes]
rs11051768	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11051769	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11051777	0.85[ASN][1000 genomes]
rs11051779	0.85[ASN][1000 genomes]
rs11051781	0.89[ASN][1000 genomes]
rs11051787	0.89[ASN][1000 genomes]
rs11051789	0.88[ASN][1000 genomes]
rs11051791	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11609854	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16919225	0.80[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs2389068	0.89[ASN][1000 genomes]
rs3867163	0.89[ASN][1000 genomes]
rs4616125	0.89[ASN][1000 genomes]
rs6488030	0.85[ASN][1000 genomes]
rs7134602	0.88[ASN][1000 genomes]
rs7138326	0.88[ASN][1000 genomes]
rs7138578	0.88[ASN][1000 genomes]
rs7298142	0.89[ASN][1000 genomes]
rs7302076	0.89[ASN][1000 genomes]
rs7307717	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7310661	0.88[ASN][1000 genomes]
rs7311149	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7311255	0.87[ASN][1000 genomes]
rs7953627	0.85[ASN][1000 genomes]
rs7964630	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3363806	chr12:31872264-32410283	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3508621	chr12:31872654-32410593	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	esv3508622	chr12:31872654-32410593	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv976030	chr12:32153446-32307541	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv983498	chr12:32153446-32388092	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv898969	chr12:32224948-32375677	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1042317	chr12:32228872-32316774	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32227200-32240200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr12:32228400-32233000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr12:32228400-32242600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:32228600-32233400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr12:32229000-32240000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr12:32230000-32230800	Weak transcription	Fetal Brain Female	brain
7	chr12:32230000-32232200	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr12:32230000-32259200	Weak transcription	Right Atrium	heart
9	chr12:32230200-32231000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:32230400-32231200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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