Variant report

Variant	rs11636071
Chromosome Location	chr15:31339049-31339050
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:31324460..31327252-chr15:31338571..31340115,2	K562	blood:

Variant related genes	Relation type
ENSG00000134160	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10162731	0.87[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1035705	0.82[ASN][1000 genomes]
rs1035706	0.86[ASN][1000 genomes]
rs10851487	0.82[ASN][1000 genomes]
rs11070764	0.82[ASN][1000 genomes]
rs11070767	0.81[ASN][1000 genomes]
rs11636121	0.82[ASN][1000 genomes]
rs1991214	0.82[ASN][1000 genomes]
rs2288241	0.82[ASN][1000 genomes]
rs2288242	0.97[ASN][1000 genomes]
rs2338834	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2338835	0.82[ASN][1000 genomes]
rs2911849	0.82[ASN][1000 genomes]
rs2911850	0.82[ASN][1000 genomes]
rs2911851	0.82[ASN][1000 genomes]
rs2911853	0.82[ASN][1000 genomes]
rs2911854	0.82[ASN][1000 genomes]
rs2959041	0.97[ASN][1000 genomes]
rs2959042	0.97[ASN][1000 genomes]
rs3743234	0.82[ASN][1000 genomes]
rs4779501	0.93[ASN][1000 genomes]
rs4779808	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4779810	0.93[ASN][1000 genomes]
rs4779812	0.87[ASN][1000 genomes]
rs4779813	0.81[ASN][1000 genomes]
rs7165995	0.93[ASN][1000 genomes]
rs7173280	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7173932	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7174338	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7174872	0.93[ASN][1000 genomes]
rs7179304	0.93[ASN][1000 genomes]
rs8037421	0.93[ASN][1000 genomes]
rs8041204	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531138	chr15:30653877-31609679	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv903831	chr15:30986051-31723279	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
3	nsv1054147	chr15:31014507-31972706	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
4	nsv542306	chr15:31014507-31972706	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
5	nsv1036018	chr15:31140415-31544888	Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
6	esv33507	chr15:31183324-31471023	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
7	nsv1052722	chr15:31261834-31609680	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv542315	chr15:31261834-31609680	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
9	nsv932896	chr15:31292475-31730445	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
10	nsv903835	chr15:31312743-31384797	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
11	nsv903836	chr15:31330280-31512652	Enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31326800-31339200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr15:31326800-31342800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:31331400-31339400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr15:31332600-31341200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr15:31338600-31339400	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr15:31338600-31339400	Enhancers	Stomach Mucosa	stomach
7	chr15:31338800-31339400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr15:31338800-31339400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr15:31338800-31339400	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr15:31338800-31339600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr15:31338800-31339800	Enhancers	Placenta	Placenta
12	chr15:31339000-31339400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr15:31339000-31339400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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