Variant report

Variant	rs2733230
Chromosome Location	chr15:56861098-56861099
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1031985	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10518858	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11071278	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11634704	0.81[EUR][1000 genomes]
rs12148474	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12148781	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12441674	0.85[EUR][1000 genomes]
rs12898886	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1482066	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1600830	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2128174	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2128175	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2128176	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2128177	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2676206	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs28374324	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28379958	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28409651	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28782544	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28805712	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28813195	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28842489	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4238320	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4290423	0.81[AMR][1000 genomes]
rs4456442	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4774870	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4774876	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4774877	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4774879	0.98[EUR][1000 genomes]
rs56327619	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7165804	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs8026706	0.85[EUR][1000 genomes]
rs8031549	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8032893	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8034366	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9806469	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]

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	nsv1545	chr15:56659498-56897381	Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv471330	chr15:56659709-56896385	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv471506	chr15:56659709-56896385	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv498847	chr15:56667038-56896395	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv2525559	chr15:56669294-56897412	Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv3693203	chr15:56676457-56894478	Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv35150	chr15:56677730-56896304	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1049240	chr15:56820899-56890478	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	esv12125	chr15:56851808-56868691	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56860000-56861400	ZNF genes & repeats	Fetal Thymus	thymus
2	chr15:56860000-56861600	ZNF genes & repeats	Thymus	Thymus
3	chr15:56860400-56861600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:56860600-56861400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr15:56860600-56861600	Enhancers	HMEC	breast
6	chr15:56860600-56861800	Enhancers	Dnd41	blood
7	chr15:56860800-56861400	Enhancers	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links