Variant report

Variant	rs2664136
Chromosome Location	chr15:39849127-39849128
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	chr15:39840133..39842449-chr15:39847834..39850464,2	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1038097	0.96[EUR][1000 genomes]
rs1051442	0.92[EUR][1000 genomes]
rs10520141	0.91[EUR][1000 genomes]
rs10520143	0.86[EUR][1000 genomes]
rs1382443	0.96[EUR][1000 genomes]
rs1382444	0.96[EUR][1000 genomes]
rs16969487	0.91[EUR][1000 genomes]
rs16969491	0.91[EUR][1000 genomes]
rs16969547	0.81[EUR][1000 genomes]
rs17632916	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17633107	0.92[EUR][1000 genomes]
rs17633210	0.90[EUR][1000 genomes]
rs17705806	0.90[EUR][1000 genomes]
rs17706083	0.90[EUR][1000 genomes]
rs17706179	0.90[EUR][1000 genomes]
rs1813493	0.98[EUR][1000 genomes]
rs1988082	0.89[EUR][1000 genomes]
rs1988555	0.92[EUR][1000 genomes]
rs2228263	0.93[EUR][1000 genomes]
rs2411316	0.91[EUR][1000 genomes]
rs2618156	0.98[EUR][1000 genomes]
rs2618160	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2618161	0.96[EUR][1000 genomes]
rs2618164	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2618165	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2618167	0.96[EUR][1000 genomes]
rs2664123	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2664137	0.98[EUR][1000 genomes]
rs2664138	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2664140	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2664142	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28377784	0.91[EUR][1000 genomes]
rs28549326	0.91[EUR][1000 genomes]
rs28619289	0.91[EUR][1000 genomes]
rs28653011	0.91[EUR][1000 genomes]
rs34878675	0.86[EUR][1000 genomes]
rs41315060	0.92[EUR][1000 genomes]
rs4415979	0.92[EUR][1000 genomes]
rs4503768	0.84[EUR][1000 genomes]
rs45461294	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4923835	0.92[EUR][1000 genomes]
rs58188999	0.90[EUR][1000 genomes]
rs59578395	0.93[EUR][1000 genomes]
rs59628570	0.85[EUR][1000 genomes]
rs6492905	0.93[EUR][1000 genomes]
rs74008647	0.90[EUR][1000 genomes]
rs74008648	0.91[EUR][1000 genomes]
rs880270	0.91[EUR][1000 genomes]
rs954152	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs985808	0.82[EUR][1000 genomes]
rs9972350	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049682	chr15:39657279-40027403	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv542361	chr15:39657279-40027403	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv3373125	chr15:39691567-40061262	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv904094	chr15:39738006-39976057	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv832977	chr15:39817512-39981520	Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39844400-39851200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr15:39844600-39849600	Enhancers	Colon Smooth Muscle	Colon
3	chr15:39845800-39849800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr15:39846600-39849600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr15:39846600-39849600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr15:39846800-39850800	Weak transcription	Pancreas	Pancrea
7	chr15:39847000-39850200	Weak transcription	Fetal Muscle Leg	muscle
8	chr15:39847600-39849600	Enhancers	NHEK	skin
9	chr15:39848200-39849200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr15:39848200-39849200	Enhancers	HMEC	breast
11	chr15:39848400-39850600	Weak transcription	Fetal Thymus	thymus
12	chr15:39848600-39850800	Weak transcription	GM12878-XiMat	blood
13	chr15:39849000-39850800	Weak transcription	Fetal Lung	lung
14	chr15:39849000-39850800	Weak transcription	Fetal Muscle Trunk	muscle

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