Variant report

Variant	rs13137007
Chromosome Location	chr4:101743600-101743601
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs13102244	0.91[AFR][1000 genomes]
rs13104901	0.81[AFR][1000 genomes]
rs13107645	0.91[AFR][1000 genomes]
rs13109077	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13109446	0.91[AFR][1000 genomes]
rs13109508	1.00[AFR][1000 genomes]
rs13110644	0.91[AFR][1000 genomes]
rs13117474	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13121438	0.91[AFR][1000 genomes]
rs13122599	0.91[AFR][1000 genomes]
rs13123162	0.91[AFR][1000 genomes]
rs13129721	0.91[AFR][1000 genomes]
rs13149562	0.82[AMR][1000 genomes]
rs13150288	0.91[AFR][1000 genomes]
rs2014244	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2202773	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34080291	0.91[AFR][1000 genomes]
rs34126461	0.91[AFR][1000 genomes]
rs34754564	0.91[AFR][1000 genomes]
rs34802397	0.91[AFR][1000 genomes]
rs34810105	0.91[AFR][1000 genomes]
rs34833700	0.91[AFR][1000 genomes]
rs34839174	0.91[AFR][1000 genomes]
rs34891917	0.91[AFR][1000 genomes]
rs34906832	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34920876	0.91[AFR][1000 genomes]
rs35024886	0.91[AFR][1000 genomes]
rs35150863	0.91[AFR][1000 genomes]
rs35209788	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35481231	0.91[AFR][1000 genomes]
rs35485367	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35554164	0.91[AFR][1000 genomes]
rs35795105	0.91[AFR][1000 genomes]
rs62305804	0.81[EUR][1000 genomes]
rs62305805	0.80[AMR][1000 genomes]
rs62305828	0.91[AFR][1000 genomes]
rs62305832	0.91[AFR][1000 genomes]
rs62305833	0.91[AFR][1000 genomes]
rs62305834	0.91[AFR][1000 genomes]
rs7441213	0.91[AFR][1000 genomes]
rs7441263	0.91[AFR][1000 genomes]
rs7441325	0.91[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931418	chr4:101500167-102443207	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:101740000-101745600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr4:101741200-101744600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr4:101742600-101744000	Weak transcription	GM12878-XiMat	blood
4	chr4:101743200-101745200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr4:101743600-101745000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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