Variant report

Variant	rs7996730
Chromosome Location	chr13:37715772-37715773
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10507445	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17054900	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17054907	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17054978	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17054982	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17054985	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17054986	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56905051	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57149532	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57266283	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57806247	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59237869	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60677413	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60888296	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61559782	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6563512	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7139475	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7319636	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7325430	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7330313	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7330518	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7336363	1.00[TSI][hapmap]
rs73533929	1.00[EUR][1000 genomes]
rs73547839	1.00[EUR][1000 genomes]
rs7985176	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7994265	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7996156	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7997086	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7999228	1.00[AMR][1000 genomes];1.00[EUR][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	nsv948975	chr13:37281203-38280430	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:37709200-37718200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr13:37710800-37718000	Weak transcription	NH-A	brain
3	chr13:37712600-37718200	Weak transcription	Hela-S3	cervix
4	chr13:37713800-37718400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr13:37714200-37717600	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr13:37715200-37715800	Enhancers	NHDF-Ad	bronchial
7	chr13:37715400-37715800	Enhancers	Osteobl	bone
8	chr13:37715600-37716000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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