Variant report

Variant	rs10994075
Chromosome Location	chr10:61695175-61695176
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10994069	0.98[ASN][1000 genomes]
rs10994076	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1171811	0.88[ASN][1000 genomes]
rs1171822	0.88[ASN][1000 genomes]
rs1171823	0.88[ASN][1000 genomes]
rs1171827	0.88[ASN][1000 genomes]
rs1180659	0.88[ASN][1000 genomes]
rs11813228	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1184955	0.88[ASN][1000 genomes]
rs12243713	0.98[ASN][1000 genomes]
rs12254991	0.98[ASN][1000 genomes]
rs12256615	0.98[ASN][1000 genomes]
rs12268832	0.93[ASN][1000 genomes]
rs12784462	0.80[ASN][1000 genomes]
rs1684889	0.88[ASN][1000 genomes]
rs1684914	0.88[ASN][1000 genomes]
rs6479671	1.00[ASN][1000 genomes]
rs7070679	0.95[ASN][1000 genomes]
rs7085413	1.00[ASN][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	esv1800316	chr10:61639599-61700473	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:61694200-61695600	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr10:61694800-61695400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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