Variant report

Variant	rs61742973
Chromosome Location	chr10:52595853-52595854
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10994643	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10994668	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12259930	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12263043	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12265892	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60228766	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73326765	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73326767	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7908964	0.94[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	nsv1035197	chr10:52446582-52622349	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr10:52576800-52597200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr10:52580400-52643200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr10:52585200-52617200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr10:52592800-52598000	Genic enhancers	Liver	Liver
5	chr10:52593200-52596200	Strong transcription	Fetal Intestine Large	intestine
6	chr10:52594200-52599400	Weak transcription	HepG2	liver
7	chr10:52594800-52617200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr10:52595800-52596800	Strong transcription	Fetal Intestine Small	intestine

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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