Variant report

Variant	rs73935996
Chromosome Location	chr2:67153864-67153865
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17032640	0.90[AFR][1000 genomes]
rs56337759	0.83[AFR][1000 genomes]
rs59394315	0.90[AFR][1000 genomes]
rs73935994	0.90[AFR][1000 genomes]
rs73935995	0.90[AFR][1000 genomes]
rs73935997	1.00[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	esv2762259	chr2:67109728-67165987	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67145400-67156600	Weak transcription	Fetal Heart	heart
2	chr2:67152600-67156800	Weak transcription	Ovary	ovary
3	chr2:67152600-67157000	Weak transcription	Hela-S3	cervix
4	chr2:67152600-67157000	Weak transcription	NHDF-Ad	bronchial
5	chr2:67152800-67157000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:67152800-67157000	Weak transcription	Pancreas	Pancrea
7	chr2:67153000-67157000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:67153200-67154600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr2:67153200-67157200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:67153400-67156200	Weak transcription	HMEC	breast
11	chr2:67153400-67156400	Weak transcription	NHEK	skin
12	chr2:67153600-67154000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr2:67153600-67155600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr2:67153600-67156800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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Input of quick search could be:

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

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