Variant report

Variant rs3806591
Chromosome Location chr2:234626199-234626200
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:234617800-234631600 Weak transcription Gastric stomach
2 chr2:234620400-234659200 Weak transcription Colonic Mucosa Colon
3 chr2:234620600-234652200 Weak transcription Esophagus oesophagus
4 chr2:234621800-234626200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr2:234622200-234627400 Weak transcription Fetal Intestine Small intestine
6 chr2:234625000-234626400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr2:234625600-234626600 Strong transcription NHEK skin
8 chr2:234625800-234626600 Enhancers Liver Liver
9 chr2:234626000-234634600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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