Variant report

Variant rs10948512
Chromosome Location chr6:49536392-49536393
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:49525600-49537600 Weak transcription Fetal Intestine Small intestine
2 chr6:49531600-49538000 Weak transcription K562 blood
3 chr6:49534200-49537200 Weak transcription HepG2 liver
4 chr6:49534200-49537400 Weak transcription A549 lung
5 chr6:49534200-49538200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr6:49534400-49537000 Weak transcription Hela-S3 cervix
7 chr6:49534400-49538400 Weak transcription NHEK skin
8 chr6:49535000-49536800 Weak transcription Adipose Nuclei Adipose
9 chr6:49535800-49538200 Weak transcription Stomach Mucosa stomach
10 chr6:49536000-49537200 Weak transcription HUVEC blood vessel
11 chr6:49536000-49537400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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