Variant report

Variant rs113315942
Chromosome Location chr2:10402026-10402027
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:10392800-10407600 Weak transcription Gastric stomach
2 chr2:10396600-10407800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr2:10400800-10402400 Weak transcription Fetal Intestine Small intestine
4 chr2:10400800-10405000 Weak transcription HSMMtube muscle
5 chr2:10400800-10406400 Weak transcription HSMM muscle
6 chr2:10401400-10402200 Enhancers Fetal Stomach stomach
7 chr2:10401400-10402400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr2:10401400-10403000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
9 chr2:10401600-10405800 Weak transcription Rectal Mucosa Donor 31 rectum
10 chr2:10401600-10409600 Weak transcription Rectal Mucosa Donor 29 rectum

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