Variant report

Variant rs137522
Chromosome Location chr22:33293908-33293909
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:33277000-33302000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr22:33283600-33299600 Weak transcription Right Atrium heart
3 chr22:33287800-33309600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr22:33287800-33312000 Weak transcription H1 Cell Line embryonic stem cell
5 chr22:33289000-33297200 Weak transcription Fetal Heart heart
6 chr22:33290000-33312000 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr22:33291200-33294600 Enhancers Placenta Placenta
8 chr22:33292800-33294600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr22:33292800-33294600 Enhancers Fetal Intestine Small intestine
10 chr22:33293000-33294600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr22:33293200-33294000 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr22:33293600-33301400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr22:33293800-33294200 Weak transcription Fetal Intestine Large intestine
14 chr22:33293800-33297400 Weak transcription K562 blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links