Variant report

Variant rs10438316
Chromosome Location chr15:31380575-31380576
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:31376200-31383200 Weak transcription Pancreas Pancrea
2 chr15:31376200-31384800 Weak transcription Gastric stomach
3 chr15:31376200-31389000 Weak transcription Right Atrium heart
4 chr15:31376200-31390800 Weak transcription Brain Substantia Nigra brain
5 chr15:31378800-31383400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr15:31379000-31380600 Genic enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr15:31379600-31381000 Enhancers HepG2 liver
8 chr15:31379800-31382200 Transcr. at gene 5' and 3' Foreskin Melanocyte Primary Cells skin01 Skin
9 chr15:31379800-31388600 Weak transcription Placenta Placenta
10 chr15:31380400-31380800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
11 chr15:31380400-31381000 Enhancers Esophagus oesophagus

Quick Search:


  
Input of quick search could be:

what's new

Quick links