Variant report

Variant rs10928200
Chromosome Location chr2:144578152-144578153
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:144574600-144582200 Weak transcription H9 Cell Line embryonic stem cell
2 chr2:144574800-144591000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr2:144575000-144581600 Weak transcription HUES64 Cell Line embryonic stem cell
4 chr2:144575000-144581600 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr2:144575000-144582400 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr2:144575200-144581600 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr2:144575200-144582200 Weak transcription iPS-15b Cell Line embryonic stem cell
8 chr2:144577000-144578800 Active TSS NHDF-Ad bronchial
9 chr2:144577000-144579200 Weak transcription Fetal Stomach stomach
10 chr2:144577400-144582200 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr2:144577400-144582600 Weak transcription ES-I3 Cell Line embryonic stem cell
12 chr2:144577600-144578200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
13 chr2:144577600-144578200 Active TSS Fetal Muscle Leg muscle
14 chr2:144577800-144578800 Enhancers Fetal Brain Male brain
15 chr2:144578000-144578200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links