Variant report

Variant rs370912151
Chromosome Location chr12:40868260-40868261
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:40866400-40869400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
2 chr12:40866600-40870600 Enhancers HUES48 Cell Line embryonic stem cell
3 chr12:40867000-40869000 Enhancers H9 Cell Line embryonic stem cell
4 chr12:40867200-40868400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr12:40867200-40870600 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr12:40867400-40870400 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr12:40867600-40869000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr12:40867600-40870200 Weak transcription ES-WA7 Cell Line embryonic stem cell
9 chr12:40867800-40869000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr12:40867800-40869600 Enhancers HUES6 Cell Line embryonic stem cell
11 chr12:40868000-40869000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr12:40868000-40869000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr12:40868000-40869200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr12:40868200-40869200 Enhancers ES-I3 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links