Variant report

Variant rs11990551
Chromosome Location chr8:43780356-43780357
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:43768600-43794600 Weak transcription NHEK skin
2 chr8:43770600-43794600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr8:43771600-43780400 Weak transcription K562 blood
4 chr8:43776000-43781000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr8:43776000-43781000 Weak transcription Aorta Aorta
6 chr8:43776000-43781000 Weak transcription Fetal Kidney kidney
7 chr8:43777400-43781000 Weak transcription Gastric stomach
8 chr8:43778800-43781400 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
9 chr8:43779000-43783400 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
10 chr8:43779000-43795000 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
11 chr8:43779200-43781000 Weak transcription NH-A brain
12 chr8:43779200-43785400 Weak transcription HSMMtube muscle
13 chr8:43779200-43791600 ZNF genes & repeats HUES48 Cell Line embryonic stem cell
14 chr8:43779400-43781400 ZNF genes & repeats H1 Cell Line embryonic stem cell
15 chr8:43779400-43791600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr8:43779400-43791800 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
17 chr8:43779800-43781000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

Quick Search:


  
Input of quick search could be:

what's new

Quick links