Variant report

Variant rs7722916
Chromosome Location chr5:177880829-177880830
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177856800-177887200 Weak transcription Right Atrium heart
2 chr5:177874600-177888200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr5:177877000-177881600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr5:177877600-177881400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr5:177877600-177894200 Weak transcription Spleen Spleen
6 chr5:177877800-177895400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr5:177878000-177888000 Weak transcription Primary neutrophils fromperipheralblood blood
8 chr5:177879200-177881000 Enhancers Cortex derived primary cultured neurospheres brain
9 chr5:177879800-177881600 Enhancers NHDF-Ad bronchial
10 chr5:177880000-177881000 Enhancers HUES64 Cell Line embryonic stem cell
11 chr5:177880200-177881000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr5:177880200-177881600 Enhancers iPS-20b Cell Line embryonic stem cell
13 chr5:177880200-177882200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr5:177880600-177882600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr5:177880800-177881200 Weak transcription Fetal Thymus thymus
16 chr5:177880800-177882200 Weak transcription H1 Cell Line embryonic stem cell
17 chr5:177880800-177888000 Weak transcription HUES6 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links