Variant report

Variant rs13385521
Chromosome Location chr2:172070991-172070992
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:172067600-172071200 Enhancers K562 blood
2 chr2:172067800-172071000 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr2:172067800-172073400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr2:172069400-172071000 Weak transcription ES-WA7 Cell Line embryonic stem cell
5 chr2:172069400-172071400 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr2:172069400-172073200 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr2:172070600-172072000 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr2:172070800-172071400 Enhancers NHEK skin
9 chr2:172070800-172071600 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr2:172070800-172071800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr2:172070800-172072000 Enhancers ES-I3 Cell Line embryonic stem cell
12 chr2:172070800-172072000 Enhancers H1 Cell Line embryonic stem cell
13 chr2:172070800-172072000 Enhancers H9 Cell Line embryonic stem cell
14 chr2:172070800-172072000 Enhancers HUES64 Cell Line embryonic stem cell
15 chr2:172070800-172072000 Enhancers iPS-15b Cell Line embryonic stem cell
16 chr2:172070800-172072000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links