Variant report

Variant rs73955283
Chromosome Location chr18:30337187-30337188
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:30333800-30341400 Weak transcription Fetal Kidney kidney
2 chr18:30334200-30338800 Weak transcription Dnd41 blood
3 chr18:30334600-30337400 Genic enhancers HepG2 liver
4 chr18:30335200-30339600 Weak transcription H1 Cell Line embryonic stem cell
5 chr18:30335200-30340000 Weak transcription Fetal Brain Male brain
6 chr18:30335200-30340400 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr18:30335600-30339800 Weak transcription iPS-15b Cell Line embryonic stem cell
8 chr18:30335600-30342200 Enhancers Primary B cells from peripheral blood blood
9 chr18:30335800-30339600 Weak transcription iPS-18 Cell Line embryonic stem cell
10 chr18:30336000-30337600 ZNF genes & repeats H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr18:30336000-30339600 Weak transcription HUES48 Cell Line embryonic stem cell
12 chr18:30336200-30339400 Weak transcription HUES64 Cell Line embryonic stem cell
13 chr18:30336200-30339600 Weak transcription iPS-20b Cell Line embryonic stem cell
14 chr18:30336200-30339800 Genic enhancers Primary B cells from cord blood blood
15 chr18:30336400-30338400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links