Variant report

Variant rs10799301
Chromosome Location chr1:225567257-225567258
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:225564400-225577600 Weak transcription Fetal Intestine Small intestine
2 chr1:225565800-225568000 Enhancers HUES48 Cell Line embryonic stem cell
3 chr1:225565800-225568200 Enhancers HUES64 Cell Line embryonic stem cell
4 chr1:225565800-225568200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr1:225566000-225567400 Enhancers HUES6 Cell Line embryonic stem cell
6 chr1:225566000-225567800 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr1:225566000-225568200 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr1:225566400-225567600 Weak transcription ES-WA7 Cell Line embryonic stem cell
9 chr1:225566800-225567600 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr1:225566800-225567600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr1:225566800-225568000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr1:225566800-225568200 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr1:225567000-225567800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
14 chr1:225567000-225583400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
15 chr1:225567000-225585000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr1:225567200-225577600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr1:225567200-225585000 Weak transcription NHEK skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links