Variant report

Variant rs13144322
Chromosome Location chr4:3772578-3772579
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3769400-3773200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr4:3769600-3772600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr4:3769600-3775000 Weak transcription Pancreas Pancrea
4 chr4:3770600-3776200 Bivalent Enhancer Fetal Muscle Trunk muscle
5 chr4:3771000-3776200 Bivalent Enhancer Fetal Muscle Leg muscle
6 chr4:3772200-3772600 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr4:3772200-3773000 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr4:3772200-3773600 Enhancers HUES6 Cell Line embryonic stem cell
9 chr4:3772400-3772600 Bivalent Enhancer Fetal Brain Female brain
10 chr4:3772400-3773000 Enhancers H1 Cell Line embryonic stem cell
11 chr4:3772400-3773000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr4:3772400-3773200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr4:3772400-3773200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
14 chr4:3772400-3773400 Enhancers Brain Anterior Caudate brain
15 chr4:3772400-3773800 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
16 chr4:3772400-3773800 Flanking Active TSS HepG2 liver

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