Variant report

Variant rs569787321
Chromosome Location chr12:39634036-39634037
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:39629600-39635000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr12:39632600-39634200 Enhancers Fetal Intestine Large intestine
3 chr12:39632600-39634400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr12:39632600-39634800 Enhancers Rectal Mucosa Donor 31 rectum
5 chr12:39632600-39635000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
6 chr12:39632800-39634200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr12:39633200-39634200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr12:39633400-39634400 Enhancers HUES64 Cell Line embryonic stem cell
9 chr12:39633400-39634600 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr12:39633400-39634800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr12:39633800-39634600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr12:39633800-39634800 Enhancers HUES6 Cell Line embryonic stem cell
13 chr12:39633800-39635000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr12:39634000-39634600 Enhancers Sigmoid Colon Sigmoid Colon
15 chr12:39634000-39634800 Enhancers Rectal Mucosa Donor 29 rectum

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