Variant report

Variant rs73788637
Chromosome Location chr6:167815905-167815906
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167814200-167816000 Enhancers Fetal Intestine Large intestine
2 chr6:167814600-167816000 Enhancers Fetal Intestine Small intestine
3 chr6:167815000-167816000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr6:167815000-167817400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr6:167815200-167816000 Enhancers H1 Cell Line embryonic stem cell
6 chr6:167815200-167816000 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
7 chr6:167815400-167816000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr6:167815400-167816200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr6:167815400-167820800 Bivalent Enhancer HepG2 liver
10 chr6:167815600-167816000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
11 chr6:167815600-167816000 Bivalent Enhancer Fetal Muscle Trunk muscle
12 chr6:167815800-167816200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr6:167815800-167820200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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