Variant report

Variant rs59928993
Chromosome Location chr6:13851621-13851622
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:13847800-13864000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr6:13849400-13860000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr6:13850400-13852400 Enhancers Fetal Intestine Large intestine
4 chr6:13851200-13852000 Enhancers Fetal Intestine Small intestine
5 chr6:13851400-13852000 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr6:13851400-13852000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr6:13851400-13852000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr6:13851600-13851800 Enhancers H9 Cell Line embryonic stem cell
9 chr6:13851600-13851800 Enhancers HUES6 Cell Line embryonic stem cell
10 chr6:13851600-13851800 Enhancers HUES64 Cell Line embryonic stem cell
11 chr6:13851600-13851800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell

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