Variant report

Variant rs538277844
Chromosome Location chr11:121069032-121069033
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:121062600-121070000 Weak transcription Fetal Heart heart
2 chr11:121065800-121070200 Weak transcription H9 Cell Line embryonic stem cell
3 chr11:121066000-121069200 Weak transcription H1 Cell Line embryonic stem cell
4 chr11:121066400-121069200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr11:121066400-121069200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr11:121068400-121069200 Enhancers HUES48 Cell Line embryonic stem cell
7 chr11:121068600-121069400 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr11:121068600-121069400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr11:121068800-121069600 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr11:121068800-121070800 Enhancers HUES64 Cell Line embryonic stem cell
11 chr11:121068800-121070800 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr11:121068800-121070800 Enhancers iPS-20b Cell Line embryonic stem cell
13 chr11:121069000-121069400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr11:121069000-121070800 Enhancers HUES6 Cell Line embryonic stem cell

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