Variant report

Variant rs561082732
Chromosome Location chr11:46744545-46744546
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:46728800-46745600 Weak transcription H9 Cell Line embryonic stem cell
2 chr11:46728800-46745600 Weak transcription HUES64 Cell Line embryonic stem cell
3 chr11:46739800-46745600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr11:46740200-46745600 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr11:46740200-46745600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr11:46740400-46745600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr11:46741400-46744600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr11:46741800-46746800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr11:46742000-46745600 Weak transcription A549 lung
10 chr11:46744000-46745400 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr11:46744200-46745000 Transcr. at gene 5' and 3' HepG2 liver
12 chr11:46744400-46744800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr11:46744400-46752000 Genic enhancers Liver Liver

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