Variant report

Variant rs72686546
Chromosome Location chr4:121003946-121003947
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:120989400-121012600 Weak transcription Aorta Aorta
2 chr4:121000400-121007000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr4:121002200-121007000 Weak transcription Muscle Satellite Cultured Cells --
4 chr4:121002400-121004600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
5 chr4:121002600-121004800 Enhancers HUES48 Cell Line embryonic stem cell
6 chr4:121002800-121004000 Enhancers HUES64 Cell Line embryonic stem cell
7 chr4:121002800-121004000 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr4:121002800-121004200 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr4:121002800-121004600 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr4:121002800-121004600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr4:121003000-121004000 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr4:121003000-121004000 Enhancers Brain Substantia Nigra brain
13 chr4:121003400-121004600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr4:121003800-121004400 Weak transcription HUES6 Cell Line embryonic stem cell
15 chr4:121003800-121006800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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