Variant report

Variant rs16841784
Chromosome Location chr1:159132953-159132954
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:159131000-159133000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr1:159131400-159133000 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr1:159131400-159133000 Enhancers NHEK skin
4 chr1:159131400-159133200 Weak transcription HUES64 Cell Line embryonic stem cell
5 chr1:159131800-159133200 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr1:159131800-159137400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr1:159132000-159133200 Weak transcription HSMM muscle
8 chr1:159132400-159133200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:159132600-159133000 Enhancers Primary monocytes fromperipheralblood blood
10 chr1:159132800-159133000 Enhancers H1 Cell Line embryonic stem cell
11 chr1:159132800-159133000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr1:159132800-159133000 Bivalent Enhancer Primary mononuclear cells fromperipheralblood Blood
13 chr1:159132800-159133000 Enhancers Skeletal Muscle Male skeletal muscle
14 chr1:159132800-159133800 Enhancers HSMMtube muscle
15 chr1:159132800-159134000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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