Variant report

Variant rs61810425
Chromosome Location chr1:147368606-147368607
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:147362400-147369400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:147362800-147369600 Weak transcription Right Atrium heart
3 chr1:147363400-147368800 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr1:147363400-147369200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr1:147363400-147374600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr1:147363800-147369000 Weak transcription Fetal Muscle Trunk muscle
7 chr1:147364600-147369400 Weak transcription Fetal Intestine Small intestine
8 chr1:147364800-147368800 Weak transcription Fetal Muscle Leg muscle
9 chr1:147364800-147369000 Weak transcription Left Ventricle heart
10 chr1:147365000-147368800 Weak transcription HSMMtube muscle
11 chr1:147365000-147369200 Weak transcription Fetal Brain Male brain
12 chr1:147368600-147368800 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr1:147368600-147370200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr1:147368600-147370400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
15 chr1:147368600-147370400 Enhancers Fetal Heart heart

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