Variant report

Variant rs114272969
Chromosome Location chr1:159209865-159209866
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:159199600-159211800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr1:159208800-159210200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:159208800-159210600 Enhancers HMEC breast
4 chr1:159209000-159210000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr1:159209000-159210600 Enhancers NHEK skin
6 chr1:159209000-159211000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:159209200-159210200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr1:159209200-159210200 Enhancers HUVEC blood vessel
9 chr1:159209200-159210400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr1:159209400-159210000 Enhancers Hela-S3 cervix
11 chr1:159209800-159210000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr1:159209800-159210000 Flanking Active TSS GM12878-XiMat blood
13 chr1:159209800-159211000 Enhancers Primary monocytes fromperipheralblood blood

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