Variant report

Variant rs59992228
Chromosome Location chr19:43827567-43827568
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43815000-43830000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr19:43821200-43837800 Weak transcription Right Atrium heart
3 chr19:43821600-43830000 Weak transcription ES-WA7 Cell Line embryonic stem cell
4 chr19:43822800-43833600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr19:43826800-43827600 Enhancers Primary neutrophils fromperipheralblood blood
6 chr19:43827000-43827600 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr19:43827200-43827600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
8 chr19:43827200-43827600 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr19:43827400-43827600 Enhancers H9 Cell Line embryonic stem cell
10 chr19:43827400-43827600 Flanking Active TSS Hela-S3 cervix
11 chr19:43827400-43827800 Enhancers NHEK skin
12 chr19:43827400-43828000 Enhancers HUES6 Cell Line embryonic stem cell
13 chr19:43827400-43830000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr19:43827400-43832200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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