Variant report

Variant rs187813801
Chromosome Location chr14:69485213-69485214
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:69473000-69503600 Weak transcription Right Atrium heart
2 chr14:69481000-69486000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr14:69483200-69485600 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr14:69484200-69485400 Enhancers ES-I3 Cell Line embryonic stem cell
5 chr14:69484200-69485400 Enhancers HUES64 Cell Line embryonic stem cell
6 chr14:69484800-69485400 Enhancers HUES6 Cell Line embryonic stem cell
7 chr14:69484800-69485400 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr14:69484800-69485400 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr14:69484800-69485600 Enhancers K562 blood
10 chr14:69485000-69485400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
11 chr14:69485000-69486200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr14:69485200-69485400 Enhancers H9 Cell Line embryonic stem cell
13 chr14:69485200-69485400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr14:69485200-69485600 Enhancers Primary neutrophils fromperipheralblood blood

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