Variant report

Variant rs1188489
Chromosome Location chr1:228621772-228621773
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:228619400-228624400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:228620400-228622000 Enhancers Fetal Intestine Large intestine
3 chr1:228620800-228622000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr1:228620800-228622200 Enhancers Placenta Placenta
5 chr1:228621000-228622000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
6 chr1:228621000-228622000 Enhancers Fetal Intestine Small intestine
7 chr1:228621200-228621800 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr1:228621600-228621800 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
9 chr1:228621600-228622000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr1:228621600-228622000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr1:228621600-228622200 Enhancers K562 blood

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