Variant report

Variant rs4091683
Chromosome Location chr15:39648912-39648913
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:39641600-39649600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr15:39643800-39650000 Weak transcription Fetal Heart heart
3 chr15:39646000-39650600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr15:39646200-39650000 Weak transcription HepG2 liver
5 chr15:39646400-39649600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr15:39646400-39649800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr15:39646600-39649400 Weak transcription Monocytes-CD14+_RO01746 blood
8 chr15:39646600-39649600 Weak transcription Primary monocytes fromperipheralblood blood
9 chr15:39646800-39649400 Weak transcription HUVEC blood vessel
10 chr15:39647200-39649600 Weak transcription Primary neutrophils fromperipheralblood blood
11 chr15:39647600-39649400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr15:39647800-39650000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr15:39648800-39649200 Weak transcription K562 blood

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