Variant report

Variant rs1300266
Chromosome Location chr3:100418594-100418595
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100415200-100418600 Enhancers HepG2 liver
2 chr3:100415600-100420400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr3:100415600-100420400 Weak transcription NHEK skin
4 chr3:100415800-100420200 Weak transcription HMEC breast
5 chr3:100415800-100420800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr3:100415800-100424600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr3:100416200-100419600 Weak transcription K562 blood
8 chr3:100416400-100418600 Enhancers Fetal Intestine Small intestine
9 chr3:100417000-100418800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
10 chr3:100417000-100423600 Weak transcription Esophagus oesophagus
11 chr3:100418400-100421400 Weak transcription Fetal Intestine Large intestine

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