Variant report

Variant rs13230620
Chromosome Location chr7:79945590-79945591
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:79937200-79949000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr7:79941800-79946000 Weak transcription Fetal Intestine Small intestine
3 chr7:79941800-79946600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr7:79942000-79945800 Weak transcription Fetal Intestine Large intestine
5 chr7:79942000-79947000 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr7:79942800-79952800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr7:79943000-79947200 Weak transcription HMEC breast
8 chr7:79943400-79945600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr7:79943400-79945800 Weak transcription HUVEC blood vessel
10 chr7:79943800-79946600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr7:79943800-79946800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr7:79943800-79947600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr7:79943800-79952600 Weak transcription NHEK skin

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