Variant report

Variant rs12097831
Chromosome Location chr1:180631029-180631030
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180602000-180645200 Weak transcription Gastric stomach
2 chr1:180613200-180632600 Weak transcription Aorta Aorta
3 chr1:180619600-180632600 Weak transcription Pancreas Pancrea
4 chr1:180619600-180634600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr1:180625800-180634800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr1:180627600-180632800 Weak transcription A549 lung
7 chr1:180627600-180640000 Weak transcription Fetal Heart heart
8 chr1:180627800-180634200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr1:180628200-180631600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:180629200-180633800 Weak transcription Sigmoid Colon Sigmoid Colon
11 chr1:180629600-180632600 Weak transcription Primary T helper cells fromperipheralblood blood
12 chr1:180629600-180641000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr1:180630800-180634400 Weak transcription Skeletal Muscle Female skeletal muscle
14 chr1:180631000-180633600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr1:180631000-180634200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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