Variant report

Variant rs6689873
Chromosome Location chr1:209224026-209224027
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:209213200-209224400 Weak transcription Esophagus oesophagus
2 chr1:209221800-209225600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr1:209222000-209225000 Enhancers NHEK skin
4 chr1:209222000-209225800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:209222600-209224600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:209222800-209224400 Weak transcription HMEC breast
7 chr1:209223000-209232600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr1:209223200-209224200 Enhancers Fetal Muscle Leg muscle
9 chr1:209223800-209224400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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