Variant report

Variant rs1611222
Chromosome Location chr6:29761896-29761897
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29760400-29764400 Weak transcription Hela-S3 cervix
2 chr6:29761000-29762000 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:29761000-29763000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
4 chr6:29761000-29765200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr6:29761200-29762200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr6:29761200-29763800 Weak transcription HMEC breast
7 chr6:29761200-29763800 Weak transcription NHEK skin
8 chr6:29761200-29764400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:29761400-29763800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr6:29761800-29762000 Bivalent/Poised TSS H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr6:29761800-29766200 Weak transcription Pancreas Pancrea

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