Variant report

Variant rs61134068
Chromosome Location chr2:113631497-113631498
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113626200-113634000 Weak transcription Placenta Placenta
2 chr2:113629000-113634000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:113629200-113632800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr2:113629200-113632800 Weak transcription NHEK skin
5 chr2:113629200-113633000 Weak transcription HMEC breast
6 chr2:113629200-113637800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr2:113629200-113643200 Weak transcription Right Atrium heart
8 chr2:113629800-113632800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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