Variant report

Variant rs59040705
Chromosome Location chr1:215593837-215593838
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:215590600-215594400 Weak transcription NHDF-Ad bronchial
2 chr1:215590800-215594800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:215592400-215594600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr1:215592600-215594400 Weak transcription Muscle Satellite Cultured Cells --
5 chr1:215592600-215594800 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr1:215592600-215596000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr1:215592800-215594600 Weak transcription HUES6 Cell Line embryonic stem cell
8 chr1:215592800-215595000 Weak transcription Fetal Adrenal Gland Adrenal Gland
9 chr1:215593000-215594600 Weak transcription Osteobl bone
10 chr1:215593000-215594800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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