Variant report

Variant rs6601705
Chromosome Location chr8:8392743-8392744
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:8385600-8394000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr8:8388400-8395000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr8:8388600-8393800 Weak transcription Placenta Amnion Placenta Amnion
4 chr8:8388600-8394000 Weak transcription HUVEC blood vessel
5 chr8:8388800-8394200 Weak transcription Osteobl bone
6 chr8:8389000-8393800 Weak transcription NHDF-Ad bronchial
7 chr8:8389000-8394000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr8:8389000-8394200 Weak transcription Muscle Satellite Cultured Cells --
9 chr8:8389200-8393800 Weak transcription A549 lung
10 chr8:8389200-8394000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr8:8389200-8394400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr8:8389200-8394400 Weak transcription HSMM muscle
13 chr8:8389200-8403000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr8:8389400-8394800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr8:8392600-8392800 ZNF genes & repeats iPS-18 Cell Line embryonic stem cell

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