Variant report

Variant rs12858147
Chromosome Location chrX:54850899-54850900
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:54842600-54852000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chrX:54843200-54852600 Weak transcription HSMMtube muscle
3 chrX:54850000-54851400 Bivalent Enhancer Fetal Muscle Trunk muscle
4 chrX:54850200-54851000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chrX:54850400-54851000 Weak transcription iPS-15b Cell Line embryonic stem cell
6 chrX:54850400-54851400 Enhancers Fetal Adrenal Gland Adrenal Gland
7 chrX:54850600-54851000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chrX:54850600-54851000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chrX:54850600-54851000 Bivalent Enhancer Fetal Stomach stomach
10 chrX:54850600-54851200 Enhancers Skeletal Muscle Male skeletal muscle
11 chrX:54850600-54851600 Enhancers Fetal Muscle Leg muscle
12 chrX:54850800-54851000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chrX:54850800-54851000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chrX:54850800-54851000 Enhancers Left Ventricle heart
15 chrX:54850800-54851000 Enhancers Psoas Muscle Psoas

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