Variant report

Variant rs210429
Chromosome Location chrX:104942374-104942375
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:104939000-104946600 Enhancers Hela-S3 cervix
2 chrX:104940200-104945400 Weak transcription NHEK skin
3 chrX:104940400-104945000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chrX:104940400-104945200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chrX:104940600-104942600 Enhancers ES-I3 Cell Line embryonic stem cell
6 chrX:104940800-104942800 Enhancers iPS-18 Cell Line embryonic stem cell
7 chrX:104941200-104943800 Weak transcription HUES6 Cell Line embryonic stem cell
8 chrX:104941400-104945400 Weak transcription ES-WA7 Cell Line embryonic stem cell
9 chrX:104941600-104943400 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chrX:104942000-104942400 Weak transcription HUES64 Cell Line embryonic stem cell
11 chrX:104942000-104943600 Enhancers Muscle Satellite Cultured Cells --
12 chrX:104942200-104942400 Enhancers HUES48 Cell Line embryonic stem cell
13 chrX:104942200-104944800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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