Variant report

Variant rs188245599
Chromosome Location chrX:29793527-29793528
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:29792800-29793600 Enhancers Fetal Heart heart
2 chrX:29793000-29793800 Enhancers HUES48 Cell Line embryonic stem cell
3 chrX:29793000-29793800 Enhancers HUES64 Cell Line embryonic stem cell
4 chrX:29793200-29793600 Enhancers ES-I3 Cell Line embryonic stem cell
5 chrX:29793200-29793600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
6 chrX:29793400-29799000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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