Variant report

Variant rs2148208
Chromosome Location chr10:25397192-25397193
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:25392400-25414200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:25393400-25398400 Enhancers iPS-15b Cell Line embryonic stem cell
3 chr10:25394000-25402000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr10:25394600-25397200 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr10:25395000-25400400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr10:25395000-25401800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr10:25395000-25402400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr10:25395000-25405000 Weak transcription H9 Cell Line embryonic stem cell
9 chr10:25395400-25397200 Weak transcription iPS-20b Cell Line embryonic stem cell
10 chr10:25395800-25397200 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr10:25396800-25398000 Enhancers HUES48 Cell Line embryonic stem cell
12 chr10:25397000-25397200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr10:25397000-25397400 Enhancers H1 Cell Line embryonic stem cell
14 chr10:25397000-25398000 Enhancers HUES6 Cell Line embryonic stem cell

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