Variant report

Variant rs4755062
Chromosome Location chr11:104728524-104728525
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:104715600-104730000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr11:104727200-104728800 Enhancers HUES48 Cell Line embryonic stem cell
3 chr11:104727400-104728600 Enhancers HUES6 Cell Line embryonic stem cell
4 chr11:104727400-104728600 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr11:104727600-104728600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr11:104727600-104728600 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr11:104728000-104731000 Enhancers Dnd41 blood
8 chr11:104728200-104729800 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr11:104728200-104730200 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr11:104728400-104728800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr11:104728400-104729800 Weak transcription HUES64 Cell Line embryonic stem cell
12 chr11:104728400-104729800 Enhancers Primary T helper 17 cells PMA-I stimulated --

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