Variant report

Variant rs2892788
Chromosome Location chr4:119008469-119008470
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:119006800-119008600 Enhancers iPS-18 Cell Line embryonic stem cell
2 chr4:119006800-119008800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr4:119006800-119009000 Enhancers ES-I3 Cell Line embryonic stem cell
4 chr4:119006800-119009200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
5 chr4:119007000-119008600 Enhancers HUES6 Cell Line embryonic stem cell
6 chr4:119007000-119008800 Enhancers HUES64 Cell Line embryonic stem cell
7 chr4:119007000-119009000 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr4:119007000-119009200 Enhancers HUVEC blood vessel
9 chr4:119007200-119008600 Enhancers HUES48 Cell Line embryonic stem cell
10 chr4:119007600-119009000 Weak transcription Dnd41 blood
11 chr4:119007800-119008600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr4:119007800-119008600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr4:119007800-119009000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr4:119008400-119008800 Enhancers ES-WA7 Cell Line embryonic stem cell

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