Variant report

Variant rs374990779
Chromosome Location chr7:149510617-149510618
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:149473800-149534800 Weak transcription Right Atrium heart
2 chr7:149487600-149518400 Weak transcription Gastric stomach
3 chr7:149490600-149520200 Weak transcription Brain Anterior Caudate brain
4 chr7:149490800-149514400 Weak transcription Brain Hippocampus Middle brain
5 chr7:149503600-149511600 Weak transcription Fetal Stomach stomach
6 chr7:149508000-149512400 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr7:149509600-149511200 Enhancers Primary T cells from cord blood blood
8 chr7:149510000-149511200 Enhancers Fetal Thymus thymus
9 chr7:149510200-149510800 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
10 chr7:149510200-149511000 Bivalent Enhancer Primary T cells fromperipheralblood blood
11 chr7:149510200-149511000 Enhancers K562 blood
12 chr7:149510200-149511800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr7:149510400-149510800 Enhancers ES-WA7 Cell Line embryonic stem cell
14 chr7:149510400-149510800 Enhancers HUES6 Cell Line embryonic stem cell
15 chr7:149510400-149514200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
16 chr7:149510400-149514200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
17 chr7:149510600-149510800 Enhancers H1 Cell Line embryonic stem cell
18 chr7:149510600-149511000 Enhancers iPS-15b Cell Line embryonic stem cell
19 chr7:149510600-149512200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell

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