Variant report

Variant rs1880549
Chromosome Location chr7:14793847-14793848
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:14787400-14801400 Weak transcription Brain Cingulate Gyrus brain
2 chr7:14788400-14794200 Weak transcription HMEC breast
3 chr7:14788600-14794400 Weak transcription NHDF-Ad bronchial
4 chr7:14792800-14794200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr7:14792800-14794200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr7:14793000-14794200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr7:14793600-14794000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
8 chr7:14793600-14794600 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr7:14793600-14794600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr7:14793600-14794800 Enhancers Muscle Satellite Cultured Cells --
11 chr7:14793800-14794600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr7:14793800-14794600 Enhancers Osteobl bone
13 chr7:14793800-14794800 Enhancers HUVEC blood vessel

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