Variant report

Variant rs72674473
Chromosome Location chr1:76646956-76646957
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:76636600-76652800 Weak transcription Primary B cells from cord blood blood
2 chr1:76643800-76651800 Weak transcription Fetal Kidney kidney
3 chr1:76644400-76651000 Weak transcription Fetal Lung lung
4 chr1:76644800-76653200 Weak transcription H9 Cell Line embryonic stem cell
5 chr1:76645400-76652600 Weak transcription HUVEC blood vessel
6 chr1:76646200-76647000 ZNF genes & repeats Aorta Aorta
7 chr1:76646400-76647000 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:76646600-76647000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr1:76646600-76647200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
10 chr1:76646600-76652600 Weak transcription Brain Hippocampus Middle brain
11 chr1:76646600-76658000 Weak transcription Fetal Stomach stomach
12 chr1:76646800-76647000 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr1:76646800-76647400 Weak transcription Ovary ovary
14 chr1:76646800-76648000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr1:76646800-76652800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr1:76646800-76653200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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