Variant report

Variant rs17502345
Chromosome Location chr5:145672255-145672256
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:145649200-145676200 Weak transcription Fetal Brain Male brain
2 chr5:145652800-145672400 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr5:145657800-145676000 Weak transcription Brain Substantia Nigra brain
4 chr5:145663200-145674400 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr5:145663200-145674600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
6 chr5:145665800-145672600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr5:145666600-145677000 Weak transcription Rectal Mucosa Donor 31 rectum
8 chr5:145667000-145677400 Weak transcription HUVEC blood vessel
9 chr5:145667200-145675400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr5:145667400-145675400 Weak transcription A549 lung
11 chr5:145668400-145672600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr5:145669000-145672400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr5:145669000-145681000 Weak transcription HSMM muscle
14 chr5:145669200-145672400 Weak transcription Monocytes-CD14+_RO01746 blood
15 chr5:145669400-145673600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
16 chr5:145671400-145673200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr5:145671600-145673200 Enhancers HMEC breast
18 chr5:145672000-145672600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
19 chr5:145672000-145672800 Enhancers NHEK skin

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