Variant report

Variant rs375884380
Chromosome Location chr5:52646485-52646486
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:52642800-52656000 Weak transcription Aorta Aorta
2 chr5:52645600-52646600 Weak transcription Fetal Brain Female brain
3 chr5:52645600-52647400 Enhancers HSMM muscle
4 chr5:52645600-52647400 Enhancers NHLF lung
5 chr5:52645600-52647600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr5:52645800-52646600 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr5:52645800-52647000 Enhancers HUES48 Cell Line embryonic stem cell
8 chr5:52645800-52647200 Enhancers Fetal Stomach stomach
9 chr5:52645800-52647400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr5:52645800-52647400 Enhancers Muscle Satellite Cultured Cells --
11 chr5:52645800-52647400 Enhancers NHDF-Ad bronchial
12 chr5:52646000-52646600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr5:52646000-52647400 Enhancers HMEC breast
14 chr5:52646200-52646600 Weak transcription Fetal Brain Male brain
15 chr5:52646200-52647000 Enhancers NHEK skin
16 chr5:52646200-52647200 Weak transcription HSMMtube muscle
17 chr5:52646200-52647400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr5:52646400-52647000 Enhancers Colon Smooth Muscle Colon
19 chr5:52646400-52647400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
20 chr5:52646400-52647600 Enhancers A549 lung
21 chr5:52646400-52649000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
22 chr5:52646400-52650400 Weak transcription Osteobl bone
23 chr5:52646400-52651200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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