Variant report

Variant rs10027679
Chromosome Location chr4:3756232-3756233
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3748200-3758200 Weak transcription Aorta Aorta
2 chr4:3750000-3763200 Weak transcription Pancreas Pancrea
3 chr4:3753000-3756600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr4:3753800-3756600 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr4:3753800-3756800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
6 chr4:3754400-3757000 Enhancers H1 Cell Line embryonic stem cell
7 chr4:3754800-3756400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
8 chr4:3754800-3757000 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr4:3755000-3756600 Enhancers HUES48 Cell Line embryonic stem cell
10 chr4:3755200-3756600 Enhancers ES-WA7 Cell Line embryonic stem cell
11 chr4:3755200-3756800 Enhancers HUES6 Cell Line embryonic stem cell
12 chr4:3755600-3756400 Enhancers HUES64 Cell Line embryonic stem cell
13 chr4:3755800-3756800 Enhancers H9 Cell Line embryonic stem cell
14 chr4:3756200-3756600 Enhancers iPS-20b Cell Line embryonic stem cell
15 chr4:3756200-3756800 Enhancers ES-I3 Cell Line embryonic stem cell
16 chr4:3756200-3756800 Bivalent Enhancer Adipose Nuclei Adipose
17 chr4:3756200-3757200 Enhancers Right Ventricle heart
18 chr4:3756200-3757400 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
19 chr4:3756200-3764000 Weak transcription Fetal Kidney kidney

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