Variant report

Variant rs373803222
Chromosome Location chr4:8166486-8166487
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:8161600-8166600 Enhancers Primary B cells from cord blood blood
2 chr4:8161600-8166600 Enhancers Primary B cells from peripheral blood blood
3 chr4:8161800-8167000 Weak transcription Right Atrium heart
4 chr4:8161800-8167000 Enhancers Skeletal Muscle Female skeletal muscle
5 chr4:8162200-8167200 Weak transcription Right Ventricle heart
6 chr4:8162400-8167000 Weak transcription Left Ventricle heart
7 chr4:8162400-8168200 Weak transcription Gastric stomach
8 chr4:8162400-8168200 Weak transcription Spleen Spleen
9 chr4:8164000-8167200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr4:8164800-8167200 Enhancers Fetal Thymus thymus
11 chr4:8165200-8166800 Enhancers Pancreas Pancrea
12 chr4:8165200-8167600 Flanking Active TSS Skeletal Muscle Male skeletal muscle
13 chr4:8165400-8167600 Enhancers Fetal Heart heart
14 chr4:8165600-8167000 Weak transcription Esophagus oesophagus
15 chr4:8165800-8167200 Enhancers Psoas Muscle Psoas
16 chr4:8166000-8167000 Weak transcription HSMMtube muscle
17 chr4:8166000-8167600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr4:8166400-8166800 Bivalent Enhancer Fetal Muscle Leg muscle
19 chr4:8166400-8167400 Enhancers NHEK skin
20 chr4:8166400-8169800 Weak transcription Liver Liver

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