Variant report

Variant rs7667775
Chromosome Location chr4:10128536-10128537
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:10125800-10128600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr4:10125800-10129200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr4:10125800-10130000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr4:10125800-10130400 Weak transcription HSMMtube muscle
5 chr4:10126000-10130200 Weak transcription Muscle Satellite Cultured Cells --
6 chr4:10126000-10130200 Weak transcription Hela-S3 cervix
7 chr4:10126000-10131400 Weak transcription Fetal Lung lung
8 chr4:10126200-10130600 Weak transcription Skeletal Muscle Male skeletal muscle
9 chr4:10126200-10130800 Weak transcription Skeletal Muscle Female skeletal muscle
10 chr4:10126400-10128800 Weak transcription Placenta Placenta
11 chr4:10126400-10130200 Weak transcription HSMM muscle
12 chr4:10126600-10131000 Weak transcription Adipose Nuclei Adipose
13 chr4:10126600-10131000 Weak transcription Fetal Muscle Trunk muscle
14 chr4:10126600-10131000 Weak transcription Right Atrium heart
15 chr4:10126600-10131600 Weak transcription Spleen Spleen
16 chr4:10126800-10128600 Enhancers Fetal Heart heart
17 chr4:10127000-10130400 Weak transcription HUVEC blood vessel
18 chr4:10127000-10130600 Weak transcription Fetal Muscle Leg muscle
19 chr4:10128000-10131000 Weak transcription Left Ventricle heart
20 chr4:10128200-10131400 Weak transcription Right Ventricle heart
21 chr4:10128400-10129200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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