Variant report

Variant rs59368604
Chromosome Location chr4:10130567-10130568
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:10126000-10131400 Weak transcription Fetal Lung lung
2 chr4:10126200-10130600 Weak transcription Skeletal Muscle Male skeletal muscle
3 chr4:10126200-10130800 Weak transcription Skeletal Muscle Female skeletal muscle
4 chr4:10126600-10131000 Weak transcription Adipose Nuclei Adipose
5 chr4:10126600-10131000 Weak transcription Fetal Muscle Trunk muscle
6 chr4:10126600-10131000 Weak transcription Right Atrium heart
7 chr4:10126600-10131600 Weak transcription Spleen Spleen
8 chr4:10127000-10130600 Weak transcription Fetal Muscle Leg muscle
9 chr4:10128000-10131000 Weak transcription Left Ventricle heart
10 chr4:10128200-10131400 Weak transcription Right Ventricle heart
11 chr4:10129600-10132000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr4:10129800-10131400 Enhancers NHEK skin
13 chr4:10130000-10131600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr4:10130200-10131400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr4:10130200-10131400 Enhancers NHDF-Ad bronchial
16 chr4:10130200-10131600 Enhancers Hela-S3 cervix
17 chr4:10130200-10132400 Enhancers Muscle Satellite Cultured Cells --
18 chr4:10130200-10132600 Enhancers HSMM muscle
19 chr4:10130400-10131000 Enhancers HMEC breast
20 chr4:10130400-10131000 Enhancers HUVEC blood vessel
21 chr4:10130400-10132200 Enhancers HSMMtube muscle

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