Variant report

Variant rs558268495
Chromosome Location chr7:18601438-18601439
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:18581600-18620200 Weak transcription HSMMtube muscle
2 chr7:18593000-18606400 Weak transcription Primary monocytes fromperipheralblood blood
3 chr7:18593600-18605000 Weak transcription Brain Hippocampus Middle brain
4 chr7:18593600-18605800 Weak transcription Primary B cells from peripheral blood blood
5 chr7:18596800-18612600 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr7:18598200-18610200 Weak transcription Cortex derived primary cultured neurospheres brain
7 chr7:18598600-18613000 Weak transcription Spleen Spleen
8 chr7:18599000-18606200 Weak transcription NHEK skin
9 chr7:18599000-18606400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr7:18599000-18613200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr7:18599000-18613200 Weak transcription Monocytes-CD14+_RO01746 blood
12 chr7:18599400-18606400 Weak transcription Aorta Aorta
13 chr7:18600200-18601600 Enhancers Fetal Heart heart
14 chr7:18600400-18613200 Weak transcription Right Ventricle heart
15 chr7:18600600-18602000 Weak transcription Skeletal Muscle Female skeletal muscle
16 chr7:18600600-18604400 Weak transcription Primary B cells from cord blood blood
17 chr7:18600600-18613200 Weak transcription Left Ventricle heart
18 chr7:18600600-18617600 Weak transcription Psoas Muscle Psoas
19 chr7:18600800-18602000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
20 chr7:18601000-18610200 Weak transcription Skeletal Muscle Male skeletal muscle
21 chr7:18601400-18601600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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