Variant report

Variant rs7706429
Chromosome Location chr5:107586783-107586784
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:107546600-107590800 Weak transcription Primary T helper naive cells fromperipheralblood blood
2 chr5:107553400-107590800 Weak transcription Primary T helper cells fromperipheralblood blood
3 chr5:107561400-107595000 Weak transcription Psoas Muscle Psoas
4 chr5:107575200-107596200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr5:107575400-107617600 Weak transcription Primary B cells from cord blood blood
6 chr5:107575600-107595000 Weak transcription Right Ventricle heart
7 chr5:107576800-107595200 Weak transcription Fetal Intestine Small intestine
8 chr5:107577000-107616000 Weak transcription Primary T cells from cord blood blood
9 chr5:107579800-107589200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
10 chr5:107585000-107617800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr5:107585400-107591200 Weak transcription Skeletal Muscle Female skeletal muscle
12 chr5:107586000-107587200 Weak transcription Colon Smooth Muscle Colon
13 chr5:107586000-107587200 Weak transcription Rectal Smooth Muscle rectum
14 chr5:107586000-107591400 Weak transcription Skeletal Muscle Male skeletal muscle
15 chr5:107586200-107587200 Weak transcription Pancreatic Islets Pancreatic Islet
16 chr5:107586200-107589000 Enhancers Fetal Heart heart
17 chr5:107586200-107595000 Weak transcription Duodenum Smooth Muscle Duodenum
18 chr5:107586600-107587400 Enhancers Fetal Lung lung

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