Variant report

Variant rs6683706
Chromosome Location chr1:155007758-155007759
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:154990600-155011200 Weak transcription Right Atrium heart
2 chr1:154990800-155016400 Weak transcription Spleen Spleen
3 chr1:154999200-155010800 Weak transcription Gastric stomach
4 chr1:154999400-155009200 Weak transcription Placenta Amnion Placenta Amnion
5 chr1:155003600-155008800 Weak transcription Placenta Placenta
6 chr1:155004400-155009000 Weak transcription Fetal Muscle Leg muscle
7 chr1:155007000-155008800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr1:155007000-155011000 Weak transcription Primary hematopoietic stem cells blood
9 chr1:155007200-155008800 Weak transcription Primary hematopoietic stem cells short term culture blood
10 chr1:155007200-155009200 Weak transcription Esophagus oesophagus
11 chr1:155007400-155010000 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr1:155007400-155015800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
13 chr1:155007600-155010200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:155007600-155010200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr1:155007600-155010200 Weak transcription HMEC breast
16 chr1:155007600-155010200 Weak transcription NHEK skin
17 chr1:155007600-155010400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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