Variant report

Variant rs2514054
Chromosome Location chr11:67450364-67450365
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:67442600-67451000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr11:67448200-67451600 Enhancers Fetal Heart heart
3 chr11:67448600-67450800 Weak transcription iPS-18 Cell Line embryonic stem cell
4 chr11:67449000-67451400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr11:67449400-67450400 Weak transcription NHEK skin
6 chr11:67449400-67453400 Weak transcription H1 Cell Line embryonic stem cell
7 chr11:67449800-67450600 Enhancers HMEC breast
8 chr11:67449800-67451000 Enhancers Placenta Amnion Placenta Amnion
9 chr11:67449800-67454200 Enhancers Fetal Thymus thymus
10 chr11:67450000-67457000 Enhancers Placenta Placenta
11 chr11:67450200-67450400 Weak transcription Esophagus oesophagus
12 chr11:67450200-67450600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr11:67450200-67450800 Enhancers Fetal Muscle Leg muscle
14 chr11:67450200-67453000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr11:67450200-67453000 Enhancers Dnd41 blood

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