Variant report

Variant rs10151145
Chromosome Location chr14:69108789-69108790
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:69105000-69121600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr14:69105600-69113000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr14:69105800-69113200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr14:69106000-69117000 Weak transcription Fetal Intestine Large intestine
5 chr14:69106200-69112800 Weak transcription H9 Cell Line embryonic stem cell
6 chr14:69106200-69115600 Weak transcription Esophagus oesophagus
7 chr14:69106400-69118200 Weak transcription Placenta Amnion Placenta Amnion
8 chr14:69106400-69118400 Weak transcription Spleen Spleen
9 chr14:69106600-69111000 Weak transcription Fetal Heart heart
10 chr14:69106600-69111800 Weak transcription Rectal Smooth Muscle rectum
11 chr14:69106800-69116000 Weak transcription Ovary ovary
12 chr14:69107000-69110600 Weak transcription Right Ventricle heart
13 chr14:69107400-69108800 ZNF genes & repeats Duodenum Smooth Muscle Duodenum
14 chr14:69107800-69109000 ZNF genes & repeats Primary B cells from cord blood blood

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