Variant report

Variant rs4902623
Chromosome Location chr14:69110926-69110927
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 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 chr14:69108800-69119000 Weak transcription Duodenum Smooth Muscle Duodenum
13 chr14:69109400-69122400 Weak transcription Primary B cells from cord blood blood
14 chr14:69109800-69111400 Enhancers Fetal Stomach stomach
15 chr14:69110200-69111000 Enhancers Adipose Nuclei Adipose
16 chr14:69110400-69111200 Enhancers Fetal Muscle Leg muscle
17 chr14:69110600-69111200 Enhancers Right Ventricle heart
18 chr14:69110800-69111000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
19 chr14:69110800-69111200 Enhancers Fetal Muscle Trunk muscle
20 chr14:69110800-69111400 Enhancers Stomach Smooth Muscle stomach

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