Variant report

Variant rs4981555
Chromosome Location chr14:25299089-25299090
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:25285200-25302200 Weak transcription HSMM muscle
2 chr14:25287400-25306200 Weak transcription Brain Anterior Caudate brain
3 chr14:25287800-25306800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr14:25288000-25309400 Weak transcription Lung lung
5 chr14:25288400-25304400 Weak transcription Stomach Smooth Muscle stomach
6 chr14:25288400-25309400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr14:25288600-25302200 Weak transcription Left Ventricle heart
8 chr14:25288600-25322800 Weak transcription Placenta Placenta
9 chr14:25288800-25308000 Weak transcription Fetal Lung lung
10 chr14:25288800-25317400 Weak transcription Placenta Amnion Placenta Amnion
11 chr14:25289200-25309400 Weak transcription Pancreas Pancrea
12 chr14:25290000-25300800 Weak transcription HepG2 liver
13 chr14:25290800-25303200 Weak transcription Right Ventricle heart
14 chr14:25297400-25302000 Weak transcription Fetal Heart heart
15 chr14:25298000-25299400 Enhancers Fetal Intestine Large intestine
16 chr14:25298200-25299800 Enhancers Fetal Intestine Small intestine
17 chr14:25298400-25306600 Weak transcription HSMMtube muscle
18 chr14:25298600-25299600 Enhancers Duodenum Mucosa Duodenum
19 chr14:25298800-25299200 Enhancers Small Intestine intestine
20 chr14:25299000-25309200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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