Variant report

Variant rs73836955
Chromosome Location chr4:106972300-106972301
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:106959600-106983400 Weak transcription HepG2 liver
2 chr4:106965800-106977600 Weak transcription Primary T helper naive cells fromperipheralblood blood
3 chr4:106967600-106983600 Weak transcription Skeletal Muscle Female skeletal muscle
4 chr4:106967600-106983800 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr4:106967800-106976400 Weak transcription Psoas Muscle Psoas
6 chr4:106967800-106984200 Weak transcription Primary hematopoietic stem cells blood
7 chr4:106967800-106994600 Weak transcription Rectal Mucosa Donor 29 rectum
8 chr4:106968000-106977200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr4:106968000-106977200 Weak transcription Primary T cells from cord blood blood
10 chr4:106968000-106984600 Weak transcription Primary B cells from cord blood blood
11 chr4:106969800-106978200 Weak transcription Ovary ovary
12 chr4:106970000-106977800 Weak transcription HUES64 Cell Line embryonic stem cell
13 chr4:106970200-106973600 Weak transcription Brain Hippocampus Middle brain
14 chr4:106971800-106972400 Enhancers Fetal Lung lung
15 chr4:106971800-106973000 Enhancers Fetal Heart heart
16 chr4:106972200-106972400 Weak transcription Aorta Aorta
17 chr4:106972200-106978200 Weak transcription ES-I3 Cell Line embryonic stem cell

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