Variant report

Variant rs322779
Chromosome Location chr7:127758567-127758568
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:127744600-127761600 Weak transcription Right Atrium heart
2 chr7:127753400-127762000 Weak transcription Fetal Brain Female brain
3 chr7:127756000-127759000 Weak transcription Monocytes-CD14+_RO01746 blood
4 chr7:127756000-127761400 Weak transcription Osteobl bone
5 chr7:127756000-127762000 Weak transcription HSMM muscle
6 chr7:127756200-127758800 Weak transcription Primary monocytes fromperipheralblood blood
7 chr7:127756200-127761800 Weak transcription Esophagus oesophagus
8 chr7:127756600-127761200 Weak transcription NHEK skin
9 chr7:127756600-127761400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr7:127757000-127759200 Enhancers Primary B cells from peripheral blood blood
11 chr7:127757200-127758600 Enhancers Primary B cells from cord blood blood
12 chr7:127757200-127760600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
13 chr7:127757200-127761000 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr7:127757400-127759600 Enhancers Fetal Thymus thymus
15 chr7:127758000-127761000 Weak transcription Spleen Spleen
16 chr7:127758200-127758600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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