Variant report

Variant rs45583938
Chromosome Location chr16:30208527-30208528
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:30199800-30217200 Weak transcription Primary T helper naive cells fromperipheralblood blood
2 chr16:30199800-30217200 Weak transcription Placenta Placenta
3 chr16:30199800-30217200 Weak transcription Fetal Stomach stomach
4 chr16:30200000-30217200 Weak transcription Primary neutrophils fromperipheralblood blood
5 chr16:30206200-30217200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr16:30206200-30217200 Weak transcription Primary T cells fromperipheralblood blood
7 chr16:30206200-30217200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr16:30206200-30217200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr16:30206200-30217200 Weak transcription Fetal Intestine Large intestine
10 chr16:30206200-30217200 Weak transcription Fetal Intestine Small intestine
11 chr16:30206200-30217200 Weak transcription Fetal Thymus thymus
12 chr16:30208400-30208600 Enhancers Primary B cells from cord blood blood
13 chr16:30208400-30208600 Enhancers Primary T helper cells fromperipheralblood blood
14 chr16:30208400-30208600 Enhancers Colonic Mucosa Colon
15 chr16:30208400-30208600 Enhancers Monocytes-CD14+_RO01746 blood

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