Variant report

Variant rs112165087
Chromosome Location chr16:30207777-30207778
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:30199800-30208400 Weak transcription Primary B cells from cord blood blood
2 chr16:30199800-30208400 Weak transcription Monocytes-CD14+_RO01746 blood
3 chr16:30199800-30217200 Weak transcription Primary T helper naive cells fromperipheralblood blood
4 chr16:30199800-30217200 Weak transcription Placenta Placenta
5 chr16:30199800-30217200 Weak transcription Fetal Stomach stomach
6 chr16:30200000-30217200 Weak transcription Primary neutrophils fromperipheralblood blood
7 chr16:30206200-30208000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
8 chr16:30206200-30208200 Weak transcription Colonic Mucosa Colon
9 chr16:30206200-30208400 Weak transcription Primary T helper cells fromperipheralblood blood
10 chr16:30206200-30217200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr16:30206200-30217200 Weak transcription Primary T cells fromperipheralblood blood
12 chr16:30206200-30217200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr16:30206200-30217200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr16:30206200-30217200 Weak transcription Fetal Intestine Large intestine
15 chr16:30206200-30217200 Weak transcription Fetal Intestine Small intestine
16 chr16:30206200-30217200 Weak transcription Fetal Thymus thymus

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