Variant report

Variant rs138829786
Chromosome Location chr10:119026366-119026367
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:119017400-119034000 Weak transcription Gastric stomach
2 chr10:119019800-119031200 Weak transcription Primary neutrophils fromperipheralblood blood
3 chr10:119020000-119034000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr10:119020000-119042600 Weak transcription Primary hematopoietic stem cells blood
5 chr10:119020600-119028000 Weak transcription Thymus Thymus
6 chr10:119020600-119035000 Weak transcription Primary hematopoietic stem cells short term culture blood
7 chr10:119020600-119043200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr10:119020600-119045400 Weak transcription Fetal Heart heart
9 chr10:119021400-119043200 Weak transcription Fetal Intestine Small intestine
10 chr10:119022600-119042000 Weak transcription Fetal Intestine Large intestine
11 chr10:119023000-119031800 Weak transcription Ovary ovary
12 chr10:119023800-119043200 Weak transcription Spleen Spleen
13 chr10:119024400-119026400 Weak transcription Primary T cells from cord blood blood
14 chr10:119025200-119026800 Weak transcription HepG2 liver
15 chr10:119026000-119027000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr10:119026000-119032600 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr10:119026200-119026400 Weak transcription Pancreas Pancrea
18 chr10:119026200-119027000 Weak transcription Fetal Thymus thymus
19 chr10:119026200-119031400 Weak transcription K562 blood

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