Variant report

Variant rs73373692
Chromosome Location chr6:15684065-15684066
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:15675800-15685000 Weak transcription HUES48 Cell Line embryonic stem cell
2 chr6:15675800-15685000 Weak transcription iPS-18 Cell Line embryonic stem cell
3 chr6:15682000-15684400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr6:15682000-15685400 Enhancers Primary hematopoietic stem cells short term culture blood
5 chr6:15682800-15684600 Enhancers Primary monocytes fromperipheralblood blood
6 chr6:15682800-15685400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr6:15682800-15686800 Enhancers Fetal Intestine Small intestine
8 chr6:15683000-15684200 Enhancers Primary hematopoietic stem cells blood
9 chr6:15683000-15684600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
10 chr6:15683200-15684200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr6:15683200-15684200 Enhancers HepG2 liver
12 chr6:15683200-15684400 Enhancers Rectal Mucosa Donor 31 rectum
13 chr6:15683200-15684600 Enhancers Duodenum Mucosa Duodenum
14 chr6:15683200-15685200 Enhancers Stomach Mucosa stomach
15 chr6:15683200-15687400 Enhancers Fetal Intestine Large intestine
16 chr6:15683800-15684200 Bivalent Enhancer Ganglion Eminence derived primary cultured neurospheres brain
17 chr6:15683800-15690400 Weak transcription K562 blood

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