Variant report

Variant rs2124879
Chromosome Location chr15:51916833-51916834
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:51915800-51917000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
2 chr15:51915800-51918000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr15:51916000-51917000 Enhancers Fetal Intestine Large intestine
4 chr15:51916000-51917000 Enhancers Fetal Intestine Small intestine
5 chr15:51916000-51919200 Enhancers Primary monocytes fromperipheralblood blood
6 chr15:51916200-51917000 Enhancers Rectal Mucosa Donor 31 rectum
7 chr15:51916200-51917000 Enhancers K562 blood
8 chr15:51916200-51917200 Enhancers GM12878-XiMat blood
9 chr15:51916200-51918000 Enhancers Primary hematopoietic stem cells short term culture blood
10 chr15:51916400-51917000 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
11 chr15:51916400-51920600 Weak transcription Primary neutrophils fromperipheralblood blood
12 chr15:51916400-51921600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr15:51916600-51917000 Flanking Active TSS ES-I3 Cell Line embryonic stem cell
14 chr15:51916600-51918200 Flanking Active TSS Monocytes-CD14+_RO01746 blood
15 chr15:51916800-51917000 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
16 chr15:51916800-51917000 Enhancers Rectal Mucosa Donor 29 rectum
17 chr15:51916800-51917800 Weak transcription Sigmoid Colon Sigmoid Colon

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