Variant report

Variant rs871722
Chromosome Location chr5:17437494-17437495
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:17430800-17463800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr5:17435400-17439000 Flanking Active TSS Primary neutrophils fromperipheralblood blood
3 chr5:17436000-17437600 Flanking Active TSS Primary B cells from cord blood blood
4 chr5:17436000-17437800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
5 chr5:17436200-17437600 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr5:17436600-17437600 Flanking Active TSS GM12878-XiMat blood
7 chr5:17436800-17437600 Active TSS Primary hematopoietic stem cells blood
8 chr5:17437000-17437600 Flanking Active TSS Rectal Mucosa Donor 29 rectum
9 chr5:17437200-17437600 Enhancers Colon Smooth Muscle Colon
10 chr5:17437200-17437600 Enhancers Fetal Kidney kidney
11 chr5:17437200-17437600 Enhancers Rectal Mucosa Donor 31 rectum
12 chr5:17437200-17437800 Enhancers Primary B cells from peripheral blood blood
13 chr5:17437200-17438400 Enhancers Primary monocytes fromperipheralblood blood
14 chr5:17437400-17437600 Enhancers HUVEC blood vessel
15 chr5:17437400-17437800 Enhancers Primary hematopoietic stem cells short term culture blood
16 chr5:17437400-17438000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr5:17437400-17438000 Enhancers Fetal Adrenal Gland Adrenal Gland
18 chr5:17437400-17440800 Weak transcription Osteobl bone

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