Variant report

Variant rs1537029
Chromosome Location chr13:110385963-110385964
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:110378400-110386200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
2 chr13:110382000-110386000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr13:110382200-110388800 Weak transcription Fetal Heart heart
4 chr13:110382600-110389800 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr13:110384400-110386200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr13:110384400-110386400 ZNF genes & repeats Fetal Thymus thymus
7 chr13:110384400-110387400 Weak transcription Primary hematopoietic stem cells blood
8 chr13:110384600-110387400 Weak transcription Primary hematopoietic stem cells short term culture blood
9 chr13:110385400-110386600 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
10 chr13:110385400-110388200 Enhancers Dnd41 blood
11 chr13:110385600-110386400 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
12 chr13:110385800-110386000 Active TSS Gastric stomach
13 chr13:110385800-110386600 Bivalent Enhancer Primary T cells fromperipheralblood blood
14 chr13:110385800-110387000 Enhancers Primary T helper 17 cells PMA-I stimulated --

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