Variant report

Variant rs12095281
Chromosome Location chr1:47709831-47709832
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:47705200-47766400 Weak transcription Placenta Amnion Placenta Amnion
2 chr1:47705600-47766400 Weak transcription Primary T cells from cord blood blood
3 chr1:47705800-47714800 Weak transcription Fetal Thymus thymus
4 chr1:47707600-47716600 Weak transcription Hela-S3 cervix
5 chr1:47707600-47722800 Weak transcription Primary hematopoietic stem cells blood
6 chr1:47707800-47711400 Enhancers K562 blood
7 chr1:47708000-47715200 Weak transcription Primary hematopoietic stem cells short term culture blood
8 chr1:47709200-47710000 Enhancers HUVEC blood vessel
9 chr1:47709600-47710000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr1:47709600-47710800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr1:47709800-47710000 Enhancers H1 Cell Line embryonic stem cell
12 chr1:47709800-47714600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr1:47709800-47716000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
14 chr1:47709800-47725400 Weak transcription H9 Cell Line embryonic stem cell
15 chr1:47709800-47726000 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr1:47709800-47745000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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