Variant report

Variant rs57525972
Chromosome Location chr1:47709227-47709228
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr1:47705800-47709400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr1:47705800-47714800 Weak transcription Fetal Thymus thymus
5 chr1:47706800-47709800 Enhancers Spleen Spleen
6 chr1:47707400-47709400 Weak transcription H9 Cell Line embryonic stem cell
7 chr1:47707600-47716600 Weak transcription Hela-S3 cervix
8 chr1:47707600-47722800 Weak transcription Primary hematopoietic stem cells blood
9 chr1:47707800-47711400 Enhancers K562 blood
10 chr1:47708000-47715200 Weak transcription Primary hematopoietic stem cells short term culture blood
11 chr1:47708200-47709600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr1:47708200-47709600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr1:47709200-47709600 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
14 chr1:47709200-47709600 Bivalent Enhancer HepG2 liver
15 chr1:47709200-47710000 Enhancers HUVEC blood vessel

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