Tag | Content |
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EnhancerAtlas ID | HS098-37306 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr22:44946440-44947410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx2-5(var.2) | MA0503.1 | chr22:44946569-44946580 | CTTGAGTGGTT | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr22:44946451-44946466 | TGATCTCTTGACCTC | - | 7.23 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I044550 | chr22 | 44946336 | 44948302 |
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Enhancer Sequence | CAGGATGGTC TTGATCTCTT GACCTCGTGA TCTGCCTGCC TTGGCCTCCG AAAGTGCTGG 60 GATTACGGGT GTGCGCCACC GTGCCCAGCC TCGAAATATC TTTATTCTAC TCTCCTAGCT 120 GATCAGTGGC TTGAGTGGTT ATCCTAGGCC CAGTTCAGTC CAGGAAGAGA AGCCACAATG 180 AGCATTGTGG GAGGAGGGGC CCATCATAGG AATGAGACCT TGCACAATCC TAGGAAGAGC 240 AGGGGAGCGG AGCTGGGGAG GAGGGGAGCG GGAGAGTCAG GAAAGACTCA GCAGCCAGCC 300 CTCCTGAAGC CTGGGGCAGG AGGCCAGCTC GGAGCTTGCA GGAAAGTCAT GAGAAAGTCA 360 CGCACATCCA GCTGCACGGG TCAGGGCGCC GGGGGAGGTC TGGCCAAGAG GCTGCAGGAG 420 CTGCTGCCTC TGCAGCTGCC ACCTCTGTGG GGAAGCCCAG GGCCACTGTC GGGGCAGCAG 480 GGTCAACGGT GGGGAGCATG AGCAGGACCC AGGGTGAGGA AGAGTGCGGA CACCCTGGAA 540 CTCACGGAGC ACCTGTGCAG CGGTCTCTCC CCATCTCCGA TCACAAAGTC GCTCAGAGGA 600 GCGCAGCCTG CTTGCTTTTG CCTGCCAACA GCCCGCGAGT TGTCAGCCTG CCATCTAAAC 660 AAACCCCTTC TCACTATATT TAACTTCCTA ATAAAGACAG CAATGAAATC AGGCTGCTTC 720 CTCACACGAT GCAACTGTTC CTTATTAAAA TCGAAAGTGC ACTAACCTTC TACCCTCCCA 780 GCCTCAAAAA GAGACTTTCT CCATCTGCGA AGGGGGCAAT CCCCCTTCTG GCTGAGTCAC 840 TCCCTCTTTG ACATCCTGTG ACTTAAGTAT CAAGACGTAA GGCCAGTCAC GATGAACACA 900 GCTTATGTGA GATAGCAGGG GAATGGAAGA AGGAAATGAT AATTGGTTAA TATGGGGGCC 960 GGGCGTGGTG 970
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