Tag | Content |
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EnhancerAtlas ID | HS105-52469 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr22:22097930-22098860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr22:22098812-22098827 | GAGGTCAGGAGTTCA | + | 6.22 | Nr5a2 | MA0505.1 | chr22:22098016-22098031 | CTTGACCTTGGACTT | - | 6.29 | RFX5 | MA0510.2 | chr22:22098439-22098455 | TGTTGGCATAGCAACC | - | 6.21 | RFX5 | MA0510.2 | chr22:22098439-22098455 | TGTTGGCATAGCAACC | + | 6.24 |
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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 |
GH22I021744 | chr22 | 22098382 | 22098750 |
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Enhancer Sequence | AGGTATGACC ATGTGAGCAC ACAGGGAGAA GACGCCATCA ACAAGCCAGG GAGAGAGGCT 60 GCAGAAGAAA CAAACCCTTC TGATGCCTTG ACCTTGGACT TCCAGCCTCC AGGACTATGA 120 CAAAATAAAT TCCTGCTGTT CAAGCCGCCC AGTCTGTGGT ACTTTGTTAC AGCAGCCCAA 180 GCTGACTAAT ATACTGGATT TTGGGGGTAG AAAGATACTT ACAGCAACTC TCCTCAAGGG 240 TCGCCCAGCC TGCCTTCCAC CCAAATCCTG CCTAAATCCT TCGGGTTGGC CAAAATTAAG 300 CTGCTTGCCT TGGTGTAACT TCAGCGCGGG CTAGTAGAAT TGCTGTGGAC AGACAGGGAA 360 CTTAACCTCC TGGGTGCCAG TGGTCTCCTC GGCCAAGTGA GAGGCCGTGC TGTGCGGAGT 420 GCCCTCCAGA GCCCCTGGAG TCTAAAGTTC TGTGACTTGC TAAGACTTTC CTTTATGATT 480 GGAAAGCCCA TTAGGAAGCA GGCAGGTGCT GTTGGCATAG CAACCACAAG CCGTCTTATG 540 TTCTTTCCAA ATTAAAAATT TTCCAGCTTT AGAACTGAGG AGAGAAAGAT GTAAGAGCAG 600 AGATGAAATT AAGTTATTGA TGGAAGCGGT TGCCATGGCA TTGTGCTGTC CTTGGAGTCT 660 GCCAGCTGCC ACTTGATTTC TCCATTTTTC GTGCAAACGA AGGAGTCCAA GAGAAGATAA 720 GGACCAGCCT CCCACAGTGA GGGAGAAAAA CAAAACATAT GTGTTCATTA GAAAGAGTTG 780 ACTCATGATG GGAACCTAAA CAATATTTTA AGAGTAGCAG CTGGGCGCAG TGGCTCACAC 840 TTGTAATCCC AGCACTTTGG AAGGCTGAGG TGAGCAGATC ACGAGGTCAG GAGTTCAAGA 900 CCAGCCTGGC CAACATGGTG AAACCCCATC 930
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