Tag | Content |
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EnhancerAtlas ID | HS044-04033 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr13:113223570-113224720 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr13:113223980-113223993 | TTAATTTGCATTT | + | 6.25 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGCTGAAAG ACAAACAAAA GGATGCGGAT TGTTACCAAC CAGGTTACGT TCTGGTCACC 60 TGAAGCTTCC AGTTCAAGAC AGTGAACTAG TAATAACATC TATCTTCCAC CTCCCCAAGG 120 TCTTAACTGA GAGGACAGAA AAGCTATTAA GATATCAAAA CAGAATGAAT GAATGAAATA 180 AGAGTTCAAT AAAATAAGAA TGAGAACAGT AACACACCAG AGAGTCTGAA AAATCCTAGA 240 TGACAAAAAA CAAACTGGCT CAGTAATCAC GAAAAGAAAA GGAACAGAAA GGGTCACATC 300 CCAACACATG AACAAGAAGA GGAGGCCGGG TCAAGAGAGC CTCTGAGTAA CTCCAGGGTC 360 AACACACACA AAAAGCCAGA AGCAGGTCAC TCAACAGTCA AAATAGACAG TTAATTTGCA 420 TTTTCACCTC TAGATGAAGA TGACAGCTTA AACGCATGTG CCTCTACTCC CTTCAAAAAC 480 ACCATAAAAT TGAGGATAAA GGAGTTTTTA AAACTAAAAG CATAAACCAA CAAGGACAAA 540 GAAAACAAGG CAGAAAGGAA TCAGAGAGAA GTCAAAAAAT GTGAGAAGCT GGACTGCAGA 600 TAGATGTGTG GTAACTGATT CAAGAGGACA ATGAAACCGG AACACTAAAT GTCCGTCAAG 660 TTAAGAATGG GGAGAGGGGA GTGGGAGGAA TAAATGTCAA GAAGAAATAA CAGTTCCCAC 720 TGCAGAGCCC AGGCAGGCTC AGGAAAGGAA GGAACTGGAT ACTCTCAGGA TGCAGAAGCA 780 AGCAGGGCTG AAGGGGGAGA CCTGGCTGCA AGTTTGGACG GAAACAGACT CCTGGGTCCT 840 CCACCCAATC CCACGCTGCC AGACAACCAC CGAGACCCGC CCAGCAAGCC TGGTCTGGAT 900 GGACACTAGG GTGGCCCCGG TCACTAAGTA AAGTTAACAG ACAACTCAGG GATCCCCAGT 960 CCTTCCCAGA ACTCCAGGAT GCACAATTTG TCTATGAGAA AACTGATCAG CCCAAGAGAA 1020 AAGAGAGACA GATGGTGATG AGTGGGGATC CCCAACAAGC ACACGGGTCT TTGTCAAATT 1080 CAGACAGACC ACAGAGATAG TGCAGATCTG GTTCCAACCA CCATATTAAA GAAAATATCA 1140 CAAAAAGTGA 1150
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