Tag | Content |
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EnhancerAtlas ID | HS044-13468 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr9:91862310-91863650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr9:91862580-91862591 | CTGAGTCATCC | - | 6.32 | JUNB | MA0490.1 | chr9:91862580-91862591 | CTGAGTCATCC | - | 6.14 | MEF2A | MA0052.3 | chr9:91863114-91863126 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr9:91863114-91863126 | ACTAAAAATAGA | + | 6.32 |
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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 |
GH09I089247 | chr9 | 91862441 | 91862630 |
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Enhancer Sequence | GTTGCCTGAT TCCCTGAAAT AAACAAACAA TAACAACAAC AAAACCACAG TTTTGTTGAG 60 AACAGTAGGT GTTACAACAA AGAAAGAATT TAATAATGGC AGGGCCAGCT AAGCGAGGAG 120 AACAGGGAGA AATTTCTCAA ACTCGTCTCC TTGAGGATTC AGAGGCTGGG GTTTCTTAAG 180 GGTACTTTGG TGAGCAGGAG CCTGGGGCAC TGGAACAATG GATTGGCTGC GGATGAAATC 240 ACAGGAGCCT CTAAAGCTGT CTTCCTGCAG CTGAGTCATC CAGGGGAAAG GGAGGTTCTC 300 AAGACCAGGT GGTGTCTCTT GGTTTACTAA GATGCTAAAT CTGAAAAAAT GTCCCAAAGA 360 CCAGTTCTTT AGTTTTCACT ATAATTATGT TATCTATAGG AGTAATTGAG GAAGTTATGA 420 ATCTTGCAAC CCCCAGTTAC ATGACTCCAG GGCAGTCAGC AACTTACAGG AAAACATGCT 480 CAGCAATGGC AGGTCATTGT TCAATGCTGC CTATTCTTTA GCAAAGTTCA GGCCCTATCA 540 TAATTCTAAC CTCCTCTTAT GAATGGCTTC AGCCTCCTGA CAAGGAGGCA GGTCAGTTTC 600 CCTTGCCTCT AAGTTGAACT ATAAACTACA TTCCTCTTAT GGTTATCTTG GCCTCTGTGC 660 TAAAATATGC AAAAAAAATA GTTTAGCCTG TGAGGTTGGA AGAAAGACGG AGTCAGTCAT 720 GTTAGATTTC TCTCATTATA ATTCTGCAAA GGCAGTTTCA CTTTAAAAGT CAATATCATT 780 GGCTATAAAA GTTCTGATGC AGTCACTAAA AATAGATCTC ATTAAGTTGT AAACATAATT 840 CATGTAAAGC AGGACTAGAA AATTAAACAC ACACAATGGC ACATGAAAGG ACATCAGATA 900 AAGTCCAAAT TCCCCAGAAG GCATTCAGAG CCCCCCACTT ATTAGGTCCC CTCTCCACTC 960 TCTTAAGAGG CAAGACAAAG AATGTCTAAA GAGGAAGCTG GGAAAAACAT TGATCCACCC 1020 TGAACAAACT TGCTTTTATT TTCCTCATAT TTCATCCAGT CAGTAAACTT CCTAAGCAAT 1080 TAAAACAAAT GTACCAAATT GTAAAAAATT AAACACTAAA ATTATCTCCA TTGACCCACA 1140 GTCTTACTGT TCTCCCCACT TAAAGGAACA GATAATACTG TCACTGAAAC ACCACGTGGG 1200 TAGGCACAAT AGCTCACACA TGTAATCCCA GAACTTTGGG AGGCCAAGGC AGGTGGATCA 1260 CCTGAGGTCA GGAGTTCGAG ACCAGCCTGA CCAACATGGT GAAACTCCGT CTCTAGTAAA 1320 TATAAAAAAT TAGCCGGGCA 1340
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