Tag | Content |
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EnhancerAtlas ID | HS044-13113 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr9:419050-420400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr9:419236-419254 | CTTTCTTGTCTTCCTTCC | - | 6.27 | HNF4G | MA0484.1 | chr9:419468-419483 | AAAGCCCAAAGTTCA | + | 6.09 |
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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 |
GH09I000419 | chr9 | 419181 | 420483 |
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Enhancer Sequence | GATTCAGTTG AGGTGGGATT CATCTCTGTT CATTGATGAG CTCTGACTAT CCCTTGTGAA 60 GACAGCACTG CATCCTCCAA TGTCATTTAC TTTCACATTT CAATGTAGGG TATAGATGTG 120 CAGAGAATTT AACTTTCTTC TCCCGTGAGA AAGCAGCATC CTGACCTAAC TCTTCTTGCT 180 GGATGACTTT CTTGTCTTCC TTCCTGCACT TAGCAAGCTC CATCACCATG AGGATTGGGG 240 GGACAGTGAG GCAGGAAGAT GAGACAGAGA AAAGACATTT GAGATTTGAC ATCACCGATC 300 TTACTGTTGG AGAAATATTG TGTGACCTCC TCCACCTTTC TAATATCCGT CTTACCAAAG 360 TTAGCTGCTT GAGGTGGTAT ATGCCTTTTA CATTATTTGC CTCTAAGGGA AAAACTCAAA 420 AGCCCAAAGT TCACCTGTTA GAACATAGTC CTTGTGAGGT TGTATCTCAA GATTTCCTTT 480 ATTCTTGTCA ACAAACTCAG AATAACTAAA GTTAAAGTTG CTTTATAACC TCTATTATTT 540 CCATCCAAAA CTAACATTTC CCTCCCATAC CCACAAATTC CTCATTGCAA TTTCACCAGT 600 ACATTCCACT GGATATTAGC TACGCTGCAT GAACCAAGGG TGCAGCCTCA TTGTTGTTGT 660 TTGTGTTGAT GAGATGAGTA ACAGAGAGTG CGCTCAGCAC TTTAAAATGA ATACTTGTGG 720 CCAAAATATT AAAGCAAATA GCCTGAACCC CCACACCCCA GCCCCAGGCA AACATAAATT 780 ATGGTTAAAC TTCCATTACA GAGAACTCCA CAAACATGGA TTTGATTAAT TTGCTGAGCA 840 GTTCATGACC CTTATGTTAT ACTTTGCACT ATGTAACAAA GAAGCTAAAT CTTGAACAGC 900 AAGCTTATTC ATGGCACCCA GCCAGTTTCC TTCTCCCCTG TAAGTCTAAC CCTCTGCTGC 960 CCAGCACGAA GGAGAAATAC TTGGAGATCT TAGCAGCATG AAAGCCTCTT TGTATCACTG 1020 GGATTGCAGC ACGCATGATC AAGGCCCAGG GGTGATCACC AGGCCACACT GCTCCTAAGA 1080 CAGAGGTACT CAGATACGTG GCTGAAAGCC TAGCTCAAAT ACTGCCCCAG GTGAGCCTCT 1140 TTGCTGAGTA GCGCTACTCA AAGAACACAG CTTCCCCTGC CTAGGGAAGG CAGGGCTACT 1200 GGCAATAGAT CTCCAGCCTA GCAGTGATGT ACAGTCATGG TATTTTAAGA GAACACTTTG 1260 AATTTTTCTG TTGCTTGACT GTTAAGCCTC AAATTTTTCT GTTGCTTGAC TTCTTCCCTG 1320 GCCTCCATCC CCCAATCTGC CTCCCTTCAG 1350
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