Tag | Content |
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EnhancerAtlas ID | HS044-01227 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:229073080-229074960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr1:229073867-229073878 | TTCTTATCTGT | + | 6.14 | Gata1 | MA0035.3 | chr1:229073867-229073878 | TTCTTATCTGT | + | 6.62 | HNF1A | MA0046.2 | chr1:229074784-229074799 | AATTAATTATTAACC | - | 6.01 | HNF1A | MA0046.2 | chr1:229074784-229074799 | AATTAATTATTAACC | + | 7.28 | HNF1B | MA0153.2 | chr1:229074785-229074798 | ATTAATTATTAAC | - | 6.98 | Lhx3 | MA0135.1 | chr1:229074783-229074796 | TAATTAATTATTA | + | 6.18 | POU4F2 | MA0683.1 | chr1:229074782-229074798 | TTAATTAATTATTAAC | - | 6.11 |
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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 |
GH01I228937 | chr1 | 229073150 | 229075248 |
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Enhancer Sequence | AACACTAAAC CTGGAAGTTG TTTTCTGAAG AAGGTGAGGG GAGAGCACCT CCCCCAGGCA 60 ACCTAGATCC CTCGCATGCA CAGTTCCCAA CACGGAGTCT TGTGGAAGGG AGCGCTCAGT 120 AAGATGTCAT TTAGCTTAAA GACTGTGGAT GCCTGAGCAT GCCGCGTTTC CCGCAGCCGT 180 GCTTCTTGCT TGGTGCTCAG TCTTGGCAAA GTCATCTCCG GCCCTACGTT CTCAGGTGTG 240 AACGGTGGAG TCAGGGGTGC TGAGGGTCAT GCTCACTCAC CAACTACCCT GCACCAGCAC 300 CCTCCCCCCT GCACTGGTTT TCTGTGCTCT CGTTTGGTGT CCCCAAAATC TTGAGGCCTG 360 TAGGATTATC ACCACTACAC AGAAGAGGAA ACCGAGGGTT AGAGAGGTGG TCTGAATGTC 420 TAAGAAGGGA GATCCAGGAT TGGAACCCAG ATTTGTACAA CTCCAAAGCT CTCTTGTGAC 480 CTGTGCCGCC TCCCAAGGGG TGAGCAATCG TGCCTCCCTT TCCTCTGCTC AGCCACCCTG 540 CAGCTCACAC AGCTGCAGTA ATGACTGCTC TCGAGAGAGC TGCCCCACCC AGAGGGGTTT 600 AAGGCAGAGA AGAGCGGCCT GCAGCCTAGT TTCTCTCAGT GTGCCTTACA GCCAAAGCCA 660 AAGACTGAGG CCGACTCCCA GGACAGGGCC GCTACCCTGG CCTCAACACC ACAAATGACT 720 GGACGCAGCT GCTGGCAGAA AAAGCCGCAC TCCAGGCATT TAGTACCTAA CCGAAGAAAT 780 CCAAAGATTC TTATCTGTGC CTTGCTTCTC AACTGCAGAG GTTCTTCCCT TTTGTCCTAA 840 CACACTGGGA GGGAACTCTG CACTGATGAC AAGTAACCAT GAACGTGATT CCTTTCCCTC 900 CTGCGGTGGT CATCTTCAGC AACTCTAGCC GTGAAGCCAG CCTGCCTGTC TCTTTCTTTG 960 CTTGTGTTGG GTCATATTAC TGAAGAAAGA ATAATAGCAA CACTGTTACC CGCCTGTGTA 1020 CCAGTCTTTG TTCACGGGAG GTTTTAGGAT CTCTATGACA CACGCAGGCA GAGCATGCCA 1080 CCGTCACTTA GGAGGGGAAG CCAGAGGTCT TGGAAGTCAC ACACTAGCAG GGAAGAGACC 1140 TAGGTTTTCC CATGGCTCAC TGCAGCCTCC CTGAACTCTT TTTCCACAGA TGCTAGGCTG 1200 ACACTCCCTT GTCCCCCTCT AGAGCTCTGT GAACAGGAAG AGGTTGTCTT CTAGCTGTGT 1260 AGAGGCTGGG GGAACAGCCC ACAGTGCAAG CCACGACTAC CTGCTCTGAA GTGGAGGGGC 1320 TGTGGAGCAG ACAGCAGACT TCTCCCAGCT GAGCAGAGCT GGGCAAAACA GATCGATCTA 1380 AACCGCCCTT AGCGGATGTT CTCATTTCCC TGCTGCCCTA AAAGTGGTGT CCGCCTGAGG 1440 TGAACACTAT AAATAACTGT TCACAGGCGG GTTGTTAAGG ACTCTATGGC CTGTGTTGGC 1500 AGAGACAGAT TCCGGGAAGT CAGTGACTTG GTCACTTCCT ACTTAAAACG CAGGGCACCA 1560 AGGAGCCTAT TTTGGGCTAA ATGCAAAAGC CTGGGAATCA AAGAAGAAAC GTTAGAGGAG 1620 AGACCGACCT CTTGCTTTTA GCCACAGTTT GGAAAAGTTT TTTGTTGTTC TCAATAGTTC 1680 GATGGAAAGT GGTAAAAATG CTTTAATTAA TTATTAACCT TGGTATTTTT CTTCATAGTT 1740 CTCAACATGC TTCACACACC TTTCCTTCTT TGAGCCTCAA AGCAACACTG TGAGTAATCT 1800 TATTGTTGTG AACCCATTTT ACAGGTGAGA AGACAGAGGC AATAAACATA AGGGCTGGGC 1860 CTCACACCTG GATCTGCTGC 1880
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