Tag | Content |
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EnhancerAtlas ID | HS044-09909 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr4:122659970-122661260 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE40 | MA0464.2 | chr4:122660133-122660143 | GTCACGTGAT | - | 6.02 | TFEB | MA0692.1 | chr4:122660133-122660143 | GTCACGTGAT | - | 6.02 |
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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 |
GH04I121739 | chr4 | 122659921 | 122661633 |
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Enhancer Sequence | GACAAAAAAG TAAGAATGCA GTGATGAAGA CTACTTTACC TAGCAGAAAC ACTAGGTAAC 60 ATGATCAGTA ACTATACATC ACATATGGTC ACATATGTTC AAGGTGTTTC TCAAGTATTA 120 TTATCTGCCT TTTCAGATGG GGAAACTGAG GCACAGAGAG GCAGTCACGT GATCAATCTA 180 GGATTTAAAT GCAACAGCCT GGCTCCAGTA TCTAAGCACT GCCTCTCTAA TAGAGTAGAG 240 CTAGCCAACA GAGAGTGAGA GAAATTCATA TACTAGAGAA TGGAATCAAT CATTGTGAGA 300 TCATTTCAGT TGCAAATAAA ATGAGAGAAA AAAAGTGAAA TTCATGTAAG ACAGGCATCC 360 TGGGCAGGCA TTAGATAAAA TAATGCAGTT TAATTCAGAG AAATAGCTGG CACAGAGACA 420 AAATGTAGTA CTGATTGATT ATTTCAGCTG TTAGAAAATC TGTTGTCCAA ATGTCCTCCC 480 TTCCTCTGTG TGGGTTCTGA GAAGCCACAG CTGGTGAAGG CAGTTTTGCG TCAAAGCTGC 540 AAGGAATGTG GAGGAATCAT GGAGAACAGG GTGAGAACCA CAAGTTTAGG GGCTGGCTGG 600 CAAATGGTCC TCTTTTCAAA AAGCAGACAG AGTGGGCTGG GGTGAGGAGA GGAGTCTGGA 660 AATTATGAAA GAACAAGTTT AATGTCAATC CATATCAAAA TTCTATGTTT AAAAATAGAG 720 TCTGTGAGCA TTTAGAAGTG CAGCCATCTG AAAACCACTA AGTCGTACTT TGTATTTTGT 780 AGGAGTGGAG ATCAAATTCC AAATGTAGGC CAATCATTTC CAGTTTCTTC ACAGTAGATA 840 AGACTGGCTA AAATCTACTG TGCCCACCAG GTTAGAAAGT ACACCAGCTA TCTCAGCATG 900 GCTGTTTGTG TTGGCAATAA GGAATCTGGA ATCAGTGACT TGCTGTCACT GACCAGACAC 960 CCAGTGAGCC CAGAGTAAAA TTCTGATTTA CAGCCTATTT CTATTCATCA CCATGTTGGC 1020 CTAGACCGTA TGACAAGGCT TCTAACTCAC TTTTTTTGCC TAGCTCTCTA ATTCCAGTTT 1080 GTCCTAGAGG CTTATCCTTT GCTCTAGTCC ACTAGGTTCA GCTTCCTTTA GTCCTGGCCT 1140 CTGACCCAAT GTAAATGGAC TGATTATCCA GATGTACAAT GCTACCCACT GCCTGGATAC 1200 CTACTCTCAG GCTTCACCAC ATAAGTCTGC CTAAAATGTA CACTAATTCA ACACCTGTCT 1260 TTGAACACTG CATATGGTGG AGGCAGTCCG 1290
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