Tag | Content |
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EnhancerAtlas ID | HS180-03610 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:169731730-169732910 |
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) |
EBF1 | MA0154.3 | chr1:169732668-169732682 | AGTCCCTAGGGACA | + | 6.34 | Mecom | MA0029.1 | chr1:169732052-169732066 | AATATAAGATAATA | + | 6.2 | RELA | MA0107.1 | chr1:169732584-169732594 | GGGAATTTCC | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 169732198 | 169732248 | chr1 | 169731860 | 169731960 |
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Enhancer Sequence | AGCTGGGTTA GAGAGAGATG AGACAGAGTA AAAAGGAAAG AGATTCAGGG CATGAAAATG 60 ACTCTACCCA CTGTTGCTGG CTTTGAAGAT AGAGGAACTA GGCCACAAAA CAAGGAGTAT 120 GAGTGGCCTT AAGAAATAGG AAAAAGCCCT CATCTGACAG CCAGCTAGAA AGCAGTCCTC 180 TGACCACAAG AAATTGGATT CTGCCAACCA CTCAAATGAG CAAGGAAATG GATTCTCCCC 240 TAGAACCTCC AGAAAGGAAC ACAGCTCTGT AATGCCTTGA TTTTAGCCAG GTGAGACCTG 300 TTTCAGACTT TTGACCTATG GAAATATAAG ATAATAAAGT TTTATTGTAT GCTGCTAAAT 360 TTGCGGTAGT TTATTACTGA AGCAATGGAA AGCCAATACA GACAGAATAT ACAGAGAGAA 420 AGAGAATGAG TTCTTTCCTG ATAATTTGTA AATATTTGGG TCTTCACTGG ACAAGCTTCA 480 CAGAGGATTC ACTGGTTCCC TAGCAAACCA GCATGTCCAG TCCTGCAGCC TCCCTTTCTT 540 AGGCCCAGCA TATGTCAGCT GTGTGCATAG AAAAATCAAA GCAGGACCCT GAGTAGTTGG 600 AAAGAAAAGA TGGTTGGAAA TGGGTTGCAC TTCAAGTGAG GAAACAAGAG GTAGGAGACC 660 GGCATCTCTT TCTCATATGT CCCAGGCTGA CTCTTGTGAG TTGTTTTCCC TTGGAGGCTA 720 TCGATGACAG TCACAGTAAC CTGATGGAAC CTGGATCATG ATGAAAGAAG TAAGTGTCAA 780 TGGCTCCGAC TTCCAAGGAC TCTGATGTCC CACAGCACTA GCTAAACAAA GCCAGTTGGA 840 AATGAGCTTA AATGGGGAAT TTCCTGAATA TATTCCCTAT TGTTAGGAAG CCAGGTTGGC 900 TTCCTTGCCT ACAATTATGC CAAGCAGTCA CACTATAGAG TCCCTAGGGA CATGATATTA 960 AGTGATTCTT TTAACACAAA CAACTTAATA ATCATTTATA CTAATAGCAA AACGGCCAAC 1020 GGCTGATATT CCACTTGAAG TAGAATTGGC TATCCAACTG GAAGAGAAGA CAGGAAGACG 1080 TGATCTCCAG GGAGCCACTA AAAGGATTGG CACCTGCCTC TGGATTCCCC TTTTCCTTAT 1140 ATTACCTCTC AGCACTGGCA GGCCTTTATT TCAGGATACA 1180
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