Tag | Content |
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EnhancerAtlas ID | HS101-27864 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr20:57638300-57639600 |
Target genes | |
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) |
RUNX1 | MA0002.2 | chr20:57638740-57638751 | AAACCACAAAC | - | 6.02 | TBP | MA0108.2 | chr20:57638397-57638412 | TCCCCCTTTTTATAC | - | 6.44 | TP53 | MA0106.3 | chr20:57639518-57639536 | AACATGCCTAGACTTGAC | - | 6.15 | TP53 | MA0106.3 | chr20:57639518-57639536 | AACATGCCTAGACTTGAC | + | 6.18 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH20I059063 | chr20 | 57638656 | 57639542 |
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Enhancer Sequence | AGAATACATT AAAACAGCAG AGAATGTAAG GCCCATTTTT AGAGGGAGTT CAGAAGTTGA 60 TAGATTATCC GAGGAAAACA AAGTGAACAG ACTTTTTTCC CCCTTTTTAT ACTAAACGGC 120 CCAAATGGAG GAAAATCACT TTCAAATGAT TACATATAAT ATGCATAACG ACAAATCCGA 180 CACTGCCAAA ATCATATGCA CAACCTCAGT TTTCCTTCCG GCAAGATAAA CAAATCGACA 240 CCGATAAATC TGAGTGGAAA CAGGGCTGTC AAATGTTATC TTCCGGACTT GGGATTAGAA 300 ACAAGGGGAA TGTCGCAGAA GTCATTTGGC ACCAGGAGGG CTGTGCATGC CCTTGTCTCT 360 CTGCCTCATC CTTTGCTGCA CTTTCCTCCA ATACGTGAGT ACATATGTAT ATATTTCTCT 420 CACAGCCCCT CCTAATTCCC AAACCACAAA CACCGAAGCC TTATATAATT TCACTGTGAT 480 TTCTTTTCTG TTTTTGATTT ATCTGAAGTG TTGCTTGACT GCTTTATCTT TCTCTACACA 540 GCCTCTTAAA TTGCTTCAGC AGATCTAACC TCTCCAGAGA CCGGAGACAG GCACAAAGCT 600 TTACGCCGGA CACTGCCAGG CCCACGTCCG TGTGGGCGTT GAATGGATGC TACGTGATGG 660 CAGAATGAGT CACTGAGATT TAGGCGGAGA GTTTGGAGGA AGGTGCTAAT GAAAAGGGCT 720 CTGGTGCTGC AGGAGACATA CGCAGGTCAG GAATAATGAC GTCAGCCCGG AGCCAGTGTT 780 TAAAAATAGT GAAGCTCTTC TATGAATCAA AATGATTCTA TGGGGAAAAA ACTAAACTGG 840 TGATGGAAGG TTATATTGCT TTGTAAAAGA AAAAGTAATT TATGCTCGAC TTCAAGAAAA 900 GCAAAAGTTA CAAATCAAAA TAAACTCAGA AGTGCTTGAA GTAGGCAGAA ACTCATCAAA 960 ACAGTTGGAG TGAACTTACC ATGTTCTGTA CACTAACTAA AGAAAATTGC TAGGGGATAG 1020 TGAATAGCAA AGATGCCTGG CTTCCTTCCC TATCGCAGTC ACCTCTGCAA GTAGGATTAC 1080 CAGCTTCTGC TTTGTGACAG CTTTTGCTGT TTCTGATGGG TCCTTATGCT GAGGGTACAG 1140 TCGACAGACC ATTCACTGCT GAAGCTGTCA GAATTAACCC CAAAGAAAAA CGGAGCTGAA 1200 TAGGCTTTAT GATTACATAA CATGCCTAGA CTTGACCAGC CCAGGCTGTT TGTTTATATA 1260 TGTCTGGCAT GCCAGATTCG ACCTGGCTTA AGTGGTACCT 1300
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