Tag | Content |
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EnhancerAtlas ID | HS078-10958 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr20:57638290-57639930 |
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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I059063 | chr20 | 57638656 | 57639542 |
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Enhancer Sequence | ATAAAATGTT AGAATACATT AAAACAGCAG AGAATGTAAG GCCCATTTTT AGAGGGAGTT 60 CAGAAGTTGA TAGATTATCC GAGGAAAACA AAGTGAACAG ACTTTTTTCC CCCTTTTTAT 120 ACTAAACGGC CCAAATGGAG GAAAATCACT TTCAAATGAT TACATATAAT ATGCATAACG 180 ACAAATCCGA CACTGCCAAA ATCATATGCA CAACCTCAGT TTTCCTTCCG GCAAGATAAA 240 CAAATCGACA CCGATAAATC TGAGTGGAAA CAGGGCTGTC AAATGTTATC TTCCGGACTT 300 GGGATTAGAA ACAAGGGGAA TGTCGCAGAA GTCATTTGGC ACCAGGAGGG CTGTGCATGC 360 CCTTGTCTCT CTGCCTCATC CTTTGCTGCA CTTTCCTCCA ATACGTGAGT ACATATGTAT 420 ATATTTCTCT CACAGCCCCT CCTAATTCCC AAACCACAAA CACCGAAGCC TTATATAATT 480 TCACTGTGAT TTCTTTTCTG TTTTTGATTT ATCTGAAGTG TTGCTTGACT GCTTTATCTT 540 TCTCTACACA GCCTCTTAAA TTGCTTCAGC AGATCTAACC TCTCCAGAGA CCGGAGACAG 600 GCACAAAGCT TTACGCCGGA CACTGCCAGG CCCACGTCCG TGTGGGCGTT GAATGGATGC 660 TACGTGATGG CAGAATGAGT CACTGAGATT TAGGCGGAGA GTTTGGAGGA AGGTGCTAAT 720 GAAAAGGGCT CTGGTGCTGC AGGAGACATA CGCAGGTCAG GAATAATGAC GTCAGCCCGG 780 AGCCAGTGTT TAAAAATAGT GAAGCTCTTC TATGAATCAA AATGATTCTA TGGGGAAAAA 840 ACTAAACTGG TGATGGAAGG TTATATTGCT TTGTAAAAGA AAAAGTAATT TATGCTCGAC 900 TTCAAGAAAA GCAAAAGTTA CAAATCAAAA TAAACTCAGA AGTGCTTGAA GTAGGCAGAA 960 ACTCATCAAA ACAGTTGGAG TGAACTTACC ATGTTCTGTA CACTAACTAA AGAAAATTGC 1020 TAGGGGATAG TGAATAGCAA AGATGCCTGG CTTCCTTCCC TATCGCAGTC ACCTCTGCAA 1080 GTAGGATTAC CAGCTTCTGC TTTGTGACAG CTTTTGCTGT TTCTGATGGG TCCTTATGCT 1140 GAGGGTACAG TCGACAGACC ATTCACTGCT GAAGCTGTCA GAATTAACCC CAAAGAAAAA 1200 CGGAGCTGAA TAGGCTTTAT GATTACATAA CATGCCTAGA CTTGACCAGC CCAGGCTGTT 1260 TGTTTATATA TGTCTGGCAT GCCAGATTCG ACCTGGCTTA AGTGGTACCT GCTTTAATTA 1320 ATTTAATTGG TTTTCTTTTC TTGATGGAAA ATAGAAAGAT ATTTAACTAC TCCAAAATCT 1380 CTTCCCTACC CCATGAAAGC CTTTGTAAAT TCTATTTGAT GAGGTGGTTA AGTTATTCAG 1440 TGAATGATTC TATGCAAGCA TATACTCACA AAAATAATAT TTAAACAATA CTATAGCTGA 1500 CATGGAATAA ATACCAAATA ACTAGTCAGA CCACATCTGT ACTTTTACAG TTGATCTTAG 1560 CCAAAGGCTA AGAAGCAATG CACCTCTGTA CTTCTAAATA CAAAATCAAT TCTGCAACAT 1620 AAAAACATTC ACCTATGGGA 1640
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