Tag | Content |
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EnhancerAtlas ID | HS102-17287 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr4:99980590-99982040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arid5a | MA0602.1 | chr4:99980613-99980627 | TTAATATTGCAAAA | + | 6.1 | ONECUT1 | MA0679.1 | chr4:99980730-99980744 | AGTATTGATTTTTT | - | 7.19 | ONECUT2 | MA0756.1 | chr4:99980730-99980744 | AGTATTGATTTTTT | - | 6.93 | ONECUT3 | MA0757.1 | chr4:99980730-99980744 | AGTATTGATTTTTT | - | 7.14 | ZNF263 | MA0528.1 | chr4:99980879-99980900 | TTCACCCCCTTTCCCTCCTTT | - | 6.15 | Zfx | MA0146.2 | chr4:99981757-99981771 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 99981779 | 99981885 | chr4 | 99981301 | 99981707 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I099057 | chr4 | 99979047 | 99984268 |
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Enhancer Sequence | GTATTTTCTT TTTAGCCTGG GATTTAATAT TGCAAAAGTA GTTTACTTCA CTACAGAGTT 60 TATGTTCTGG GATTTGTCTG TCTGAGGCAG TGAGTCCTAG AGGTAATATG TTTCACCTAA 120 AGATTACTCA AAATGAAGAA AGTATTGATT TTTTTTTAAC ATCTAATTTT GAAAGAAGAA 180 AGCTCGCAAA TACATCTTTT ACAGTAGTAT CTAGAATTGC CTTTCTCATT CCACCTCTGC 240 TTCACATTCT CTTGGGCCTT TGCTTTCTGC TTTCCCTCAT TATGACCCCT TCACCCCCTT 300 TCCCTCCTTT CTCTGAGTTT TCTTTCATGG CCTCCCAGAT TCACTGTCCC TTTGCTTCCC 360 TTCTCTGGTT TCAACTCCTG TCCAGACCAT TCTGCTTCAT ATTTTTCTTA TGCTCTCACA 420 CCAGTCTTTC TTTTGCCCCT CTTTCTGATT CCAGGGGTAT AGTTCACAAA AATTTCACTG 480 TATAATCTGT TCTCACCATC TGTTTGTGTG CCTACCATTT TGAAATTATA TCAGGAATTG 540 AATGCTGTAA TAAAACTGTA AACATTTACA TGATTTCCTT CACAATATAT GCTGAGTATA 600 GTTTTGTCAG ATGCCCAAGT TATACTAGGA AAGAGCTAAA TTCATTCAAG TTTTTTTTCT 660 GATTTTTTAA TTGTAAAATA CACATCTCAT TTTTAAATGT ACAGTTCAAT ATTATTAAAT 720 ACATTCATAA CGTTGTGCAC CCATTACCAC CATCCATCTC CAAAAGTCTT TTCATCTTGT 780 AAAACTGAAA CTCAACCCAT TAAACATTCC CTTCCTATTG CTCACTACTC CCAGACCTTG 840 GCACCCACTG TTCTGCTTTC TATCTCCATG ATTTTGACTA CTGTACTCTA CCTCATAGAA 900 GTGGAATCAT TAAGCACATG CTTTTTTTTT TTTTTTTTTT TTGAGACGGA GTCTTGGTCT 960 GTCGCCCAGG CTGGAATGCA GTGGCGCGAT CTCAGCTCAC TGCAAGCTCT GCCTCCCAGG 1020 TTCATGCCAT TCTTCTGACT CAGCTTCCCG AGTAGCTGGG ACTACAGGCG CCCAACACCA 1080 TGCCCGGGTG ATTTTTTGTA TTTTTAGTAG AGATGGGGTT TCACTGTGTT AGCTAGGATG 1140 GTCTCAATCT CCTGACCTTG TGATCTGCCC GCCTCGGCCT CCCAAAGTGC TGGGATTACA 1200 GGCGTGTGCC ACCGCGCCTG GCCAAGCATA TGCTTTTTTA TGACTGGCTT ATTTCACTTA 1260 GCATTATGTT CTCAAGGTTC ATCTGTGTTG TAGCATATTG CAGAATGTCC TTTTTAAAAA 1320 ATTTCCTGTT TTAAAATGGA CAATTATTGT ACATATTCAT AGGGTACATA GTGATGCTTT 1380 GATACATATA ATGATACATA TAATTAATTA AGGTTGTTAC TCAAAGTTGT GGTGATTGGT 1440 ATCAATATGT 1450
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