| Tag | Content |
|---|
EnhancerAtlas ID | HS059-32473 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr3:72586440-72588120 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ONECUT1 | MA0679.1 | chr3:72587911-72587925 | TTTATTGATTTTTT | - | 6.89 | | ONECUT2 | MA0756.1 | chr3:72587911-72587925 | TTTATTGATTTTTT | - | 7.52 | | ONECUT3 | MA0757.1 | chr3:72587911-72587925 | TTTATTGATTTTTT | - | 8.12 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATCGTCATCC CCATTTTACA GATGCAGAAA GCAAGGCTGG GAGGGTGAGC TTTGGCACTG 60
TTCCCACAGC CACACAGCTG AAGGGCATCA GAGATGGGAC CAAAAGTGTG CTCTGAACCC 120
TCCCTGTGAA TCAGAATCTC CTGGGGAGAT TTTAAAAAGT ACCAATTTGC CTAGATCTCC 180
GCCAGGCCAT CTGCATTCTG TTTGTCTGAG TTGGGCCCAA GCATCAGGAT GTTTCAAAAG 240
ATCCTCATTG GCTCCAGTGT TCAGGCAGGA GGAGAACCTT GCACTCGATG GTTCATGTAA 300
AGTGCGTAGC TCAGCACCGG GCTCAGAGCC GGGCAGTAAT CAGCCCAGTT AGCATCAGCT 360
GCTGTGGATA TTTTTACTAT GCAAACTCAA GCCCTATGAC ACCATGCTGT CGCCCACTGG 420
TTCTCAAACT CTACCAAGCA TCAGAGTCAC CTGGAGGGCT TGTTAAAACA CAGAAAGCTG 480
GGTTCACCCC CTGAGCTTCT GGGGTCTGGG TTAGGAATCC AGAAGGTGCC TTTCTGACAA 540
GCTGCCTTTC TTAATGCTGC TGTTCCAGGG ATCACACTTT GCGAACCAGC TCTGTAAACA 600
AAGCAAGGCA AGACGACTCA AAAGGGCACA TGATTTTCAA TCCTTCCAAC TTGGGATCAA 660
GTGGCCAGAC TGAGTGGGGC CCTTCCAGTG GCCTGCCATG ACAGATGGCA GGACTGGGTG 720
TTGGGCGACC TTTGGCAGGT ACATCGCCTA GCAGGTGTGA CTAAGACATT GCCGGTTCGT 780
GGCCGACATT CTGGGACCTG GTCCTACATT CAATGGCTGA CAGGAGCCTG AAATGGATAG 840
AAAACACCTG TAGCCTAGGC AACACAGTCT GGCTCATACA ATTACAGACT ACTTGAAAAA 900
GAGAACAGTG AGGAGGAAGG GAGGAAATGA ACATGTGTAA GAAAAGAGGA GCTCAGTGTC 960
AAATGTTCCG TATGCTTGCA TGTTCATACA TGCTCTCACA GACACACGTA GACACTACTG 1020
CATACTATAC ATATTCTTTC AACCTGGGCT GGGAAAGAGG AACCAAGACA AGGGTTCTGG 1080
AACCTACTTT GGCTTTTCTG CTCTCAGGCA AGAAGCCAGA CATTGTCCCA TTTGAGTTGC 1140
CATAAATTGG GTCATGGGAC CACCCCCATC ACCATCACCC TGACCACAGT CTGGTCAGAT 1200
CTGCTAGCCC CAAACTGCCA CGTGTAGACA TAAGGGAGCC TGGCAGCCAA TGAGGAGGCC 1260
TGGTGCAAAA ACTCTGACTG ACAGAGAAGC CCTGCAGTAG ACAAATGGGA ACTATCCAAG 1320
TTAGGGCTTA CCCTCTGGGG GACACATAGA GTGGAGGGAA ACAAGCCGAG GTGGCAGAAA 1380
GGGAAGACAG AAAGAGTAGG TGGGGCTGAG TCACCACTCA ACAGTCTTTT TTTTTTTTTT 1440
AAATCGTGGT ATTTTTTCTA CCATAAGCAT TTTTATTGAT TTTTTTTTTA TTTATTTATT 1500
TTGTAGAGAC AAGGTAATGT TGCCTAGGCT GGTCTTGAAC TCCTGAGCTA AAGTGATACT 1560
CCCTGTTTGG CATTCCAAAG TGTTGGGATT ACAGGTGTCA GCCACTGCAT CTGGTGGTGG 1620
CTGATGCCTG TATTTTTATT TTTAAATTTT AAACAAAATT TAATGTTTAA TTTAATTTAT 1680
|
| |
|
|
|
