Tag | Content |
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EnhancerAtlas ID | HS133-00671 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:24164160-24165620 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:24164314-24164332 | GAAAGGTGGGAAGGAAGT | + | 6.22 | EWSR1-FLI1 | MA0149.1 | chr1:24164373-24164391 | GAAAGGTGGGAAGGAAGT | + | 6.22 | EWSR1-FLI1 | MA0149.1 | chr1:24164258-24164276 | GAAAGGAGGGAAGGAAGT | + | 7.55 | KLF16 | MA0741.1 | chr1:24164514-24164525 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:24164514-24164524 | GCCCCGCCCC | + | 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 | 24164299 | 24164463 | chr1 | 24164266 | 24165101 |
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Enhancer Sequence | AATTGCTGGG AAGGGAAGAG CATGGTCCCT ATAAATGACA TAAAAAGGAG CGAAGGAAGT 60 GCTGGGAAGG GAAGAGCGTG GTCCCTATAA ATGATAAGGA AAGGAGGGAA GGAAGTGCTG 120 GGAAGGGAAG AGCATGGTCC CTATAAATGA TATGGAAAGG TGGGAAGGAA GTGCTGGGAA 180 GGGAAGAAGA GCATGGTCCC TATAAATGAC ATGGAAAGGT GGGAAGGAAG TGCTGGGTAG 240 AGGAGGACGT GAGAACGTGG TCCTTGACTG CAGCTCCACC CCCACAGACC TAGGTGAGGA 300 CAGGCATTTT TGTTTTCCTG TCCCAATGTT GCGTTTCCCA AGACCACCCG GCCTGCCCCG 360 CCCCCATCCT GTGCCTATAA AAACCCCCAA GACCTTAGCA GGCAGACACA CAGGTAGCCG 420 GACATGGAGA GGAGCACATC AGTGGAGGAA CACACAGGCG GCTGGACGTC CAGAGGAGCA 480 CATCAGCAGG CACTGGCACG CCAGCAGGCC GCTGACCAGC AGAACGACGC AGAGTTTGGC 540 TGGGACTGTG GAAGGGGGTC CCGGGCTGCT GAGTGGCCCC ACTCCAGGGG AAAACCTTCC 600 TACTCCATTC TCTTCTGGCT TCCAACATCT GCTAAGAGCT ACCTCTACTC AATAAAACCT 660 TGCACCCATT CTCTAAGCCC AGGTGTGATC CAATTCTTCT GGTACACCAA GGCAAGAACC 720 CGGCATATAG AAAGCCCTCT CTGTCCTATG ACAAGGTTGA GAGCCCACTC GAGCTGGTTA 780 ACTAACACAA GTCGCCTATA GACAGCAAAA CTAAAAGAGC ACCCTGTAAC ACACGCCCAC 840 TGGGGCTCCA GGAGCTGTAA GCATCCACCC CTACATGCTG CCGTGGGGTT GGAGGCCCAC 900 AGCCTCTGCC TGTCTGTATG CCCCCCTAGA GGTTTGAGCA GCCTGGCACT GAAGAAGCGA 960 GCCACACCGC CCTCGCACGC CACACTCCCC TCGCACGCCA CACCCCCGTC GCACGCCACA 1020 CCCCCCTCGC ACGCCACACC CCCGTCGCAC GCCACACCCC CCTCGCACGC CCTGAGAGGG 1080 GGAAAAGGAA CTTTACCCGT TTCAGTTGCA CAACATTGTG AAAATAATGC CACTGAATTG 1140 TACACTTAAA AATGTTTAAA GTGACAAGTT TTATGTTACA TATATTTTAT CACACACAAC 1200 AAAAGGGGTT AAACATACAG TTACCATATG ACCCAGTAAT TTCGCCTCTA GGTATATGAG 1260 GGGACTTTAA AAACTTATTG GAAAATGGAA TCAAAATATT AAAATAAAAA ATATAAACCT 1320 CATTTCTCAG TATAAGCTCT ATCAAGGGCA AGACATTTTT GTAAAGCTAT GATATGCATT 1380 TAGTTTACCT TTAAAGGGCA GAGGGTCCTG GGAATTAAAC CACGTCAATG CAGTCTTTTT 1440 TGCATTATTA ACTGAAGAAA 1460
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