Tag | Content |
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EnhancerAtlas ID | HS133-00680 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:24371930-24374000 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr1:24372296-24372306 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:24372296-24372306 | GGCACGTGCC | - | 6.02 | MEF2A | MA0052.3 | chr1:24373541-24373553 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr1:24373541-24373553 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr1:24373540-24373555 | TTCTATTTTTAGTAC | - | 7.16 | Myod1 | MA0499.1 | chr1:24372076-24372089 | AGCAGCTGTCTCT | + | 6.32 | Myog | MA0500.1 | chr1:24372075-24372086 | CAGCAGCTGTC | - | 6.14 | Nr2f6(var.2) | MA0728.1 | chr1:24371999-24372014 | TGAACTCCTGACCTC | - | 6.22 | Tcf12 | MA0521.1 | chr1:24372075-24372086 | CAGCAGCTGTC | - | 6.02 |
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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 |
GH01I024045 | chr1 | 24372096 | 24374241 |
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Enhancer Sequence | CTGTGCCTGG CCTTAATTTT TTGTATTTTT AGTAGAGACA AGGTTTCACC ATGTTGGCCA 60 GGCTGGTCTT GAACTCCTGA CCTCAGGTGA TCCACCCGCC TTGGCCTCCC AAAGTGCTGG 120 GATTACAGGC ATGAACCACA GCGCCCAGCA GCTGTCTCTG GTAATTGAAC AGTTTAACTT 180 GATTCTGTCC CACAGAAATA TAACAAGAGC CATATATAGA ATTTAATTTT TTTTTTTTTT 240 TTTGAGACAG GGTGTCCCTC TGTCACCCAG GCTGGAGTGC AGGGGCATGA TCACAGCTCA 300 CTGAGGCCTC GAACTTCTGG GCTCAAATGA TCCTCCTGTC TTAGCCTCCT GATTACTAGA 360 ACTACAGGCA CGTGCCACTG TGCCCAGCTA TTTTTATTTT TGTAGAGACA GGGATCTCAC 420 TGTGTTGCCA GGGCTGATCT CAAACTCCTA GGCTTAAGCA ATCCTCCCTC CTTGGCCTTC 480 CAAAGTACTG AGATTACAGG CGTGAGCCAC TGTGCCCAGC TGAATTTTCT AGTAGCCATA 540 TTAAAACAAT AAAAAGAGGC CCTGCAAATC ACTGGCAAGC TACTTAACCT TCTTGATCTT 600 CCACTCCCTC TTGGGTAAGA TATCCACCAA AGGGCAATTG TAAAGGTCAG ATGAGGTAGC 660 ATATAGGAAA GATACACATG AAAATGATTT GCTAGTGCAA CATCTGATAG TCAAAGTGTT 720 ATTTTTATTT TTCTGGAAAT AAACAAATGA TTTGAAAAAG TATCATGTGG TGAGCACCAG 780 ATGGATAATG AGACAAGTTT ATTAAACATC TTAAACTGTG CAGTCAGTGA CAAAAGCAAG 840 TGGGAAGCAA CTAAAGATGT TAGAGCTGGG AAAGCCGCCT CATCTGGTCA AAGTCAGGAG 900 GAGCAAATCC CTCTGAGCCA CCAGCCCGTT TGCCCACTTG GCTCGACCCC AGCTGACAGC 960 CCGTGCAGGA GTTATTGCTG CTTGGGAGAC TTGAGATTTT GGCCAGTAGC ATTCTTTTGT 1020 AATCTTCTAT GTGACTGTAT CCGCCCACAT TTCTGACTCA GAATGAACAG GGAAAGGCGC 1080 TGCTGGCAGC TGAATTACCT CAAAACCCAG CTCCAGCCAA CCCTTTGAAT AGTGATGAGA 1140 GCAATGTGCT CCTCCACACA TCACCTAAAT AGGGAGGCCC ATTTGTTATC ACCACTTGGC 1200 AGATGAAAGT ATTGTTTCAC AGCGGTTAAG TGATTAGGCC TGGATAAGCA AGCAGAATTT 1260 CGAACCCAAG TAGCCTGACC GTGGGCCTTG TGCTGTTAGC CCTGAGGCTG CTTTAGGGAC 1320 CAGAGATTAC GTTATTAGGC AAATATTAAA TAAACTCAGT GCATTTAGTT GCCTTCCCAC 1380 CCTCAGAAAG CAACCTGGAC TCAACCACTT TATTACTGAT TTATTTATAT CACTCTATTT 1440 TGCAGATGAA AAGCATCATT GAGTATCTCT CCCTCTCTCT TTTTTTTTGA GACAGGATTT 1500 TGCTCTGTCG CCCAGGCTGG AGTGCAGTGG TGCAATCATG GCTCACTGCA GCCTCGACCC 1560 CCTGAGCTCA AGCAATCCTC CTTCCTCAGC CTCTCAAGTA GCTTCAGTGA TTCTATTTTT 1620 AGTACTTTTA GTGGTCACCC CACACCTCTA AAGGAAGGTT TGGGCCAAGC ATGGTGGCTC 1680 ATGCCTGTAA TCCCATCCTT TGAAAATAAA CTCACCCTCA TAGCTCAGTA ATTTGTTGCT 1740 GCTGAGATGA TTGAAAAGAA TGGACCTTGA GTTCGAACTG TTCAGTTGTG GTTGTCACTT 1800 AAGGTCCAGC TTGCTGGGCT TCTCTGGAGT GCTGAGGCAA GGGGTGCCCC GCCCTATCCA 1860 AAATCTGTGT TATGAGTCAG AAGGCAGAGA CGCCAAAAGT CCATGGGGCA ATTCCCAGGA 1920 GGAGGGCCTG CTCTGAGTGA CATGTCCTCT TGGTTCTGTG GACTCCTCAC CTGGAGGGGG 1980 CATCTGAAGA CAGAATCCAG GACAGTAAGT CCCAATGAGG AGTTCCATTC ATGGTGTGGC 2040 AAGTAAGCTC CAACTGGACT GATCTCCGGG 2070
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