| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00040 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:1496320-1498980 |
Target genes | | Number: 47 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr1:1498280-1498294 | AGTCCCTGGGGACT | + | 6.28 | | EBF1 | MA0154.3 | chr1:1498280-1498294 | AGTCCCTGGGGACT | - | 6.93 | | Nr2f6(var.2) | MA0728.1 | chr1:1498695-1498710 | GAGGTCAAGAGTTCA | + | 7.64 | | RARA | MA0729.1 | chr1:1498695-1498713 | GAGGTCAAGAGTTCAAGA | + | 6.45 | | RREB1 | MA0073.1 | chr1:1497304-1497324 | CCCCCCACCACACACCAAGA | + | 6.46 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATCAGAAATT CTGCGAGGTG GGCATGCACA GAGAAACCTA AGCCCTGGCC ACATGGCAAG 60
TAGGCAGATG GCAGTGGTGG GGTCCCCCTC GACCCCGGCC CTGCCTCTGA ACAAGCAGCA 120
TTTTCCTCCC AAGTCACACT GTCCTTCCTT TTTTATTTTT TTGAGACAGA GTCTCACTCT 180
GTCACCCAGG CTGGAGTGCC GTAGCGCGAT CTCGGCTCAC TGCAGGCTCT GCCTCCCAGG 240
TTCAAGCAAC TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ACTACAGGCG TGCACCACCA 300
TGCCCGGCTA ATTTTTGTAT TTTTAGTAGA AATGGGGTTT CACTATGTTG GCCAGGCTGG 360
TCTCTAACTT CTGACCTCAT GATCCACCCA CCTCGGCCTC CCAAAGTGCT GGGATTACAG 420
GCCTGAGTCA CCGCGCCGGC CCGTCCTTTG TCTTGACGCT GTGAACACTC GACCAAGTGC 480
TGCGTCTTAT CTTTGGGCCG CATCTTGAAC CCCGTCTTGC TTCCACTGCA GTTTACGGCG 540
ATGACTTCTG CCAACGCACC GGCTGCTGTG GGGCAGATTT GCTTTCGGGC TCTCACTTGT 600
AACAGTCACT TCCCGCGGCC CCCCTGCACC CATCACTAAC CAGGAAACGT TATCGGGGTC 660
CTCCCGACCT GCACATCTCA ACACCCCTGA GGCCCCACCC GGCATCGTGC CAGTGTCCAC 720
AGGGAACTGC CTGGGGACTT CACTCCTCTC CAGGCCAAGG GCATCATGTG CAAGAGCTTT 780
AGCTAAGTGG CAGGCTTCCC ATTCTGCACC TTCTGCCCCC ACCTAGGGGG CAAAGACGCC 840
CCCCGAGTGA AATAAGGTAA TGAAGGCACG CTCCTCCTAG AGCCTCCTGA GGGGCCACCA 900
CAGGCAATGC CTTTCCCACA CGAGGTCCCC AAAGCAGAGC CCGTGGCTGA CAGTGTCCCA 960
GCGCCACCCC TGCTGCCACT CCTTCCCCCC ACCACACACC AAGAGCACAC ACACGCACGC 1020
GGGGTTCTTC TGGGCCGATG CTTCCTGGGA GATCACCAAC CCCTACAGTC CCTCTGTAAA 1080
GGAGGAGCTT CCGAATTCTG GGACACTGGG CTCAGCTCCT TCTTTTAGAA TGACCAGAGA 1140
CAGGCTCATC CTCTGCCTAT ACCAAGTCCT TCCGGATGAG ACTGCTGAAG CTGGACTCAG 1200
TCCTTGCAGA ACGTGGCAAG TACTTCCCAG GTCTGGAACC CAGGAGGTCA CAGTGGGCTG 1260
ACATGAAGGG GCTGAGCTTA CACCAATCAA GGGAGTGTGA GGATGTGCGT CACTCTCTGC 1320
TTTTCTTTCT CTTACTGAAT ATACAAGAAC TTAAAAATAA ACAGTGCTAA CTGAAGAGTA 1380
ATTGTCAAAA ACAGGATGTC AGGCTAAGCT TCATGGCACA GAGTTTAATG TGAATCATGA 1440
GATGAGACAA AAGCCTCCTC CAGGGCGATG GGAAGACCCA GCCCCAAACC AGACTCTTGA 1500
GCACGCAGCC CTAAACCAGA CTCCGGGAAG GGGCTGCGTG GTCATGCACC GCCTAAGACT 1560
CAGAGGTGAA GATGGGAAGA CCCAGCCCTA AACCAGACTC CTGGAAGGGG CTGCGTGGTC 1620
ACGCATCGCC TAAGACTCAG AGGTGAAGAT GGGAAGACCC AGCCCTAAAC CAGACTCTTG 1680
GAATAGGCTC TGTGGCCACC CATCGCCGTA AGGCTCCGGG ATGGAGACAG CATGGACAGG 1740
GACCTCGCAC AAAGGCATGT CGGGAGGGCC TCCTTTCCAA GGCACAGCCC CACCTGCTCC 1800
TTCTCAGCCC ACGACGGGAG CAGAGCCATG TCGAAGCCGT GCCCCACACA GGGTGGACAA 1860
GGACATGGCC TGACAGCTCC TCAGAAATCC TTAGAGATTT TTCCAAACGC AGGTTACCAG 1920
GGCTTCTGCA GAGAGAGGGG CAGCAGGACG TGCTGCTGAC AGTCCCTGGG GACTTACACT 1980
GACTTGCAGT GAGAGCCCAC ATCTGCCACC AGGATGGCTC CCAGCACCAC CGCGTCACAA 2040
GCACCACACT CTCCACCGTG GGACGCCCAG ATGGCTCGGC AGGCAGGCCG GGCTGGGGAG 2100
CTGACAGCAG ACGCCTGGGA CTCTGCCCAG CGTCCTCACC CACAACCTTT TAACTGTAAC 2160
TGGCAGAGGA GACAGCAGGG AGGGCAGAAG GTACAGTGAT GGCTAGGATG CAGTTCTAGG 2220
TTTTGCCAGA CATACTTTCA GGGGCCACTC CTGGCTACCT AATTAATCTA CCTGTGTATA 2280
AGAATTTTTT AGCTTATTAA ATATTCCAAG AGGCCAGGCA TGGTGGCTCA CGCCTGTAAT 2340
CCCAACACTC TGAGAGGCCG AGGCAGCTGG ATCACGAGGT CAAGAGTTCA AGACCAGTTT 2400
GGTCAAGATG GTGAAACCCC CGTCTCTACT AAAAATACAA AAATTAGCCA GGCATGACAG 2460
CGGATGCCTG TAATCCCAGC TATTCGGGAG GCTGAGGCAG AGAATCGCTT GAACTTGGGA 2520
GGGGGAGGTT GCAGTGAGCT GAGATCAAGC CGCTACACTC CACCTTGGGC AACAGGGTGA 2580
GACTCTGACT CCATCTCAAA AAAAAAAAAA AAAAAAAATA CAAGAGTAGG GCTGAGCATG 2640
GTGGCTCACG CCTGTAATCC 2660
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