| Tag | Content |
|---|
EnhancerAtlas ID | HS133-10350 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr15:75397060-75398840 |
Target genes | | Number: 25 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr15:75398669-75398687 | GGGAGTAAGGAAGCAAGA | + | 6.26 | | EWSR1-FLI1 | MA0149.1 | chr15:75398665-75398683 | GGAAGGGAGTAAGGAAGC | + | 7.18 | | GLI2 | MA0734.2 | chr15:75398538-75398553 | CGTCGTGGGTGGCCA | - | 6.49 | | KLF4 | MA0039.3 | chr15:75397508-75397519 | CCACACCCTGT | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr15 | 75398506 | 75398605 | | chr15 | 75397173 | 75397774 | | chr15 | 75398293 | 75398660 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I075104 | chr15 | 75396502 | 75399119 |
|
Enhancer Sequence | GGGACAGAGT GAGACCCTGT CTCAAAAAAA AAAAAAGTGA GGCTCACCTC ATGTGCATTC 60
CTTCTCCAAC GACCATAACC CTGCATTGGC TGCTGTCCAG TGCCTACAAA CTGTTGTTGG 120
ATATTCTATT TTGCCCAGTA TTTATGGTTG TTTACCATGG TAGGGTAAAT CTGAGATCAA 180
TGAGTCTGCC TTGGCTGGAA TCAGGTTTCT CCCTCAGGGG TTTGAGTGGT TGAGGCTAAG 240
TTGAAAGGGT GTGTTTCAGA GCAGCCACAA AGCTGTCTGG ACTCTGAGGT CATGCCCAGG 300
AAGCTGAGAG ATGAGGAAAT GGAAAAAATG AGTTTGCGGA AGCTGGGAGG ACAAGAAAAA 360
GCTGAACAAA TGCAGGGTGG TTGTGGGGTG TTTGTGAGGG AAGGGAGCGG ATGCTGAGAG 420
AGCTCAGGAA GTGCCATAGG ACCACTCACC ACACCCTGTT GTCTTGAATC CCTAGTGCCC 480
ACACGCAGTA CCACTCTCCA GCCCCAGGGT CCATGCCTGG ACAAGGTCCA GGTCCTACTC 540
TTGGAGTCCT GTGAGGGCCT GTCTCCCTTA CTGATAATAA TCCCCCAGAC TCAAGGGAAT 600
CCAAGGGACC TGCTGATCTG GCAACCAAAA GGACTCAACC TCCCACCACC CCAACAGGTA 660
AAGAAACCAA GGCACAGAGA GGTTAGGTTC CCTTCTGAGG GCCACACAGG AATAAGTTGT 720
ACAGCCAGGA TAAATACCCA CATACTGTAA ACTCATGAGC CTGAGCTCTT AACAAATGGG 780
TTCTCCTACC TCCCATGAAC AAGCACAATC CAGTCTCTTC TCATGAAAGA AAACCTTCTG 840
GACTCAAGCC CCCAAGGCGG CCCATGAGCT CAAGTAGCCT GTGCCCCCTG CACCCTTGGA 900
AGGCATGAGC TTCCTTGGGC CTATACATGG AAGACAAGGC TCTGAACAGG TAGCAAAAGG 960
TCTGGTTATG AACCTTGCTC TGTTAATGAT TTGCTCGGGA ACCCCAGGCA AGTCACCGTC 1020
CTTCTCTGAG CCTCAGTTTT CCCCAACACT TGTGAGGCTA TTGTAAATTG ATGATAAACC 1080
CATGTGGGAG GCTGGGCATG GTGGCTCATG CCTGTAATCC CAATACTTTG GGAGGCCGAG 1140
GCTGGTGGAT CACTTGAGGT CAGGAGTTGG AGACCAGCCT GGCCAACATG GTGAAACCCC 1200
GTCTCTACTA AAAATACAAA AATTAGCCAA GCATGATGGC GCACACGTGT GGTCCCAGCT 1260
ACTCGGGAGG CTGAGGCTTG AGAATTGCTT GAACCCGGGA GACAGAGGTT GCAGTGAGCT 1320
GAGATTACGC CACAGCATTC CAGCCTGGGC AACAGAGCGA GACTCTGTCT CAAAAAAAAC 1380
AAAACACAAA AACCTATGTG GGAAACAGCC CTTGGGGCTC CCGGTGCCCA GCAGTGCCGG 1440
GCCTGTCACT GACCTTGCTC TAGGATGATT CACAGGGACG TCGTGGGTGG CCAGAGGGCT 1500
CGTGGGTGGC CAGAGGGCCC CTTGCCTGCA GCAGCAAGAG CAGAATGGCT GGTGTGCCAA 1560
GCTTCGGGGC ACCAGTGGGC AATAGGAGAA TTCTGTCAGT GCTGGGGAAG GGAGTAAGGA 1620
AGCAAGAACA GCCTTCAGGC GTGGGTCTCC CAGCCACAGG GGCTGTAGGG GAGACCCCGG 1680
AAGGAGGATG GGGCAGCTGT CTTAGAATAC CAATCACCCA AAGGAGCCCA TATTCCATGT 1740
TTACCAGGAG TACCAGGGTC CTCAATATCG TCTTCACTTG 1780
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