| Tag | Content |
|---|
EnhancerAtlas ID | HS133-12802 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:47336810-47338640 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:47337127-47337145 | GGGAAAAAGGCAGGAAGG | + | 6.31 | | FOSL1 | MA0477.1 | chr17:47338191-47338202 | CATGAGTCACC | - | 6.62 | | FOSL2 | MA0478.1 | chr17:47338192-47338203 | ATGAGTCACCC | - | 6.14 | | JUNB | MA0490.1 | chr17:47338192-47338203 | ATGAGTCACCC | - | 6.32 | | JUND | MA0491.1 | chr17:47338191-47338202 | CATGAGTCACC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr17:47336855-47336870 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 47337000 | 47338436 | | chr17 | 47337469 | 47337918 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I049259 | chr17 | 47336904 | 47338798 |
|
Enhancer Sequence | TATTTTCAGT AAAGACAGCG TTCACCATGT TGGCCAGGCT GGTCTTGAAC TCCTGACCTC 60
AGGTGATCAC CCACCTCAGT TTCCCAAACT GCTGGGATTA TAGGCGTGAG CCACTGCGTC 120
CGGCCTTAGT TAGCTTTATT AATGAGAAAA CAGGAGTGCT GGTCCTTAGC CTCCAGTCCT 180
GATGGGGTGC AGCGAGGAAA TGGAGCTCTC ACTGGAAGCT GTGGCCCTGC CAGGACTACA 240
GCCCTCGGTT TTTTGTGTTT TTTATGTTTT TTTTTTTTTT TTTTTTTTTT CACCCAGGCC 300
TGTGCACTGA GGGGTAGGGG AAAAAGGCAG GAAGGGGAGG GTGGAGTCAC CTCGCAAAAG 360
GAAGCCAGGG GAGCCCAGAA CAGGATCCAG GGTCTCCCTC CCCCGTGGTC TGGAGATCCT 420
TGACATCTGC CATCCCCTTA GCAGAAGCTG CAGCCAGAGA AAGAGGGCGA CGGTCCCGTC 480
ACATTCTGAG CCCAGCAACG GAGGGCTTTC CAGGCCGGGA CTGCGGGCAG ATGGGAATTC 540
TCCTCTCCTT TCTGCTGGAC GTATCTCCCC TCAGTTTCGC TATCTGTAAG ATGGGGCATT 600
GTCCCTGCCA AACCCGCAGG CCAGGACGGC CTAAGAGGAT CAAACGAGGA GAGGCAACGA 660
GGATTGGTGC CTGGCTTTTC CTGAAAACAG ATTCCTCCCC CGCCCCCGGG ACCTGTCCCA 720
CAGGGGCGTC TGGAAATTCC ACAGAGCCAG CCAGTCTCAG AGTGAAACAA TCGGATCCGC 780
CGCGACACAG CAGCTATTCA GACGTCGGGG GCGGGGGCCG GGCCGCTGAG CGAGCAGAGC 840
AATGCCGCCC TCGCGTCCCC TCCCGGCCCA CGCGGCTGCC CCGGCCGCCC TCCCCGCGGA 900
GCCCCGGCCT CGCACGGGCC TCGGCGCCCG CCGGGCGTCC CCCAAGCTTC CTTGTTTGTG 960
GCCGAGCGAC CGCGGAGCGT GGCACGTTCA GGAAGGACGA GTCGCCCCAC GGCGGGGAAC 1020
CGGCGACCGG CGGCAGCCCC AGCCCAACCC CGGCCACGCC TCGTTAGGCG CCACGTCCCG 1080
TCCCCGGGCG CCCGGAGCAC TGTGCCCCGC CGGCCCCTGC CCGCCGCTCG CTGTAGGAGG 1140
GAGCCTTCTG CGTCGGCTCC CGACACTCGC TCACTGGGGC GCGGGCACTT GAGAGTAGGC 1200
AACCTGGGGG CCCCAGAAGG GGATGGGGCT CCGACAGCTT CAGCCGGGCG TCCCCTCAGC 1260
TGCCTTAGCT GGCGTCTGAG AGCGACTCCT CCGTCCAGGG CTGACAGTTC CCTTGCCCCT 1320
TAAGAGCCAA TCGGAGAATC ATAGGATCTG ACATCCTGTG GCTCAGCCGG GTCTAAGAGC 1380
TCATGAGTCA CCCTGTGTGC TTTGCTGATG AGGAAACCGA GGCCCAGAGA CGGGGGCTGA 1440
CTTATTCGAG CCACGTTTGT GTCTCCTAGC CCTGTGCCCT TTCTCCAACA CTCTACTATC 1500
CTACCTCAAA TCAAATCCAC TCTGGGGCTA AGGACATCTA GAAGTGTGCG TGTGTGTGTG 1560
TGTGTGTGTG TGCGCGCGCG CCAAGAGTGG CTTGGCTACA TTAGGGAAAT GCCAGAAAAA 1620
TGGAAGGTTT CTAATAAAAG CTGCTCTCCA CGGGCCCAGA GTGTGGGGCT CCCACCCATT 1680
GGCTCCACAA ATCACCTGTA CAACCTTGCC AGACATTGGC CGCCTGGCAG CTCCAGACTT 1740
CACTCCACCC ACACTCCCCA CACACATACA GACAATGGCA TTTTTTTCTA TGGCATCTGG 1800
AAGGGGCAGA AATGCCCAGA GACCTGGTTT 1830
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