Tag | Content |
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EnhancerAtlas ID | HS133-15896 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr19:47867340-47868330 |
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) |
FOSL1 | MA0477.1 | chr19:47867726-47867737 | AGTGACTCATG | + | 6.14 | Klf12 | MA0742.1 | chr19:47867510-47867525 | GGCCACGCCCAACCG | + | 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 |
chr19 | 47867637 | 47867786 | chr19 | 47867367 | 47867809 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I047363 | chr19 | 47866669 | 47868209 |
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Enhancer Sequence | TCCTTCACTC TTGTGGCTCT ATAATCTCCC CAGGGGCTTT TCCTGCATAT GTGTCCAGCC 60 AGCCAAAGGG TCAAGGGCAT GGGAAGTGAG TACAGGAGGG TTTGCGGGTC GAGCCTGCAA 120 ATGGTGCACT TGCCTTGCAC TCACCACTCC TGGTCAGTCC TCAGTCTCGT GGCCACGCCC 180 AACCGTGAAG GAGGCTGGGA AGTGTAGTCC TTGTGCTCAG GAACAAAAGG AAAAGGAAAG 240 TTGGGAGCAG CTGATGGTGT CTGCCACAGG CTCACGTGCG GGTGTAGCAC AAACCAGTGG 300 CCTTCCTGCA GGAGGTGCAC ACTATTTTCT ATTCTGTTTG ATTTCATCTT TTAAAAAAAA 360 AAATACTAGT GCTGCCGGGC ACAATGAGTG ACTCATGCCT GTTATCCCAG CACTTTGGGA 420 GGCTGAGGCA GGAGGATTGC TTGAGGCCAG GAAGTCGAGA CCAGCCTAGG CAACACGGTG 480 AGGCCCTGAC TCTAGAAAAA ATTTAAAAAT TAGCCCAGTG TGATGGCACA CACCTGTGGT 540 CCCACGCAGG AGGCTGAGGC AGGAGGATCG CTAGAGCCCA GGAGTTCGAG GCTGCAGTGA 600 GCCTTGATTG CATCACTGCA CTCCAGCCTG AGTGATAGAG CAAGACCCTG TCTCATAAAA 660 AAACAAAGTC CATGGGGTAG GTAGTCTTAC CCTAATTTTT GGACCAGAAG AAGGATGCAG 720 AGAGAGAGAA AATATTGCCC CAGGTCACAC AGCTGGCAAG TAGTAGAGTC AGGGCTCCAT 780 CCGAGGCCAC CAGGCGTCAG AGCCTGCTTC GTGAGTGGCC GCTGGCTCCA GGCACAGTGG 840 GCGTCACCTC CTCCTCCTTT ACCATCCGGA GGCAGAAGCA AGGAACTGCC CTTCTCTGTG 900 GGTCTAATTT TTAAGGCCAC AGGAACATTT TCTAGACTCC TCTGGCCAGT CTCTCATCCT 960 CTCTTGTCAG CAGAACCGGG TCATATGTGT 990
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