| Tag | Content |
|---|
EnhancerAtlas ID | HS133-14098 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr18:20948840-20950170 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr18:20949904-20949918 | GAGGCCGAGGCGGG | - | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH18I023368 | chr18 | 20948881 | 20949737 |
| Enhancer Sequence | GAGGGAAAAG TATTTAATAT TCAAAACCAG TTACTAGTTC ATTTTAAATC ACACACATTT 60
TCACCTGTGG GCAACTGTTT CCCACATGTA CATTTGTCAC TTTCAAAGGA GTGTCAACTA 120
TCTCAGGCCA CTGGACTGGC TTTTGGGGCT ACCATATTTA ACAAATAAAA ATACAGGGCA 180
ATCAAACACA TTTGAATTTC TGATAAAGAG TAATGTTTTA GTGTAAGTAC TGTATGTTCC 240
AAATATTACA AAAATTATTC GAGGCTTATC TGAAATTCAA ATGCAACCAG GCATCCTGTA 300
TTTTATCTGG CAACTCTACT GGCTTCTTGC TACAAAAACA CTTTATTAAA AGAACAAAAG 360
GTGCTCCAGG GAGTGGAAGC CCCACATTCT CAGAGTGGAT GACCTTCTCT CAGGAGTCAT 420
TCCCTTCAGA CCTTTTCTCT TTAGGCCTTC AGCAGGCCCC AAAACCTGGA GGCCAGCTGG 480
CCAGTCTAGG GGCACTGGCC TCAGCGCTCC AGGCCTGAAG TCTTGTCTTT TCTCATTTAC 540
ATTCACCAAA GCTGCTCCAT TGACTGGCTG CAACAAAGGC CTCATTTTGC CCAAGAATGA 600
GCTAGTAAGT GGAGACTTCT GGGTCTAAAG TAAGTCAAAT TAGGACGGGG CTGGGGAAAC 660
AAGAAAAAGT ACTGTCCCTC TGTGCTTGAT GCAGCCGATT GGCACCCAAA GCAGCTGGCC 720
ACATACATTT CATTCACATG TCATCTGAGA GGTGACATGT GAATCCCCTG AAGGAAGGAG 780
ATTGAGACTT CCATGCCTCT TCACACATGG CTAAAGGCAG ACATGTTCCA GGTGTTGGTG 840
GACACAGCCT GGAGTGGCCC AAACAGCAAG AAGAGGGCCG GCTTCAAGGA CTAAGTCCCC 900
TGCCCTCAAC ACAACCCAGG CCTGTAGAGT CTCTGGCTGA ATGGAAGAAT CTCATGATAC 960
CACAAGTCTC AGCCCTTTCC TTTAACCCAA CCACAGCTCA CCAAACATTA AGAGTTTATC 1020
CTGGCCGGGT GTGGTGGCTC ACGCCTGTAA TCCCAGCACT TTGGGAGGCC GAGGCGGGCG 1080
GATCACCTGA GGTCGGTAGT TCCAGACCAG CCTGACTAAC ATGGAGAAAC CCCTCTCTAC 1140
TAAAAATACA AAATTAGCCA AGCATGGTGG CGCATGCCTG TAATCCCAGC TACTCGGGAG 1200
GCTGAGGCAG GCGAATCGCT TGAACCCGGG GGGTGGAGGG TGCGGTGAGC TGAGACCGCG 1260
CCATTGCACT CCAGATCACG CCATTGCACT CCAACAAGAG CTAAACTCCA TCTCAAGGAA 1320
AAAAAAAAAA 1330
|
| |
|
|
|
