| Tag | Content |
|---|
EnhancerAtlas ID | HS133-22041 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:24186510-24187820 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr3:24187454-24187465 | TGATTAGATTA | - | 6.32 | | FOSL2 | MA0478.1 | chr3:24187622-24187633 | GGATGACTCAT | + | 6.62 | | IRF1 | MA0050.2 | chr3:24187309-24187330 | TTTATCTTTCTTTTTCTTTTT | + | 6.45 | | JUNB | MA0490.1 | chr3:24187622-24187633 | GGATGACTCAT | + | 6.62 | | ONECUT2 | MA0756.1 | chr3:24186946-24186960 | AGATAATCAATAAT | + | 6.05 | | ONECUT3 | MA0757.1 | chr3:24186946-24186960 | AGATAATCAATAAT | + | 6.37 |
|
| | 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 |
| GH03I024144 | chr3 | 24186039 | 24189305 |
|
Enhancer Sequence | GGATTGTCAA AGTCATGTGA GCGCTTACAA ATGAGGAAAA TATGAATGAG CCCTGTTAAG 60
TCATTTTGGT TCAGTTACTA AAGGGAAAGG AGGAATGGTA ATAATACCCT CAACCCCTTC 120
CCAAATGCTT CCGGTGTGCC AGGGACTGTT GTATTTGATG AACATTATCT AATTTAATCT 180
TGAAAACAAC TCTACAAGGT AGGCAATGAT TTCACAGAAG GAAAATCTCA GCTTAATTCC 240
AAAGGTCACA CAGCTAGTAA GTGACAGATC TGGGACTCGA ACAGAAGTTT TTCTGATTAG 300
AAAGCCTGAG CTCTTAGAAT CCCTCACAAG CAAGTAAAGG GCACTCAAAA TTTATTTCCA 360
TACAGTCTAG ATTAACACTG AGTTTTTAAA CCTCATAGAC ACTAGTATCT TAAACTTCTC 420
AATAGAACAC TGAAATAGAT AATCAATAAT AAGTTTGTCA TAGTGGCATA TCTAAGTATT 480
TGGCTGTAAG TCAATCATAT TCACATATCC CTATCAGGCA TATTGTTGGC AAGGGCTAAA 540
GGCCTTTAAG AGATAAAGAT AAAGAAAATA CTCAGCCAGA GGTGGGGATT AACCCAGGAT 600
TTCCAGCCTA ACACTCTAAC ATAACCCTCT TCCTTTTTAA AGATTCTCCA TTCCTTCTTC 660
TTTAATGGGC AAACCAGAAC ATTTCACAGA TTTTTTTTTC TCAGTGAAAG AACTCTATTT 720
CTCACATAAA ATGTGAGTCA TGATTACTTC TTTCATCAGG AAAAATCCTC ACTGTATTTT 780
CTTTTTTCTT TCTTCATTTT TTATCTTTCT TTTTCTTTTT AATTTTTAAC TAATAGTTGG 840
AATCTCTCAC TGATGTGCAA AAAATTTATG CCAGTAGAAT CATTAATACT GATGCCTGGC 900
AAAAGGGAGG CCACACATTC TGAATGACAT GATTCTTATT TTTATGATTA GATTAATTAA 960
AGTGACTGGT GTAAATCCCT CGCACAGTGT GGGGAGAAGA GACCCCAAGG GCTAATCTCG 1020
CCACCATATG CTGTAGCACT TTGAAAACTG GGTAGGACGA CTTCAGCTCG GAATGTCTTT 1080
ATTGCTAAAA ATATAACAAA CAACCAACTG CAGGATGACT CATGCAATAG CACTCAACTT 1140
TGCATTCTTC AGAAATTTCT GAACACGATG TTTTCTGCCA GCGCCCCATC TCCAAAAATG 1200
TCCATAAAAT AAATTCCTGT CTTTGCTCTT GAAAAAATAT TAGGACTAGT CCCTGAGGCT 1260
CTACCCCATG TGAACACTGT GTATAGAATG ATACCTTATC AAGGTAAATG 1310
|
