| Tag | Content |
|---|
EnhancerAtlas ID | HS133-19302 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:48391250-48392350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLIS2 | MA0736.1 | chr20:48392171-48392185 | GGTTGCGGGGGGTC | - | 6.37 | | JUN(var.2) | MA0489.1 | chr20:48392044-48392058 | ATGAGTCATTCTCC | - | 6.4 | | MEF2A | MA0052.3 | chr20:48392244-48392256 | TCTATTTATAGA | - | 6.74 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_01358 | chr20:48390996-48392247 | Adrenal_Gland | | SE_10052 | chr20:48391381-48393333 | CD14 | | SE_23623 | chr20:48391391-48392368 | Colon_Crypt_1 | | SE_26706 | chr20:48391001-48392376 | Esophagus | | SE_35046 | chr20:48383102-48394150 | HeLa | | SE_50537 | chr20:48391359-48392319 | Sigmoid_Colon | | SE_53571 | chr20:48391382-48394015 | Spleen | | SE_59121 | chr20:48392206-48441118 | Ly3 |
|
| | 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 |
| GH20I049762 | chr20 | 48379421 | 48394150 |
|
Enhancer Sequence | AGTTACAATG AGCCGACATT GGACCACTGC ACTCCAGCTT GGGTGACAGG GCGAGACTCT 60
GTCTCCAAAA TAAAAAAGTG AGAAGAAAAA TAAATAAAAT TTAAAATAAC AAAAAGTAAG 120
AAACAGAAAC ATACACACAC ACAAAAGCAA ACAAAAGAAA ACAAGAAAAG GAAAAAATGA 180
AACAAACTAG AAAAAACAAA ATGAGAAGAA TGTAGACTGT CATCATGTGC CTTGGCCATC 240
CCTCCAGGAA GATGTCTTGG AGCTGGGATT CGTGGATAAA CAAGATAAAC AAGATGTATA 300
CATTTTCCTG TGTGCTTGCA GCTACACACA CACACACACA CACACTTGTG CATGCATTTG 360
GACACACAAA CACTGGGGCC AGAGAGAGGC CCAGCCTCCC CTTAGACACA TTGTTGTCCA 420
ATGTCCCCCA CCCCCAGTTG GGGTTCTGTA AGTAAAAAAG AAGGAACAGG ATGAGTATTC 480
AACAGGCAAC CTTTAGGTTT TCCATGGACC TCACCTCATT TGATAGACAG AAAAGTTTCT 540
ACAGCAAGTT CATTGGCAGG ACTAGGCCTT GAGCCCACTC CCTGGGACAG CGGACTCCAC 600
ACCACCTGTT ACAACTGGAG ATTGAGTGTC TGCCGGAAGC TGTTTCCTGG GGAACTGCAG 660
CCAGCTGCTG GCCACACAGG AGCTCTTTAT CCCCCACCAA CTCACCTCCC TGGGATCTAC 720
CCAGGACCTG CCTTCTTGAG TAACAGGATG TGACCCTATG TCACCAGGGC ACTTGCTGCC 780
CATTGAAAGT CCTCATGAGT CATTCTCCAA GGTTCCAAGG GAAAAAAAAC TCCTAGATAG 840
GGGCCCATCC CAGAAAGAAA TAAAACACTG GCCCAGGGCC GAGACTTTCA GAGAAACCAG 900
CTGGCCTGCT TGTGAGTGGG AGGTTGCGGG GGGTCACCTT GAACCGAGGT CTCTCTGGAC 960
AGAACTGTTT TCTTATTCAA TCATTCATTC ATCATCTATT TATAGACATG ACATTTATTC 1020
ATGGATTCAG CTAATATTTA TTAGGAGGGG CAAAATAACT CTCACTTCTA ACCTACACAT 1080
TTTTGAGTTG TTTACATTCA 1100
|
