| Tag | Content |
|---|
EnhancerAtlas ID | HS133-21772 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:46748260-46749660 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr22:46749088-46749099 | GGATGACTCAT | + | 6.62 | | JUNB | MA0490.1 | chr22:46749088-46749099 | GGATGACTCAT | + | 6.62 | | ZBTB18 | MA0698.1 | chr22:46748414-46748427 | CTTCCAGATGTGG | + | 6.11 | | Zfx | MA0146.2 | chr22:46749457-46749471 | CCAGCCCAGGCCTG | + | 6.19 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27556 | chr22:46748448-46750040 | Esophagus | | SE_41347 | chr22:46741374-46751402 | Left_Ventricle | | SE_65618 | chr22:46746316-46750951 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 46748367 | 46748503 | | chr22 | 46748818 | 46749289 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I046353 | chr22 | 46749041 | 46749190 |
|
Enhancer Sequence | ATGCCTAGAG CTGTGGCGTT TCAGCTCTGG GAGACTAGAC CAGAGTTCCT GTCGTCCCTT 60
CCACTTGGCT GGAGAATTGT AGAAGGCTCT GTGGGGCGGC CGGGGGCGGG CACGGCCTAG 120
GGTGGAACAG TTGCCTTGAT GGTGGCTGGG TGCACTTCCA GATGTGGCCT CAGCTGAGAT 180
GCTGGAGTTC ATGAAAAGCG CGCCTCTGAC TTGGAAGGAC TATACTCTGT GAGTTACGTA 240
TCAAGTCCCT GTAAAAAGAA TGATTTCCTT CCTGTGTAAG GAAAATGTTA AACTACACAA 300
AACTCCACTC TGATTCAGGG AGTAAGGTGG ACGTCCCGGC ATGGTGTGAA TGATTAAGGA 360
CCACATGCAG CGATGGGATC AGGCGTCCGC GCTGGCCAGA GTGCTGCTCG CTCATGTGCA 420
GACCCTTACT GCGGTGAGGC CTGCGTGAGC CTGTGCTGTG CCTGGTGTCA GGGGACAGGC 480
TCCGAGTCAG TCACAGTGTG CAGTCCTGCT GTGGGGACAG AGTGCAGCCA TTGTTGGGTT 540
AGTACAGTGG CGGGGATGTG CCTGCCGGCG TGATGATCAG GCAGGTCTTG ACACAGCACA 600
GACCTGAGCT GTGGGACTGG CCAGGAGAGC CAGGCTGCAG CTCAGGTGTA GGGCGTCTTG 660
CAGTGAATTG CACTTGGAGA TCTTCCACCT CTTGTGGAGG GGAGACGGCA GGCGGAGCCG 720
GGGCTAGGCA TTCCTGAGAC AGGTGGAGGT GACAGCTTTG CTTGGGACAG AACTGCCAGA 780
CAGGATTGCC CATGTATCTG CCAGCCCTGG CCCCAGCAGG AGCCAGTTGG ATGACTCATG 840
GCTTCCACCT GCAGTTCACT TCACTGAAGA AGGCTGCCGG CCCAGGCCAC GTGGTAAATC 900
CCATGAGGTT CTCTCTGCCT GTGTGCCCCA CTGCAGGGGA GGGAGGCAGT GAGTTTGCCA 960
TCTGCTGTGT GACATTGTGA GGGTGCGCAG AGCAGCTGGG GGTAGCCCTG ATGCAGTTAC 1020
TGCATTAGAT GGACACTGTG AAGACGTGCA GCTATGTCAT GGGCTCAGCA AGAAGGGCCC 1080
CTGGCGTCAC ACAGGGCACC CAGCCGCATC CTGGGCCTAG GGTCAGGGGC TCCTACAGCT 1140
GGAACCTGCA CCTTCTGGGG CACAAGGTGC CTTCTTTGTG GCCACCACAC CCCATGTCCA 1200
GCCCAGGCCT GGACAATGAT GAGATGTGCT CAGGTGCTTG GTCAGGGCTG GCTTTGGTGG 1260
TTGGAGAATC GTATCTTCCT AGTGAGTTAC ACCATTGCTG GGCCTGCTCT GGGCTGCCCT 1320
CCCAGCATCT GCCTTCATGA TGAGGCGTGA CATGTGGGCT GTAACTTGTT GCCCAGCCTC 1380
ATGGAGAAAC TGTCTTTCTG 1400
|
