| Tag | Content |
|---|
EnhancerAtlas ID | HS148-08031 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr18:21561550-21562730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr18:21562139-21562157 | AAAAGAAAGGGAGGAAGG | + | 6.1 | | ZNF263 | MA0528.1 | chr18:21562086-21562107 | GAAGGAGGGAGGAGGAATGAA | + | 6.01 | | ZNF263 | MA0528.1 | chr18:21562129-21562150 | GAAGGAGGGAAAAAGAAAGGG | + | 6.42 | | ZNF263 | MA0528.1 | chr18:21562093-21562114 | GGAGGAGGAATGAAAGGAAGG | + | 8.01 | | ZNF263 | MA0528.1 | chr18:21562588-21562609 | CTCTCCCCCTCCCCCTCCTCT | - | 8.59 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_62548 | chr18:21544867-21602342 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr18 | 21561703 | 21561858 | | chr18 | 21561939 | 21562030 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I023981 | chr18 | 21561162 | 21563569 |
|
Enhancer Sequence | GTGACTGGGG AAGTTTGCAA AGGATTTCCC GAGCAGGCAG CGGGCAGCTC TCTGCAGCAC 60
TCCCTCTGAC AGCTGCTCAG CATTAGGGAC AGAAGGTGCT GCAGGGAACC CTGACACTGC 120
CAGGGCTGCA CTCCCTGCAG CTCCCCTGTG CTTCCACTCA GGAATCGATG CAGCACATCT 180
TTGGAAAGTT TGTTTCCTCT AAAAACAAAA GGTTGTTCAG AGGAGATTTA GTCTGCATCG 240
CATTAGATGG CAAGTCAGTA AGCATATGAA TATCGCCATC CCTGTACCTC CACAGTCACA 300
GCAGGTTATG GGCTGCTGGC CCCCATGCCT CCCAGTGTCA GGGTGACAGC ATTCGGGAAT 360
TGAAGGATTA AAGCCAGCCA CCCATTCAAG AGAAGGAGAG AAGCAGGGAA ACACTAAGCA 420
CTTAAAATGC TCTGCTCCAA GATGCTGCGC AGGACAGCCA AGAGAGAGGG CTGTGAACTG 480
AGGGTTGGGG TTTATGTAAT TATGTGTCTC TAAGGGAAGG ACAGAGGAAG AGAAGAGAAG 540
GAGGGAGGAG GAATGAAAGG AAGGAGGTAG AAGTGAATAG AAGGAGGGAA AAAGAAAGGG 600
AGGAAGGCTT TGTTCCAGAA TCTGGAATTG GTTCTGAACA AAACGTTGAA ATGTGTGAAG 660
TTAGACTCCG AGGCCTCTCC ATCTCTCTGT ATTGTGTTAG GAAACCTTTC TCCCCCAGGG 720
GCACAGATCC TCCCAGGGGC GATAACCATG GCAACCTCAT TTGAGTGGGA TGGGTCCCAC 780
TTCTCACCTT GCTCCTTGTC AGAGTCGGCC TGTCCAGCAT GCCACTCTCT GTCCTGATGG 840
CTGCCTGCTC ACAGAGGGGC AGCGATGGAC AAATGAAGAC ATCATGGCAA CCAGCTAACA 900
TGTTCCATCT CTGAGAGAAA ACAGCTTCTC TCTTCGGGCA AAGCTACAGA AAATGTGCCT 960
TCCCGTAATA ATGATTCCCC CTGGACTGCC CAGCCAAGGG CCTGCGTCAG CGCTGGCCAA 1020
TGTCCGGCGT CTGTCTGGCT CTCCCCCTCC CCCTCCTCTC GGCGGTGACT CGCTCTCATT 1080
TCACACAGGC TCTGCTTAAA GGTCACCTCC TTAGAAACAG CCTCCTTGGC TACACCACCT 1140
AAAACCACAC CCCATTCATC TGTATCCCTT TACCTTGCTT 1180
|
