| Tag | Content |
|---|
EnhancerAtlas ID | HS024-11172 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr22:39752310-39753320 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr22:39752622-39752640 | GGGAGGGAGGAAGGGAGA | + | 6.09 | | NFIA | MA0670.1 | chr22:39752671-39752681 | ACTTGGCACC | - | 6.02 | | ZNF263 | MA0528.1 | chr22:39752585-39752606 | GAGGAAGGGAAGAGAGGAGGA | + | 6.34 | | ZNF263 | MA0528.1 | chr22:39752620-39752641 | GAGGGAGGGAGGAAGGGAGAG | + | 7 | | ZNF263 | MA0528.1 | chr22:39752613-39752634 | GGAGGAGGAGGGAGGGAGGAA | + | 8.4 | | ZNF263 | MA0528.1 | chr22:39752616-39752637 | GGAGGAGGGAGGGAGGAAGGG | + | 8.61 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27409 | chr22:39752084-39753501 | Esophagus |
|
| | 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 |
| GH22I039356 | chr22 | 39752085 | 39753501 |
|
Enhancer Sequence | CGGCCTCCCA AAGTGCTGGG ATTACAGGTG TGAGCCATCT TGCCTGGCCT GAATGCAAGT 60
TTAAAAGGCC TGCCGTAAGT CTGCTGTGGT GCGTTTTGTT ATCCCCTCCT TAGATGAAAA 120
GCTGAGGCCC AGAGAGGTTA ACTGGAGTCA CTGGGATCGG AACCCATGGC CCCTGCTCCA 180
GGGAGTCCCC AGCCATGTGG GGAGTCCCAC ATGAGCAGCG TGTGCAAAGC TGTTGGGCGG 240
GCCTGAGCCC CAGGGAGAAA AAACAGAGGC TGGGAGAGGA AGGGAAGAGA GGAGGAGAAG 300
CCAGGAGGAG GAGGGAGGGA GGAAGGGAGA GGCAGATGGC AGGGCTGTTG GAGGGAGCCA 360
CACTTGGCAC CCAGACCGGA AGAACCAGCT GTCAGGTGGG AGGGGAGGCA GGGTAGGCGC 420
AGAGGAGTGC CTTGGCCTGG AGACCTGAGG CTGCGTTCTG CACCCTCTCT GCCAGTGATT 480
GGCTGTGTGA CTGGAGCAAG AGGCCCATGC TCTCCTGGCC TTGGTTTCCC CATCTATCAA 540
ATGGGAAAAG GATAGTTGGA TTGCTCTGGT GGATCCCGAC CTTTCCACCC TTGAAGAACC 600
CCACTCTTGC TCCTAGTGGA CTCCAGGTTG GGAACTTTGG ATTGGTCAGT CTTTAAAGAA 660
GTGATGTTGG GGCCAGGCGC GATGGCTCAC ACTTGTAATC CCAGCACTTT GGGAGGCCAA 720
GGTGGTTGAC TCACTTGAGG TCAGGAGTTT GAGACCAGCC TGACCAACAT GGTGAAACCC 780
TGCCTTTACT AAAAATACAC AAATTAGCCG GGTGTGGTGG TGCCTAGGAT TATGCTTGTA 840
ATCCCAGCTA CTCCAGAGGC TGAGGCACGA GAATCGCCTG AACCCAGGAG GCGGAGGTTG 900
CAGTGAGCCA AGATCCCACC ACTGCATTCC AGCCAGGCAA CAGAGCAAGA CTCTGTTTCA 960
AAAAAAAAAA AAGTGATGTT TGGAGCCATC CCCTCATGCT TTGTAGGAGC 1010
|
