| Tag | Content |
|---|
EnhancerAtlas ID | HS182-15234 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr22:43198950-43199900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr22:43199874-43199892 | CCTTCCTTCCTTCCTTCC | - | 10.83 | | EWSR1-FLI1 | MA0149.1 | chr22:43199866-43199884 | GATTGTTTCCTTCCTTCC | - | 6.31 | | EWSR1-FLI1 | MA0149.1 | chr22:43199882-43199900 | CCTTCCTTCCCTCCCTCC | - | 8.45 | | EWSR1-FLI1 | MA0149.1 | chr22:43199870-43199888 | GTTTCCTTCCTTCCTTCC | - | 9.07 | | EWSR1-FLI1 | MA0149.1 | chr22:43199878-43199896 | CCTTCCTTCCTTCCCTCC | - | 9.47 | | TFAP2A | MA0003.3 | chr22:43199603-43199614 | TGCCTGAGGCA | - | 6.02 | | ZNF263 | MA0528.1 | chr22:43199874-43199895 | CCTTCCTTCCTTCCTTCCCTC | - | 6.24 | | ZNF263 | MA0528.1 | chr22:43199878-43199899 | CCTTCCTTCCTTCCCTCCCTC | - | 7.27 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_33525 | chr22:43198926-43200330 | H2171 | | SE_41938 | chr22:43199221-43199832 | LNCaP | | SE_66955 | chr22:43198926-43200330 | H2171 |
|
| | 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 |
| GH22I042803 | chr22 | 43199096 | 43203764 |
|
Enhancer Sequence | TTCATGCAGA CAAATGAAGA GAAAAAGTAT TTCCAAGATT ATAAGAACAA GTTTGGGCAT 60
TGTTTGTTTG AGACAGGGAC TCCCTCTGTT GCCCGGGCTG GAGTACAGTG GTGTGATCAC 120
AGCTGACTGC AGCCTCAATC TTTTGGGTTC AAGTGATCCT CCTGCCTTAG CCTCCGAGTA 180
ATTGGAACTA TAGGCATTAG CCATCGCACC TAGCTAATTT TTTTATTTTT TAAATTTTTT 240
GTAGAGATGG GGGTCCCACT ATGTTGTCCA GGCTGGTCTG GAACTCCTGG GGCCACTGCA 300
CAGCTATACT GTCTGACAAG CACACATGGC AATAACCAAA CCAGACTGCC TGATGCAGAC 360
TGAGGGCAGT GCTTTCGAGG TCACACTCCT AGACCCTGGG CTGGAGCAAA GAGAAAAGGA 420
GACAGTGGTT AAGGGACCTC ACAAACAACC TACCACTTGA CCCCACGATG CACACAAGGA 480
AGGGGTGCAG GTGTCTGCAC TCCCATGCAG ACGTGCTCTC ATTCAAACAA TCAGAATTGG 540
CTTTCTGGGA GGAAACATGC TGAGGGGGCA GCTGGGTTTT AAGCTTTTTG TTGTATCCTG 600
GCTCTCACAC AGCTGCCTCC ACTCTGTCAT CTGGTGTCTG AGTGCCTCAC GCCTGCCTGA 660
GGCAGTGCCC AGCTGATGGC AGTCCCCCAG CTCTAATGAC CCTGTCCCAT GGGTGTGACC 720
ACAGGGACTG TTGCTGTGCC AGGTCAGGTT GGCTGCAGGC ACTTACATGC GCTTCCCACT 780
CAATCCTTCA GCTACAGTGA AAGAGAGTGC CCGTAAGAAC GGCCGCAGGT CTCCTGGGCT 840
AGAAACACCC CCAGAAAGCA GCTTACCTCA CCAGAAGCGT TTCACATTTG GAAATTAAGA 900
TAAGGAACAC AGAACTGATT GTTTCCTTCC TTCCTTCCTT CCCTCCCTCC 950
|
