| Tag | Content |
|---|
EnhancerAtlas ID | HS091-19036 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:16215970-16216860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr17:16216224-16216245 | GAAAGAGGGGAGGGGGAAGGG | + | 6.15 | | ZNF263 | MA0528.1 | chr17:16216232-16216253 | GGAGGGGGAAGGGGGGGGGAG | + | 6.24 | | ZNF263 | MA0528.1 | chr17:16216248-16216269 | GGGAGAGGGAGAGGGAGAGGG | + | 6.44 | | ZNF263 | MA0528.1 | chr17:16216235-16216256 | GGGGGAAGGGGGGGGGAGAGG | + | 6.71 | | ZNF263 | MA0528.1 | chr17:16216246-16216267 | GGGGGAGAGGGAGAGGGAGAG | + | 6.95 | | ZNF263 | MA0528.1 | chr17:16216236-16216257 | GGGGAAGGGGGGGGGAGAGGG | + | 7.09 | | ZNF263 | MA0528.1 | chr17:16216229-16216250 | AGGGGAGGGGGAAGGGGGGGG | + | 7.54 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28022 | chr17:16216124-16217657 | Fetal_Intestine | | SE_28895 | chr17:16216081-16217967 | Fetal_Intestine_Large |
|
| | 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 |
| GH17I016312 | chr17 | 16216254 | 16217805 |
|
Enhancer Sequence | GTCTGCAATC CCGGCACCTT GGGAGGCCAA GGCTGGCAGA TCACTTGCGG TTAGGAGCTG 60
GAGACCAGCC CGGCCAACAC AGCGAAACCC CGTCTCCACC AAAAAAATAC GAAAACCAGT 120
CAGGCGTGGC GGCGCGCGCC TGCAATCGCA GGCACTCGGC AGGCTGAGGT AGGAGAATCA 180
GGCAGGGAGG TTGCAGTAAG CCGAGATGGC AGCAGTACAG TCCAGCTTCG GCTCAGCATC 240
AGAAGGAGAC CTTGGAAAGA GGGGAGGGGG AAGGGGGGGG GAGAGGGAGA GGGAGAGGGA 300
GCTATTTGTT TTTTCTTTAA TTCATTTGTG TAGAAATGAA ATGTTGGAAT ACAGACTGAG 360
CTTGTAGTTA ATAAACAGAT ATTGATATAG CTGTGAAAAT GGAAACAGAG GCAATCTATG 420
AATAAATACA CTTTTTCCAT GAACTCAACC CCAGGACACG GTGGACATTG TCCTTCAAAG 480
CTTTTTTTGC CCTCAGTATG GCATGAGAAA AAGAGAACCA GTAATTCAGG CTGTATCTGC 540
ATAAACAGAG TTCACTTAGA AGCTAGCCAG GAATTCTAAA TGTGCTAATA AATGGCTAAA 600
CCAATAAGCA ACAAAGATAT TCTGAACCCA AGTTACTATC ATGGCTGAAT TCCACTCTGC 660
TCCACTGGCT AGGAACAAGA GTAAAACATC AAACCCTGGA AAACAGTCTC TATGTGGTCA 720
ACCACAGCAC TAGCTACACA CCACTGATCT GCTCAGAAGT CACTTCAGAT AGATGCTGCA 780
TTTGAAAAGT TTCAGGGTTC TGTTCTCTCC TTCCCAAGGG AAGGAGACAG CTCCATTGAA 840
GTTGAGGTGG TGGAGAAGGC ATTCAGTGAA AACCCTGTGT TTCTCTACAG 890
|
