| Tag | Content |
|---|
EnhancerAtlas ID | HS044-02900 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr11:129731350-129732550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr11:129731420-129731430 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr11:129731420-129731430 | GGCACGTGCC | - | 6.02 | | RREB1 | MA0073.1 | chr11:129732499-129732519 | CCCCTAACCACCCAACAACT | + | 6.32 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_27353 | chr11:129731037-129732709 | Esophagus | | SE_27846 | chr11:129730398-129732763 | Fetal_Intestine | | SE_35121 | chr11:129730409-129733029 | HeLa | | SE_36539 | chr11:129730682-129732779 | HMEC | | SE_57651 | chr11:129732057-129732417 | VACO_503 | | SE_64293 | chr11:129730399-129732758 | NHEK |
|
| | 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 |
| GH11I129860 | chr11 | 129730176 | 129732734 |
|
Enhancer Sequence | TGGAGACCAG CCTAGCCAAA ATGGTGAAAC CCCATTTCTA CCAAAAATAC AAAAATTAGC 60
AGGGCGTGGT GGCACGTGCC TGTGATTGAT CCCAACTACT CAGGAGGCTG AGGCAGGAGA 120
ATCACTTGAA CCCAGGAGGC GGAGGTTGCA GTGAGCTGAG ATCTTGCCGC TGCACTCCAG 180
CCTGGGCTAC AGAGTGAGAC TCCATCTCAA AAACAAAAAC AAAAACAAAA CACTCACCAT 240
AGCTGTGCCA TTCATCTATC AGAAACCTGA AGCCAGCATA TGAAGGAAGC AAGTGTGGCA 300
CAAATCCTGG GCTGTCACCG TAAACAGCTC CAGTAGGAAG TTCCCATTCT CCGCTATTGC 360
CATTCCACCC ACAGGCTGGA TAGTGCCGAA GTTACACTTC TGAGGAGTCA GCATCCTGAC 420
GCAGCCTAAA CTTTACACTC ACTCCCTGCT CTCCAGAATG CACACGTCTG CCTGTGCAAA 480
AACGACAAGC AGAGTCAGGT GACCTCAGCT AACAGGAATG TGGGCAGGGC TGCGGCTGAA 540
TGCCAGAGCT ACTTTTATTA AATTCCTTGT TAAGTAAATT CAAAAGGGGT TTGTTTGTAG 600
CTGGCAGTAA ATACCTAAGA CAAGATCTCT GGAATTTCTA CCTTTTTTTT TTTTTAATTT 660
AAAAACTGTC ACATGGCTTT CTATGTGAAA TGTGATTCTT GAAAATAACA GATACGCAAA 720
TATCAAAGGA TTATCAAACG CAGACACACT CGCCTTTCTC AGGTGGAAAG GCCCATTTCC 780
CCGCACTGCA TCCTACCTCT CCCCACTGCC AACCTCATCC CGTGCCAGTC TACTTGCCCA 840
TCACAAGCTC AACCTGGGAG GCCCATTCAC CTCTGCTCTC TGCAATGCAG GCCTCCCACC 900
TCCTAAGACT GGATCGCCCC CAGGCTCGCC AGGATACATC ACAGCCCTCC TGCCCGGAGG 960
AAGGCAACAG AGAGAGACTT GACTTAGAAT CAGAAGCTTC TCTTTAACTT CAACTCAGAC 1020
TCATGTCTTC CAACGGTTAA AGGGGAATGA TGACACTGAT TTTACAAAAT TGCTCTAAGA 1080
ATTAAACAAA ATGTCTGTGA AACAGCTGTG GAGCCAACCA GCCTCCCAGA CCCTCCTCCG 1140
CTTCGCAACC CCCTAACCAC CCAACAACTA AGCCAGGCTG CCTCCATCCC ACATCCTTCA 1200
|
