| Tag | Content |
|---|
EnhancerAtlas ID | HS034-06135 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr11:129731450-129732600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| 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: 2 | Chromosome | Start | End |
| chr11 | 129731556 | 129732597 | | chr11 | 129731747 | 129732130 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I129860 | chr11 | 129730176 | 129732734 |
|
Enhancer Sequence | CAGGAGGCTG AGGCAGGAGA ATCACTTGAA CCCAGGAGGC GGAGGTTGCA GTGAGCTGAG 60
ATCTTGCCGC TGCACTCCAG CCTGGGCTAC AGAGTGAGAC TCCATCTCAA AAACAAAAAC 120
AAAAACAAAA CACTCACCAT AGCTGTGCCA TTCATCTATC AGAAACCTGA AGCCAGCATA 180
TGAAGGAAGC AAGTGTGGCA CAAATCCTGG GCTGTCACCG TAAACAGCTC CAGTAGGAAG 240
TTCCCATTCT CCGCTATTGC CATTCCACCC ACAGGCTGGA TAGTGCCGAA GTTACACTTC 300
TGAGGAGTCA GCATCCTGAC GCAGCCTAAA CTTTACACTC ACTCCCTGCT CTCCAGAATG 360
CACACGTCTG CCTGTGCAAA AACGACAAGC AGAGTCAGGT GACCTCAGCT AACAGGAATG 420
TGGGCAGGGC TGCGGCTGAA TGCCAGAGCT ACTTTTATTA AATTCCTTGT TAAGTAAATT 480
CAAAAGGGGT TTGTTTGTAG CTGGCAGTAA ATACCTAAGA CAAGATCTCT GGAATTTCTA 540
CCTTTTTTTT TTTTTAATTT AAAAACTGTC ACATGGCTTT CTATGTGAAA TGTGATTCTT 600
GAAAATAACA GATACGCAAA TATCAAAGGA TTATCAAACG CAGACACACT CGCCTTTCTC 660
AGGTGGAAAG GCCCATTTCC CCGCACTGCA TCCTACCTCT CCCCACTGCC AACCTCATCC 720
CGTGCCAGTC TACTTGCCCA TCACAAGCTC AACCTGGGAG GCCCATTCAC CTCTGCTCTC 780
TGCAATGCAG GCCTCCCACC TCCTAAGACT GGATCGCCCC CAGGCTCGCC AGGATACATC 840
ACAGCCCTCC TGCCCGGAGG AAGGCAACAG AGAGAGACTT GACTTAGAAT CAGAAGCTTC 900
TCTTTAACTT CAACTCAGAC TCATGTCTTC CAACGGTTAA AGGGGAATGA TGACACTGAT 960
TTTACAAAAT TGCTCTAAGA ATTAAACAAA ATGTCTGTGA AACAGCTGTG GAGCCAACCA 1020
GCCTCCCAGA CCCTCCTCCG CTTCGCAACC CCCTAACCAC CCAACAACTA AGCCAGGCTG 1080
CCTCCATCCC ACATCCTTCA GCTCCACCTC TTCAACCCAC AAGAGCTTCA ATACACTCCA 1140
AAAATTAAAG 1150
|
