| Tag | Content |
|---|
EnhancerAtlas ID | HS145-05134 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr11:129723640-129724450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr11:129724313-129724328 | AGGTGACTCAGCACA | + | 6.38 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27353 | chr11:129722906-129725277 | Esophagus | | SE_27846 | chr11:129723063-129724609 | Fetal_Intestine | | SE_35121 | chr11:129721033-129725996 | HeLa | | SE_36539 | chr11:129723345-129724382 | HMEC | | SE_64293 | chr11:129722901-129725891 | 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 |
| GH11I129852 | chr11 | 129722635 | 129725772 |
|
Enhancer Sequence | TTCCTGGGTC ATTTCCACAA CTTCCTGACT CTGTGTGTGG GAATTCAAAA AGGGTCTGGC 60
TTGAGAAACA AGTATCTGGG AAACGGAGTC CAAAATGTCA TCATGGAGGA TTTCTTCTAG 120
GCTTCCCCAA GAACACTTTG GGTACCAGGC ATAAAGACAA ATCTTTTGCC TTCCAAATTA 180
GCTGATAAAA GTAGAAGGGA TAAGAACTAA GAGCTATCCT GTGTCGCAGT TTCGTCATTT 240
TCTGGCCCAC ATCCTGGGGC CTCTGCCTTG TTTACCCGGT GTTTTAAAAC ACACAGCTGG 300
GAGGGGCGCA GGGCTTGCAG AGCTGGCTCT GTGCCCAGGA AGGACACGCA CTCAAAATCA 360
GCCCTGCAGA CACGCACCTG GGAGCCGCTT CCCTCCCTTG GCACGTACAG GTATCTTCAT 420
TACCAGTGTG TCTCTGCTCA GATTCTGCTT TCAGCCTAAT TGTTTCTGTC TGGGATTTCT 480
TTCACTGCTC ACTTGGCAGG GAAGCCCAGA GATTATTCTA TCAGCCACAC TCCGACTTAA 540
GTGATGATGT CTTGCTCATC TCTGCTCCTG GACAAACCTC CTGGGGATCT ATGTGTGTGT 600
GGTTGTGTTC ATTGATTCTT CTACCCTCAA CCCCAAACCC CTAAAAGGAA CAACAATGGC 660
AAGATGTCTA CACAGGTGAC TCAGCACACA CCCTACTTTA TACTGAAGCA GCTGCACCTG 720
AGGCAGCAAA GTAGCTCTGC TGACCCGCGG GCCACCCTCA CCTCACCCCA TCTCCGCTTC 780
GCTCATGCCT TTGGGTTATT CCTTGCTCCT 810
|
