| Tag | Content |
|---|
EnhancerAtlas ID | HS105-16383 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:119438380-119439800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr11:119439058-119439073 | GTATGACTCAGCATG | + | 6.73 | | Nfe2l2 | MA0150.2 | chr11:119439056-119439071 | AAGTATGACTCAGCA | + | 7.48 | | RELA | MA0107.1 | chr11:119438566-119438576 | GGGAATTTCC | + | 6.02 | | RREB1 | MA0073.1 | chr11:119438713-119438733 | GCATTGGGGGTGGGGGGTGG | - | 6.03 |
|
| | 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 |
| GH11I119567 | chr11 | 119438347 | 119439690 |
|
Enhancer Sequence | GAAAATTAGG TGGGAAGAAG CTGATTCTAG GTTTTGCAAG TAAAGGGGGA CCTAGTACTG 60
CTGGGGCCAG CTTGCACCCA GGAAGTGGCT GGTAGCTGAG CAGAATGAGC CACTGATGAC 120
AGCTTTGGCT CTTTGGCCTT AGGCCTAGTG GGTCCCCAGG GTTCTGCTGA TCTGAGCATT 180
TTGCTGGGGA ATTTCCCTTT TCTGAAAGGG CTCCACAATA AGGTGGTGGC ATCAGCTGGG 240
GCCTAGGCCA GGCACCTTCT GTCTATGGAC TCTGGCCTGA GTTTCAGGGA CATCTTGACT 300
CACAAGGGGA GCTTTTCCCT CCCACCAATC ATGGCATTGG GGGTGGGGGG TGGGCAGCCA 360
CCCTGGATAA CGTCACTCAG TGCATACCAC TGCTGGCCCC TGTGGCTGTT GCATGAAGAG 420
GAGACGGGGC TCCATTTTCC AGAAATCGTC TGTGCTAGGC ATCCCAGTGA GGGGGCTGAG 480
CCAACCTCTA AGTTTCCTCT AAGACACTAG GAAGCATTGG GGGAACCCTG GATGCACCCA 540
AGCAGGGACT GGATGGGGGA GGCTTGAGCA TTCGCTCTTT TCTCCCACAT GGGTTGGAGG 600
CCACTCTGCC TCATTATCGT CCTCTACATT TGCATGACTG CTGTCCTGTG AAAAATCTCC 660
GCTTGTGAGC CAGCACAAGT ATGACTCAGC ATGTCTCTTT AATTCCCTTC GGGCACGACC 720
ATCAGAGTCA GTTTACAATA ACCAGACGCC TGGCTTTACA ATCACTCCTC ATTGTTGACC 780
CAAAACAGCA TCCTGCAGCT TGATCATTGC CCATGTGCCA GACTTCTCTC AGAATGACTC 840
TTATTTAAAA AAAAAAAAAA ATCACATCTG GTCCATTTAG TGGCCTAGAG CACATACCCT 900
TGAGAATTCA TCAAGGCAGA AAGTATTTGT TATTCGAGGA TGGGTTTGAT TTTTGGCAAT 960
GATGTTGAGG CTCTCTGAGT CAAGTCTGGA GGATTATGCA GCAGGGAGAG CTCTTTGCTT 1020
AGACCACTGC ATCAGACCAC CCTCCTCAAT CTCAGGGCTC AGCTACCACT TCCCTTCTAT 1080
AGCTCCCCCA GTCGCCATGG CAGATGTGGC CAGACACCTC ACTCTCTTGC CATCCGCCCA 1140
GGGTTTCTCT GACACCAAGG CCATGCCCGC CTCTTCCTTG TCTCAGGTGC ATTTTGCATG 1200
GTTCTTCAGA GGTTCCCTAG CAGGATGGAG CCTCAGTGAC CCACAGTGAT GACCAGCTCA 1260
GTTAAGAAAA CTTAGCTTGG CCTTTCTGCT TCCCTGTTTT ATGCTTCCCA ATCCCCCTTG 1320
GGATTCTAGG GAACCATTGC TTTTCCCTAG AATCTCTTTC CAAAATAAGC TACTTGAACC 1380
AAAGGCTCTT TATGTGGGGG AACCCAGGCA AGGACAGCTG 1420
|
