| Tag | Content |
|---|
EnhancerAtlas ID | HS176-08289 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr11:119438360-119439770 |
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 | TCCCCACCCC TTGGGGTTTT GAAAATTAGG TGGGAAGAAG CTGATTCTAG GTTTTGCAAG 60
TAAAGGGGGA CCTAGTACTG CTGGGGCCAG CTTGCACCCA GGAAGTGGCT GGTAGCTGAG 120
CAGAATGAGC CACTGATGAC AGCTTTGGCT CTTTGGCCTT AGGCCTAGTG GGTCCCCAGG 180
GTTCTGCTGA TCTGAGCATT TTGCTGGGGA ATTTCCCTTT TCTGAAAGGG CTCCACAATA 240
AGGTGGTGGC ATCAGCTGGG GCCTAGGCCA GGCACCTTCT GTCTATGGAC TCTGGCCTGA 300
GTTTCAGGGA CATCTTGACT CACAAGGGGA GCTTTTCCCT CCCACCAATC ATGGCATTGG 360
GGGTGGGGGG TGGGCAGCCA CCCTGGATAA CGTCACTCAG TGCATACCAC TGCTGGCCCC 420
TGTGGCTGTT GCATGAAGAG GAGACGGGGC TCCATTTTCC AGAAATCGTC TGTGCTAGGC 480
ATCCCAGTGA GGGGGCTGAG CCAACCTCTA AGTTTCCTCT AAGACACTAG GAAGCATTGG 540
GGGAACCCTG GATGCACCCA AGCAGGGACT GGATGGGGGA GGCTTGAGCA TTCGCTCTTT 600
TCTCCCACAT GGGTTGGAGG CCACTCTGCC TCATTATCGT CCTCTACATT TGCATGACTG 660
CTGTCCTGTG AAAAATCTCC GCTTGTGAGC CAGCACAAGT ATGACTCAGC ATGTCTCTTT 720
AATTCCCTTC GGGCACGACC ATCAGAGTCA GTTTACAATA ACCAGACGCC TGGCTTTACA 780
ATCACTCCTC ATTGTTGACC CAAAACAGCA TCCTGCAGCT TGATCATTGC CCATGTGCCA 840
GACTTCTCTC AGAATGACTC TTATTTAAAA AAAAAAAAAA ATCACATCTG GTCCATTTAG 900
TGGCCTAGAG CACATACCCT TGAGAATTCA TCAAGGCAGA AAGTATTTGT TATTCGAGGA 960
TGGGTTTGAT TTTTGGCAAT GATGTTGAGG CTCTCTGAGT CAAGTCTGGA GGATTATGCA 1020
GCAGGGAGAG CTCTTTGCTT AGACCACTGC ATCAGACCAC CCTCCTCAAT CTCAGGGCTC 1080
AGCTACCACT TCCCTTCTAT AGCTCCCCCA GTCGCCATGG CAGATGTGGC CAGACACCTC 1140
ACTCTCTTGC CATCCGCCCA GGGTTTCTCT GACACCAAGG CCATGCCCGC CTCTTCCTTG 1200
TCTCAGGTGC ATTTTGCATG GTTCTTCAGA GGTTCCCTAG CAGGATGGAG CCTCAGTGAC 1260
CCACAGTGAT GACCAGCTCA GTTAAGAAAA CTTAGCTTGG CCTTTCTGCT TCCCTGTTTT 1320
ATGCTTCCCA ATCCCCCTTG GGATTCTAGG GAACCATTGC TTTTCCCTAG AATCTCTTTC 1380
CAAAATAAGC TACTTGAACC AAAGGCTCTT 1410
|
