| Tag | Content |
|---|
EnhancerAtlas ID | HS105-23277 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr13:111292490-111293750 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr13:111293051-111293066 | CCTGCTGAGTCACTG | - | 6.14 | | Nfe2l2 | MA0150.2 | chr13:111293053-111293068 | TGCTGAGTCACTGAC | - | 6 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09490 | chr13:111292213-111293723 | CD14 | | SE_55064 | chr13:111292408-111294399 | Stomach_Smooth_Muscle | | SE_65828 | chr13:111292403-111294485 | Pancreatic_islets |
|
| | 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 |
| GH13I110640 | chr13 | 111292902 | 111294139 |
|
Enhancer Sequence | GCTGCAATAA AGCACCTTGA AGGATAAGCC CAAGGCAGCC CCTTCTTTCC TTAGGAAATA 60
GAATTCAGCA GTCACAGGAA CTATTCGTCT GGTTTTTGTT CTAAGTAAAA CATCCCTTTG 120
CTTAAAGGAG AGAATGGGTT TTTTTACAAG CAGCTCATTG CTTCCATGTT CTTTCTCAAA 180
CCCACGTATT TCACGCACTC GCTCCAGCCG GACACGCTCC CAGGAGCTTC CCTGGACCAG 240
GAGAGCAACG GGAAAGTGTG GGGGGGTGGG CGGCCCGTAA TGCCCCAGTA CTGAGCAGCC 300
CTGTCGAGAT GCCTCATTGT AAGGAGCCCT CTGGGGACTT TTTCTATGTG GGTAGCTTTA 360
CTAGGGTGAT TTTCTAGGTG AGTGACTTCT GAACTGTAGA CAGGAGACCT GTACCTCAGG 420
GTCACGGTTA AATGATGAGC AAGCCCGTAT CCCCAGTCAC GGGTCCCGCT GCTGCCTGTG 480
CCCTTGGGAT TCAGAGATGC CAGTGTGACA GGGAGAGGCC TGGCCCAGGG TCTGCGAGCA 540
GGAAGAGTGG AGAGGGGTCA CCCTGCTGAG TCACTGACAG CTGTGGCGCT GGGCTTACCA 600
CAGAAGGGTG AGATCAGGAG CAAGGTGGGT GCTTCAGGAG GCCACCGGTC CTGTAGCCCA 660
GGCAGCCTGC CGTGTGCTGG CCGCCACCTC CCGCTCAGGA ATCCTGTCTG TCACAGCTCG 720
CCAGCTGGCT TTCAGCCTGG CTGCCCTGAC TCCTCCGGAA CCAACCTTTC CCAGGCCCAG 780
CTCGACCCCA TCACTGCTCT GCACAGACCA TGACCACCAA GATGGCCTGC AGCTGCCAGG 840
ATGTTAACTG CAGCGGGACT GCAGACGGGT TCTCAGCTGC ATTTTTCCTA TGCTGAATAC 900
GTTACTTTTG TAACCAGAGA GAAAACGTAA GATTGTGTTC TTGCTGGGGG AGGTGTCCCG 960
GGGTTAGCAT TGCTGGCGTC CCACCTCTGC TTCAGACTAT GCTGCGTGGC CCACCCACCT 1020
CACCCATCCC CAGCCCCTCC CTCAGGAGGA AACAGGCTGC ATTCTGCCGC CTCCCGGGGT 1080
CCCTGCTCTT CTGTTGGCTG TGTTGTCTGT TCCCTGGGCA CAGGGCCAGC AGGTCTCACG 1140
CACAGGCACG TGTGCTGCTG GATGCTACTG AATGTCTGAC ACTACTTCAC TCAATCGACG 1200
GTGAGTCTGT AGCCACAGAA CGCAGTGAGT GTTTAGGCTC AGTTACTAAC AAACAGACGC 1260
|
