| Tag | Content |
|---|
EnhancerAtlas ID | HS092-15317 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:111292460-111293750 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
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 | GGCCTCCTCG CCAGCGCCTC TCCCGTGGTG GCTGCAATAA AGCACCTTGA AGGATAAGCC 60
CAAGGCAGCC CCTTCTTTCC TTAGGAAATA GAATTCAGCA GTCACAGGAA CTATTCGTCT 120
GGTTTTTGTT CTAAGTAAAA CATCCCTTTG CTTAAAGGAG AGAATGGGTT TTTTTACAAG 180
CAGCTCATTG CTTCCATGTT CTTTCTCAAA CCCACGTATT TCACGCACTC GCTCCAGCCG 240
GACACGCTCC CAGGAGCTTC CCTGGACCAG GAGAGCAACG GGAAAGTGTG GGGGGGTGGG 300
CGGCCCGTAA TGCCCCAGTA CTGAGCAGCC CTGTCGAGAT GCCTCATTGT AAGGAGCCCT 360
CTGGGGACTT TTTCTATGTG GGTAGCTTTA CTAGGGTGAT TTTCTAGGTG AGTGACTTCT 420
GAACTGTAGA CAGGAGACCT GTACCTCAGG GTCACGGTTA AATGATGAGC AAGCCCGTAT 480
CCCCAGTCAC GGGTCCCGCT GCTGCCTGTG CCCTTGGGAT TCAGAGATGC CAGTGTGACA 540
GGGAGAGGCC TGGCCCAGGG TCTGCGAGCA GGAAGAGTGG AGAGGGGTCA CCCTGCTGAG 600
TCACTGACAG CTGTGGCGCT GGGCTTACCA CAGAAGGGTG AGATCAGGAG CAAGGTGGGT 660
GCTTCAGGAG GCCACCGGTC CTGTAGCCCA GGCAGCCTGC CGTGTGCTGG CCGCCACCTC 720
CCGCTCAGGA ATCCTGTCTG TCACAGCTCG CCAGCTGGCT TTCAGCCTGG CTGCCCTGAC 780
TCCTCCGGAA CCAACCTTTC CCAGGCCCAG CTCGACCCCA TCACTGCTCT GCACAGACCA 840
TGACCACCAA GATGGCCTGC AGCTGCCAGG ATGTTAACTG CAGCGGGACT GCAGACGGGT 900
TCTCAGCTGC ATTTTTCCTA TGCTGAATAC GTTACTTTTG TAACCAGAGA GAAAACGTAA 960
GATTGTGTTC TTGCTGGGGG AGGTGTCCCG GGGTTAGCAT TGCTGGCGTC CCACCTCTGC 1020
TTCAGACTAT GCTGCGTGGC CCACCCACCT CACCCATCCC CAGCCCCTCC CTCAGGAGGA 1080
AACAGGCTGC ATTCTGCCGC CTCCCGGGGT CCCTGCTCTT CTGTTGGCTG TGTTGTCTGT 1140
TCCCTGGGCA CAGGGCCAGC AGGTCTCACG CACAGGCACG TGTGCTGCTG GATGCTACTG 1200
AATGTCTGAC ACTACTTCAC TCAATCGACG GTGAGTCTGT AGCCACAGAA CGCAGTGAGT 1260
GTTTAGGCTC AGTTACTAAC AAACAGACGC 1290
|
