| Tag | Content |
|---|
EnhancerAtlas ID | HS105-74067 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr7:76234730-76235810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr7:76235762-76235774 | AAGTAAACAGAT | + | 6.74 | | FOXP2 | MA0593.1 | chr7:76235762-76235773 | AAGTAAACAGA | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr7:76234984-76234999 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr7:76234732-76234747 | GAGGTCAAGAGTTCA | + | 7.64 | | RARA | MA0729.1 | chr7:76234732-76234750 | GAGGTCAAGAGTTCAAGG | + | 7.63 | | SPI1 | MA0080.4 | chr7:76235520-76235534 | CACTTCCTCTTTCT | - | 6.51 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_00592 | chr7:76234056-76240067 | Adipose_Nuclei | | SE_36622 | chr7:76234572-76239823 | HMEC | | SE_55997 | chr7:76234590-76237294 | u87 |
|
| | 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 |
| GH07I076605 | chr7 | 76234319 | 76237516 |
|
Enhancer Sequence | ACGAGGTCAA GAGTTCAAGG TGACTATAGG GAGAAAAATT ATATTTCAAT AGAAAAACGA 60
TAGTTTACCT GTTATTATAG TAATGTTCAT TGTTTGAGTT ATTTATCTAC CTGTAGACTG 120
GATTAGATTC TAGATTCTTC CAGTTTTCTC TAATGTCTGG CTACAATCTC CAGTGAAGAA 180
TGAGAACTGG CTGGGCGCGG TGGCTCATGC CTGTAATCCC AACATTTTGG TAGGCCGAGG 240
CAGGAGGAGC ACTTGAGGTC AGGAGTTCAA GACCAGCCTG GCCAACATGG TGAAACCCCG 300
TCTGTACTAA AAAAATAAAA TAAAATTAGC TGGGCATGGT GGCATGCCCC TGTAATCCCA 360
GCTACTTGGG AGGCTGAGGT GGGAGGATGG TTTGAACCAG AGAAGTCGAG GTTGCAGTGA 420
GTTATGGTGG TGCCACTGCA ATCCAGCCTG GGCAACAGAG TGAGACCCCA TCTCAAAAAA 480
TAAACCCACA CCCAAAGTGT TGGTTTACAG AGGCTTTCCA ATGCAATAGG AAGCTTCTGG 540
AAACTTTAGG GAAAGAGGAG GATTAAGCAA TGGAGTCTAG AGAACCCTCA GTGGCTTGCC 600
ACTGCCTTTC ATTTCCAGTC TAGTTCCCCT GGGAGGCAGA CAGGCCGAGC CCTCTGACAT 660
TGCTGCTGGA GGCTGTCTCT CCTGGCAAAG GCCCAGGGAA ACTATCCTGC TGAGGCCCAT 720
CTGGAGCTGG CAGGGAGCTG ACATTCACGG CCACATCTTA GTCATAACTC CTCCCCTCCC 780
CTGACACAGC CACTTCCTCT TTCTGCTGAG AAAAGAAGTT GAATGAAGGA CAAGCTCTCA 840
GAAAGTTGCA ACCCCTAAGA ACTTGAGTAC AAGGAAGAGA CGGATGTTTA TTGCAAGAAC 900
CGTTCCCCGG TGTCTCCTGG CTCATAGAGC AGCTCCAACA ACACGTGCTT GGATGCCAAG 960
TGTGCCATGG AGACCAATCC TTGCTATAAT CCTGATGGAA AGAACTTCCC CATCTGAAAA 1020
GAGGATGGTG ATAAGTAAAC AGATTGTCAG GGGTAGAAGT ACCCGTCGGA CCCCAAGCCT 1080
|
