| Tag | Content |
|---|
EnhancerAtlas ID | HS187-22823 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr7:76234890-76236100 |
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 | | HES2 | MA0616.2 | chr7:76235963-76235973 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr7:76235963-76235973 | GGCACGTGCC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr7:76234984-76234999 | GAGGTCAGGAGTTCA | + | 6.22 | | 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 | CTACAATCTC CAGTGAAGAA TGAGAACTGG CTGGGCGCGG TGGCTCATGC CTGTAATCCC 60
AACATTTTGG TAGGCCGAGG CAGGAGGAGC ACTTGAGGTC AGGAGTTCAA GACCAGCCTG 120
GCCAACATGG TGAAACCCCG TCTGTACTAA AAAAATAAAA TAAAATTAGC TGGGCATGGT 180
GGCATGCCCC TGTAATCCCA GCTACTTGGG AGGCTGAGGT GGGAGGATGG TTTGAACCAG 240
AGAAGTCGAG GTTGCAGTGA GTTATGGTGG TGCCACTGCA ATCCAGCCTG GGCAACAGAG 300
TGAGACCCCA TCTCAAAAAA TAAACCCACA CCCAAAGTGT TGGTTTACAG AGGCTTTCCA 360
ATGCAATAGG AAGCTTCTGG AAACTTTAGG GAAAGAGGAG GATTAAGCAA TGGAGTCTAG 420
AGAACCCTCA GTGGCTTGCC ACTGCCTTTC ATTTCCAGTC TAGTTCCCCT GGGAGGCAGA 480
CAGGCCGAGC CCTCTGACAT TGCTGCTGGA GGCTGTCTCT CCTGGCAAAG GCCCAGGGAA 540
ACTATCCTGC TGAGGCCCAT CTGGAGCTGG CAGGGAGCTG ACATTCACGG CCACATCTTA 600
GTCATAACTC CTCCCCTCCC CTGACACAGC CACTTCCTCT TTCTGCTGAG AAAAGAAGTT 660
GAATGAAGGA CAAGCTCTCA GAAAGTTGCA ACCCCTAAGA ACTTGAGTAC AAGGAAGAGA 720
CGGATGTTTA TTGCAAGAAC CGTTCCCCGG TGTCTCCTGG CTCATAGAGC AGCTCCAACA 780
ACACGTGCTT GGATGCCAAG TGTGCCATGG AGACCAATCC TTGCTATAAT CCTGATGGAA 840
AGAACTTCCC CATCTGAAAA GAGGATGGTG ATAAGTAAAC AGATTGTCAG GGGTAGAAGT 900
ACCCGTCGGA CCCCAAGCCT GGAGCATTTT GCCAGAGACC TTTTTTTTTT TTTTTTTTTG 960
AAACGGAGTC TCGCACTGTT GCCCGGGGTG GTGCAATCTT GGTTCGCTGC AACCTCCGCC 1020
TCCCGGGTTC AAGCGATTCT CCTGCCTCAG CCTCCCAAGT AGCTGGGACT ACAGGCACGT 1080
GCCACCACGC CTGGCTAATT TTTGTATTTT TAGTACAGAT GGGGTTTCAC TATGTTGGCC 1140
AGGCTGGTCT CGAACTCCTG ACCTCGTGAT CTGCCCACCT CAGCCTCCCA AAGTGCTGGG 1200
ATTACAGACA 1210
|
