| Tag | Content |
|---|
EnhancerAtlas ID | HS105-14932 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:69955980-69957260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:69956280-69956301 | GTTCACTTTCTTTTTTTTTTT | + | 6.86 | | Nr2f6(var.2) | MA0728.1 | chr11:69956512-69956527 | CGATCTCTTGACCTC | - | 6 | | STAT1 | MA0137.3 | chr11:69956932-69956943 | TTTCCAGGAAA | + | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_01662 | chr11:69947719-69956165 | Aorta | | SE_01662 | chr11:69956504-69958769 | Aorta |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I070101 | chr11 | 69947720 | 69956165 | | GH11I070110 | chr11 | 69956758 | 69959201 |
|
Enhancer Sequence | CGGGGCAGAT AGATGCGGGT CCTCCTCTTC AGCCCTGCTT CACCATGACA CCTTGTCTGA 60
GAGTCGACCC ACCTCTAAAT TCATCCGCAA GTGCTGAGGA TTCCCGTCAC CTGCCAAGTT 120
GTGTCCCATA GTCTTGCAGG ATGAGCAGGG TGGGGCTAGC TGCGGGATTT AGGAACTGTG 180
ATGAGAGAAG GCCTTCCAGA TGGAGGGAGT GGCACATGCA AAGGCCCTGC GGCAGGCAGC 240
ACCAGGTTAG CAGCATTCCA GCAACAGGAA GGAGGCCAGC GAGCCTGGCT GAGGGCCTAT 300
GTTCACTTTC TTTTTTTTTT TTTTTTTTTT TAGACAGAGT GTTGCTCTGT CACCCAGGCT 360
ATAGTGCAAT GGCACAATCT CAACTCACTG CAACCTCTGC CTCCTGGGTT TAAGCAATTC 420
TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC TACAGGCGCC CGCCACCACG CCTGGCTAAT 480
TGTTTGTATT TTTAGTAGAG ACGGGGTTTC ACTGTGTTAG CCAGGATAGT CTCGATCTCT 540
TGACCTCGTG ATCCACCTGC CTCAACCCCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC 600
TGTGCCGGGC CCCCATGTTC ACTTTCTATT GCAGACAAAC TTTTCACTCA CACATGTGGC 660
TTAAGCCCCT TCCTCTGGTT TTGACTTCTA AGCATCCCTT AGTCCCCTGA TCATTCCAGG 720
TCATTGACCA CAGAGATGGC CCATTTTCAA GGGGATTTCG GGAGGTCATT TTCCCGCCGC 780
TATCAGGTGG AGTCTCAGAG GGTGGTCCGC CCAGGCTGCT GTGAAAAACT TAACGCTCTT 840
ACTGCCTAGG AAGCCTCTTC AGCCAAGCAG GGGGTTCCAT GAGCAGCAAA GGGCCCCATG 900
GAAACGCCCC CGCCTGGCTG GGCCCCCACG ATGTATTTGG AGCAAGATCT GATTTCCAGG 960
AAACCCTTCC CCACACATGG CCCTGGCTTT CCGGTCCTCT CTCGCAGTCT CCTGGGGCTG 1020
GGCGCCCGCA TGCGCACCTG TTAGGACACA CAGGCATGGT GTTTTTATAA TGTGCCCAGT 1080
GCAGGCCCTG GGGGCCACGT AAAAAGGGGC CCTGCCAGCA TTCCACTGCC TCCAGGAGCA 1140
CTGGACGGCT GTGAGTCCGC CAGAATCACT GGCCACTGAC GCTTGCTGCC CCAAATGTAG 1200
CTTTGATCCT GTCAGGCCCT TCCACCTCAC TAATAGCCAA TGTATAAACA GGGCAAGGCG 1260
AGGGAAGAAA GAAGGACTCC 1280
|
