| Tag | Content |
|---|
EnhancerAtlas ID | HS182-22393 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:140639900-140640960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr9:140640708-140640718 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr9:140640708-140640718 | GGCACGTGCC | - | 6.02 | | NFE2L1 | MA0089.2 | chr9:140640360-140640375 | ATTGCTGAGTCATGC | - | 8.55 | | Nfe2l2 | MA0150.2 | chr9:140640362-140640377 | TGCTGAGTCATGCCT | - | 7.3 | | SREBF2 | MA0596.1 | chr9:140639950-140639960 | ATCACCCCAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_10754 | chr9:140638878-140640811 | CD19_Primary | | SE_11232 | chr9:140638468-140641129 | CD20 | | SE_32711 | chr9:140638399-140641999 | GM12878 | | SE_59172 | chr9:140631350-140657613 | Ly3 | | SE_62965 | chr9:140561512-140658488 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 140640542 | 140640735 | | chr9 | 140639929 | 140640461 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I137744 | chr9 | 140638883 | 140641502 |
|
Enhancer Sequence | AGTTTTTTCT CCTCTTATAT GAAGAAGCAT GAGGAAGAAA ACACAGCATC ATCACCCCAT 60
TGTCCTGGTG GCTCTGGCAC TCTGAAACAG TCACTACAGG AACTTCCTTA GACGTGCCCA 120
GCACAGCCCA GCCCTCCCCG AAGGACAGGC AGCCCTGACT GCACCGTGGG GAAGCAGCTA 180
CCCCAGCAGC TGCCGCGGTC TCTGCACACA CGTGTCTGTC GCTCCAGTGC ACTGTCTGTT 240
CAGCTGTGTT ACGCTCTTTC TGTCAAGTTA CAAGGGGTAT TCAGTGTCAC AGTTTTGCTG 300
AGTATGCCGG AGGCTCATAA GTGCTGTCTG CATTTACAGT GTAGCACTTT GATGTCACCA 360
GGCCACCTCT GACTGTATCC TTCCACCTGC AGAGACCTGA GGGGTGTGGT TTCCTCACCT 420
TCCCCAGCAG GGCTGCCTTC TTGGAGTCCA GCAGCTCTTC ATTGCTGAGT CATGCCTGGG 480
GCTGAGCAGC CAGCCACCAG TGTTTGTTCC TCTGTAAGCC GCTTGCTAAA TAGCCCCTGC 540
TCATTTTTCT TCTGGATTTT GCATCTTTTG AATGTAGTCT GACGATCTTT TTTGTCAACG 600
AAGAGTTGAT CTGTTGGCTC CAGTATGAAT GGAGGTTTTT TCCCCAGGTG GATTTTGGGT 660
TTTTTGTTTT GTTTTTTATT TTTTGGGGAC AGGGTCTCAC TCTGTTGCCC AGGCTGGAGT 720
GCAGTGGCGT GATCACGCTC AGTGCAACCT TGAACTCCTG GGCTGAAGCG ATCCTCCTGC 780
CTCAGCTTCC TGAGTAGCTG GGGCTACAGG CACGTGCCAC CATGTCCAGC TGATGTTTTT 840
TTATTTTTTG TAGAGACAGG ATCCCACTGT GTTGCCCAGG CTGGTTGAAC TCCTGGGCTT 900
AAGTGAACCT TCCACCTCAG CTTCCAAAAG TGCTGGGATT ACAGGCGTGA GCCACCACGC 960
CCAGCCGATT TTGTCTTTTG ACCTTGTCTG TAGTGTCAGA ACTCCCAGGT ACTAATCAAT 1020
TTCTTTATGA TTTCTGAGTT CTGTGTTCTA ATTATGATAA 1060
|
