| Tag | Content |
|---|
EnhancerAtlas ID | HS098-00313 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:9138080-9139210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Pou2f3 | MA0627.1 | chr1:9138259-9138275 | TATAATTAGCATATAA | - | 6.49 | | RARA(var.2) | MA0730.1 | chr1:9138283-9138300 | AGGACAACCAGAGGTCA | + | 6.62 | | STAT1 | MA0137.3 | chr1:9138117-9138128 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr1:9138117-9138128 | TTTCTGGGAAA | + | 6.32 | | Stat4 | MA0518.1 | chr1:9138117-9138131 | TTTCTGGGAAAGGG | + | 6.56 | | ZNF263 | MA0528.1 | chr1:9138512-9138533 | GGAGGCGGGAAAGGGAGAGAA | + | 6.3 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_58674 | chr1:9120585-9146230 | Ly1 | | SE_59733 | chr1:9120065-9146380 | Ly4 | | SE_61311 | chr1:9121391-9143632 | HBL1 |
|
| | 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 |
| GH01I009077 | chr1 | 9137781 | 9141591 |
|
Enhancer Sequence | TGTTCTTTGC TAAACAAGGG GAGGATTATC CACTAGTTTT CTGGGAAAGG GGTGGACAGT 60
TCCCCGGAGC TGAGGGCTCC TCCCGCTTTT AGGCCATATA GGGTAACTTC CTGAGGTTGC 120
CATGGCATTT GTAAATTGTC ATGGCACTGG TGGGAATGTC TCTTAGCATG CTAATGTATT 180
ATAATTAGCA TATAATGACA GTGAGGACAA CCAGAGGTCA CTTCCATCAC CATCTTGGTT 240
TCGGTGGGTT TTTGTGGCTT CTTTACCACA TCCTTTCATC AGCAAGGTTT TTGTGACCTT 300
GTGCTGACTT CTTATTTCAT CCTGTGACTA AGAATGCCTA AACCTCCTGG GAATGCAGCC 360
CAGTAGGTCT CAGCCTCACT TTACTCGGTC CCTATTCAAG ATGGAGTCGC TCTGGTTCCA 420
ATGCCTCTGA CAGGAGGCGG GAAAGGGAGA GAAGACTTTG TATTGGGTAC AGTGTACAGC 480
GCTTGGGTGA TGGGTGCACC CAAATCCCAG AAATTACCAC TAACGAATTT ATCCATGTAA 540
CCAAGAACCA CTTGTATCCC CAAAAACTAT TGAAAAACAT TTCATTTAAA GAAGAGACAG 600
TTCTTTACCA AGAATTTACA TCAAAACCAT GTAAACTGTA GATCCACACT ACATTGTTCT 660
TTGTACCATG AATTCCAAAA CCCTGAAGAA AATGGGTGAG GCAGCTATCA GGAACAAAGT 720
GTCGTCAAAT AGCTGCCCTG GACATGGGTG GGGAAGTGAC TCAAGTTCCC ACTCACGTCT 780
CTCTGGGCCT AATAAATTTT GCGAACCTCA CAGGGCTCAC ACTGCTCAGC TGTTTTTCTT 840
TTCCCACATT CCAGATTTAG ATAAGGAAGG AATCATTAAC AGATTCAGAG TGGACCTGAC 900
CACCCCACAG TGCCCTTGCT TTGCTTTTGG CACAGGCAGT GTATCTCGTC TGGGGAAGGG 960
AGAGGAGTGC ATCCAGTCGG TTGACACAGG ACCTCCCAAC CCCAGTGCCC ACGCGCGGTG 1020
TCTCCCTCTT CCTCTTCTGT GAAAAGCCAC ACCCCACCTT GGGCATGCCA CCTGGCCGCC 1080
GGAACCCAAG TCTGCAGGGA GGGTCCAGAA AACGTGCGCC TTCCAAGTTT 1130
|
