| Tag | Content |
|---|
EnhancerAtlas ID | HS060-09463 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr13:50818540-50819590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr13:50818555-50818573 | GGAAGGAAGGAAGGCCAC | + | 6.44 | | EWSR1-FLI1 | MA0149.1 | chr13:50818551-50818569 | TCAAGGAAGGAAGGAAGG | + | 7.71 | | JUN | MA0488.1 | chr13:50818927-50818940 | ATTACATCATCAC | - | 6.24 | | JUND(var.2) | MA0492.1 | chr13:50818926-50818941 | TATTACATCATCACA | - | 6.07 | | RARA(var.2) | MA0730.1 | chr13:50818745-50818762 | TGACTTCTGATTGACCT | - | 6.19 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_59092 | chr13:50782479-50820345 | Ly3 | | SE_61075 | chr13:50782509-50861156 | HBL1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 50818584 | 50818600 | | chr13 | 50819119 | 50819505 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I050243 | chr13 | 50817934 | 50820152 |
|
Enhancer Sequence | TTATTAGAGC CTCAAGGAAG GAAGGAAGGC CACAGGGTGA AAACCATTGC ATATTAAGTA 60
GCTAAGCCTA ATAGAAGCCA AAGGAAACAG CAGCAAACTG TTACAGAAAA TTCTTTTGAA 120
CTGCCCTCCG CCCACTCTCT CCCCGCTGCT GTTGGTGACA CGTGGACAGA AATCCCCCTG 180
CACGTAGACA CACATATGCC TGCCTTGACT TCTGATTGAC CTTATCCCTT GAACATCAGG 240
CTTAGGCCAC TTTCATGGAT TCTCATGTGA ACGTTCATGC CTAATGCCTG ACTGCATGCC 300
CTCCGCACCA GCCACTAATA AGAAGAAGGA GGCTTCCCCT GGCCACCCAA GATGAGGCAG 360
TGCCCACCTT CCCTCTTGTC ACATTCTATT ACATCATCAC ATTTTATTTC TCTGCCTAGG 420
ACTTACCACT GTCTCGTGTA TTCATTAGTT GACTTGTTTA TTATCTGTCT TCCCCAACCA 480
GAATGTAATT CTGCGGAGAG GCTCTGTCTG GTTTAGTGTA ATCTCCAAGG CCTAGCACTG 540
TCCTTGGCAT GGAGTAGCCC CCAGGAAATA TTCGTTGACT GACTGACTAT GAAATGGTGG 600
AAGAGGAACT TTGCTCCATG AGTTGTGAGT GTATGCACAG CACAGGTGTT CAGAGTGATT 660
TTCCCTCCCC CACGTTCACT ACAAAAAGTA CCCTCAGTTA CAGGCCCAGG GGTAATGGCA 720
TCACCGCATT GTTGACTCAA CTTGTAACTG ACTTCTAGCT CTGTTTCTGA CTTAGTTTTG 780
GCCTTTGGGA CAGGTCAGGA GGGTGCAGCA AAAACAAATA CACCAGATGA CTAGAAGCTG 840
GGATCTTGGG TTGCAGGCTT GGTTTCAGCT CTGACTCACT GTGTAAACCA TGGGTGACTC 900
ACTTAACCTC TCTAATTCTG CTTCTTCATC CATCAAATAT AGAGGTTAGA TAGATGACAC 960
TTCAGATCCC TTGTAATTCT TCCATTCTAT AATGTTCCCC TTTACCTTTC TTTAAGTGTG 1020
AGCACAGCCT AGTCTCTTCA TGCAGGAGTA 1050
|
