| Tag | Content |
|---|
EnhancerAtlas ID | HS108-20442 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:40904720-40906440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr19:40905748-40905766 | CTTTCTTTCCTTTCTTTC | - | 6.33 | | EWSR1-FLI1 | MA0149.1 | chr19:40905838-40905856 | CTTTCTTTCCTTTCTTTC | - | 6.33 | | EWSR1-FLI1 | MA0149.1 | chr19:40905752-40905770 | CTTTCCTTTCTTTCTTTC | - | 6.34 | | IRF1 | MA0050.2 | chr19:40905800-40905821 | TCTTTCTTTCTTTTTCTTTCT | + | 6.14 | | IRF1 | MA0050.2 | chr19:40905846-40905867 | CCTTTCTTTCTCTTTCTTTCT | + | 6.59 | | SP2 | MA0516.2 | chr19:40904892-40904909 | CTTATCCCCGCCCCCTG | + | 6.36 | | TP63 | MA0525.2 | chr19:40906356-40906374 | GGCATGTTGGCACATGTC | - | 6.01 | | TP63 | MA0525.2 | chr19:40906356-40906374 | GGCATGTTGGCACATGTC | + | 6.71 |
|
| | 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 |
| GH19I040398 | chr19 | 40904179 | 40905586 |
|
Enhancer Sequence | CCCCTGCGGG CGAGGTGGAG GTGCGCAGCA CGTGGGCATC TCCCGGCTCC GCCCGGGCCT 60
AGTTCTGCCC ACTTGCACGG AGCCCTCGCG GTGAGGACCC GCCCCAAATT TTAGTTTCTC 120
CAATCCCCAG CGCAGGATTA AGTCGCAGTT ACGCTAGTCC CCGCCCCATG ACCTTATCCC 180
CGCCCCCTGC AATGAACAAA GCCGCGCCCA CTCAGGCCAC GCCCGCACCT TGTCGCTCCC 240
CTACCCATCC TTACGTTTCA GATACTGACT TTGCTTCTTT TACCGAGAGA ACAGAATCAG 300
AAGGGAACTT CCAGAATCTC CCACACTGTG TGTTCACCCC CTTTCTCCTG CGGCGACTTA 360
CTCCATTCGC CTTCCTGTTC CTGGGGATGA ACTAACCCCA CTCCTAGCTC AGGGCAATCT 420
CTCCACCGCC TTCTCAGGGA CATCCTCCAG CAATTCTCTC CTCTTCCCAC GTCATCAGTT 480
GTCCTTCTCG TCTACATTAT TCCCATCAGC ATACAAACAT ATTATTATTT CTCGCATAAG 540
AAAGGTTGTC ATGGCCTCAC TCCCCCGGAG CTCCTGCCCC ATTTATCTGT TCACCTTAAT 600
AGGCAAAAGG TATTGAGTTC TCCAGTGGCA TTGTTACCAG TTCTCCAGTC ACACCTCTGA 660
CCCTGCTTTC CAACACGCAC ATCTGAACTG CTCCTCTCAA GGTTCCAGGC AGTGACCTCT 720
GTATAGTAAG TCCAAGGGTC AAGTCCCAGG CCTCATCTGC TTAAACCACT CAGCATCTGA 780
TCTAACCTCA CTCTCTGTCA TATCCTTGCT TCCCTTGGCT TCCAAGGTGC TACACCCTCT 840
GGAGCGTCTC TGGGAGTTCC TTGTCAGTCT CCATAGATGT TTGCTTTCCC TCTCCCTGAT 900
TTCTTTCTTT CTTTTCTAAA CAGTCTCACT ATGTTGCCCA GTCCAATCTC AAATTCCTAG 960
GCTCAACTGA TCCTCCCACC CCAGCCTCCC AAAATGCTGA TATTACAGGC GTGAGCCACT 1020
ACACCCAGCT TTCTTTCCTT TCTTTCTTTC TTTCTTTCTT TCTTTCTTTC TTTCTTTCTT 1080
TCTTTCTTTC TTTTTCTTTC TTTCTTTCTT TCACCCAGCT TTCTTTCCTT TCTTTCTCTT 1140
TCTTTCTTTC TGTCTGTCTG TCTTTCTTTT CTTTTCTTTT CTTTTTTAGA TGGAGTTTTG 1200
CTCTTGTTGC CCAGGCTGGA GTGCAATGGC GCGATCTTGG CTCACTGCAA CCTCTGCCTC 1260
CCGGGTTCAA GCGACCCTCC TGCCTCAGCC TCCTGAGTAG CTGGGACCAC AGGCATGCAC 1320
CACCACACCC AGCTAATTTT GTATTTTTAG TAGAGACGGG GTTTCTCCAT GTTGGTCAGG 1380
CTGGTCTCGA ACTCCCGACG TCAGGTGATC TGCCCGCCTT GGCCTCCTAA AGTGCTGGCA 1440
TTACAGGCGT GAGCCACCGT GCCCAGCCCC TCCTCTTTTT TTTTTAAGAC AAGATCTCGC 1500
CAGGTGCGGT GGCTCATGCC TGTAATCCCA GCACTTTGGG AGGCCGAGGC AGGTGGATCA 1560
CCTGAGGTCG GGAGTTCGAG ACCAGCCTGA CCAATATGGA GAAACCCTGT CTCTACTAAA 1620
AATACAAAAT TGGCCAGGCA TGTTGGCACA TGTCTGTAAT CCCAGCTACT AGGGAGGCCG 1680
AGGCAGGAGA ATCACTTGAA CCCGGGAGGC GGAGGTTGCG 1720
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