| Tag | Content |
|---|
EnhancerAtlas ID | HS108-26711 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr22:30577370-30578390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK1 | MA0028.2 | chr22:30577881-30577891 | ACCGGAAGTG | + | 6.02 | | ERG | MA0474.2 | chr22:30577881-30577891 | ACCGGAAGTG | + | 6.02 | | ETS1 | MA0098.3 | chr22:30577881-30577891 | ACCGGAAGTG | + | 6.02 | | FEV | MA0156.2 | chr22:30577881-30577891 | ACCGGAAGTG | + | 6.02 | | FLI1 | MA0475.2 | chr22:30577881-30577891 | ACCGGAAGTG | + | 6.02 | | Gata1 | MA0035.3 | chr22:30578186-30578197 | TCCTTATCTGT | + | 6.14 | | MIXL1 | MA0662.1 | chr22:30577531-30577541 | GTTAATTAGA | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 30578133 | 30578264 | | chr22 | 30577545 | 30577597 | | chr22 | 30577606 | 30578240 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I030181 | chr22 | 30577606 | 30581842 |
|
Enhancer Sequence | GCACTTGAAC CATGCTTCCA ATTGCCTCTG TTCTCAGAAC CCTCCCCACT CCTTTCCCTA 60
AATCGAAACT CCCTTTCCAT CAAGATAGTT CAATGGGAGA GAAGCATCAG ACGAAGCTTA 120
ATATGCTGCC CTCCCACATT TGCATTTTAA AACAGAAGCT TGTTAATTAG AAAAATGAAT 180
CTCACCTAGG GATTGTGATA TGAGAACAGA CTGAATAAAC AAGGAAGAAG AAAGTTTAAA 240
GGGAACTTTG TAGCTGTCTT TAAATTTATG AAAGTCTGTC ATAAAATGCA GGTAACCACA 300
GACACATTCT GTGTTGTTCC AAAGCGTAGA ACATAGACCC AATGGGAGGA CATCCCAGGG 360
ATGCGGATTT GGCCTCAACC TATTAAAGAA TTTTCCCCCA ATGCTCTAGC AAATTGCCTG 420
GCACATGGAA GGCAATCAAC ATTTGACTGT TTTTGATAGC AATGAAAACT GTCAGATGGT 480
GACTGCTTCT GGCTGTAATG AGTTCCTTAT CACCGGAAGT GTTCAAGACT AGTTGTGCAA 540
GATGTCCATT CGGATAAGAA TTGAACCAAC TGAATACTGT AGTCTCTTCT AGCTATAAAA 600
CTCAGTGACA CTTCTATAAA TAGTTGAATT TCAATGGAGA TTTTAGAGCA AAGGAACATT 660
TTATCAATCC TTTTTCCAAA AGGCAGCAAA GTGGTTAAAA CTGAGGGTTC TGGAGTTAGA 720
CGTTATCTGG GTTCAAACCC TGGTCACCCT ACTTACTAGC TGTATGACTC TGTTCGACAA 780
TTTTAATGTT TTACTTGCTA TCTCTGTACA TCAGCTTCCT TATCTGTGAA ATGGGGGCAA 840
TAGTAGTGTC TTTCTCACAG AGCTATTGTG AGAGCTCAAT GAGTTAATAC AGGAAAAGCA 900
CTTAGAAGAA TAGCTGGCAC ATAGAAAGTT AATGTTCAAT AAACATTAGT TATGAGGTAT 960
CATCTGATAC CCTTGCCACT TCTACAGCTT TTTACGTCTT TTCAGTATGT GGAGGGAGGT 1020
|
