| Tag | Content |
|---|
EnhancerAtlas ID | HS108-11170 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr13:31264140-31265170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr13:31265044-31265055 | AAGTAAACAAA | + | 6.62 | | IRF1 | MA0050.2 | chr13:31264420-31264441 | ACAGCGAAACTGAAAGAGCAC | - | 6.16 | | Klf1 | MA0493.1 | chr13:31264564-31264575 | AGCCACACCCT | + | 6.02 |
|
| | 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 |
| GH13I030689 | chr13 | 31263676 | 31265628 |
|
Enhancer Sequence | ACACCTGCAC ACCATCGACC AGCGGAACGA GGCAGAGTGT GGCTGGAGCA GTCGGAGGGA 60
AGCCTGGGCC GCTGACTCCA GGGGAAAACC ATCTCCTTTC TGGCTCCCCC CTCTGCTGGG 120
AGATACTTTC ACTGAATAAA ACCTTGCACT CATTCTCCAA GCCCACCTGT GATCCGATTC 180
TTCCTGTACA CCAAGGCAAG AACCTGGGAT ACAGAAAGCC CTCTGTCCTT GTGATAAGGT 240
AGAGGGTCTA ACTGAGCTGG TTAACACAAG CTGCCTATAG ACAGCGAAAC TGAAAGAGCA 300
CACAATAGCA CACACTCATT GGGGCTTCAG GAGCTGTAAA TATCCACCCC TAGACGCTGC 360
CATGGGGCGG GAGCCCCACA GCCTGCCCGT CTAGAGGTTT GAGCAGCGGG ACACTGAAGA 420
AGAGAGCCAC ACCCTCATCG CACGTCCTGC GAGGGAGACA AGGGAACTTT TCCGGTTTCA 480
CTTCTGCTTG GCTTGAGCTG GCACTGAAGC ACCCTTTTCC CTCCTCACTG AGGGAGCAGA 540
GGGGAAAAGC GGTAGAACTA ACAGGCTAAC AATGCTCCTC CGAAAATATA TCGTATTTTT 600
GGATCCCTAG AGATAGGTGA TCACGGCAGC CGCGGAGTGC ATTTGGGTCT CCTTTCAAGA 660
AAGAACTTGC TGCTCAGCGT TGAAGAATGC AGTTGGCCAA CAGCCTCCAG CTGCTCTGTC 720
TTCAGCATCT GCCATGGCAT CTGAGCTGAG GTCATGTTCT TCCTGGGAGG TCCCCAGCAG 780
AAGGATCACG TGGAAGCTCC ACAAGCTCCA CAGATGTTCC AGGAGAGGAA TAGGCAGCAT 840
TTGGAAGACA TATCCTGCCA TAACAGAGGG CATTTGCTAG TAGAGACAAC AAACAGCAAC 900
AGCCAAGTAA ACAAACACAC AAGCACAAAG CACTTTCTCC CATTTCCCCT CATTGATCCT 960
GTCCGGGTAG AAGCTGGGGA GGAAGTAGAA TAGGGTGAGG CGGGGTGGGG CTGGGGGGCC 1020
TACACCTTCT 1030
|
