| Tag | Content |
|---|
EnhancerAtlas ID | HS197-16913 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr5:67294460-67295300 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr5:67294643-67294659 | ATTTGTTTACATAACC | - | 7.17 | | FOXP2 | MA0593.1 | chr5:67294644-67294655 | TTTGTTTACAT | - | 6.14 | | IRF1 | MA0050.2 | chr5:67294467-67294488 | AAGAAAAAAAAGAAAGCAAAA | - | 6.2 | | IRF1 | MA0050.2 | chr5:67294473-67294494 | AAAAAGAAAGCAAAAGAAAAA | - | 6.84 |
|
| | 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 |
| GH05I067998 | chr5 | 67293897 | 67295950 |
|
Enhancer Sequence | AAAGAAAAAG AAAAAAAAGA AAGCAAAAGA AAAAAAAAAA AGAACTTTCC AGGCCAGAAA 60
AGAATCTCCC TTCTAGGCAG GAACAAACCC CTGTCATCAC CCACTGTGTT CCCTGCTTAC 120
GCACACCCTG GGACACAGGA AAGGCATGTT AAAGCCAGTG GCCCTGCGTG GATTGTTCCT 180
CTTATTTGTT TACATAACCC ATGACAGATG CCAAGTCAAG CAGTGGAGGA AGAGCAGGCA 240
GCACAGAGTG TCACTCAGAT GAGCCCTTCC CTGCCCTTGC CTTTTCCACT TTCCATGAGG 300
AGGCCAGCAG ACACTTTGGG GCTGCTGTAA ACCTTCAGTT AAATGGCAGC TCAGTGACAA 360
TGACAGCAAA GCTGCATTCC CCCATGGCAG ACACGCCATG TGGGCACTTC CTCAGGTCTG 420
CTGGGAAAAT CGGAGCGTCA TGTGCAGACC CTGCTGGAGG CACAGCAGGA AGTGACCAGG 480
CACAGGCTGG GCAGTCCTTC TTCCGCCCCT GAGTCACTGC CACATGCATG AGAAGGGAAC 540
TCAGTGCAGG CTAGACAGAA AAGGTGGAGG CTCAGGCAAG AGGATCAGGA AGACATTTAG 600
ATAAAGAGGA TGACGAAGTT AACACAACAC CCACAACCCC ACGCACACAG AGATTTACAC 660
TCACACACGC ACTTGGCATC TGTCCTCAGT GAAGAGCAAT TAAAGACACA CCCCCTCAGA 720
TTCAAACAAG CAAGCATTAA ACGGATTGCA ATTATTCTGG AACAAACATA ATTCCAATTT 780
GTGTTCCCAG TATCTATGCA GCAAACCCGA ATTTCCTAAA CTAGCACCAA CTTCCTTTTA 840
|
