Tag | Content |
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EnhancerAtlas ID | HS145-20798 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr5:67294480-67295190 |
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 |
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| 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 | AAGCAAAAGA AAAAAAAAAA AGAACTTTCC AGGCCAGAAA AGAATCTCCC TTCTAGGCAG 60 GAACAAACCC CTGTCATCAC CCACTGTGTT CCCTGCTTAC GCACACCCTG GGACACAGGA 120 AAGGCATGTT AAAGCCAGTG GCCCTGCGTG GATTGTTCCT CTTATTTGTT TACATAACCC 180 ATGACAGATG CCAAGTCAAG CAGTGGAGGA AGAGCAGGCA GCACAGAGTG TCACTCAGAT 240 GAGCCCTTCC CTGCCCTTGC CTTTTCCACT TTCCATGAGG AGGCCAGCAG ACACTTTGGG 300 GCTGCTGTAA ACCTTCAGTT AAATGGCAGC TCAGTGACAA TGACAGCAAA GCTGCATTCC 360 CCCATGGCAG ACACGCCATG TGGGCACTTC CTCAGGTCTG CTGGGAAAAT CGGAGCGTCA 420 TGTGCAGACC CTGCTGGAGG CACAGCAGGA AGTGACCAGG CACAGGCTGG GCAGTCCTTC 480 TTCCGCCCCT GAGTCACTGC CACATGCATG AGAAGGGAAC TCAGTGCAGG CTAGACAGAA 540 AAGGTGGAGG CTCAGGCAAG AGGATCAGGA AGACATTTAG ATAAAGAGGA TGACGAAGTT 600 AACACAACAC CCACAACCCC ACGCACACAG AGATTTACAC TCACACACGC ACTTGGCATC 660 TGTCCTCAGT GAAGAGCAAT TAAAGACACA CCCCCTCAGA TTCAAACAAG 710
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