Tag | Content |
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EnhancerAtlas ID | HS176-31687 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr5:67294590-67295180 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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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 | GGACACAGGA AAGGCATGTT AAAGCCAGTG GCCCTGCGTG GATTGTTCCT CTTATTTGTT 60 TACATAACCC ATGACAGATG CCAAGTCAAG CAGTGGAGGA AGAGCAGGCA GCACAGAGTG 120 TCACTCAGAT GAGCCCTTCC CTGCCCTTGC CTTTTCCACT TTCCATGAGG AGGCCAGCAG 180 ACACTTTGGG GCTGCTGTAA ACCTTCAGTT AAATGGCAGC TCAGTGACAA TGACAGCAAA 240 GCTGCATTCC CCCATGGCAG ACACGCCATG TGGGCACTTC CTCAGGTCTG CTGGGAAAAT 300 CGGAGCGTCA TGTGCAGACC CTGCTGGAGG CACAGCAGGA AGTGACCAGG CACAGGCTGG 360 GCAGTCCTTC TTCCGCCCCT GAGTCACTGC CACATGCATG AGAAGGGAAC TCAGTGCAGG 420 CTAGACAGAA AAGGTGGAGG CTCAGGCAAG AGGATCAGGA AGACATTTAG ATAAAGAGGA 480 TGACGAAGTT AACACAACAC CCACAACCCC ACGCACACAG AGATTTACAC TCACACACGC 540 ACTTGGCATC TGTCCTCAGT GAAGAGCAAT TAAAGACACA CCCCCTCAGA 590
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