| Tag | Content |
|---|
EnhancerAtlas ID | HS180-38815 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr5:67294520-67295220 |
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 |
|
| | 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 | AGAATCTCCC TTCTAGGCAG GAACAAACCC CTGTCATCAC CCACTGTGTT CCCTGCTTAC 60
GCACACCCTG GGACACAGGA AAGGCATGTT AAAGCCAGTG GCCCTGCGTG GATTGTTCCT 120
CTTATTTGTT TACATAACCC ATGACAGATG CCAAGTCAAG CAGTGGAGGA AGAGCAGGCA 180
GCACAGAGTG TCACTCAGAT GAGCCCTTCC CTGCCCTTGC CTTTTCCACT TTCCATGAGG 240
AGGCCAGCAG ACACTTTGGG GCTGCTGTAA ACCTTCAGTT AAATGGCAGC TCAGTGACAA 300
TGACAGCAAA GCTGCATTCC CCCATGGCAG ACACGCCATG TGGGCACTTC CTCAGGTCTG 360
CTGGGAAAAT CGGAGCGTCA TGTGCAGACC CTGCTGGAGG CACAGCAGGA AGTGACCAGG 420
CACAGGCTGG GCAGTCCTTC TTCCGCCCCT GAGTCACTGC CACATGCATG AGAAGGGAAC 480
TCAGTGCAGG CTAGACAGAA AAGGTGGAGG CTCAGGCAAG AGGATCAGGA AGACATTTAG 540
ATAAAGAGGA TGACGAAGTT AACACAACAC CCACAACCCC ACGCACACAG AGATTTACAC 600
TCACACACGC ACTTGGCATC TGTCCTCAGT GAAGAGCAAT TAAAGACACA CCCCCTCAGA 660
TTCAAACAAG CAAGCATTAA ACGGATTGCA ATTATTCTGG 700
|
