| Tag | Content |
|---|
EnhancerAtlas ID | HS148-14285 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr5:67294500-67295230 |
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 | AGAACTTTCC AGGCCAGAAA AGAATCTCCC TTCTAGGCAG GAACAAACCC CTGTCATCAC 60
CCACTGTGTT CCCTGCTTAC GCACACCCTG GGACACAGGA AAGGCATGTT AAAGCCAGTG 120
GCCCTGCGTG GATTGTTCCT CTTATTTGTT TACATAACCC ATGACAGATG CCAAGTCAAG 180
CAGTGGAGGA AGAGCAGGCA GCACAGAGTG TCACTCAGAT GAGCCCTTCC CTGCCCTTGC 240
CTTTTCCACT TTCCATGAGG AGGCCAGCAG ACACTTTGGG GCTGCTGTAA ACCTTCAGTT 300
AAATGGCAGC TCAGTGACAA TGACAGCAAA GCTGCATTCC CCCATGGCAG ACACGCCATG 360
TGGGCACTTC CTCAGGTCTG CTGGGAAAAT CGGAGCGTCA TGTGCAGACC CTGCTGGAGG 420
CACAGCAGGA AGTGACCAGG CACAGGCTGG GCAGTCCTTC TTCCGCCCCT GAGTCACTGC 480
CACATGCATG AGAAGGGAAC TCAGTGCAGG CTAGACAGAA AAGGTGGAGG CTCAGGCAAG 540
AGGATCAGGA AGACATTTAG ATAAAGAGGA TGACGAAGTT AACACAACAC CCACAACCCC 600
ACGCACACAG AGATTTACAC TCACACACGC ACTTGGCATC TGTCCTCAGT GAAGAGCAAT 660
TAAAGACACA CCCCCTCAGA TTCAAACAAG CAAGCATTAA ACGGATTGCA ATTATTCTGG 720
AACAAACATA 730
|
