| Tag | Content |
|---|
EnhancerAtlas ID | HS082-28229 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr5:67294280-67295830 |
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 | chr5:67294454-67294475 | AAAAAAAAAGAAAAAGAAAAA | - | 6.09 | | 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 | CTCTACTAAA AATGCAAAAA TTAGCCAGGC ATGGTGGTGC ATACCTGTAA TCCCAGCTAC 60
TCGGGAGGCT GAGGCAGGAG AATCGCTTGA ACCCAGGAGG CAGAGGTTGC AGTGAGCCGA 120
GATCGTGCCA CCGTACTCCA GCCTGTGCAA CAGAGTGAGA CGCTGTCTCA AAAAAAAAAA 180
AAAGAAAAAG AAAAAAAAGA AAGCAAAAGA AAAAAAAAAA AGAACTTTCC AGGCCAGAAA 240
AGAATCTCCC TTCTAGGCAG GAACAAACCC CTGTCATCAC CCACTGTGTT CCCTGCTTAC 300
GCACACCCTG GGACACAGGA AAGGCATGTT AAAGCCAGTG GCCCTGCGTG GATTGTTCCT 360
CTTATTTGTT TACATAACCC ATGACAGATG CCAAGTCAAG CAGTGGAGGA AGAGCAGGCA 420
GCACAGAGTG TCACTCAGAT GAGCCCTTCC CTGCCCTTGC CTTTTCCACT TTCCATGAGG 480
AGGCCAGCAG ACACTTTGGG GCTGCTGTAA ACCTTCAGTT AAATGGCAGC TCAGTGACAA 540
TGACAGCAAA GCTGCATTCC CCCATGGCAG ACACGCCATG TGGGCACTTC CTCAGGTCTG 600
CTGGGAAAAT CGGAGCGTCA TGTGCAGACC CTGCTGGAGG CACAGCAGGA AGTGACCAGG 660
CACAGGCTGG GCAGTCCTTC TTCCGCCCCT GAGTCACTGC CACATGCATG AGAAGGGAAC 720
TCAGTGCAGG CTAGACAGAA AAGGTGGAGG CTCAGGCAAG AGGATCAGGA AGACATTTAG 780
ATAAAGAGGA TGACGAAGTT AACACAACAC CCACAACCCC ACGCACACAG AGATTTACAC 840
TCACACACGC ACTTGGCATC TGTCCTCAGT GAAGAGCAAT TAAAGACACA CCCCCTCAGA 900
TTCAAACAAG CAAGCATTAA ACGGATTGCA ATTATTCTGG AACAAACATA ATTCCAATTT 960
GTGTTCCCAG TATCTATGCA GCAAACCCGA ATTTCCTAAA CTAGCACCAA CTTCCTTTTA 1020
CTACACCCAC ACCTACTTTC CTATTTCAAT ACGGTCCCCA AGATACATGG AATTTGGAAA 1080
TATATCAATC CCATTCTTTT CTCCTTGCAT TGACTTTTTC CATTCCTCCC AATCTTCCAG 1140
AAAATATTTG GCCTCTCTCT CTAAATCTAT TCCTGGATTC ATGCAATAAG TATTTTTTGA 1200
GTATAGTGAG TAGCTGTTAC ATGCCAGGCA CTGTACTAAG TGATAGGAAC ACAGCAATAT 1260
GCAGAAGACA CCAGAGCCCT GTTCCCACAG AGTCTGTTAT CTTAATGCAA ATTCCTATTT 1320
CTTTTCTTTT TTTTTTTTCT TTTTGAGATG GAGTTTCACT CTTGTTGCCC AGGTTGGAGT 1380
GCAGTAGCAT GATCTCAGCT CACTGAAACC TATGCCTCCT GGGTTCAAGC CATTCTTCTG 1440
CGTCAGCCTC CTGAGTAGCT AGGATTACAG GTGCCTGCCA CCACGCCCAG CTAATTTTTT 1500
GTATTTTTAG TAGAGATGGG GTTTCACCAT GTTGGCCAGG CTGGTCTCGA 1550
|
