| Tag | Content |
|---|
EnhancerAtlas ID | HS080-28790 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr5:97767770-97768900 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr5:97768106-97768119 | CAAAGGTCAAAAG | + | 6.87 |
|
| | 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 |
| GH05I098432 | chr5 | 97768140 | 97768787 |
|
Enhancer Sequence | CAGAAATTTA AATAAGCAGT TGCAGCAATG TGATGAGCCT TATGATGGTA GAAGCACAAG 60
ATGCTGTGGT AGTGCAAGGC AAAGACACCT GCCCAGGTCA GGAGGGTCAA GGAAGCATCT 120
CAAGAAAAAC AAGTTAATTC TTCAACAACG GTTATAAGTT AGCAGGTGCC ATTGTACAAT 180
GGAAACATGA AACTGCTGCC ACACTGGGAA GCCTGTGGCC TTATAGGAAG GCACGTCTGA 240
AGGCAGCAAT AACTGGGAGC AGCCAGCAAA ATGACTGTTG CCAAACATTT CCAAGTGAAA 300
AGCTAACCAT TTCAGGCAAA TTATGAGGCC ACTGACCAAA GGTCAAAAGA AGGGGAAAGG 360
GAGCTGAGGC TTTCCTAGAG TCAGTGAAAG GTAGGACTGC CATTGAGGTT AACAGCAAGG 420
AATGTATCAG ATAAAGGGAA TGGAGCCTAA GATAAAGGAT GGGGTATTGC AGCCTTTTGA 480
AGCTTCCGCA TCAATAATTA CGACTGGAGG TCAATCCGTC AGAAGTTCAA ACAGCTAAAG 540
CTTCAAATGA AGAGGATTTG TTCTCATGCA AATGTCTCTT AAAATGCAAA CTAAGGAAAA 600
AAAAGGTAAG AGAATGTGGC ATGAAAGACA GGAGAGTGTC TTATTCAACA GCAATTTCTT 660
TAAATTAAAA AAACAACTTG CAAATGGATG GGAAAAACAT CTCTTTACAA CAGCAAGTGG 720
CTAAGTATGT TCCATGTAGA TGGCATTCTG CTACAACTCT CTAAATTCCA CCTTTCGAAA 780
CATTACTCTA AATTCTTTCT TTTAAAACAC TGATTTGCCA AATAGAATAA GGCTTAAGAA 840
CATTTCACTC TATAATTTCA ATAGAGCAGG CATTTGGGGT CCACCAATGC AAAAGAAATA 900
TTCTTTAAGT AACAGATTGA CTGTGCTGTG ACCACACTGG ATGAGGTCTC CTGCTTAAGG 960
GTTTTGACAA AAAAGAGTAG ATTTAAAGAT AGTGTACTTG CCTCCAAAAA CGGTGCTGCA 1020
AGACTGAATA TTACTTCATT GTGGGCTGTA GGAAATGTGT TTTGCCTGCT CTGTTTAATT 1080
CTGGGGTTAA AAGCAGTAGT CAAATCATGA CAGCAAGGAG CTTTCTGCTC 1130
|
