| Tag | Content |
|---|
EnhancerAtlas ID | HS062-05168 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr14:90701370-90702350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr14:90701863-90701882 | CGGCGCCCTCTGCTGGTGA | - | 7.62 | | Nkx2-5(var.2) | MA0503.1 | chr14:90701939-90701950 | AAGCACTCAAG | + | 6.02 |
|
| | 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 |
| GH14I090235 | chr14 | 90701545 | 90702017 |
|
Enhancer Sequence | ACGCACCAAC CTCAAAGCAC CGTGGTGAGG TCGGATGAGC CAGTCTAAGA GAGCAAAGAG 60
CGGGCATTCA GCAAGTTTAA GTGGAATCTG AAGTCTGGCT TTAGCTCATC TCTTGGTATC 120
AAGTGCCCAA GTCATGGGCC TGGGGTCCAA TGACATGGAG TGGTCTGGCT CCAGTCTGAA 180
AGTGCCAGTC TCTCTCCAGC CAGTCCCGGG TAGCCAGGTG GAGCCTGGAC AGAGAGAGGG 240
AGGATGAGCC TGCAGATTGC AGAAGCAGCC CTGAAGACCA GGCTTTGAGC AGGATAGAGG 300
CAAAATACTA GCCTTTCGGC CAAAGGGCTC AAGGGCCACG GTGAGAAAGA GCAGGCCAGC 360
CCCGGGAGTG GGTGGGCAAG GAGCGTCCGG TCCGAGAGCG CCCAGGGCGT TTGGAGGCTC 420
GAGGGGCAGA CAAGTGCTCC ACAGAGCACT TCTTAGGCAG GGAGGAACCG GCCCCTGCGC 480
GGTATTTGGT ATGCGGCGCC CTCTGCTGGT GAATATCTGA ACTGCATGCA CCTGTCAGAA 540
CCCGGGAAAA TTCATTCCTT CTTCACAGGA AGCACTCAAG ACAGTCACAG GCCGCCCGGG 600
CTCTAAAGCT GAGTTTAGTT TTGGTGGCAG ATTACCAAGC CTCAGGTCAT TTTACCTAAA 660
CGCTTCATTT GAAAAAAAAC TTTTAACAAA CTTGCCTGCC GGGCACTGTT TTAGGTACAT 720
TACAAATGCC ACCCAGCTTT TTATTCAAAG TTATGTGAGC AGGGTCTATT AGCATATCCG 780
TTTTACAGAT GAGGACACTG GTGCCAGGGC TTACACGCTG ACATGTAAGC ATGCATGTAA 840
GCTGACATGC GGCAACCGGG GGGCACCCAG GAAGCCCGGC CACAGGGTGC CTGCACTTCA 900
CCATTCCAGT ACCTGCCCCC CTTTTTTTTC TTTTTGATAT AACAGCTTAA TTGAGATATA 960
ATTCACATAC CATACAATTC 980
|
