| Tag | Content |
|---|
EnhancerAtlas ID | HS148-11512 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr21:42589260-42590230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxq1 | MA0040.1 | chr21:42590091-42590102 | TATAAACAATA | - | 6.32 | | STAT1 | MA0137.3 | chr21:42590020-42590031 | TTTCCAGGAAA | + | 6.62 |
|
| | 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 |
| GH21I041217 | chr21 | 42589070 | 42590850 |
|
Enhancer Sequence | ACATCCACAC TGTCCTCTTC TCAAGCCCTA GTATTCTCTG ATTTGCCTTG TAAAGGAATT 60
TTTGTGTGTT TGTTTTCTGT CTCTCCTTTA CCTCTTTACC CCCCTCCTTT CCCTCTTTAC 120
CCCGTTTTAG CCAAGCAACT TCCAAATTCA TCTTGCCTCC AGAAAGCATT TAAATCCCCA 180
ACACAGAGAC AGTGGTGAAC ACTCAGGGCC CTGTGCCTTC CCTGTGGCAG CTCATGGCAG 240
CTTTGGCGAG GTATCTGCTG GTTGAGCCTC GGTGCTTTCC AGCCTGGGTG CTGGACACGT 300
TGTACTTTGG AGCCCCCTCC CAGTGATGGT TTAGGTCCCG GCCCTTGCTC TTTTCACATC 360
AGCCATAGAA GTGGCTTTTG CTCTTGTGAT AATCCTAAGC TGGATGCAAA GAAGGTGTCA 420
CAGAGCCAGC TCGGCAGGCA GCAAGGAGGC CTGGAGGCCG GCAAGCCTTG AAGATGGACG 480
GAGCAAGTAA AGGCGGCGGC CAGCAGCAAG TGAGTGGGAG GCCTGGGGAC ACGCCTCCAT 540
GACACAGCCT GAGGGCTGCC AGCCCCTACC AGAAACTGGG AGAGACAAGA AGGGCCCTCC 600
CCTGGAGCTT CTGTGGGAAG CGCAGCCCCG CCCACACCTA GATTTTGGAC TTCTGACCTC 660
CAGAACTGCC AGAAAATAAA TGTATATTAT CTCATGCCAA CCAGTTTGTG GCTGTTTGTT 720
AAGGCAGCCA TAAGAAATTA ATGTAAAAAG TGAGTCCCGT TTTCCAGGAA ACTTGAATCA 780
GACCAACCAA TGTTAAGATA TGTCAGTAAA ACTACAGAAC GATGGTTCTA ATATAAACAA 840
TACAACTATA GAACTTTGTG GCTATGGAAA GAATTCTTCA GTAACCAAGG AGAAAAAGTC 900
ACGTGTAATG AGGAAAAATA AGACATGCTT TAGATTTCTC CACAAATACT CACTGTTGAA 960
ATACACTGGA 970
|
