| Tag | Content |
|---|
EnhancerAtlas ID | HS150-05938 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr2:100056440-100057230 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PHOX2A | MA0713.1 | chr2:100056768-100056779 | TAATTCAATTA | + | 6.14 | | Phox2b | MA0681.1 | chr2:100056768-100056779 | TAATTCAATTA | + | 6.14 | | TEAD1 | MA0090.2 | chr2:100056983-100056993 | ATGGAATGTG | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 100056956 | 100057060 | | chr2 | 100056540 | 100056696 |
|
Enhancer Sequence | GCCATGTCAA TGTGTGGGGG TAATTCAGTA AAATTTACAC CTAGAAAAAT AAGGACGCTT 60
GCCTTACTGA GAAGGGAAAT TGCACTTCAT TTCTAAGAAA TGCATATTTA GATGCCAGGG 120
TGGTACAAGG CAATCTGGAC CAAGTTTCCT GATGACAGCT TTATAAATGC AGAACCCATG 180
ACAAATGTTA TGCTAAAGTC ACATCCTGGC TCCTCTAGAC GTTTGTTTAG AAATGCATTC 240
ACGAGAATCA TCTAAGTAAC AAAAACAAAA ACCTGAATTA CAAAGCAGTA ATTCATTCTA 300
CTTAGGAATG TCCAAATGTC CATAGCATTA ATTCAATTAC AGCGCAGGCT CCAGATGAAG 360
GGCTGCCCTA CAGAGTAGTA AGCCACAGGT GAAATTACCA CAGTATTATC AGGTTCCACC 420
TAAAGCCCCT CACCCTAATA CCAACTTGGT TTATTAGTAA TGAGAGCCTG ACTACACAGA 480
AAAGTCCCAC AAGCTGGATG ATCACCCATT TCTGGGTTAG CTCAGGCTCT GGCTAAACAT 540
CATATGGAAT GTGACAGGCA ACTGTGAGTA GATGCCATGC TCACAGATGA TCATGCCAGT 600
GATGGGGAAA AAGACAAAGT AGATATGATT AAAAGAAGAA AAAAAGAAAA CCTAATTTGT 660
CACATGCAGA GAAAGTTCAG CCTCTTGAGA TAAACAGAAT GCAAGGGAGC AAGAAGTCAC 720
AGATGAGCAT TTCAAAGAAA TGTACAAAAT GTACTGAATA TACCCCCCAA AAAAACCCCA 780
GAAAACAACA 790
|
