| Tag | Content |
|---|
EnhancerAtlas ID | HS047-23530 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr3:27756150-27757120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr3:27756433-27756444 | CTAATCCTCTT | - | 6.62 | | ZNF263 | MA0528.1 | chr3:27756325-27756346 | GAGGGACGGAGGGGAAGGGAG | + | 6.09 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_20664 | chr3:27753478-27764471 | CD56 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGTCATCCA CAGTACATAT ATCTTAAAAA GCACATCTTC AACGCTTTTG TCCTTGGCTC 60
CCCGGTAAAG TTCGGGGCGC CTTTGCCAAA GTGTTTTGAG TAGGCCGTTC GGAAACGCGG 120
AGCAGGAGTT CGAGCCCCCA AGGTCACGGG TGGCGCGGGA AGAACTCGGG CCCCAGAGGG 180
ACGGAGGGGA AGGGAGACAG GACAGTCGAG GTACAAGGTC CTGGCGGCCT TAATTGGGCG 240
CAGAAGGGGA GGAGGTCTCG GCTGATTGCT CGCCTCCCAG CAGCTAATCC TCTTAGCAGC 300
TGCATTTCCG CGCTACACAG TTAGCAGAAT GATCCTCCCA GCTAGACCTT TACCCCGGGA 360
GGGTCCAGGA GGGGGCTGGA AAGGTTTGCA ATCTGGGCCT GAAGCCGTCT GCAGATAAGC 420
CTGGCGGGAC GTCTGGCTGG GGGGACAAAG GGGACCCTCC ACCCCACTCT TTGGACCTCC 480
CAGGGTTCAG CCAGGGGATG GGCTGTCCTT CGTCTTCCCG TGGAGCGTGG GCCAAATAAA 540
CGGAACTAAG CGCAAGGTGA ACTGCTCCAA GGTCACTGTT TGCAGAGCGG CAGTGCACGG 600
AACGACTGGA ATCCTCCTTT GTAAGTGCCA CGCCCGTCCC TAGCCTGCGC CTCAGACCGA 660
GTCCGGGCGG AGTTTGACTG CAGCTACTGA GGCCGGCAGC CGGCGGCGGC GGGTGCGCAG 720
CGTCTGGGTT CAGAAGAAAG CCGCAGGTGG GCGCAGAAGC TGAGCTGTGT GCAGCCCCCC 780
GCTCCGCCGC GCCCCAGGGA CCCTGAACTG GTGGGCGCTC AAAGGGCCAC GGGGGTTCCC 840
AGGGAGCCTA GGTGGGCCTA AGGATGGGTG GCCCCAAGTA AGCCTAGAAA AAAGCCCAGA 900
GAACTTAGTG GCCAGGCGCT CTGACAGAGC CTGGTCTCCA AGAGCCAGAA GCGGAGGTTT 960
TCGAGGCTTG 970
|
