| Tag | Content |
|---|
EnhancerAtlas ID | HS040-25446 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr3:47063640-47064610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr3:47063742-47063753 | AGTGACTCATG | + | 6.14 | | Foxq1 | MA0040.1 | chr3:47064083-47064094 | AATAAACAATA | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 47063642 | 47063910 | | chr3 | 47063994 | 47064606 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I047022 | chr3 | 47063732 | 47065053 |
|
Enhancer Sequence | CATGCCATTG CACTCCAGCC TGGGAGACAG AGCAACAATC TGTCACACAC ACACACACAC 60
ACACACACAC ACACACACAC ACAAATTTAG CACGTGGGGT TCAGTGACTC ATGCCTGTAA 120
TCCCAGCACT TTGGGAGGCC AAGATGGGGA GATTGTTTGA GCCCAGGAAT TCGAGACCAG 180
CATCTCTATA AAAAAACTGA AAAATTAGCT GGGCATGGTG GCTATGCCTG TGGTCCCAGT 240
TACTTGGGAG GTTGAGGTTG GAGAGTTGCG CGAGCCTAGG AGGTTGAGGC TGCAGTGAGC 300
TGTGATCATG CTACTGCACT CCAGCCTGGG CAACAGAGTG AAATGCTGTC TCCAAAAAGA 360
AAAAAAGCAC TTTTAAGGAA ACCACCAGAG AACAGGGTAG GGGCTCTGAT ACATAAAAAA 420
GCGAGTGCTT CCAGATCCTC AGCAATAAAC AATAATCAGT TTGCCTTTTC TCTGTGTTGG 480
CTTATATAGA GTATCAGTCA ATTAAAGATT CTGGTGGAAA TCTATGTGAG GCCGTGGACA 540
GTTAAGAGTA CACAATGAAA TGAGCAGGCA AAGGGCCTGG CAGAAAGCCA GAGCTTACTG 600
CCTTTAGAAG CTGACCCTGC TGTCAGCCTT CACCTGTGGC ACATTTGGAT TCCTAGGAAA 660
TCTGTTCTGA TTATGACAAG GCAGGCCTGA GTACCTTTAT ATTACCCAAG GTGAAGCTTG 720
AGACCTTCTG GATTAGTTGG CAATGGCCTT AAGCTTATTG GGCAGTTCTG GTAACCATAC 780
ACAGGCTGTG TAACACAACA GAATCACCCT TTATTATAAA TATTGACATG ACTATGTCAC 840
AAAGCCCATG TGACTTGGAA CCAAGAGGGT ATGGCTTGAG TTACAGAAAT GAGTCCTGAC 900
AAAGGCAGAG CAGGACATAC CCAGCTAATA CTTCTCTCTC CCTGTATTTA ATTAAATACT 960
GATTAGAGGG 970
|
