| Tag | Content |
|---|
EnhancerAtlas ID | HS012-21896 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr7:129209040-129210060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr7:129209472-129209484 | AAACAAACAAAC | - | 6.32 | | HES2 | MA0616.2 | chr7:129209328-129209338 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr7:129209328-129209338 | GGCACGTGCC | - | 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 |
| GH07I129569 | chr7 | 129209123 | 129210534 |
|
Enhancer Sequence | AAGAGAATGG CGTGAACCTG GGAGGCGGAG CTTGCGGTGA GACGAGATTG CACCCCTGCA 60
CTCCAGCCTG GGTGACAGAG CAAGACTCCG TCTCAAAAAA AAAAGTCAGC ATCATTAGTC 120
ACATGAAAGG CTCTTTAGGC CAGGCACAGT GGCTCATATC TGTTATCTCA ACACTTTGGG 180
AAGCTGAGGT AGGAGGATCA CTTGAACCCA AGTGTTCAAG ACCAGCCTGG GCAACAGAGT 240
GAGGCCTGTC TCTTAAAAAA AAAAAAAAAA AGTGACATGC CTAATAGTGG CACGTGCCTG 300
TAGTCCTAGA TACTCAGGAG GCTGAGGTGG AAGGATCGCT TGAGCCCACG AAGTTGAAGC 360
TACAGTGAGC CCTGATAGCA CCACTGCACT CCAGCCTGGG TGACAGAGTG AGACCCTGGA 420
TCAAAAAAAG AAAAACAAAC AAACAAAAAA GAAGGTTGTT TAAAGACTAT GGGATTCATA 480
AGTCCCCCCC AGCCATGTCG GCAAAAGCCA AACATAGAGA AAAGGTTATC TTGAAAGGAT 540
TTGTGCACAA GCCTCTTATC TAATGGAATG AATCCCCATG ACATTCACAG GAAACCCACT 600
AGGCTCTTGA GAATTTTATT CCAGCAGAAA TACTGCCAGC TTGGACTGAA AGGGAGAGAG 660
AGAGGATGAA ATGTAAGAAG GCTGTGGATC CCCAAAATTC TACTGGCAAG AAACAGGCTG 720
GTAAAACTAT TCAGCTGCAA ACACCAGCCA TGTTTCATGA AAAAGGAATG ATGACTCAGA 780
GGGCGAAGGT TTGAGCCCAG AGGGTGGGGT GGAGCCTTGA ACCACAGAGG ATCATTACCA 840
GGTCTGGAAA ACTAATGTTT GCCCAGATAG ATTTTTTTTT TTTTTTTTTG AGACAGTCTC 900
ACTCTGTCAC CCAGGCTGGA ATGCAATGGT GTGATCTCGG TTCACTGCAA CCTCCACTTC 960
CCAGGCTCAA GGGATCCTCC CACCTCAGCC TCTTGAATAG CTGGGACTGC AGGCACACAC 1020
|
