| Tag | Content |
|---|
EnhancerAtlas ID | HS044-08542 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr22:31434950-31436120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr22:31435502-31435513 | GGGTGACTCAG | + | 6.02 | | JUNB | MA0490.1 | chr22:31435502-31435513 | GGGTGACTCAG | + | 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 |
| GH22I031038 | chr22 | 31434104 | 31437311 |
|
Enhancer Sequence | AAAATGTCTA ATCCAACCAT GACATTTCCC AGATGGGACA AGTGAGGCCC AGAGAAGGCT 60
ACTAATTTTC CTGGAGTTAC ACAGCAGCAA AAGATGGTTC TAAGACTCAG GGCCAGGGTT 120
TGAACTCCTG GGCCAGGGCT TTTTCAGGGG TTCTCAAACT GTGTTCCACA CCCAATGGCA 180
GGTTTCCTAG AGAAGTGGTT AGTGAGGGAA CAAGAGGGAA GCTACATCAC TGGGCAACCT 240
CTACCCCTCC TCCTTCCATC CCGTAAGCTC CACTTTGACC ATTTTGTACA TTGACCTTCA 300
ACTTAAGGAC CCTCTGCAAC AGGGTTCATC TCTGGAAAAA CTCTTTTTGA AAGCCACTCA 360
GTTATATTGT AGGATTTACA CATTTTCCTC CCTGGAAAAC TTTTGTTCCC ATGGAGAAAA 420
CTTAACTTTT TCTTTGAACC ACATTCTCCC CCTCTCTAAT GGATTTTTAC ATATTTGGAA 480
AAACAGAGGC ATGCATGGGC CTTTTACAAG CCAGCAGTTA AACTGAAAGG CTCGTTCACT 540
TGCAGGAGAG CTGGGTGACT CAGGGCGTCA GTAACAACTG GCCCAGATGT GAAATCTCAT 600
GCTCATTGCT TAGAAAAATG TTTAGAAAAA TGCTGCTGTT TGGGATCACC GGACGGAAGC 660
TGCAGTGAGG GCCCAGGAGA GCCCCAAGGT CGACAGTTCC GAGGGAACAG GATGGAGGGG 720
GGCGAAGGGT GGTGAGACCG TCCAGAACTC AAGGCTAAGC AGTGCAGGGG GCTGATGGTA 780
AGATACGCCT TTCCCCCAGA TGTCTCATTT TAAGCTGAAA CAGACAAGAT CCAAAGCCAG 840
GAAAATATCC GGGATGGACC CCCAAAGTGG GAGAAAGACA AGAAACACAA CAAAGCCAAG 900
TGCGCAGCCT TTGTCCATAG GGATCCTGGG CTCTGCATGG AGTGAGTCTA GGCTTAAAGG 960
AAGGGCCAGG AGGCAGAAGC TGATTCCCCA AAGCAGAAGG GTGAAAGCCT GGACTTGATA 1020
CTTGATGGAA CTGGATTTGA ATCCCAATTC AGCAACTCAC AAGCTGTGTA ACCGTGGGCA 1080
AGTTATCCAA CCTCTCTGAG CATCCTTTTC TCATTAGCAA AATGTAGACT GTCGTGATGC 1140
CTACCTTATA GGGTAGTGAA GGGTTAGAAA 1170
|
