| Tag | Content |
|---|
EnhancerAtlas ID | HS105-39533 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:18451530-18452920 |
Target genes | | Number: 35 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr19:18452266-18452283 | GGGGTCATTTTGACCTG | - | 6.51 | | RREB1 | MA0073.1 | chr19:18452164-18452184 | CTCCCCCCCACCCCCAAACC | + | 6.01 | | SREBF2 | MA0596.1 | chr19:18452866-18452876 | ATCACCCCAT | - | 6.02 | | ZEB1 | MA0103.3 | chr19:18452039-18452050 | GGGCAGGTGGG | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGGCTGATG GGGGCTGTAG CGGCAGCGGC CGGGGGCAGA GGCGGGGGCG GCTCCGGGAC 60
TGCGGGGCCG AGAGGGGCAG GTGCTGGAAG TCCTCTCAGA TTTGGAAGGT GTCATCACCC 120
GCGGGAGCCC CGCGCAGCCC AGGCTTCCTG GAAAGTGGAG GAGGAGGAGC CTTGGGGGTC 180
CCAGGGTCGG GAGTCAGGGC AGTCGGGCGC GGGGCTTGGG GGGCCGGGCA AAAGCCCGGC 240
GCTGCGCAGG CCCCCCTGGC GTCCTTTCCT CCCAAGGTGG GGATGGTGAC CCTCCTGGCA 300
CCTGCCTCCT CTGTCTGGCC TGCGGGCTGG ACTGGACCCT TCCTCCCTGC CCCTTCCGAG 360
GTCCAGCCTG TCCCCACACC GCTCCCCCAA CCCCTGGCCC CAGGGGACAA AGGCCGATTT 420
GCGGGCAGGA AGTGTCCCAG TGACAAATGA ACCTCCCAGT CACTGCTCGC CGCGCCCTGC 480
GCTCCTGGGG GGCTACTCTC CCAAGGCAGG GGCAGGTGGG GGTCCGGGGA CCTCGGGCTC 540
TCCCAGCTGT CCCAGGGACT GTCTTCAGCG GAAACCTTTT TGTGTTTTGT GCCAGGGCTG 600
TTTGTTGGTG AGTCAGGGCC CCTGCTGTCA CCGACTCCCC CCCACCCCCA AACCAACTGT 660
TTCTCCTCCC TGAGACTCCG CCTCGGGGCC ACGTGGGGCG CCAACTTCCG CTGGGGCCTC 720
AGAGTCAAGG AGTGGGGGGG TCATTTTGAC CTGCTGTCTG GAGGGGTCAG AGTGGGAAAT 780
CCAGCAAAGG TGCACACAGG TGTTTTGTGG CTGTTGAAGG GAGATTGAGG CTGATCCAGG 840
AGATTCAGGG AAGAAGGAAG AAACAAGGCA CCTGCTTAAC AGGTGTGTAT AATTGGGAGG 900
AGGGTCACTG CCCCCATCCC TTCCAGCCTT CCTTTATCTG GTTATTTATT CCAGCACTTT 960
TTGCATGAGC TGATTACATC TTTACTGTCT CCATTTTGCA GAAAGGGAAA CTGAGGCTCA 1020
CAGAGGTCAT CCAGTTTGTA AGGGGCTGAG CTGAGACTCA AACTTTGGCT GTACAGAAGG 1080
ATAGAGTTAG GAGGTCCCCT CCTGAGCCAC AGCCCCTACC TGCTATCCCA GGCTACAGCA 1140
TCTCTGCATA GCATTCATAT CCTGTGGGAT CACTGGCCCA GATGGACCGT ATTTTTTTTT 1200
TTTTGAGACG GAGTTTTGCT CTTGTTGCCC AAGCTGGAGC ACAACGGCGC GATCTCGGCT 1260
CACTGCAACC TTCGCCTCCT GGGTTCAAGC GATTCTCCTG CCTCAGCCTC CTGAGTAGCT 1320
GGAATTACGG GCACGCATCA CCCCATCTGG TTAATTTTTT GTATTTTTAG TAGAAACGGG 1380
GTTTCACCAT 1390
|
