| Tag | Content |
|---|
EnhancerAtlas ID | HS003-24076 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr19:48372090-48373720 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:48372312-48372331 | TGGCCACCAGGGGGCAACA | + | 8.23 | | Foxd3 | MA0041.1 | chr19:48372997-48373009 | GATTATTTGTTT | + | 6.07 | | MEF2A | MA0052.3 | chr19:48373217-48373229 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr19:48373217-48373229 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr19:48373216-48373231 | TTCTATTTTTAGTAG | - | 6.57 |
|
| | 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 |
| GH19I047869 | chr19 | 48372261 | 48372430 |
|
Enhancer Sequence | CAAAAACAAC AAAAAACCTC AGACTGCTTC CCTGAAATTC TTCTAAAGAA AATGCCTGAC 60
AGGAAATAAC TTAAGGATAT TGTGGGTTTT TATTGTTGCT ACTTCGAGAT GCAGTTGTAT 120
CTCTAGAGAC ACAGTGGGGT CAGATCAGAG ATGGGGTTCA TTCAGGGGCA CCCCCAGAAC 180
TGGGAGAGTC CTCGGCTTCC ACATACCCGT TATGGTGCTC CGTGGCCACC AGGGGGCAAC 240
AATACGTCAC TGTTCCAGCC CAGGGAGCGG CCAACCAGAG CTTGGACCTG GGGTGTCCCA 300
GGAGCCACCT AGACCGGCTG GTTCCTTCCA TACAAAAGAC CTCCAGGTGG GATGGGGGAG 360
AGACACCCCA CATTCGAGTG GGAGAAAAAC ATGGAAAAGA CACAGAGGCA ACATTATATT 420
TCTTTCCACT TGTGTAATTT AAGCTAAAGC CAAACAGCTA GAAAATATAC TTTTTTTTTT 480
TTTTTTTTTG GAGACAGTCT TGCTCTGTTG CTCAGGCTGG AGTGCAGTGA TAGGATCATA 540
ACTCACTGCA AGCTCCGCCT CCCGGGTTCA AGCCATTCTC CTGCCTCAGC CTCCCAAGTA 600
GCTGGGACTA CAGGCACCCG CCACCACGCC TGGCTAATTT TTGTATTTTT AGTAGAGACA 660
GGGTTTCACC ATGTTGGCCA GGCTGGTCTC AAACTCCTGA GCTCAAGTGA TCCACCTACC 720
TTGGCCTCTC AAAGTGCTGG GATCATAGGC GTGAGCCACC TTACCCGGCC TTCTTGTTGT 780
GGTTTTAATT TATATTTCTC TAGAGGCAAA TGATGCAAAA CATCGTTTCA TGTGCTGATT 840
TGCCATCCCT GTGTCCTCTT TGGTGAAATG TTTGTTCAAA TCTTTTATTC TTTTTTTTCT 900
TTTAAAAGAT TATTTGTTTA ATGCTGGGTT TTAGGAGTTC TTTATGTATT CTAGAAACAA 960
GTCCATTGCC AGATATGAGA TTTACAAGTA CTTCCTCTCC ATCTCTGGTT TGTCTTCTTG 1020
TTTTCTCATT TTGTTTTGAG ATGGAGTCTC ACTTTGTTGC CCAGGCTGGA ATGTAGTGGC 1080
ACAATCTCGG CTCACTGCAA CCTCCGCCAA CACATCTGGC TAATTTTTCT ATTTTTAGTA 1140
GAGACAGGGT TTTACCATGT TGGCCAGACT TGTCTTGAAC TCCTGAGCTC AAGTGATCCA 1200
CCTGCCTCGG CCTCCGAAAG TGCTGGGATT ACAGGCATGA GCCACCGCAC CTGGCCTATC 1260
TTTTCATTCT CTTTATAGGT TCTTTGGTTC TTTTGCGGAA CAAGACTTTA GTTTTTTTAT 1320
TTTTTATTTT TGAGATGGAG TCTCCCTCTG TTGCCCAGGC TGGAGTGCAA TGGTATGATC 1380
TCAGCTCACT GCAACCTCCA TCTCCTAGGT TCAAGCAATT CTCATGCCTC AGCCTCCCGA 1440
GTAGCTGGGA TTACAGACAT GTGCCATCAT GCCCAGCTAA TTTTTGTATT TTTAGTAGAG 1500
ACAGAGTTTC ACTATGTTGG CCAGGCTGGT CTCAAACTCC TGACCTCAAG TGATCCGCCC 1560
TCCTTGGCCT CCCAAAGTGC TGGGATTACA GGTGTGAGCC ACCGCACCTG GCCTTATGAA 1620
AGTTTTAGAA 1630
|
