| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00018 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:1172610-1174180 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxa2 | MA0047.2 | chr1:1172971-1172983 | CCAGAGTAAACA | - | 6.11 | | PLAG1 | MA0163.1 | chr1:1173433-1173447 | GGGGCCCAAGGGGT | + | 6.47 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41703 | chr1:1170354-1174245 | LNCaP |
|
| | 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 |
| GH01I001235 | chr1 | 1170967 | 1178914 |
|
Enhancer Sequence | CCCTCCCCAA GGATCTGAGC CTCCCTCACC GAGGTTCCCA GTGGAGGTAG ACAGTGGATG 60
AGTGATCCCA GGAGAGCTGG CTGCAGCCAA GGGGCTGAAG GGAGGTGGAG GCGGGAGGGG 120
CAGGAAGGAG GATCTGGAAG GCCCCAGGCG CTCCCCACCC ATCCAGCCTC GGCCTCTGTC 180
CTGGTCGCGT TGCCCAGCGA GGCCTCTCCT TGGGCTGGGG CTCGGGTACT CTGCCCTGGT 240
CGGGGCCACA GATGCCGCAA AGTCCCCTCA ACTCAGCTAG CCAGGGTGCA AGACCGCGCC 300
CACAGCTGAG AAGCCAGGGG TTACGAGTGT GGCCCTGCCA GGACCTCCTC AGCTGCATCC 360
TCCAGAGTAA ACACAGGTGG CCGCAGATCT TCCAGGGCCG GCCGGGCAGG CAGGACAGGA 420
GCCCAGGAGG GCCGCAGTCC AGCTCCCCTC CCCGCTGACC CAGGGCCGGA CCCAGCCCGG 480
TGACTGGAGC AGAAGGAAAC CCAAGCCCCA GGCCCTCCCT CCGGTGGCAT CCGAAGGTCT 540
CAGCGGCCCC AGCCTCCCCC AGGGGCCCCG CACCCGCCAC CGCCCACCTC AGACCGGAGA 600
GAGAGTGAGG GATGGGCAGA GCCAGGCCCA AGTCCCCGCC GGGGCGACGG TCACGGTGCC 660
TCACCCTCAA CCGCCTCACC CAGACCTTCC GACCCAGGAA CAGCTGAACT CAGCCTAAAA 720
AGCACCCGTC CCGAGGGCCT GAGTCCGGCC GTGGTGCCTC CTGCTGCAGA GATGTGTTTT 780
GCACACTCCT GTGTGGCAGG GAGAGGCCCG GGCGTGCGGG CTGGGGGCCC AAGGGGTCTG 840
GAGACGCTTC CCTGCGGAGA CGGGGTTTGC CCAGCCCCCA CCTGTCACGC TTCTCGTCAC 900
CCCCAAGTGA GGGCCGTGGG CGCGGGCGGG GTGGGCAGGA GGCCCTGCTG GGCTGGGTCA 960
CACGCATGAC ACCTGGCTGT CGCAACACAG ATATCATCAC GCCCGGGCAC CCGTGAGTCA 1020
CTGGCCCAGA GCAGGGGCTG CCCCCAGCCT CCCAAACAAA GACCCTTTGT CCCCAGGCCT 1080
CTGGTGCCAG GCCCACCTGT ACAGCAGTCA GATGCGCAGG CGGACAGACA CGCCGGTGGC 1140
TCGGCAGGCA CAGGCAGGGC CAGGGCGTGT TCCCGCAACC AGACACGCTG CCATTCCTGG 1200
GTCAGGGTCA GGCTGAGGGA GACCCCTGGG GGACAGGCCC TGAGGTCACC ATAGCTCAGA 1260
GTGACCTGAA CTGGGAGTCC AAGCACAGAC TGGCCAAGCC CAGCCCGTGA GCGACGGCCC 1320
CAGGACGCGG CGCCGAGCTC TGCCCCCAGC TCCAGCTCCC AGCGGCGTCG GAGCACAGCA 1380
GATCCCAGGG CAGCGCTCTG CAGGCAGGAA AGAGCTTCCC CTTGGGACAG CGCGCTGAGC 1440
AGCCCCCAGC TGAGGGTGGG AGCCCCGTCC CTGGACCCCT TCACGCAGTT CAGGGAGCCC 1500
CACATGCCGA AGCAGCCGTC ACAGCTCCAT GGGCCCCTCT GCTGTCCCTG GCAGGACCGA 1560
AGCTATGTGG 1570
|
