| Tag | Content |
|---|
EnhancerAtlas ID | HS003-08315 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr11:67230550-67231810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr11:67230936-67230947 | TCCTTATCTGT | + | 6.14 | | NR2C2 | MA0504.1 | chr11:67231356-67231371 | TGCCCTCTGCCCCCA | - | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27544 | chr11:67231042-67233407 | Esophagus | | SE_42089 | chr11:67231301-67232191 | LNCaP |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 67231285 | 67231800 | | chr11 | 67230800 | 67231000 | | chr11 | 67230654 | 67230827 |
|
Enhancer Sequence | GGAGTTCCTG CATCCAATGG GTGCCCCCTA AGTGCCTTGA ATGGGGGATG AGGGTGGGAA 60
GTCTGCGGGG CCTGGAAAGG TGGGAGCGAG AGCAAGAGTC TGGGTGTCCA TTCCTCTAAC 120
TCAGAATCCT GAAGGCCCCG CTGTGTTGGG TGCTGCAGAC AGTGGTTTGT GGGACCCGTG 180
TTTTGGTGGG GGAGATAGAC AGTACGGGCA GGTGCACCAA CAGGGCCTCC CAACCCTTGC 240
TCACTCAGCC AGCCTCTTGG TTGGCCGGTA GGGGAGACCA GCTCAGTGCC GGTTTCCTTC 300
TCCCTCCCCG ACAGTGTCAT GGGAAGAGCC CTGGGCTACG TTCCTAATTC TACCTACCAC 360
CTGCTGGCTG TCCTTGGGTG AGTCAGTCCT TATCTGTAAA ATGGGACGGA GGTAGTGAAG 420
ATTACAAGAT ATAACCCGTG TTCAGTGCTT AGCGCAGGGC CTAGTATATT TTCTTTTCTT 480
TTTTTTTTTT TAAATAGAGA TGGGTTCTCG CCATGTTGTC CAGGTTGGTC GCGAACTCCT 540
GGGCTCAAGC GATCCTCCCA CCTTGGCCTC TCAAAGTGCT AGGATTACAG GCTTGAGCCA 600
CCGTGCCCGG CCATCCTGGG GTCTTTCAAC AAATTGATAA CTGGTAGCTA CTATGATCTC 660
AGATTTCAGG TTTCTCAAAG ATTCTGTTTC TTGTTTCGTA AGATTCTGAA ATGCTGATGT 720
TCCAAAATTC TGAGATGGTT TGTTTCTAAC GTTCTGCATT TCTAAGTCTT TGACCACTGA 780
GGGTGTCTGT CAGGCGCGGC TTCCTATGCC CTCTGCCCCC AGGTTCTCCC AACCTCTGGG 840
ACTGGGAAGG AGGGCAGTGG GTGGAGGGGG CTGGGCCATT GCCTTGACAT GGCCCACATT 900
CAGGGCTGGC TGTGGCAGCC CAGGGCCCCA GAGCCAGGCT GGAACTAGGA TACCAGCCTC 960
CAGGTCCCAG GCCTGCGTCA TCTCTGCGTG CCCTCGGCCA GGGCCACCAG ACAGAGACGG 1020
GCTGGTTGAG TCATCCAAGG GCTGGGGGTG GGGCAGGCTG TTCCGGCCGG CTCCTGGCTG 1080
GCAAGGCAGG AGTCCTACGC CCAGCTCTGC CCCTAACATG CCCCGTGCCC TTGGGCAAGC 1140
CTCAGCATCA GGGCTGCCAC GCGTTCGGTG GTGCTCGAAG CCCTTCAGCG TCAGGGTCAG 1200
TCCTTGGGAG GGGGGCTGTG GTCAGGCTGG TGGGCTGGGC TAGCAGTGGC AGGACAGGAG 1260
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