| Tag | Content |
|---|
EnhancerAtlas ID | HS127-05803 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr11:67230440-67231810 |
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 | GGCATGAGGC ACGGCACCCG GCTAGTTCTT CTTATGAAAG TACTGGACCG TGATGGATTA 60
GAAATGAAAA CTGGTCCTTT ACCATAGCTA GTTGGGGGAC CACTGGTTTA GGAGTTCCTG 120
CATCCAATGG GTGCCCCCTA AGTGCCTTGA ATGGGGGATG AGGGTGGGAA GTCTGCGGGG 180
CCTGGAAAGG TGGGAGCGAG AGCAAGAGTC TGGGTGTCCA TTCCTCTAAC TCAGAATCCT 240
GAAGGCCCCG CTGTGTTGGG TGCTGCAGAC AGTGGTTTGT GGGACCCGTG TTTTGGTGGG 300
GGAGATAGAC AGTACGGGCA GGTGCACCAA CAGGGCCTCC CAACCCTTGC TCACTCAGCC 360
AGCCTCTTGG TTGGCCGGTA GGGGAGACCA GCTCAGTGCC GGTTTCCTTC TCCCTCCCCG 420
ACAGTGTCAT GGGAAGAGCC CTGGGCTACG TTCCTAATTC TACCTACCAC CTGCTGGCTG 480
TCCTTGGGTG AGTCAGTCCT TATCTGTAAA ATGGGACGGA GGTAGTGAAG ATTACAAGAT 540
ATAACCCGTG TTCAGTGCTT AGCGCAGGGC CTAGTATATT TTCTTTTCTT TTTTTTTTTT 600
TAAATAGAGA TGGGTTCTCG CCATGTTGTC CAGGTTGGTC GCGAACTCCT GGGCTCAAGC 660
GATCCTCCCA CCTTGGCCTC TCAAAGTGCT AGGATTACAG GCTTGAGCCA CCGTGCCCGG 720
CCATCCTGGG GTCTTTCAAC AAATTGATAA CTGGTAGCTA CTATGATCTC AGATTTCAGG 780
TTTCTCAAAG ATTCTGTTTC TTGTTTCGTA AGATTCTGAA ATGCTGATGT TCCAAAATTC 840
TGAGATGGTT TGTTTCTAAC GTTCTGCATT TCTAAGTCTT TGACCACTGA GGGTGTCTGT 900
CAGGCGCGGC TTCCTATGCC CTCTGCCCCC AGGTTCTCCC AACCTCTGGG ACTGGGAAGG 960
AGGGCAGTGG GTGGAGGGGG CTGGGCCATT GCCTTGACAT GGCCCACATT CAGGGCTGGC 1020
TGTGGCAGCC CAGGGCCCCA GAGCCAGGCT GGAACTAGGA TACCAGCCTC CAGGTCCCAG 1080
GCCTGCGTCA TCTCTGCGTG CCCTCGGCCA GGGCCACCAG ACAGAGACGG GCTGGTTGAG 1140
TCATCCAAGG GCTGGGGGTG GGGCAGGCTG TTCCGGCCGG CTCCTGGCTG GCAAGGCAGG 1200
AGTCCTACGC CCAGCTCTGC CCCTAACATG CCCCGTGCCC TTGGGCAAGC CTCAGCATCA 1260
GGGCTGCCAC GCGTTCGGTG GTGCTCGAAG CCCTTCAGCG TCAGGGTCAG TCCTTGGGAG 1320
GGGGGCTGTG GTCAGGCTGG TGGGCTGGGC TAGCAGTGGC AGGACAGGAG 1370
|
