| Tag | Content |
|---|
EnhancerAtlas ID | HS017-06090 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr11:67230660-67231810 |
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: 2 | Chromosome | Start | End |
| chr11 | 67231285 | 67231800 | | chr11 | 67230800 | 67231000 |
|
Enhancer Sequence | TTCCTCTAAC TCAGAATCCT GAAGGCCCCG CTGTGTTGGG TGCTGCAGAC AGTGGTTTGT 60
GGGACCCGTG TTTTGGTGGG GGAGATAGAC AGTACGGGCA GGTGCACCAA CAGGGCCTCC 120
CAACCCTTGC TCACTCAGCC AGCCTCTTGG TTGGCCGGTA GGGGAGACCA GCTCAGTGCC 180
GGTTTCCTTC TCCCTCCCCG ACAGTGTCAT GGGAAGAGCC CTGGGCTACG TTCCTAATTC 240
TACCTACCAC CTGCTGGCTG TCCTTGGGTG AGTCAGTCCT TATCTGTAAA ATGGGACGGA 300
GGTAGTGAAG ATTACAAGAT ATAACCCGTG TTCAGTGCTT AGCGCAGGGC CTAGTATATT 360
TTCTTTTCTT TTTTTTTTTT TAAATAGAGA TGGGTTCTCG CCATGTTGTC CAGGTTGGTC 420
GCGAACTCCT GGGCTCAAGC GATCCTCCCA CCTTGGCCTC TCAAAGTGCT AGGATTACAG 480
GCTTGAGCCA CCGTGCCCGG CCATCCTGGG GTCTTTCAAC AAATTGATAA CTGGTAGCTA 540
CTATGATCTC AGATTTCAGG TTTCTCAAAG ATTCTGTTTC TTGTTTCGTA AGATTCTGAA 600
ATGCTGATGT TCCAAAATTC TGAGATGGTT TGTTTCTAAC GTTCTGCATT TCTAAGTCTT 660
TGACCACTGA GGGTGTCTGT CAGGCGCGGC TTCCTATGCC CTCTGCCCCC AGGTTCTCCC 720
AACCTCTGGG ACTGGGAAGG AGGGCAGTGG GTGGAGGGGG CTGGGCCATT GCCTTGACAT 780
GGCCCACATT CAGGGCTGGC TGTGGCAGCC CAGGGCCCCA GAGCCAGGCT GGAACTAGGA 840
TACCAGCCTC CAGGTCCCAG GCCTGCGTCA TCTCTGCGTG CCCTCGGCCA GGGCCACCAG 900
ACAGAGACGG GCTGGTTGAG TCATCCAAGG GCTGGGGGTG GGGCAGGCTG TTCCGGCCGG 960
CTCCTGGCTG GCAAGGCAGG AGTCCTACGC CCAGCTCTGC CCCTAACATG CCCCGTGCCC 1020
TTGGGCAAGC CTCAGCATCA GGGCTGCCAC GCGTTCGGTG GTGCTCGAAG CCCTTCAGCG 1080
TCAGGGTCAG TCCTTGGGAG GGGGGCTGTG GTCAGGCTGG TGGGCTGGGC TAGCAGTGGC 1140
AGGACAGGAG 1150
|
