| Tag | Content |
|---|
EnhancerAtlas ID | HS007-03000 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr11:67230900-67231810 |
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: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TACCTACCAC CTGCTGGCTG TCCTTGGGTG AGTCAGTCCT TATCTGTAAA ATGGGACGGA 60
GGTAGTGAAG ATTACAAGAT ATAACCCGTG TTCAGTGCTT AGCGCAGGGC CTAGTATATT 120
TTCTTTTCTT TTTTTTTTTT TAAATAGAGA TGGGTTCTCG CCATGTTGTC CAGGTTGGTC 180
GCGAACTCCT GGGCTCAAGC GATCCTCCCA CCTTGGCCTC TCAAAGTGCT AGGATTACAG 240
GCTTGAGCCA CCGTGCCCGG CCATCCTGGG GTCTTTCAAC AAATTGATAA CTGGTAGCTA 300
CTATGATCTC AGATTTCAGG TTTCTCAAAG ATTCTGTTTC TTGTTTCGTA AGATTCTGAA 360
ATGCTGATGT TCCAAAATTC TGAGATGGTT TGTTTCTAAC GTTCTGCATT TCTAAGTCTT 420
TGACCACTGA GGGTGTCTGT CAGGCGCGGC TTCCTATGCC CTCTGCCCCC AGGTTCTCCC 480
AACCTCTGGG ACTGGGAAGG AGGGCAGTGG GTGGAGGGGG CTGGGCCATT GCCTTGACAT 540
GGCCCACATT CAGGGCTGGC TGTGGCAGCC CAGGGCCCCA GAGCCAGGCT GGAACTAGGA 600
TACCAGCCTC CAGGTCCCAG GCCTGCGTCA TCTCTGCGTG CCCTCGGCCA GGGCCACCAG 660
ACAGAGACGG GCTGGTTGAG TCATCCAAGG GCTGGGGGTG GGGCAGGCTG TTCCGGCCGG 720
CTCCTGGCTG GCAAGGCAGG AGTCCTACGC CCAGCTCTGC CCCTAACATG CCCCGTGCCC 780
TTGGGCAAGC CTCAGCATCA GGGCTGCCAC GCGTTCGGTG GTGCTCGAAG CCCTTCAGCG 840
TCAGGGTCAG TCCTTGGGAG GGGGGCTGTG GTCAGGCTGG TGGGCTGGGC TAGCAGTGGC 900
AGGACAGGAG 910
|
