| Tag | Content |
|---|
EnhancerAtlas ID | HS050-03697 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:112462450-112463690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr1:112463036-112463048 | TCTAAAAATAGC | + | 6.52 | | MEF2B | MA0660.1 | chr1:112463036-112463048 | TCTAAAAATAGC | + | 6.22 | | MEF2C | MA0497.1 | chr1:112463034-112463049 | CTTCTAAAAATAGCC | + | 6.31 | | Myod1 | MA0499.1 | chr1:112463208-112463221 | AGGGGCAGCTGCA | - | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_08557 | chr1:112459974-112465123 | Brain_Inferior_Temporal_Lobe | | SE_33589 | chr1:112460773-112465003 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 112462702 | 112463337 | | chr1 | 112463593 | 112463664 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I111919 | chr1 | 112462399 | 112463621 |
|
Enhancer Sequence | TTAGGATTCA AACCGATTTG AAACAGGTGC CACTCATTTC TCCAGGCTCT AAGCAGCATG 60
TGAATGAATG ACACTGCCCT TGAAGGGGCC AGCCTGGATG GAGGGAGATG GGGAATGTTT 120
CAAGGTTCTC ATTAGGAGCT CAGGTTGCTG CTATAACATC TCCCTCTCGT CTCTACTTCT 180
TACTCCTCCT TAGGAACAGG GAATGAAGGA CAGCTTTGCC CCCAGGCCAC TGGACCAATG 240
ACCACCTGAT GCCCTAGGGA ACGTAAGGGA GTGGGAGAGA ACCCCACCTG GCCCCTCCAG 300
CTGGTAGACA AAATGGAGGC CTCCAGTTCC TGCCAATGTT CCATCTGGGG AAGGTCATGC 360
AGACCCTGCA CTCACAATCA ACTGGGCAGA AGCAAACCCT TGGGGAGGGC AGGGCATGCA 420
GCTGCATGGG CGCCATCTGC ACGTGAGTCC TGACCTGGGG GAGGAGAGGT CGTCTTCCTA 480
CAGCCCGACC TCACACATTC CTTCAGCATC TCTGGGAAAT AATCACACTC CCCACACTGA 540
AGAAACACAG TCAACAGATT CTGGTTTCCT AGATACGCCA GTGGCTTCTA AAAATAGCCA 600
GGCAATGACA AAGCAAATTG GCATATGGAC TGCAAATAAT TCCAGTACCA GCTTGCTTGG 660
CAGCACTCAA GCCTCCCAGT GCTGGGTGCT TCCTCCTCTT CCCTCCCGTT TCTGAAACAG 720
TCTCTTGCTG CTGAAAACCC CAGGCCAAAT GTGAGCGAAG GGGCAGCTGC AGCCCCTGTG 780
GGGGTCCAGC CCAGGGCTGG TGCACTCTGC TGGGCTGAAG CCACTCCAGG CTCCTCCTAC 840
TTCCCTCCTC ATCCACTCCA CATGCTCTGC GGGTCCCCAC TCACGCTGAA GGTCCACTGC 900
CAGTCAAGCC ACCGGTAGCT CTGTGTGTGC CCCAACACTC CCAAGCAACC AACCTCTTCC 960
TTTGTGTAAC CAAGATGGGG CTGCCTTGAC CTTCTCACTC CAGGACTCCT CTTCTGGGGA 1020
TAGGCCACTG TCCACGGTAC CTCTTACTTT GACTCAATCC CTCCCCTGGC CCCAGCAGGG 1080
AGTCTTTGCA AAGTATCCTC TTTATCTGCC TTTCTTCATT CTCTAAACCC TGTGTATGGT 1140
TGTGTGCAAT GTGCCAGGCT TTGTGGTGGG CAGCATACCC AGCAGTGGGA ATTCCAGGGG 1200
GAAGAAGACA GGTCTGTGGC TGGAAAGAGT AAGGAAAACT 1240
|
