| Tag | Content |
|---|
EnhancerAtlas ID | HS134-00041 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:3246840-3248150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr1:3247125-3247140 | CTGCTGCCTCAGCAG | - | 6.04 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_01548 | chr1:3245969-3247500 | Aorta | | SE_40807 | chr1:3243784-3248075 | Left_Ventricle | | SE_65787 | chr1:3246865-3248824 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I003327 | chr1 | 3244561 | 3248729 |
|
Enhancer Sequence | AGAGCAGGAG GCCCCGGACT CTTCAGAAAC TGAAATTGGA AATTGGAGAT GCTTTTTGTG 60
TCTAAGTCTT CATCCTTTAA TTGTCACTTG GCAAGGCGTC CGCTCAAGGC CTTCTCTGGT 120
GGCCTTGTAA GAATGCAGGG ACAAAATAAT GCCAATGACA GTGGCCCTGA ACAGAGAGCA 180
GAGGCCTCAC ATGGCGCCCA TTCTCTTCTG CTCTTCTTCC CATCTGCCCC TCGCTCCCTA 240
GGCATCCCCA CCACATCCCC TCTCAGCTCA GCGGGGGCTG CCTGGCTGCT GCCTCAGCAG 300
GGGCCACTTT TCTAATCCTG GGGTCTCAGA CACACCCTTG TGCCTCCACC TCAAATCCCA 360
AGGCAATATC TGCCCCACAG CCTCAGGACC CACTTGCCAG TCCAATGGCA GAACAAACAG 420
CCCAGAGAGG TTGTTGGGGA GGGTGGGTTT TTGAGAAGCT CTTGCAGTCA TCACGACAGA 480
GCCTCCTAAG CGAGGGCGAG TCAGACCCCA GAAACCTTGG ATCTCTGGCC GAGTGGAGGT 540
GCCCCTGGTT CATACAGGCC CGAGCTGCCC TCAGGGCCCT CCTCCCTCTG CCTCCAGCCA 600
GAGACTTTCT CACCTGCTGC TCTGGGGCAG AAATCGGAGC CACCTGGAGT GTGCCTGCCA 660
GGGTCAGGGG GTGAGGAGAT AAGGGCCTGG CTTTCAGCTC ACAGGAAGTG GGCCTGAATG 720
CGGAGAATAG CAGCAATTCC ATCTGATAAG GCCCCGCTAA ACCCCACATT GACAGGCCCC 780
ACCGCCCACC CGGGCTCCAG GGGCCAAGGG AGGGGCCGCC AGCCCACTCA GCCCTGCAAG 840
CTGCTCCTGC CCTTCGGCCT GGGAGGGGGC CTTCCTCTGC CCTGGCCTCC ATACCTCCAG 900
CACTTGGGTG GGCTTTGATC ACCTGTGGAT TGCAGGGGGG AAGCTGCGCA ACTTCTCCAC 960
TGCCCCTTCC CCCTGCCAGC CTGGGGGGGG CGCATACTGG GAGTCTGGAG AAAGGCAGCC 1020
CCCCCCCGGC ACACTTGGAG GTGGGGGGCA TTCCTAGCAA CCCCCTTCAT CCCCGAGTCC 1080
ATTGATGAAT GGACCCTCTC TGCAGAGAAC ACAGCCCACC AGGGAATCCC CCAGATCAGG 1140
ACCCCAGGTA CAGAGGGGTT CAAAGCACGT TTGTTGAATG AATGAATGAA TGAATGAACA 1200
GATGAGCGAA TAGCCCAGGC TCCACTTCCA GGCTGAGTAA CTACTACAAA GGGACACACA 1260
TGGGACGGGG GCTGCCAGGA GGGACTTCTC TGAGCCTCGT TCTTCAAGGA 1310
|
