| Tag | Content |
|---|
EnhancerAtlas ID | HS037-05830 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr11:2812450-2813700 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr11:2813305-2813316 | GCTTCCCGCCC | - | 6.02 | | Foxa2 | MA0047.2 | chr11:2813152-2813164 | TGTTTACTTTGC | + | 6.27 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_31950 | chr11:2811885-2814051 | Gastric |
|
| | 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 |
| GH11I002791 | chr11 | 2812631 | 2813630 |
|
Enhancer Sequence | GGCCGGAGCC CGCAGCGGCC GAGCCCTCAC TGGGCACCGT GTGCGGATCT ATAATCGACA 60
GCATCAATTG CGGGAGTCCG GCTGGGCTGG CCGCCTGCAG GGGCCAGGGC GTGAGGGCGG 120
TGCGGAGCCT TGTCTGTGCG GCAAACCCTG CCTGGCTGCC CTGGCCAACC TCAGAAAAAC 180
ATGTATTTTG GTCAAAATGG GCCCCTTTTC AAACTTGTCA CCCCGTGGGT CAGGGCACAG 240
CCTGCCCCCA GCCGGTTCTG CATATTAAGC AGTGGCTTGG TCACCATCAA AAATAGATGT 300
CCCGACCCGA GCCTCCCCTC CCTCCCGGGG AGGGGACCTG GCCGTGCCGG CTGGGCTGGG 360
AAACCGCGGG CGGGGAAGGA AGGACGGGGC GAACCGGCGG CACAGGCCCA GCACGTCCCG 420
GGCCCTCCCC GTCAGGTGTG GACCCCGAGG TTGTGCGGGG GCTTGGCGGC AGCTGCGGGT 480
GGGGGTGGGG GGCCCGGGCC TCCCGGGCTC GGGTTCTGGC CCCAGGTCAG AGGTGGCGCT 540
GGCGGCAGGT GGATGCCCAG GTCCTCGCCG CGCCGCTCCG GGCGGTGGGA CCGGCTTCCT 600
GCCCTGGCTC CGAGCCCGCA GGTGGGGGCT TCCGCCTCAC TTTGGACGGT GGCGTCCACA 660
AAATGGCTGA CGCGGCGCAC GGCCGTCCCT GCACGGAGCC GGTGTTTACT TTGCCGCGCG 720
AACAGCCTTT CGTTGCCCGG GTTCCGAGTG CTCCAGAGGC AGATGGAAAT TTTTGTGGAT 780
TAAACACGGG GCCGAGGCGC GCTGGGCTGT TTGGGTTGGC AACCTGAGCC CTCCCCACCC 840
CGTTCCGCGT CCGCTGCTTC CCGCCCTGGT CCGGCGCTTC CATTCATGCC TTCCCGGGTC 900
CCTCCGCCAC CCCTGCAGGC CCGGCGTCCC CTCCCGCACT CCCGCGGCCT CCAGGGGGTG 960
GCCCTGCAGG CCCAGAGCAG CGTGGGCCTG AACCCCTCTC CACGTGTGGA AGACGCTGCA 1020
GCAATAGGAA GGGGCTGCTC CTTTGAGGGC CCTTCTCAAA CCTGGAGCCC CTCTGGCCGC 1080
CAGATCTTTG TCTGTGAAAC AGCAGCCAGT GTGTGGACCA GGCAGGAGTG GATGGGGTGT 1140
GTGCCCACAA GTCCAGCACC CAGAAAACCC CCAGCACACG GTCCCTTTTA CAGTGGCCTC 1200
TGCTCTCAGG AAGGTGGAAA GCGCCAGGTG GATAGGAGGG ACGGGGCCGT 1250
|
