| Tag | Content |
|---|
EnhancerAtlas ID | HS050-11967 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:45067280-45068660 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr11:45067769-45067780 | AGCCTCAGGCA | + | 6.32 | | ZNF263 | MA0528.1 | chr11:45068427-45068448 | TGTCCTGCCTCCTCCTCCTCC | - | 6.68 | | ZNF263 | MA0528.1 | chr11:45068430-45068451 | CCTGCCTCCTCCTCCTCCTCC | - | 6.82 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_33426 | chr11:45060876-45080805 | H2171 | | SE_66866 | chr11:45060876-45080805 | H2171 |
|
| | 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 |
| GH11I045045 | chr11 | 45066690 | 45069025 |
|
Enhancer Sequence | TGCCCTAGCA CACAAAGTAG GTGCTCAAAA AAGACTGGAG AATGAGTGAC TCTATTATTA 60
TAGAATTACG TTCTCTTTTT TCCTTTTACA TGAATGAGGG AACTAGAACC CAGAGACGGT 120
AAGTGTTCAG CCAGCCACAC ACAGTGAGTT CCTGCCCACT GAATAACTTC CCTCCTCCAC 180
TCCTGTCCAC TCTGCTCCCT GGTGGCTTGT TGGCAGCAGG GAACTGATTA AAACCAATCA 240
GCCAATTTAC CCTGGAGAAT CCGGGATGTG GTGCTCCAGG TCGCAGCTGG CATGGGCTGA 300
GACTGCAGGT GAAGGCATAG GTGTCTGTGC TGCCTCCACG AGCCAGTGGG GGTGGACGGA 360
GATCCACGGG GTGCGTGAGT CACAGGATAT TGCTCAAGAT GACAACAGAC AAAAAACAGA 420
CTAAAGCCCA GGAGACGACC AAGTGATTAC TTTTTAAATC AAGAACTCTT TACAGATTTC 480
TGCTAGGCCA GCCTCAGGCA ACAGGGGTCA AAGAAGAGTC TAGCTGGGAA TTGTAAAAGG 540
AAACAGGAAA CTTGTTTCCT GCCGATTGGC AGGAAGTGTG AGCAGGAGTG GTTTATATTT 600
GGAAAGAGAA AGGTAAGGAG GGGGACCTAG GGAGTCTCTG TGGTCTGAAA ATGCTGTTGA 660
CGTGGACAGT CCACCTTGCT GAGCTCAGCG TTGCCCCGAT CTCCTGGGAG TGAGGACGGG 720
CGCGGTTCCG ATGCTTCACA GCGTGAATCT GCATCTTTTA TTCACCTTCT CTAAGCCTCA 780
GTTTCCTCAT CTGCACAATG AAGAGAAGGA AGCCCACCCC CCACCCCCAG GAGATGTGAA 840
ATGTCAATAG ACCAGTGTAT GAAGTGCCCT GCACATAGCC GGTGCTTAGC AAATGGTAGC 900
TTATGATATT ATTGTCATCA AAGTCTCCGG GTGCTGTGAA AGATAGGAAG GTCAGAAAAT 960
ACTTTTCTGA GCTCGTGACA AACTGGGCCT TGGACGAGCA GGCAAGGTGA GAAGGAAGCG 1020
CCAGGCAGAG GGAACAGCCT GACCAAAGGC TCAGAGGTGG GACGGGGGGG AGCTTATTTG 1080
GGCCACACAA CTGGCAGGTC CTGATTCTCA CCCCACTCCC AACTATGACT TTGGGAGGCT 1140
GTCTGTCTGT CCTGCCTCCT CCTCCTCCTC CCAATGGCTA TCTCGGTGGG AGTCCTAGGG 1200
AGCAGGGTGA GGGCACTGGG GGAAGGAGAG GCAGGTTTTG GCGGCTCGGG CAGGTGGCAG 1260
TGGCAAGGGC CAGAGAGAAC AGGCTGTGGT CTAGTTAATC AGCCCGGACA CATCTGATTA 1320
CCAAGAGGGG ACGAGGACAG TCCCAAGGAG GGGCAGGACA TCCTACATCT CTCCATCTAG 1380
|
