Tag | Content |
---|
EnhancerAtlas ID | HS134-00520 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:22677130-22678460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr1:22677408-22677419 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:22677408-22677418 | GCCCCGCCCC | + | 6.02 | MYC | MA0147.3 | chr1:22677946-22677958 | GGCCACGTGCTG | + | 6.37 | SP1 | MA0079.4 | chr1:22677405-22677420 | CTAGCCCCGCCCCCC | + | 6.67 | SP2 | MA0516.2 | chr1:22677404-22677421 | CCTAGCCCCGCCCCCCT | + | 7.39 | SP4 | MA0685.1 | chr1:22677405-22677422 | CTAGCCCCGCCCCCCTC | + | 7.14 | ZNF263 | MA0528.1 | chr1:22677426-22677447 | CCTTCCCCTCCTTCCTGCCCC | - | 7.23 |
|
| 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 |
GH01I022349 | chr1 | 22675891 | 22678331 |
|
Enhancer Sequence | TAGATCACGC TCCTAAATAA GCTGAGATTT ATCCCCGGAT CCTCTCCGCA GGGGCCAGCT 60 CCATAAATCC TGCGCGACCC TGTCCCCTGG CCAAGGGATG GGGGAGGGGA GGCCAGAGTG 120 GGGAGGGGCG AGGTGTAGCA GGGCAGTTCC AGGTACAGAA GGATGGAGCT GAGCAGGGGC 180 TGCAACAGGG GCCAAGAAAG GGGGCAACAG TGGGCCCAGG CGGCCTGCCC CTGACCTCCC 240 GCTCACTTGC CCAAGCTCCT TACCCCAGCC CTCTCCTAGC CCCGCCCCCC TCGCATCCTT 300 CCCCTCCTTC CTGCCCCCTC CCCCGCCCCC ACCCCGCCCC CACCCTCTCT CCTGGCCCCT 360 GCCTGCCTAT AATCTCGTTC TTGACATTAA AACAATATAA TGACTCCACT GCTGGAAAAG 420 ACAAGCATCT GTAGCTTCTA AATGGGCAGC TCAGCCACAG CTGAAATTGC CTTTGTCTGT 480 GGGATGCGAG GGCCCTCTGC GAAGAAAAAT GTATTGTAGG AAAATGCAAA TTTACAGGCC 540 AATAAATTAG GGGGTGATTA GTCACGTTGC AATCCTTCTT CAAAGGATTC TTTAAAAGCT 600 AAACTCGTTC ATTTAGGTGT CTGTTTATAG CTCAGTAACT TCCAGACAGA GAGGCTGGGA 660 GGCCCCACGG GACACAGCCA GGGAAACTGG GAAGATGCAG AGAAAAAGGG AGAAGTCTTC 720 CGCGCTTAAC CAGCTTGCGG CTAAAACATC CCAAAAGGGT CCTCCCATCA CCTGGCTCGT 780 GTCGATTCAA AACGGGTTCG TCCAGCATCT ACTACAGGCC ACGTGCTGCC TCCAACACGG 840 GGGAAGCGGC CAGACAGGAA CCCCGGGCTC TCATGGCGTT TACAGGGTGT TGGGGGGCCG 900 GGAGGTGGGG AACAGGGAGA GTCACATTCA TTCGATTCTC ACTGGCTCCA GGTTGACAGG 960 ATGTGATTTA CAGGCGGCTG TCTCTGAACA CACTCATGGC CAAATGTCAG GGACGGTCCA 1020 TATGCACGAC GGCGGAAGGA GGGGTGAATA ATCAAAGATG GGATTTGAAA AAGGGCAAAA 1080 CAAGCATAAA TGCCATGGCT TCTCCAGCTT TTCCCAAAGG ACAAACACAA AGTTCGGCCT 1140 TCACTGAATC AGTGTCCTGG AGTCCCCTGT TCTGTGTCCT GGATGAAATC CCGTAGCCAC 1200 TCAGCACTTA ACGCCATTTA CTGCAGGCAG ACAGGGAGAG ACCAGCTTGC GCCCCGGCCA 1260 CTGGGATCGT GAAGGAATCT CTTCTGAGGG TGAAGTAAGC TCGGCTGGGT CGGCACTACT 1320 CGCCCTCCTT 1330
|