Tag | Content |
---|
EnhancerAtlas ID | HS050-06734 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:247523540-247525090 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr1:247524474-247524486 | GAGCACGTGGCC | - | 6.92 |
| | 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 |
GH01I247359 | chr1 | 247522981 | 247525159 |
| Enhancer Sequence | TGTAGAGGTG TGGTCAGCTC ATAAAAGGGA AGAAAGTTTT GTTATGGGGA AATCAAAACT 60 TAAGTGGGGA AGAGGACGGG GTATAACTTT GTAAGGGGGA TAATGAAAGT TAGGCGATGT 120 CCGGGAAGAT TGTAACCCCA CAGTACTCAA CCAGTGAGGA ACTGGGGGAG GGACTTGTGT 180 GCTAGGACAT AAATTACCCG TTGTGACCGC CCTGGTTGTG CCTGCTCACC AGACACCCGA 240 TCTCGCAAGA CCGTTATGAA AAGTCTCCCT TTCGCTGTTC TTTGTGCCTC TAAGTCCATT 300 CTTTGGGTTT GGATGGGTGA GTGTGTTTCT CACAAATGCA CCACTGCACC CCTGCCTAGG 360 TGACAGAGAC AGACTGTGTC TCAAAAAAAT GAAAATATCA GGGAACTCAA TGCAAAAGAC 420 TGCGGCGCTT TAGACTTGAG AGTAACCTGC CCATGACCCT TGGGGCTCCG TGAGGAAGAC 480 AAAAGACCCC CAAAAGGAGG GTGTATGGCA CCTTTTTCTG GTTTCTCAAG GGGTCTCAGG 540 ACTGCTAGAA GTTCCCTCTT GATTTCTTCG TGTGTTATTG AAGGTGGCAG AAAGGAAGAA 600 GGGCCAACAG TAAATGGGAA AACAATTCTT AGAGGGCTCA ATTTGGGAAG ATTTTAAACT 660 TCCCAAAAAG GCCAAGGATG TTTTACATTT TTCTCAGTAA AAATCATGCC GACAACAACA 720 ACAACAAAAA AGTGAACAGA TGGAAGGAAC ATAAAATTGC TTTTTAACAA AATTTCAGTT 780 GACTGAAAAG AATTCCCAGG GTAGGAACAG GATCCAAAGA GAAAAAGCAT TGCTCTATAT 840 ATCTGCCAGG GAAAAATCCC CCAAAAACTA AAAGAAAAAA GAAAAAGCAG AAGGGTGTGT 900 TGAAAATACA CAAGCAGCAA GCTTTCTGTT TCATGAGCAC GTGGCCTAAC ACTGGAGTGG 960 AAAGAATTTC GGCTGTGGAG CGCTCCCACC CGCTCTGCTC ATGGGAGGAG CCCTGCCTCT 1020 CTTCAGCTTC CCAGCAGTGG TGGGAGACAC ACGTCTCTTC TGCCCACGGG AGGAAGCGAG 1080 ACAAAAGAAA AAAGTTGCTA TCACACTCTA AATACAAACC AGTTTTCTAT CAAAGGTATA 1140 CCTGAACAAA TGACTCAACG CCAAGTGAAA TAAGCACCAA GGAGACCAGA ACCAAGAAGC 1200 CTTTCACGGC TTTCACCAAG GTCTCCAGAG AGGAGGCAAA AGTTGCAACC CTGCTCAGAT 1260 CCAGACCACT CCAGGCAGCT CAAATAAAGG AGAATTTTAG TAGCTGCAAA TGGGGCTACT 1320 GTCTGGCCAT ATTATCTAGG GTTTCAGCCT CTCAGCTGGC TGACTGCACA CAAAGGCCTG 1380 ACAACCCGTA TCTCCCACAG ACGGAAGATT GCATGGCAGT TTGTAAGATG GGAAGTCAAA 1440 AGCTGTCTGT GGGAATAGAC AGGATTGCAA AGTGAAAGGG TACCCCAAAA GGTCAGAGTT 1500 ATGCAAATAC CAAACTAACT TTTTACAAAT GTTTCTATTT GTTTTGTCCT 1550
|
| |
|
|
|