Tag | Content |
---|
EnhancerAtlas ID | HS050-24826 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr16:3898960-3900290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYCN | MA0104.4 | chr16:3900212-3900224 | GGCCACGTGGTC | + | 6.52 | MYCN | MA0104.4 | chr16:3900212-3900224 | GGCCACGTGGTC | - | 6.52 |
|
| 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 |
GH16I003848 | chr16 | 3898951 | 3900980 |
|
Enhancer Sequence | TTTCCGACAT TCACAGGGTT TTGCATCCGT CACCCAACGC TCTCATCAAC CTTCTGGGGA 60 AACTGTGTTC TACTCTTATT CTCCCTCACC CCTACTTGGG ACTAAACAAA TCCAAAGAAC 120 AGCCCAAACT GATTTTCTGT TCTGGGATGT GCTGAATTCC ACTGCCTGAA GACGTGCCTG 180 GTGGCTGCTG TTGAGAAGCC TCTGGCCGCA GAGCATCCAC AGTGTTTGTC ACTTCAGTGG 240 GAATAGGCTG CCCTTCCTTC TCTGTGCTCC TGTCAGTCCT GGGCTTTTCC AGCTGTCTCA 300 CATCTATCCA GGCATCTGCC TTCCCCCTTC TCCAAGTCCA GTTCCTACTC TAGAAGGCAG 360 CTGCAAGGCT GGTGGCTGCA AATCCCAGTC CAGGCCTTTC CCTAGCAGAG CTCTTGGCCG 420 TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 480 TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG ATGTGCGTGA 540 CCTTGGAGCC ACCTGGAGGC TGCTGCTTTT TTTTTTTTTT TTTTTTTTTT TCCAAGAGAC 600 AGGGTTTCGC CACATTGCCC AGGCTGGTCT CAAACTCCTA GAGTTGAGCT ATCCACCCAC 660 CTTGGCCTCC CAAAGTGCTG GGATCACAGG CGTGAGTCAC TGTGTCCAGC ACCCATCTGG 720 AGGCTTCTTA AAGCCCAGGC CCCACGCCGA GCTTCTGAGT CAATAAAGAA GTCTGCATTT 780 CTAACAAGCT TCTAGGGGAT GCTGCTGCTG CTGCTGGTCC AGGGGACCCC ACTTGAAGAA 840 CCACTGCACT GGTGTTTCCT CTGGGACCCG AATGCCTGTG CTTCTCCCCG GCTCTGCCAC 900 CTCTTCCTTG TTAACATAGC AGGGAGTGAG CTGACAACCC TGGAACACAG CTTTCTCATT 960 CAGTGAAATG GATACTGTGC CAACAGATAC TTCACTGGAT GGCCACAGAG GAGCATACAG 1020 ACCAGTGATC ACCTCCTCAG TGGGCAGTAC ACAGGCAGAA AGCAACCTCT ACCAGGTTCA 1080 CGGACACATT AGGCCCTGTA CTTTCCAACT GCCTGACCTG CAAGCTGTCC TACTTCTTTA 1140 AGAATTCTCA TTTTAAAGAC AGAAATGGGG CAGAGATCTT TATCCTAGAA AGAAATCTGT 1200 CTCTTCCAAG CATGAGTGGC ACGTGGAGAG CCCAAGAGGA AAAACAGGAG TGGGCCACGT 1260 GGTCCCATTT TACGCATTAC TCGGAGGGAA AGCCCGCGGT TAGGTAGGAA GTATTGAAAG 1320 TGCTTCAGTT 1330
|