Tag | Content |
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EnhancerAtlas ID | HS098-19293 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr15:51435710-51436810 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr15:51436394-51436405 | TTTTATTGCTT | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I051144 | chr15 | 51436397 | 51436598 |
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Enhancer Sequence | TGATATTAGT TCAGTTCTAG AGTTTTCCTT AGGTTTGTGT TTATATAATA CATCTTTTTC 60 CTTCCTTTAC TTGACCTTCC TGCATTGTGA TATTTAGATG TGTCTTTTAT AAGCAGCATA 120 TAATTGGGTT TTATGAAAAT TTCTGTCTTT TGTTTGATAT ATTAGGGCCA TTTACATTTA 180 ATGTAAATTA TTGATGCACT GGATTTAATT CTACCATCTT GCTTTTACTA TTTTTTTTTT 240 TTTTTGGTCC CATCTGTTGT GTATTTCTTT TCCTCTTTTT TTGTTGCCTT CTTTTGGAGA 300 AATCAAGTAT TTTTAACATT ATTATATTTT TTATTTTTGT TGAAGTGAAA TTCATCTAAC 360 ATAAAATTAA CCATTTTAAA GTGAACAACC CATGGCACTT CACAATGTTG TATAACCAAC 420 ACGTCTATCT AATTTCAAGA CATTTTCGTC ATTCCAGAAG GAAATCCCAT ATCCGTTAAG 480 CAGTTGCTCC ACAATTTTCC CTTTCCCCTG TCCCTGGTAA CCACAAATCT GCATTTTGTC 540 TTTTTGGATT ATGGACAAAT CAAGTATTTT AATAATTCCA TTTCCTCCTC TAACCACTTG 600 TTAGTCATAC ATTATTTTAC TGTTCTTTTA GTGATTACCT CAGAAATTAC AACACACATT 660 CATGATTTCA CTGTAAGTTA GTACTTTTAT TGCTTCTAGG GCAAAGAAAG CATTTAGCAC 720 ACACTCCAAT TTTTGTCTCC TCAATTCTGT GCAGCTGCTG ACAGCTAAGG TGAGCTTCCT 780 AAACTCTGAA ATACCATCCA TCCACTTACA GCCAACTGCT TATGAGTCAG CAAGCACTTT 840 GTTGGGGAAA GTGCTGGCAG ATTGTTGAAC TCACGTCAGT CTGGTTCCCT TCCCCCAAGG 900 TCCTATCTCC TCAAGTCCTG GCTGACAAGG CATCTCTCCA ATACTTTTTG TGTGTGTGCG 960 TGGCCTTTTG TATCGTCTAG TTTTTTAAGA TATTCTCAGT GGGAGGTTGG TCTTCAACAA 1020 GCTGCTCTGC TGTTATTTTT TTATTTTGTA CGTTTTATTT TTTGAGACGG AGACTCACTC 1080 TGTCGCCCAG GCTGGAGTGC 1100
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