Tag | Content |
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EnhancerAtlas ID | HS044-03930 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr13:96193000-96194090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYCN | MA0104.4 | chr13:96193264-96193276 | GGCCACGTGGCC | + | 7.22 | MYCN | MA0104.4 | chr13:96193264-96193276 | GGCCACGTGGCC | - | 7.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 96193155 | 96193520 | chr13 | 96193580 | 96193928 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I095540 | chr13 | 96192765 | 96193893 |
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Enhancer Sequence | CTTGAGTAAT TGATATAGGG AGTGAAGTTT TTTTGGGGGT TGGGGAGAGA CATTGCTTTT 60 TTCCACTGAC ACTGACGATA CCAGTTTACT ACTATGTGAC ACTTTTTGCT TGAACTAGAA 120 GAGATAAGTA GTATTTTTCA AGTTTTGAGG TTTGGGTGTT CTGCTCTTGT GGACGTGTCA 180 TGTTTAATAA AGCTTGTTCA CAACTACTGG CTTAGGAAGT GGCTTGCAGT TGACAAGTAT 240 GTGACTTGGA ACACTGGGTG GAATGGCCAC GTGGCCCAGT GGCCCAGGGC CCACACTGAG 300 AATGCAGCAG CTGTGCATGC TAAATCTGGC TCTGTCATTA ACCTGCCGAG GGACCTTCTA 360 CAAATGCTTA ATTCCAACCA TGAAAGCAAA CATAGGCACC GATGCTTGAG AATAGTTGTA 420 AAGGAAATCA GGCCTTGTGC AGAAAATAAA CGGAACTCGT CTGCCTTTCC TTTCTAACAC 480 TTGTTGGAGG CAGGGAGGAA TTCAGAATGA CCAGGCTGCA AGTTACTGTT CTTTGCTTCT 540 AATTAAGAGG CAACTATACG CAAGTGAGCA TAATTAGGAG AAACTGGGGC AGCTGGGGCA 600 AGTATGGGCA AAACTTAAGC CAACTTTGAA AACTAAAGGG CAAATCTCTG GAGTAGTGAG 660 AAAGAGATTT CTCCCTGGTT CCCTCTCTTG CTAGCTGCAT ATGTGTACAA TGACCCCATC 720 ACACTCTGCG TCTGAGCCTC CCTCTCTTTC TAGTTTTTTT CTGTTTCCCC TGTTCCTTCT 780 TGTTTTTCCT TTGTTTGCAC TGTCTGAAGG GGAGGAGGAG ACAATATTCT CCCATTGCAT 840 TTTTTATTAC TTCCTCTATC ACTAGATCTA GGCAGAGCTT TTGAGACTTG TTTTGACACA 900 CTCACTTTTT TTCCACACTC ACTTTTTAGA CGGGAAAAAT GGGCCCAATC AAATGTAAAT 960 GAACAGCAAG GTAGTGACAG CTAGAATAGA TGGCAGGTCA TTTAAATGCC AGTCCAGTGC 1020 TATTTCCATA CATTGCACCC AAGTTTAATG ATTAAGAACA AACAATAACA CTCCCAAGGC 1080 TGAACTGACC 1090
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