Tag | Content |
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EnhancerAtlas ID | HS044-10688 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr5:133155630-133156720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GCM1 | MA0646.1 | chr5:133156166-133156177 | GTACCCGCATA | - | 6.32 | ZNF263 | MA0528.1 | chr5:133155839-133155860 | CTTTCCACCCATGCCTCCTCC | - | 6.29 |
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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 |
GH05I133819 | chr5 | 133154909 | 133156506 |
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Enhancer Sequence | TCCATTTTTC ACATGAGGAG GTGGCCGCTC ATAGGTACAC TGACTTGCTC AAGGTCACAC 60 AACTATAGAA AACGGCAGAA GGAAGACTCA AACTTGGGTC TTCTTGCTCC AAATCCTCTT 120 CCCAGCACGG CACGGCGCAG GTTCTGCAGT GCCTCGTGTC AGCAGGCCTG AGGGGTTGCA 180 GTCGCAGAGG CCTGTGTCCT CCAGGGCCCC TTTCCACCCA TGCCTCCTCC CCCAGAAGTC 240 CTTCCCCACA GAGCAGCACA GCTTCCCCGG GCCGGCTGGG AGGGTCCAGC TGTCACGCTG 300 CATTTCTCTC CACTTATTTC TGCTTCCCTC ATGACCTCCG TTTCAACAAG ATGTGCCTTT 360 AAATTAGATC CCAGAAGGAA CTTCAAGGCA AATTCCCACA TTTGTGACGT TTATGGAACT 420 TGTCATTGTT TATGCTATTA TAGTGCCATC AGCTGTGAGG GCACATTCTT CCTGGTTACA 480 ACATTGTTTT TCTTCCCTTT GGGAGGGAAG CACCCTTGAA ACCAGAGGCT TGTCTGGTAC 540 CCGCATAACC TCCTTATTCC CTACTCCACT TATGTATATT TTTCTCTGTG GATCATGTAC 600 ATGGTCTTTC AATTTCATGT CTGTGATTTA TACATTGCAG TGTTTGCTAT CCTCTGTACA 660 ACAGAGAGAA AATAGTTACT TTACAGGAAG AACAATGTGA CAGGCTCCCA ACTCTGCAAC 720 ATTCGCCAAA CCCGGAGTCA AGTGCAGCTT TAGCTTTCGT AAGTGTTGGA ATTTAGGCTT 780 CATGTTTCAC TTACTCTTGC AGGCAACTGA AGAGCAGAAA CCAACTGTTT GTGGCCAGCC 840 CTGAGCTAGG GACCAAGGAA GAACCAAGAC ATGTAATATC TTATATCCTC TCCCTGGGGA 900 CTTCTCAACT TGTTGGAGGG AAAAAAGATA CATTAAACTA TTAGAAAACA ATGCAATGTA 960 TGTTATTGAT AGTGTATTCT AATAAATAAG CTGCTATTTT CAGAAAAGGG TGGTAATAGG 1020 AGATGTTTCG GATTTGAAGG GAAGTTATAC AAGAAAACAT TGATTGTGTT TGAAAACTAT 1080 ACATTTTCTG 1090
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