Tag | Content |
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EnhancerAtlas ID | HS044-08390 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr21:43990830-43991810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr21:43991174-43991190 | GGTCACCATGGAAACG | + | 6.19 | RFX1 | MA0509.2 | chr21:43991174-43991190 | GGTCACCATGGAAACG | - | 6.2 | RFX2 | MA0600.2 | chr21:43991174-43991190 | GGTCACCATGGAAACG | + | 6.36 | RFX2 | MA0600.2 | chr21:43991174-43991190 | GGTCACCATGGAAACG | - | 6.45 | RFX5 | MA0510.2 | chr21:43991174-43991190 | GGTCACCATGGAAACG | - | 6.14 |
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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 |
GH21I042570 | chr21 | 43990514 | 43991761 |
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Enhancer Sequence | ACTAGGTGAA AAAACACATT TTTCTTCATA TTCTCAAAAT GAGAGGGAAG CAGAAGTCTG 60 TGGCTAAGGG TGGAGACCCT GCGTCTGTGA ACAGAGGCCA CTGCCCACCA CTGCCCCCAA 120 GCAGGTGGAG GGAGGCACAG TTCTGAATGC CTTTGGCCCC TCACAAGGAA GGTGGCACAC 180 ACACCGGACC CCCTCTGGCC TTCTGTTAAC CTGCACCAAG TCCTGACTGT CCGCGGAGCT 240 GCCGCGCCCA CCTTGATGGC TGCTGCGTTA CACCAGAGGC AGGACCAGGA CCTGACTCCT 300 CCAGGCTCCA CTGCCCATCA GTGCCTGCTG CCTGCTCAGT GAATGGTCAC CATGGAAACG 360 GCGCTCAGGC CTACCCACCC CCACCACCAC GCCTTGGTCA TTGTTCCTTC CATGAGTGAG 420 TGCTGCCCAG CAAGACAAAG TACAGGCTCC AGTGGGAAGG CCACCATGTC AGCCAAGTCC 480 CTTCCCGAAG GAGGTGCCCG CATGCTTATT CAGTGTCACT GTCCACTCCT TGGCAGTGAC 540 TCGGGTGGAG GCGAAACATG ACTAATCGTA AATCACCCCT GCCTTCTCCC AAGTGCCACA 600 CGGTTTGTTG ACACGGTGTG CGCCTGGGGC GTTCACAGTG CTTAGAATCG CAGAGGTTGC 660 CGTTTCTGTA CATTTCATGC AGAGCAATTA AATAGGGCAC TGCATTTTTC TTCAAGTTAA 720 TTTTTATTTA TTAAAGTAAA ACATAATGTA CCTTAGAAGC TAGACAGTCC TACAAGCTTA 780 TTATGTTGTA CAGCGGCGTT CCGTCCCCCT CCCCAGCCCT CTCTTTCTAG AGGCAGCCAA 840 TTTCAGCTGC CTCTCTCTGC TTACCTACGT ATTTCCATGT TTCTTGGTTC ATCATCTGAA 900 CGTCATCAGC TGTGCTCCTC TTACGGAAGA GGGGACCTGG CTCCCTTCCA CCCCGACATT 960 GCCCACCCCT CCTCCTCCTC 980
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