Tag | Content |
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EnhancerAtlas ID | HS012-12152 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:123639790-123640940 |
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) |
NFYA | MA0060.3 | chr12:123640168-123640179 | TCTGATTGGCT | - | 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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Enhancer Sequence | GAATAAAGGC ACTTGATTCT AATTATAAGT AATTTTGATT AGCCTGAAGT CTTCAAAAGT 60 TGCAGAGTAG GGAGCAAAGG TTCAACTGCA CTGTCAGACA GGCCACCCTC CTTGCTGAGA 120 AGGGAGCAGG GCTGTGGACC CCTGGCCTGG GGACCAGCCA GGTGAAGGGT GCTCAAAGGT 180 CATTTGAGAG CCTGCTTGGA ATAACTGGGA TGGCTTGGTT CATTCTAACT ACTTATTATT 240 AAGAGCCACA TAAAGAGGAA AAGCTCAAAA GCAAACCAAA ATTTAAAACC TGAGCATGTT 300 TAGTACGAAT CCATTTTGAA AGTTTGGATG AGTCTGTTTA TCAACATGTA CCGAGCTGGA 360 ATATGTGGGG CACTGCGTTC TGATTGGCTA CCAAAAACTA AGTAGTTACA CAGCTCCAAC 420 TTAACCAGCA GTCCCAACAC AAACCTGCCA ATGCTCCTGG ATCAGAGGAG AGACTCCTGC 480 CCACGTGCTA CTTCTGAGAG CCAGCGGCTA CCACAGAGGC AGTGGGCTGG AGCCCTCTGC 540 AAGGCCGAGG GGAAGGCACC AGGCTCCATC CGGACACACT CCCTGTCCAT TAACAAATAC 600 AGTAGATTGT GATGATCTAA AGTCTAGTGT TCTTACAGCA CCTACAGTGG AAATATTTTC 660 CTTTTGGCCA GGGTGAAGGA GTGGAAAGGG GTGAACATAT CCAGATGACA ACTATGACGG 720 ACAGCTGAAG CCATGCACAC TAAGAAAACC AGGCTGCCCT CTTAATCCCT CACGGGGTGG 780 TGGCTTGTAT TTCAAAGGGT TTATCTGTCC ATTTATTGTC CAGGGTGGGA CACAAGTTAA 840 TTCAGAACAA TGGGCAGAGA GCTACTCTGA GAGCCCTCCA GAGAGGGCTC TCCAATTGTT 900 TAACTTTTTT AGAAAAGATA AAATTAGAGA ATTACAATCT CTCTTTTTTC TCTTACAGAC 960 AATAAAGTTT AAAGAAAATG AGTTATATTC ATGTAGTTTT CAAAGCTTTC CAAGAGTCCA 1020 TTATTACTAT TCTGATATTC ACTCTAAGAC ACGTTTCAAA TACGAATTGC ATTATCATTT 1080 TTTAAAAACC TCAACACAAC TGAAATCCAA GGTACACTGT AATTGTTTAT GTATTCAGCA 1140 TGTACTAGTC 1150
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