Tag | Content |
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EnhancerAtlas ID | HS012-18043 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr3:37180320-37181550 |
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 | chr3:37180379-37180390 | TTTTATGGCTT | - | 6.62 | NFAT5 | MA0606.1 | chr3:37180667-37180677 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr3:37180667-37180677 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr3:37180667-37180677 | ATTTTCCATT | + | 6.02 |
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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 |
GH03I037138 | chr3 | 37179788 | 37181797 |
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Enhancer Sequence | GCACACAATT TTTTTCCTTA CTAAGTTGAG AACTTTCACC TTTTCACTTA AAGAAAGAAT 60 TTTATGGCTT CTCTTTGGCA TATCCAAACT GCCAGAGTCA CTCTTGCTCT TTGGGGTCAT 120 TATTAAATAA ACTAAAGGTT ACTCAAACAC AAACAATGTG ATACCATGAC AGTCAACCTG 180 ATAACAGAGC CGGCTCCTGT GAGACTATCT AGCAGGTAGC ATACACTGTG TGGATACACT 240 AGACAAAGGG ATGATTTATG TCCTGTGCAG GATGATGTGA GATTTAATCA TGCTACTCAG 300 AACACTGCAC GATTTAAACA AAAATAAACA AACTGTTTAT TTCTGAAATT TTCCATTTAA 360 TATTTTCAAA CTGTGGTCAA ACATAAGTAA CTGAAACCTC AGAAAGCAAA ATCACATGAA 420 GGAGAGGCTC TGCACAATGA ACCATACAAG GTTTTTAAAA ACAAAATGGG TACCAATCAA 480 TGTGTAGCCT ATTTAAAAAA CAACAACAAA ACAGGAAGGT ATTTCCAAGA TATATAATGT 540 AAATGATCTG AATTATCAAT GGAAAAAGTT TCTCTGCAAG ACCTTATCAG TTCAGCACTT 600 CTTTCATTAT TCCAGTTCTG ACACTTTTAG TATTTCCCCT CCTGTGCCAA TGTTTTCATG 660 ACAGAAGGCA TTTTAAGGTC TGAAGAAGGC ATTCGCTTCA CACCCTCCAA AGCCACTAAC 720 AGACTTCCCA GTCTTCCCTT CTTTCTTACT TTCCCTGTGG TTCTACTGAA GAGCTGCCTC 780 TTCTGTTGTT GAAAGTCAAA CCCTCCCAAG CCCCGTCACA CACACTCACA CACATACACA 840 CCCTCCATTT TATGATGTCC TCCCCAGGAC TTTGTCCCAA CTATCTGATC TCTCTTCTGG 900 GTCTTTGCTC TCTACTTCTA TTGGTTCACT CTCTTCATCA TAACTAGGTT CAAAGTCTCT 960 CTGATCTTTA AAAGGCAAGC AAAAAATCTC ACCCTGGTCC AATTCTACCC TATCTTCTCT 1020 TTACAGCTAA GCTTTCTCAC ACCTCCCTCT TCACTTCTCA CTCTCTTCAA ATGACTGCAA 1080 TCTGGCTTCT GCTCATATCA CCTTATTGAA ATTGTTCATC ACAAAAGTCA CTAATGACCT 1140 CTAACTACCA AACCCAATAG AATTTTTCTA TTCTTATCTC ATCTGTCTTT TCTGGACTTT 1200 CAATATCACT AAACACATAT TCTTTCTTAA 1230
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