Tag | Content |
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EnhancerAtlas ID | HS108-27745 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr3:37180330-37181450 |
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 | TTTTTCCTTA CTAAGTTGAG AACTTTCACC TTTTCACTTA AAGAAAGAAT TTTATGGCTT 60 CTCTTTGGCA TATCCAAACT GCCAGAGTCA CTCTTGCTCT TTGGGGTCAT TATTAAATAA 120 ACTAAAGGTT ACTCAAACAC AAACAATGTG ATACCATGAC AGTCAACCTG ATAACAGAGC 180 CGGCTCCTGT GAGACTATCT AGCAGGTAGC ATACACTGTG TGGATACACT AGACAAAGGG 240 ATGATTTATG TCCTGTGCAG GATGATGTGA GATTTAATCA TGCTACTCAG AACACTGCAC 300 GATTTAAACA AAAATAAACA AACTGTTTAT TTCTGAAATT TTCCATTTAA TATTTTCAAA 360 CTGTGGTCAA ACATAAGTAA CTGAAACCTC AGAAAGCAAA ATCACATGAA GGAGAGGCTC 420 TGCACAATGA ACCATACAAG GTTTTTAAAA ACAAAATGGG TACCAATCAA TGTGTAGCCT 480 ATTTAAAAAA CAACAACAAA ACAGGAAGGT ATTTCCAAGA TATATAATGT AAATGATCTG 540 AATTATCAAT GGAAAAAGTT TCTCTGCAAG ACCTTATCAG TTCAGCACTT CTTTCATTAT 600 TCCAGTTCTG ACACTTTTAG TATTTCCCCT CCTGTGCCAA TGTTTTCATG ACAGAAGGCA 660 TTTTAAGGTC TGAAGAAGGC ATTCGCTTCA CACCCTCCAA AGCCACTAAC AGACTTCCCA 720 GTCTTCCCTT CTTTCTTACT TTCCCTGTGG TTCTACTGAA GAGCTGCCTC TTCTGTTGTT 780 GAAAGTCAAA CCCTCCCAAG CCCCGTCACA CACACTCACA CACATACACA CCCTCCATTT 840 TATGATGTCC TCCCCAGGAC TTTGTCCCAA CTATCTGATC TCTCTTCTGG GTCTTTGCTC 900 TCTACTTCTA TTGGTTCACT CTCTTCATCA TAACTAGGTT CAAAGTCTCT CTGATCTTTA 960 AAAGGCAAGC AAAAAATCTC ACCCTGGTCC AATTCTACCC TATCTTCTCT TTACAGCTAA 1020 GCTTTCTCAC ACCTCCCTCT TCACTTCTCA CTCTCTTCAA ATGACTGCAA TCTGGCTTCT 1080 GCTCATATCA CCTTATTGAA ATTGTTCATC ACAAAAGTCA 1120
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