Tag | Content |
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EnhancerAtlas ID | HS007-05053 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr14:63355860-63357020 |
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) |
ALX3 | MA0634.1 | chr14:63356952-63356962 | TCTAATTAAA | + | 6.02 | TBP | MA0108.2 | chr14:63356834-63356849 | CTATAAAAACCCTGG | + | 6.19 |
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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 | ATATAAGTTA TGTACCTGAT GACAAAGGCT ACTCATGGAA ATGCAAAAGT GAGAGTTAAA 60 ATAAAAAGAT ATAGACAAAA GTCCAAGGAT TTTACTCAAC AAATACTTAT TGATTGAGAG 120 TCAGCTACCT GCCAGACACA CTGTTCTAGG CACTGAGGGC ACAGAATTGA ACAAAAGGAA 180 TGAAAACCTC CCCCTCACAG AGCTTACATC CCAGCAGAGC ATCACATGGG GGCCAAGCCA 240 GGAAAAGCAG AGACTGCACC AAAAAAAGCT CAATTGCAGA GGAGAAGAAT ATCATGCATG 300 ACAAAGCCAC ATGGCAGGAA GCAAGGGAAA AGTCAACAAC TAAGAGCAGA GATATTGGGG 360 GATGATGATG CAGTAGTCGA GAGAGCAGCC GATGAGCACA TTAACTGACA GAGCCGGCCT 420 GGAGTTTTAG ATGCTGGCCC TGTTCCCATT CCTCTGCCTC TCCGATTCCT AAGAGAGTAG 480 AATCTCCATA AGACAAGCAG CCAGGACAGA TTCCAGACTC TGACATTCAG ACTACTTCAG 540 TACCTATAAT GTTTGGATGT GAGAAAAAAC TTGGCTCATT AAGTGCCATA TTCTACACAA 600 TAACAATTCT GTATGGTAAT AAATTATCCT GCATAGTACT ATTGCATTTC AATTGAATGT 660 ATAACTACAT AGGAGAGAAG CTAATTATCC ATGGGTATTA AAGATGGTTG TTTAAAAAGG 720 CATTAGAAAA CTAAGTAGAA AAATTAGAAG ACGAAGTTCA TAAACATGTT CTGATTCAAC 780 CAGCCATCAA ATTAATATAA CCCATCTTCG GCAAAGTTGA CAAAAACAAG CAATGGGGAA 840 AAGACTCACT ATTCAATAAA TGGTGCTGGG AGAACTGGCT AGCCATACGC AGAAGACTGA 900 AACTGGACCC TTTCTTACAC CATATACAAA AATCAATGCA AGATGGATTA AAGATGTAAA 960 TGTAAAACCC AAAACTATAA AAACCCTGGA AGACAACCTA GGCAATACCA TCCTGGACGT 1020 AGGAATGGGC AAAGATTTCA TGACAAAGAC ACCAAAAGCA ATCGCACCAA TAGCAAAAAT 1080 TGACAAATGG GATCTAATTA AACTAAAGAG CTTCTGCACA GCAAAAGAAA CCATCAATAG 1140 AGTAAACAGA CAGCCTACAG 1160
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