Tag | Content |
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EnhancerAtlas ID | HS040-25519 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr3:49334140-49335300 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr3:49334417-49334428 | TGGGTGTGGCT | - | 6.14 | MSC | MA0665.1 | chr3:49334834-49334844 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr3:49334834-49334844 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr3:49334834-49334844 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr3:49334834-49334844 | AACAGCTGTT | - | 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 |
GH03I049296 | chr3 | 49334281 | 49334430 |
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Enhancer Sequence | TTGTCAATTC AAATTCATCT ATAAAAGAAT TTGTTTTTCC AATGGTTGGC CCATAGGCCC 60 TCTGAAAATT CCTTTGTTGG TGGTCTGCTA AGCTCCCCAC AGGGTAATCC TCCAGTTCCT 120 TTCAGCTCAG GTGTGTGAAA ACACTACTTT CTGGAATTTA CAGAGACCAT GTTAAGGGCT 180 TGGGGTTATA TGTGAAAGTG GACTTTCCCA TGTTCTAGCC CTTGGCACAG TGTCAGCTCT 240 TGGCTGTGTC TGTGCAAGTG AGAACAGAAA TAGATCTTGG GTGTGGCTAG GAACTATTCC 300 TTTTAGAGAG ATCTAGAAGT CATAGGCCCA AAAATGTAAA GGGAAGGAAC TATCTCCTTT 360 ACATACTGAA TTCCTCAGCC AAAAACAAAA ACCAAAACAA AATCCTAAAA CCCTTTCTCA 420 GCAGAGGCAA GTTCCTGAGT GAGAGGTAAA GAGGGAGGGA CAGTACGGCT GTGCTCCATA 480 CTTCCTGGGC AAGTGGCTGC CTGGGAGCAG CAGGCAAGTT CATGTATGGG AGCAGCCGGC 540 AAGTTATTAC ACCACTGTGC CTGGAAGAGG GACACACACA CAATTACACA GAGCAGCCAT 600 GAAGCAGCAT GTGGGAAGGC AGAGGAGGCC TTTGTATTGT CCTCACAGAG ATGAAGAAAC 660 TCAGTCTCAG AGCTTACAGA ATGTTTGAGC TGAAAACAGC TGTTTAAATC AGCCCTGTCA 720 TTTCTGCATT GGGGATGGTA GTATCATGGT ACTCGCTGAG AAGCTACAGC CTGTGGCAGA 780 GAAAGGACAA GATCCTTCCG TACCACACCC CTACTACCAT CTTCCCATCA CACAGCTGGG 840 ATTCCTCTTA AGAAAGGCAT CTCTGATGGT AGGACCATCT GTAGGAGCAG TGATTTGGCC 900 TTCTTCATAG GCAAAACTGT TGAAAAAAGG CTGTGGCTGT GCTGAGGAGA GTTATCAGAA 960 TGTTTAGCTC TGCAGGGCAG GAGGGGTTGA GCACTGATGG CTGCCCACGA TGCCCTCAAT 1020 ACCCATCTCT TGCACCCAGG GGTCAGGGCC AATCCACATG AGCAATGACT GCCCACATTT 1080 TTGTTCTGGA GATATGAATG CAGCAAAGTC TCTAGAATGT GTCCTCTGAC CTGACCTGCA 1140 GCAGAAACTG CTGAGTACTC 1160
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