Tag | Content |
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EnhancerAtlas ID | HS062-02961 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr11:65473460-65474470 |
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) |
PAX5 | MA0014.3 | chr11:65474285-65474297 | GTGGTCACGCTC | - | 6.62 | TCF3 | MA0522.2 | chr11:65473980-65473990 | AACACCTGCT | + | 6.02 | TCF3 | MA0522.2 | chr11:65474129-65474139 | AACACCTGCT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 65473895 | 65474200 | chr11 | 65473826 | 65474214 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I065705 | chr11 | 65473401 | 65474271 |
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Enhancer Sequence | AAGGAGAAGT CAAGCAAGAA AGACAAAGAA AAAATAGACT GCATTAAAAA AACATGTATT 60 ATGAGCTGGG CGCAGTGGCT CATGCCTGTA ATCCCAGCAT TTTGGGAGGC TGAGGTGGGC 120 AAATTACTTG TGTGGGTGGC AAGCCACCCA GGCGACGAGG CAAGAGACAG AGGACACAAA 180 CTGTTCCAGC ATAATAAAAT ATAAAACAAG AACAGTTATA CCAGATATAG ATCTTAAATA 240 TGATTATATA TATCATTAAT TAGTTTGTAG CAATTACTTT TTATTCCAAT ATTATAATAA 300 TCCTCGCTCT ATAATCATAG CCTAGGAAAA ACCAGGCCAT ACAGAGATAG GAGCTGAGGG 360 GACATAGTGA GGTGTGACCA GAAGACAAGA GTGCAAGCTT TCTGTTATGC CCGGACAGGG 420 CCACCAGAGG GCTCCTTGGT CTAGCGGTGA CACCAGCGTC TGGGAAGACG CCCGTTGCCA 480 GGCAGATGGT GGTCTAGCGG TAGCGTAAGT GTCAAGGGAA AACACCTGCT ACTTAGCAGA 540 CCAGGAAACG GAGTCTCCTT TTCCCCGGAG GAGTTTAGAG AAGACTCTGC TCCTCCACCT 600 CTTGTGGAGG GCCTGACATC GGTCAGGCCT GCGGACCGTG GTCTAGCAGT AGCGTAAGTG 660 TCAAGGGAAA ACACCTGCTA CTTAGCAGAC CGGGAAAGGG AGTCTCCTTT TCCCTGCAGG 720 AGTTTAGAGA AGACTCTGCT CCTCCACCTC TTGTGGAGGG CCTGACATCA GTCAGGCCTG 780 CCCGCAGTTA TCCAGAGGCC TGTCTCCCTG TGATGCTGTG CTTCAGTGGT CACGCTCCTA 840 GTCCGCCTTC ATGTTCTATC CTGTACACCT GGCTCTGCCT TCTAGATAGC AGTAGTAAAT 900 TAGTGAAAGT ACTAAAAGTG TCTGATATGC AGAAATAATG GCATAAGCTG TCTTTCTCTC 960 TGTCTCCTCT CCCTCTCTGC CTCGGCTGCC AGGGAGGGAA GGGCACCCTG 1010
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