Tag | Content |
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EnhancerAtlas ID | HS047-09588 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr13:99724720-99726170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr13:99725938-99725956 | CCTTCCTGCCTTCAATCC | - | 6.91 | MAX | MA0058.3 | chr13:99725437-99725447 | ACCACGTGCT | + | 6.02 | ZNF263 | MA0528.1 | chr13:99725622-99725643 | TCCTCTCTCTCTCTCTCCTCT | - | 6.75 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 99725130 | 99725560 | chr13 | 99725845 | 99725895 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I099073 | chr13 | 99725341 | 99725490 |
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Enhancer Sequence | TTCCTGACTT CGGGGACAAA GCACTGATGA AACTGAGGGA AACTAAAGAT GGGGTTTAGC 60 ATCAGCTCAC CCCAACCAGA GCATTCTTTC ATGCATCCCC AGTGATCACA AAACCCCATA 120 CCACTACCTC GCTGATGCTA TCTATACCCA CTAACCCTGA GGCTTTAGTC AGATAAAGAA 180 AACACCCATT CTAAATTGTT CTTCTGTGTT CTCAGAATGT TTAACCATGC CTTTTACTTA 240 AAGAATTCCA GGGGCCAGGC ATGGTGGTAC ACATATGTAA TCCTGGCACT TGGGACGCCG 300 AGGCAGGAAG ATCACTTGAA CTCGAATTTG AGACTAGCCT GGGCAACATG GCAAAACTCC 360 ATCTCTACAA AAAATACAAA ATTGAGCCAG GCATCATGGC ACACACTTAT AGTCCCAGCT 420 ACTTGCAAGG CTGAAGATGG GAGGATTGCT TGAGCCCGGG AGGTCAAGGC TTCAGTGAGC 480 CAAAATCACA CCACTGCACT CCAGCCTGGG TGACAGACCC TGTCTCAAAA AAAGAAAAAA 540 GAATTCCAGG AATTGGCCAT AGGAGATCCA AAATATGGAA CCAAGGTTGC AGAGTGTCTC 600 ACCTCAGGAA GGAATGCTGA CCAACTGATT TATAGCCTTG TTGCCACCGG CCAGACCACC 660 ATGTGGCCCA TCACTCAAGA TAACCATCGC AACCAGATAT TCTGACCCGC ATACCCTACC 720 ACGTGCTTTG CCCAGCCCAC CCTGCATATC CTACCCCTGA TGTCAATTCC CATGCTTTGC 780 CTAATAGAAA ATCCCTACAG GCTCAGAGAG TCAGCTAAGG AATTCTCTCA TTCTCATTCA 840 TTCTCTCTCT CTCTCTCTTC TCTCTCTTCT TTCTCTCCTC TCTTCTTCTT CTTTTCTCTC 900 TCTCCTCTCT CTCTCTCTCC TCTCTCTCTC TCTCTTTCAT GCTTCCTCCC TTATGCTCAG 960 GCATAAGCTC CAATGAAGGC TTTTCTTTCG GCCTCGGGTC GATTTCTATT GCATTGAGGG 1020 CCCAAGAACC CATGGCTGGT AACAAAACCA ATCCAGAAAA AGGGTTCTCC TTGACCAGGT 1080 CTTCTTATAC AATGAACAGA CTGGCAGCTG GCATTGATCT TTTCCCTTTA AGGCTAGGGG 1140 GTTGGCAGCT TTATAGAAAA GGGCAGTCCT GATCATAAAC CTGATTGCAT TTGCACAAAA 1200 CAGTAGAGTT GGCCTAACCC TTCCTGCCTT CAATCCTGGT GTTCACTTTT CTTCCTTACT 1260 AAAAAATGTC CTTTGTGGCA TTTTTTCCAG AATAGGGACT TTAATCTGTA TTAAAACCCT 1320 GTTCGGGCAG ATATCCTTTC TCCTCAATGA CTTTCTTAAC GACATCTGGG AGCTTGTATG 1380 CTGCCTCTTG GTTGACAGAA CTGCTTCTCC TGTTATCTTG ATATTTTTAA AGCCAAAACT 1440 CTTTCTAGAA 1450
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