Tag | Content |
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EnhancerAtlas ID | HS182-02309 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr10:18950460-18951240 |
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) |
NFAT5 | MA0606.1 | chr10:18951023-18951033 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr10:18951023-18951033 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr10:18951023-18951033 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28380 | chr10:18946186-18951042 | Fetal_Intestine | SE_29347 | chr10:18945942-18951317 | Fetal_Intestine_Large |
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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 | CTTATTCATT CATACAGCCA TAGGCCAGTC TTCAGAGTTT AGCATAGGAG ATACAAAATT 60 AAAGAATAAA GATACCTTAC TTCTTGGCAA AGTATTCAAA CATCAATAAA CGAGACAAAC 120 ATGAAAAAAA ATGCAGTGTG GTAAATTATT TAACAGATAT GTGTAAAAAT ATAACGTTGG 180 CTGCAGCACA AGGTATACTT GGACGTAATG TAATGATGAG TAGGAATTTG GGTGGCATGC 240 TAGACAGACC GAATAGAAGG GACGTGTTAT TCTAGGCAGA AGAGCTAATA TGCAAAAGGG 300 AGAGGAATGA GCTAGTTTGG TACTTTTAGG GAAGCTGAAA ATAGTTGAGC TTGGCTGTGT 360 GTTAGTTTGC TTGCGAGGAG TGAAGAGGAG ATGAGATTGG AAAGACAACC AGGAGAACCT 420 TATCACAGAG GGCCTCCAGT GTTGACTAAG ACATTAAACT CTCTAGAGCA AGGAATGGGA 480 CTCACTGAAG GGTTTAATCC ACAGATGTAT CTTAGCCTAT ATTTTTGTTT TCTGCATCAA 540 CAAAATTAAC TACCAATCTC AGCATTTTCC ATTTTTGTAA CTATATTTAT CTATTCCAGT 600 GGAATTAGAT ATATTAGAAT AACAGGCCCA AAGCGCCACC TCACACCAAC TAAATTAGAT 660 TGGGGTGAAG AGGCCTGGGC ATCACTGCCA AGGTAAATCG AATGTGCAGC CAGTGTTAAG 720 AACTACTGAT CTTACTTTAT GTGCTCCTTT CCCGTGTCTT TCTTCCAGTA TTTCCACATT 780
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