Tag | Content |
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EnhancerAtlas ID | HS176-28146 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr3:182903370-182904080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr3:182903973-182903983 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr3:182903973-182903983 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr3:182903973-182903983 | AATGGAAAAT | - | 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 |
GH03I183185 | chr3 | 182902881 | 182904031 |
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Enhancer Sequence | TTGTGTTGTG TGTGCTGCTA ACCAATTTCC CCTCTCTGTC TTCTAGGATT TAATACATGG 60 TGTCACATTC TGTCTGATCC ATCCCAGTAG CTCTCCAGAG CTCCCAACAG GAGAGAGTTC 120 CAAAATGTTT CCAGGGGTAC TAGGCTCGGT TACAATATTT TGCTTGGTGG CCCAGAGTAT 180 AAACGTGGAT ATCTTAGGCT GGTCTATAGC TGAAACGTCT ATTTCATTTG CAAGCCTATC 240 TTTGGCTAAG AGGAAGTGAA TCATTCTTGA GAACATCTAA TTAATTGCTT TCAGATTCCA 300 CATGTTGACA TTCTCAGGGC ACATTTTTTT TTTCCCGTGC ATTTCTGTTG TCAAAGTCCC 360 TGCCAGCTCC TAAGGCAGTC TGAGCTGGCT GTCTTAGACT TTCAGAGCTG CTGGAAGCTT 420 GGGGGAGGGA GGGGCTGTAG GTCAAAGAAA CTTTATAACC TAGCTTTACC TCCCAGCTCA 480 GCCACCAGCT GCCCTCAAAT GTTCTGGATT GGAATAAGCC CAAAGATGAG TGGCAGGAGG 540 GAAGGGCAAG CCAATACGTC TAGTTTGGTT CAGTCAAAGC CTTGCCCATT TCATCAGAAT 600 TTTAATGGAA AATTTCCAAT AAGATTAAAA TATAAGGTCA CCCCAATTTT AGTATGGCTC 660 CATTTAAAAA AAATCATGCA TATCTTTGTT TTGCAATGGG GCCTTACTCT 710
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