Tag | Content |
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EnhancerAtlas ID | HS187-14920 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:241551770-241552730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP4 | MA0691.1 | chr2:241552165-241552175 | AACAGCTGAT | + | 6.02 | ZNF263 | MA0528.1 | chr2:241552192-241552213 | AGAGGAAGAAGGGGAAGGGCA | + | 6.11 | ZNF263 | MA0528.1 | chr2:241552627-241552648 | GAAGGAGGAGGAGAGGGGACA | + | 7.16 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 241552102 | 241552293 | chr2 | 241552389 | 241552597 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I240611 | chr2 | 241551051 | 241552738 |
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Enhancer Sequence | GAGGCGGAGC TTGAAGTGAG TGGAGATCAC GCCACTGCAC TCCAGCCTGG GCGACAGAGC 60 GAGACTCTGT CTCAAAAAAA AAAAAAAAAA AAAAAGGACT AGGGACTTAC TGACTTGGCC 120 AAAGGCTGCT GGTGGGTGCG TGGAGGTGCT GCCTGTCAGC TGTGCTCTGG GCTCTAGGGA 180 CATGGGAGTC CAAAGGGCTC TCACCTCCTC AGTGAGAGGT TCTGGTGGGC TGACCATGGT 240 GGGATCCAGA TTTCAGCAGG TGGACCCCGA GGGGGTGTGA GGAAATGGAC TCTGTGAGTG 300 GGAACTTCTC TTTCAGAGGA ATTTGCAAGA CTGGCCTGAG CCGCACACGG CTCTTCAGCA 360 GGGCTTGGCA GCCAGCGGGG CCTCGGGAGG AGGCAAACAG CTGATCAAAT CCGGGCTTCT 420 CCAGAGGAAG AAGGGGAAGG GCAGGTCTGG GGAGGTCAGA GCGTGGGTGA GAACCGTGGC 480 CATGGGTGGG ATCCACATCC CAGCCTGCAG GGCCTCCTGG TGATGGTTCT CCAGAATTCT 540 GCGATTGGAG CTGTGCTCAC AGAGTCACTG TCCCCGACCT CCCAGGGGCG CGGACATAAC 600 CCAGCCTCAG CTGCAGACAG CAGAGACTCT GCACAACTGC AGAAGCTGAG CAATCAGCCT 660 CATCAGTGGC AATTCCTGGA ACTCCAACCT CAACTGTAAC ATGAGCTGTG GCAGACCTTC 720 AGTAACCCCA GACAAGGAGT GAGGCAGAGC CTGATAGCTC AGGGACCAGC TGGGATGCTC 780 AGTAAACAAG AGCTCCAGAA GATACGCGGA ACAGGAGAAG GTGAAGTGTG GGGACAGCAG 840 GCGCTGCAGG CCACCCAGAA GGAGGAGGAG AGGGGACAAG AAACACTGAC CAGGCCTTCA 900 AGATGAGGAG TGAGCAGAGA GGACAGCAGA ACATGGGAAA ACCTACCTGG CACTATGAGG 960
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