| Tag | Content |
|---|
EnhancerAtlas ID | HS089-09261 | Organism | Homo sapiens | Tissue/cell | Hela | Coordinate | chr3:126208220-126209090 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr3:126208795-126208806 | AGCCTCAGGCA | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTGCATGGAA GGACAGAAGC TGTCAGCCAA CAGTGTCCAC CATGGCTTCC TGGTAAAGAC 60
TGAGGACAAG GGGCAGGTCA CACCAGAACC CGCTGGATTT CTCCTCCTGG AAAATAGACC 120
CTCTTCACAA CTATTTCTGA TGTCATCTGT AGCCTGGAAT AGATTCACGT GTGCCCGGCA 180
GCACTCGTGT GTAATACATG TGTGAGCTCA CCGAGCACTC ACAGCCACCC TGTTCAGATA 240
GGCACAACCA TTATCATGCC CACTTCATAG ATGAGAAAGC GGAGGCACAG AGAGGAGAAG 300
AAATTTCCCC TATATCACAG AGCGAGTGAG TCGTGAGCTG GGGTTTAACC CCACACGTGT 360
TATATGCCGG CGCTCCTCGT CTTACGATGG TGCTACATCT TAATAAGCCC ACTGTACCCT 420
AAGTAAAAAA CGACTTAAGA GTATTTTTAA CTTACGATGT ATTCATTTGG ACGCAACCCC 480
ATTGTATGTC GAGGAGAGTA CTAAACAAGT GTCACTTCAC ACCATTGTAA AGCAGAAAAA 540
TTGTTAAGTC CGAGTGTCCA CTTAGTCTGG GCTCAAGCCT CAGGCAGCCT GGCCCCTGAC 600
CTGTGCAATA GAGACGTGGC TGGCTGATGG CCTGGAGGTG TTGGAGGGCC TCACTGGGGG 660
AGTATTTGGC AGTACCTACC ATGAGACCTT GGGCAGGTCA CTTCCGTCTG GGAATAGCTC 720
TTGGTTTCCT GGATGAGGTA ATTGCTAAGA GCCTTTTCGT GCTGCCAGTC TCTCTGAGGA 780
CAAAGACTTT TCGCACAGAG AAAGCATTCA TGCTGAGTTT GATTTTTTAA TACACTCATC 840
GGCAGCACTC CTTGTTCCCC AGGAATCTCC 870
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