| Tag | Content |
|---|
EnhancerAtlas ID | HS188-00622 | Organism | Homo sapiens | Tissue/cell | Th2 | Coordinate | chr1:109583400-109584480 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX5 | MA0510.2 | chr1:109584418-109584434 | GGTGACCATGGCAACC | + | 6.19 | | RFX5 | MA0510.2 | chr1:109584418-109584434 | GGTGACCATGGCAACC | - | 6.33 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCCAATGCAA CATATGCCAA CACTGGAGAC AAAAAAATTC TACTTGAATT TACTGTGAAA 60
AAAAGATTTA TAGCATTTTT TAAACCTACA TGTTCATTTC TGTGCCATTA ACTTTTTGAG 120
GCATTCTACA GAGTCTCCAA CAAAGAGAGA AATAAGTATT AGGATCACAA CCTACGAATC 180
TGGGTGGAAC AAAGACTTCT CCTTTCATTA TGCAGAGAAA ACCAAGTTGC CAAAAAAAAA 240
AAACGGTCCC CTCAGATACC ATGCACGGTT ACTAACTGCA CGTCTGGGTA CAGAGAAGGA 300
AAAATCATCT GGTCAAAAGC CCAAATGCCG CCCCGGCCTA CCCTCGCCCC CCGCCCCCGC 360
CCCCTTTGCC CATGGCCTCG CCCCAGAGCT AGAGTTCCAA TATTTTTCTC CCCAATAAAG 420
GGAAGCGGTT TAACCCTTTG AGTTCCACAA CCTTGCGTTC TTCTACGCAG GCGCCCCTCC 480
AGCGCAATCC CAGTTCTAAA TCGAGTCGCT GCCCCTTTCC GCGACCACAC CCAGATCCCC 540
AAAGGCCTGC TCCCATCCCG ACCATTGATG TGAGAAAGGC CAAAACCGGC CCCAGCGGGG 600
CTCCCAGCCC CGCCGCTCCC TCTCTTCCTC CGGGCCAAGG CGTGCCCAGA AAGGGACGCG 660
AGCGCGCCCC TCAGTTCTCG CACGGGCTCG ACCAAGGGGC GAGGAAGGAA GAATCGGCGC 720
AGCGGCGAGA TGGGCACGAA CCTCGCGCTC ACTTGCTGCT CAGTGCCAGG GCGAGGGGCG 780
TCGCTCTGCC CCCAGAATCC AACTGGTAAT GTGGGAAAGG TGTGGTCCAG GACCGGTGAC 840
CTCGAACCGG GGCCCAGCAG TTCGCAGATC CTCACCCCGC GATGCTGGGG CCTCACCCAC 900
GACCCCAGCC CCCTCCCAGT CGGCACCCAA GCCCACTAAA GACCCCTCTC CGGGGCCGCA 960
AACACAGTCC TCGGGGCCGC CCGGTCGGAG CCGTGTCAGG TGGTGACAGG AGGCGACGGG 1020
TGACCATGGC AACCCGAGGT GTGCAGCGGA CCGACCCAGC CTCCGACTCC CGGAGTCACC 1080
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