| Tag | Content |
|---|
EnhancerAtlas ID | HS187-10152 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr17:18835720-18836780 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6 | MA0677.1 | chr17:18836333-18836347 | TGAGCTTTGACCTC | - | 6.18 | | Rxra | MA0512.2 | chr17:18836333-18836347 | TGAGCTTTGACCTC | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCCAAATCCA GTTAATGATA GAGCTATTTA CTTTGAAGAA GTGTCCTTGC TTTCTGTGAA 60
CCTGTCCCTA GAAATGGGGC CTCTCGATCT TCGGAATGAA TTGGCTTAGG GCATGGGATG 120
GTAGCTGGTG GCTTCTTTGC CAGTGCAGCT CTGTCAGTTG CAGGCTGGAG ACCACCCAGT 180
TTCCACATTT GGAAGAAGAG CTTTGGGAGC AAGGTGTCAC CACCCATGAG AGTGGAGCCT 240
GCCTGTGGTG CCAGGACCTC CCACTGTTGC TGTGAAATGA GCTGAAGAGG CTTCAGTAAA 300
TCTCACAGCT CCAGCCTCTG ATGGGTTTGG GTTTTTTCTT ACCTTCTGCC GTTTGGATGC 360
TGCCTAACCA TTTGCTACTA TAGATGACGG TTGAAGTTGC CATGTGGTTT GGCTTTATAA 420
CAAGTGACAG GCACTTCCTG AACAGCCATG GGGCATCCCC TGGGGTGGCT GTGCTGGCAC 480
AGTGGCCCTC CCATGGTTTG GGAATGGTGG TGCTGCACTA GCACGGAGGA CAGGTTCTGC 540
TCTGGGTTCC TTGGAGATGC AGTGGGCTCT CAAGCTCCTT CAGTGGGAGG TTTCCTCCTG 600
CCACTGTGTC CAGTGAGCTT TGACCTCTGG TTTTTCTTGG CATGTCATCC TTCATGAAGA 660
AAAGTCATAT TTACAGAAGT GAATGGAAAC ATGTTTTATG GGAGTGTTTT CCTCTGGGTA 720
ATGAACTTGG CTAAAGCTAG GATCCTTCAC ACCCACAGAG ACTCGAAGGT CTGCCCTGAG 780
TTGGCTCTGG AAGAACATGA AGATGAGTGC TGGGAGGAGC CACGGGTGGG GCATGTGCCA 840
GGGGATGGCT GACAGGGCTG AGGCCCAGGA AAGACAACTG GCAGATGATG GTGGAGGAGA 900
GTGGAGTGCC ACGTCCTGGC CCGCCGGGCT GGGGCAGGAG GATGGAAGCC TTCAAGGGGC 960
AAGTCAGGTT CTGTGGTGTG GTGGGGAGTG CTGGGGGACT CTCAGGGCTT CAGGAGTGCC 1020
CAGTAAGGAC ACCCAAACCC CTCAGCCATC CTCTTCCCTG 1060
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