Tag | Content |
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EnhancerAtlas ID | HS106-00887 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chr17:108990-110630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MNX1 | MA0707.1 | chr17:109655-109665 | TTTAATTACC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 110526 | 110586 | chr17 | 109180 | 109478 | chr17 | 109497 | 110447 |
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| Number: 3 | ID | Chromosome | Start | End |
GH17I000259 | chr17 | 109561 | 109750 | GH17I000261 | chr17 | 109817 | 110111 | GH17I000260 | chr17 | 110121 | 110190 |
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Enhancer Sequence | CGTGAGGAGC AGCAGTTCCT AAGTCCCAGC ATCAGGGGAC CACAGCACAC AGGTGTATCA 60 TCCAGTACAG GAGGTGCACC CATGCAGATG TGCATAAAAC ACACTGTCAG TATTTCTGAA 120 AATGCCTTCC GCAGGGGAGA GCAGATCTGT TGAGGTGAGG TGCAAAGGAC CCCACACCCA 180 CAGGCCTTCT CTCTCCTGGC TGCCCGCCCC ACTCTGCAAA ACACACCACG GCAGCCTTAA 240 TCACGTAACT TCTGCTCTGT GCATCTGGGC CTGTCACCCG CTGCCTGGCA TCCACATCTA 300 CCCCTCCCCG CCCAGGAATA GTGGCAGGAA AAGCCCTCAT GGGAATTAAC CCCAGGCCAC 360 CCCGCAGATT GAAAATCAGT TACTTTCTGG AGAAGCCGAG CAACTCTGCA AAACCCTACT 420 CGGCTCCCCA CGTGTGGTTT GCTGTGATAA GGCCGGCAAA GCAGCCAGCC TTGAAAATGC 480 CATTTAATGA GAAAAGACCC ACAGCCGCCG TGGCGGTGGC CGGGGTGTCC GGCAGCAGTA 540 AACGCTCCTG GTACCGCTGC TCGCCCTGCT CTGTGCTCCG CTTCCAGGTT TGCATTACGG 600 TTTCAGCTCA CGGCCAATCT GACTGCAGAT TCTCATGGAT ATTCGCCAAG CTGTTCCCAG 660 GGAATTTTAA TTACCATGAT AACAATTGCT AATCACTGGC ATTTCCTAAA TGGTTGTGGC 720 TGGAGAAGGT GGTAATTGTC AGGCTGGTGC TGGAAAGAAG GGGAGTCTCA CAGACCTGCC 780 ACTGGAGGGG GTGGGACAGG GGAGCCTGAA GACCCCTCTC TCTGTCCATT GTCCACCCCT 840 TCCATGTGTC ACTCCCTCTC CCGTGCCACC CTGAGAGTGC ACCTGGCTTG AGCTCTTCAC 900 TGGCCCAGGC ATCCATCCTC TCTGCCCCAA CCCCACGAGT CACAGCAGGG GACGGTCTGT 960 GGCCTGTGCA CCTGCTGTTC CTTCCCCCTG GAGTGCCTTT CATCAGCATC TCTAACAGGC 1020 AGTCACGCTT CCCCGGAGGG CTTCAGTGGG TGCCCCTTCA TGCAGAATCA GGGCCCCTCT 1080 GTCGTGCTCC CAGAGGCCAT GTGGTCCCAC TGGTACAGCA CGCCACACCT GGGCTGGAGC 1140 TCAGACTCGC CCACCTTCCT GAGCAGGAGG CTGTGAGCTC TTCAAGGGCA GGGCTGTGCC 1200 TGAGCCATCT CTGGATTCCC GGGACCCAGT GAGGAGCCTG CTATGTTACT GACCGACCAC 1260 ATGAACAAAG AAGGGAAAGC AGAGGCACTG TCTCCAGGGG ACAGAGGGGA GACCTCGCCT 1320 TCAAGGGAGA CTGCGTTCTG TCTGCCTAAC AAGCTCCAGA CTGAATCAGT CTTGGAGAAC 1380 CACGGGAAAA GACCTGTGAC TGAGCGGTCT TCTCAATTAC ACTGCAGCTA CTTTAAAGGT 1440 CTCTTCAAGG GTCAACCCTC TCTGGCAGAG GAGAGGCAGT ACCTCTCCCT CCTCCATTAC 1500 CTGACACACA CTCACAATGC TGGTCTCCCA GGAACCCTAA GAGGCAAGTT AAACAAGTCC 1560 GCAGCAGGCC AACAACACCC CAGGACCCAG CCTCCCTCTC AGCCTCACCT CTCACCTCCC 1620 CCACCCCCAT CACCAGGCAC 1640
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