Tag | Content |
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EnhancerAtlas ID | HS103-09671 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr17:108540-110850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MNX1 | MA0707.1 | chr17:109655-109665 | TTTAATTACC | - | 6.02 | MYC | MA0147.3 | chr17:108815-108827 | GGCCACGTGCCT | + | 6.07 |
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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 | TCAACCCGTT TTTTTTTTTT TTTTTTTTTG AGACAGGGTC TCACTCTGTT GCCCAGGCTG 60 GAGTGCAATG GCACGATCAT GGCTCACTGC AGCCTTGACA CCCTGGGCTC AAGTGATCCT 120 CCCACCTCAA CCTCCCGAGT AGCCAGGACC ACAGCAACAC GCCACCATGC CCGGCGAAGT 180 CAACCACTTT TGAACTATCA AAAAAGCCCG TCAACTTCAT ACGATTCACC CCAATATTTA 240 TGCCCAGAAG GGGCAATAAT CCCACAGGCC AGGCAGGCCA CGTGCCTCCC CGGGGCTCTG 300 TGGGCAGGAC CATGAGCACC CGATGGATCA TTCCCTGTGA GTTCATTGTA ACGGGGCCTC 360 GCTCCGATTC TCTCCTGCTG TCACTGTAGT CCAGGTGGAA GGTCTAAGAG CTCACCCTGA 420 CCATCCAGCA TGGCTGGTGA TCTGGACCAG CGTGAGGAGC AGCAGTTCCT AAGTCCCAGC 480 ATCAGGGGAC CACAGCACAC AGGTGTATCA TCCAGTACAG GAGGTGCACC CATGCAGATG 540 TGCATAAAAC ACACTGTCAG TATTTCTGAA AATGCCTTCC GCAGGGGAGA GCAGATCTGT 600 TGAGGTGAGG TGCAAAGGAC CCCACACCCA CAGGCCTTCT CTCTCCTGGC TGCCCGCCCC 660 ACTCTGCAAA ACACACCACG GCAGCCTTAA TCACGTAACT TCTGCTCTGT GCATCTGGGC 720 CTGTCACCCG CTGCCTGGCA TCCACATCTA CCCCTCCCCG CCCAGGAATA GTGGCAGGAA 780 AAGCCCTCAT GGGAATTAAC CCCAGGCCAC CCCGCAGATT GAAAATCAGT TACTTTCTGG 840 AGAAGCCGAG CAACTCTGCA AAACCCTACT CGGCTCCCCA CGTGTGGTTT GCTGTGATAA 900 GGCCGGCAAA GCAGCCAGCC TTGAAAATGC CATTTAATGA GAAAAGACCC ACAGCCGCCG 960 TGGCGGTGGC CGGGGTGTCC GGCAGCAGTA AACGCTCCTG GTACCGCTGC TCGCCCTGCT 1020 CTGTGCTCCG CTTCCAGGTT TGCATTACGG TTTCAGCTCA CGGCCAATCT GACTGCAGAT 1080 TCTCATGGAT ATTCGCCAAG CTGTTCCCAG GGAATTTTAA TTACCATGAT AACAATTGCT 1140 AATCACTGGC ATTTCCTAAA TGGTTGTGGC TGGAGAAGGT GGTAATTGTC AGGCTGGTGC 1200 TGGAAAGAAG GGGAGTCTCA CAGACCTGCC ACTGGAGGGG GTGGGACAGG GGAGCCTGAA 1260 GACCCCTCTC TCTGTCCATT GTCCACCCCT TCCATGTGTC ACTCCCTCTC CCGTGCCACC 1320 CTGAGAGTGC ACCTGGCTTG AGCTCTTCAC TGGCCCAGGC ATCCATCCTC TCTGCCCCAA 1380 CCCCACGAGT CACAGCAGGG GACGGTCTGT GGCCTGTGCA CCTGCTGTTC CTTCCCCCTG 1440 GAGTGCCTTT CATCAGCATC TCTAACAGGC AGTCACGCTT CCCCGGAGGG CTTCAGTGGG 1500 TGCCCCTTCA TGCAGAATCA GGGCCCCTCT GTCGTGCTCC CAGAGGCCAT GTGGTCCCAC 1560 TGGTACAGCA CGCCACACCT GGGCTGGAGC TCAGACTCGC CCACCTTCCT GAGCAGGAGG 1620 CTGTGAGCTC TTCAAGGGCA GGGCTGTGCC TGAGCCATCT CTGGATTCCC GGGACCCAGT 1680 GAGGAGCCTG CTATGTTACT GACCGACCAC ATGAACAAAG AAGGGAAAGC AGAGGCACTG 1740 TCTCCAGGGG ACAGAGGGGA GACCTCGCCT TCAAGGGAGA CTGCGTTCTG TCTGCCTAAC 1800 AAGCTCCAGA CTGAATCAGT CTTGGAGAAC CACGGGAAAA GACCTGTGAC TGAGCGGTCT 1860 TCTCAATTAC ACTGCAGCTA CTTTAAAGGT CTCTTCAAGG GTCAACCCTC TCTGGCAGAG 1920 GAGAGGCAGT ACCTCTCCCT CCTCCATTAC CTGACACACA CTCACAATGC TGGTCTCCCA 1980 GGAACCCTAA GAGGCAAGTT AAACAAGTCC GCAGCAGGCC AACAACACCC CAGGACCCAG 2040 CCTCCCTCTC AGCCTCACCT CTCACCTCCC CCACCCCCAT CACCAGGCAC AGCTGCTCTC 2100 ACCGCCTTGA CCACACTAAG CTCTCCTTTT GGACACGTTG TTCCTTCTCC CTTCCCTGGA 2160 CTAGCTCGTC TCCAGCCTTT GGGAAATCAC TTTTATCCAG AAGCTTCCAG ACATAATCTT 2220 GCATGTTTCC ACAGCTATGC ACACTCCCTG GGTTATGATC ACCTGTTTCT GTGTCTGTTT 2280 CCTGAGGATG GAAGACCCCA TGATGGCGGG 2310
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