Tag | Content |
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EnhancerAtlas ID | HS076-05666 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:225898020-225900340 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx3-2 | MA0122.3 | chr1:225900180-225900193 | ATTAAGTGGTTTT | - | 7.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I225710 | chr1 | 225898621 | 225898770 | GH01I225712 | chr1 | 225899903 | 225900557 |
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Enhancer Sequence | CAAAATGAGC CTGTCCTGGG CTCCTGGCAC TAGAAGTTTG GGGGTGGTAG AGAAACAAGG 60 GCTTTTTTAA AAGAAGGCCT CCAAAATTGT CCAAGCTTCA GGCCCCTCAA AATGTGAATC 120 TGCCCTTAAC TGGATATGGA TAAATCTAAA TCAGCTCATA CTTTATTTTC TCTCACATTT 180 ACAGACTACA GAGCCTAAGT CAAAGCTTGT TCTTGGACCC AGGAAATATG TCAAATCCTT 240 CCAGTGAATG GTATGTCTTC CTAAATGACG CACTTGTGAG AACAGCTGGA CCTAACTGTC 300 TAAAGGACAG CTAGCTTCCA GCCCGATTTT CAGAGCTGAT ATATCAAAAT CTAATTCCTT 360 TTACAGAATA GCCAAATAAA TATTTTCACT GTCAAATTCT TCACACCAAA TGCTGTACAA 420 GCAAAATCAT TATACCTTAG ATAATGACTG TATTATATTC GTAGATTTCT AGTGGTGTTC 480 ATTTATTCAC TCACTCACTT GATAAATACA CGAAGTCCTT ACTACAAGTC AGGTATTGGG 540 GGTAATACAT TAACTAAGAC ACAGTCCCCT TCTTCAAAGA GTCTAGTGGG GGAGTGAGAC 600 ATTTAAACAG GCGATGACAA TACATGATTC ACACTAAGAT TGGGGTTGAT GATGAGCACA 660 GCATTTTCGA AGCACTTGGG TGGAGCTCCC ACCTTGGCAA GGCAAGTCAG GGAATGCTTC 720 TTGGAAAAGC TGAGTCAACC TCTCGGCAGG GATGCTGGAG CACTGGGTGG GAGGGTGAAC 780 TGGATCAAAG GTTCCCAAAT CTGGCTGATC ATCAGAATCA CCTGGGGGAG CTTCGAGAGT 840 CCCAGGCTTG CCCCCAACCT ACTGACTCAA TTTCAGTGGG GTGAATTTCA GGAATCTGTC 900 TCCTAAAAAA TAAAAGCATG CCTGGTGGGT TTTTGATCCA CCAAATTTGG TGAAGTGGAT 960 GACTTGTGAT TTTGGGGAGA GGGCCCAGGG CAGGAAGGGG TAGATAAAAA AGCCCACGGG 1020 AGGCTGCAGA ATGCCCTATG GAAAAGGCAG AGTAAGGAGG GGCTAAGGCA CAGGTAGGCA 1080 GAGGAGACTT TCCAGGCAAG GGGAAAAAGA ACCTTCTACA TGGGCTGTTT GAAGGAGCTC 1140 AGGCCCTTTT AGAACAGTCA CTCAGCATGG CTGGCAGCTC ACAGGGCCGC TGGCTAACTC 1200 AGGTTCGGAA AATCATTTAG CAACCTGATA GAGACCACAG AGGTGGCTGT GTTTCATGTT 1260 GGGGAAAGGG GCAGGAATGC CTGCACTGTG GAGCAGGAAG GAAAAGGCTC AGACTGCACC 1320 TGTGACCCTG CAGGGACTTT GGTCCCCTGA AAGCTTTGCA CTAGTCCAAC TTCCAATGCT 1380 CTGGTTTAAG AAACCTCCTT GTGTCATTTG CCTCTTTTTT TTTTTTTTTT TTTTTTTTTT 1440 GAGATGGTCT TGCTCTGTTG CCCAGGCTGT AGAGCAGTGG TGTGATCACA GCTCATTGCA 1500 GCCTTGACCT CCCAGGCTCA AGCTATCCTC CCACCTCAGC TTCCCGAGTA GCTGGGACCA 1560 CAAGCATGCA CCACCACACA TTTTTGTATT TTTTGTAGAT ATGGGTTTTT ACCATGTTTA 1620 CCAGGCTGGT CTCAAATTCC TGGGCTCAAG CAATCTTCCT GCCTTAGCTT CCCAAAGTGC 1680 TGAGATTATA GGTGCGAGCC ACCACACCCA GCCTTTTTTT CTTTTTTTTT CTATAAATAT 1740 ATATATATAT TATATATATA TATATATATA ATACTTTAAC TTCTGGGATA CATGTGCAGA 1800 ACATGCAGGT TTGTTACATA AGTATACATG TGCCATGGTG GTTTGCTGCA CCTCTCAAAC 1860 CGTCATCTAG GTTTTAAGCC CCACATGCAT TAGGTATTTG TCCTGATGCT ATCCCTCCCC 1920 TTGCCCCCTA CCCTTTTATT TTCCTTTCCT TTCTCTTTTT TATTTTTTAG AGATGGTGTC 1980 TCACTATGTT GCCCAGGCTG GTCTCCAACT TCTGGGCTCA AGCAATCCTC CTGCCTCAGC 2040 TTCCCAAGTA GTTGGGATTG CAGGCATAGG CCAGCACATC TGGCCCCTTT TCTTTTTCTA 2100 ATAACAGCTT TACTTAGATG TACTTTACAT GCCATAAAAT TCACCCTTTT AAAGCGTACA 2160 ATTAAGTGGT TTTTAGTATA TTCACAGAAT TGTGCAACCA TCACCACTAT TTAATTTTAG 2220 AACATTTCAT CACTCCAAAA AGAAACCGGC ACCTATTAAG TCACTTCTCA TTTCCCTACC 2280 CCATCCCCAT CCCCTAGCAA CCAACAATCT ACTTTCTATC 2320
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