Tag | Content |
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EnhancerAtlas ID | HS105-38926 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr19:10812930-10814240 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr19:10812967-10812979 | TGTCAGGGGGTG | + | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTGAGAGGAC CCTGGGGAGC CGCCTCCTTA CCCTGTCTGT CAGGGGGTGA AGTTTACACG 60 GGGCCTGTTT TTTAGCTGTT GTGTGGCTTT GAGCAGGTCA CTCCTCGCTG AGCTTCAGTT 120 GAACCAACTC AAAGCGGGGG TAAATAGTAG CAGGTCTTTG GTAGAATTGT TGACAAGTAC 180 ATATGAGATG ATGTCAGTAA ATCTCCATCC CAGCCATGTA GTAGCTTAAG TATTATTATT 240 GCAGTTTTTC TCTCATTAGC AAATTAAGAC TGGACGTGGA AGCTCATGCC TGTAATCCCA 300 GCAATTTGGG AAACTGAGGC GGGAAGATCA CTTGAGGCCG GGAGTTGGAG ACCAGCTTGG 360 GCAATACAGG GAGACCCTGT CTCTACCAAA ATAAAAAATA AAAAATAAAA AAAACAAATT 420 AATTGGACAA ATATCTGTTG AAATAATGGT GGCAACAAGA GGATTGGGGA GGCTTTAGGC 480 TTCTCCCATA TCCTCAATAT CCTTCTTTTT TTTTTTTTTT TTTTTTTTTT TTGAGACAGA 540 ATTTTGCTCT TGTTGCCCAG GCTGGAGTGC AATTTTGCGA TCTGAGCTCA CTGCAACCTC 600 TGCCTCCCGG GTTCAAGTGA TTCTCCTGAC TCAGCCTCCC GAGTAGCTGG GATTACAGGT 660 GTGCGCCACC ACACCTGGCT AATTTTGTAT TTTTAGTAGA GACAGGGTTT CTCCATGTTG 720 GTTAGGCTAC TCTCAAACTC CTGAGCTCAG GTGATCCGCC TGCCTCGGCC TCCCAGAGTG 780 CTGGGATTCC AGGCGTGAGC CACCACACCT GGCTTTTTTT TTTTTTTTTT TTTTTTGAGA 840 CAGAGTCGCC CAGGCTGGAG TGCAATGGTG TGATATCCAG TCACTGCAAC CTCCACCTCC 900 TGGGTTCAAG TGATTCTCCT GCCTCAGCCT GCTGAGTAGC TGGGATTACA ACTGCTTGCC 960 ACCATGCCCA GCTAATTTTT GTATTTTTTG TAGAGACGGG TTTCACTATG TTGGCAAGGC 1020 TGGTCTCAAA CTCCGGACCT CAGGTGATCC ACCTGCTTCG GCCTCGCAGA GTGCTGGGAT 1080 TATAGGTGTG AGCCACCACG CCTGGCCCAA TATCCCCATT TCTTGATAAA GAACCATGGC 1140 AACACAGGGT CAAAACCCCT CTTCCCCTCA TCATTCTAAT AGATTGATGC TGTAGGGAGG 1200 AAGAAATATT TTTTCTTCTT AGATTCATGG CTGAAGCCCC TATAACAAAA ACCCTTATAA 1260 GAAAAGAAGC CACGTGCTGG GTGCGGTGGC CACGCCTGTA ATCCCAGCAC 1310
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