Tag | Content |
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EnhancerAtlas ID | HS098-48529 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:43692140-43693590 |
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) |
DMRT3 | MA0610.1 | chr6:43692255-43692266 | CTTGATACATT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_50764 | chr6:43691612-43694182 | Sigmoid_Colon |
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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: 1 | ID | Chromosome | Start | End |
GH06I043723 | chr6 | 43691339 | 43693949 |
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Enhancer Sequence | GCAGTCAAGA AAACCTGTTA GACTGTGTTT AACTCAGGTT TCCTGTGCTT ATTTGAGCCC 60 GTTTGCCACA ACATAGTTAG GGAAATGCTG GCTTAAGGGT GGGAAAGGGG GTGTGCTTGA 120 TACATTAACC TTCCCCAAGA GCATTTGCCC TCCCAACACA CTCCCTCCTC CACCCATTGC 180 AAGTAGTGTG TGACACATGT CTGTTGTAGA AAAGTGGGGG AAAAAACTAC AAAGAAGAAA 240 GTTACCCATC CCCTGCCTCC AGAAGAAAGT TACCCATCCC CTGCCTCCTG CTCCTTAGTC 300 TCTTCTCAAA AGAGCTCTGG CCACTGTCCT CGGTCTTCCT GGAGAAAGGG TGATGATGGA 360 GCTCCCCTCA AGGCACACCC ACTTCTACTG GGGAGAAGCC CCAAGAGGAA AGGGCCCTTT 420 TAGAGGTCAT CTTATCCACC CCTCCGTCTC CTCTCTGTGC AGATTCTTGC TTCCCTCTCT 480 TGCTGACATT CCTACAGGAA GGGAGATGGT GGTGGTGGTT TGGAGGGTGT TGAGGGGCGC 540 AGAGGGCAAT TGGGTATGTA GATCATCAGG GTGGAAGGTG AGCTTCCTTT CTAGGTGGGG 600 AAACAGGCTC AGAGAGGGGC CATGACTTAC TGGTGTTTCA CAATGAGCCA GTGGTGGAGC 660 TCACAGATCC TGGCCCCAGA CCAGGCACCC TCCTCCCCCT AACCCCCATC TCCAGCTCTC 720 AATGCCAAGA GTCTGGAGCG GGCCCTGTGC ACTCCAGGCA AGGCTGCGGT TTCTTCTGTG 780 GGACTGTGGA GCCACCCAGG GTGTGTGGGT GCTGCGCACG CGCACCACAG TTGTGTAACA 840 GGCTCTGGGG CGTGTGCACG CGCTCAGTAA CCTGATGCAA CAGGGAAGCT GTGGTCCCGT 900 GAGCTGGGGT GTGGGCGCTT GGCCGGTGCC CAAACCACAA AGAGTATTTG GCTGGTGGCT 960 AAGGAGGCCA GGCATGGGGG TCGCAGAGTT GTCTACGTCA GGGCTTGTCT ATCCCTAGTT 1020 GCCCACATCC TGGTCCCTGT GGGCGCAGGG CTGGGAATGG GGCTGCCTGG CCAGGTGATA 1080 CTGTGGAGGA GGGGTTGGGG CCTTGCCCCT TCCTCCTTCT GTTTGCCACG ATGCCTATTG 1140 TGATGAGGAT GGGGGGCAGG CGGGGCTTCC TCCCTGTGGT TCCATCTCTT CCTGGCTGTA 1200 ACCCCCCAAC CCAGTTCTGT ACCCTGCTCT CTCCACCAAT CCTGGAGCCC TCACCACAGA 1260 TCCAGGTCAT TTTACACAGC AATATCTGCC TCTCACTCCC CCACCTCCCC TGAGTCTCAC 1320 AGCCCTGCCC TCCCTACATA ATAGGCTTTC CTGGGCACCC CAAATTGGGA GAAGCAGAAC 1380 GGGGAAGGAG AAGAAGAGTG GCCACTTTGC AGCCAGCCCA GATGCTGACT TTCCGCTGCC 1440 ACTTCTGAAC 1450
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