Tag | Content |
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EnhancerAtlas ID | HS095-26136 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr6:43692210-43693760 |
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 | Nr2f6(var.2) | MA0728.1 | chr6:43693712-43693727 | TGAACTCTTGAACTC | - | 6.19 |
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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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I043723 | chr6 | 43691339 | 43693949 |
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Enhancer Sequence | ACATAGTTAG GGAAATGCTG GCTTAAGGGT GGGAAAGGGG GTGTGCTTGA TACATTAACC 60 TTCCCCAAGA GCATTTGCCC TCCCAACACA CTCCCTCCTC CACCCATTGC AAGTAGTGTG 120 TGACACATGT CTGTTGTAGA AAAGTGGGGG AAAAAACTAC AAAGAAGAAA GTTACCCATC 180 CCCTGCCTCC AGAAGAAAGT TACCCATCCC CTGCCTCCTG CTCCTTAGTC TCTTCTCAAA 240 AGAGCTCTGG CCACTGTCCT CGGTCTTCCT GGAGAAAGGG TGATGATGGA GCTCCCCTCA 300 AGGCACACCC ACTTCTACTG GGGAGAAGCC CCAAGAGGAA AGGGCCCTTT TAGAGGTCAT 360 CTTATCCACC CCTCCGTCTC CTCTCTGTGC AGATTCTTGC TTCCCTCTCT TGCTGACATT 420 CCTACAGGAA GGGAGATGGT GGTGGTGGTT TGGAGGGTGT TGAGGGGCGC AGAGGGCAAT 480 TGGGTATGTA GATCATCAGG GTGGAAGGTG AGCTTCCTTT CTAGGTGGGG AAACAGGCTC 540 AGAGAGGGGC CATGACTTAC TGGTGTTTCA CAATGAGCCA GTGGTGGAGC TCACAGATCC 600 TGGCCCCAGA CCAGGCACCC TCCTCCCCCT AACCCCCATC TCCAGCTCTC AATGCCAAGA 660 GTCTGGAGCG GGCCCTGTGC ACTCCAGGCA AGGCTGCGGT TTCTTCTGTG GGACTGTGGA 720 GCCACCCAGG GTGTGTGGGT GCTGCGCACG CGCACCACAG TTGTGTAACA GGCTCTGGGG 780 CGTGTGCACG CGCTCAGTAA CCTGATGCAA CAGGGAAGCT GTGGTCCCGT GAGCTGGGGT 840 GTGGGCGCTT GGCCGGTGCC CAAACCACAA AGAGTATTTG GCTGGTGGCT AAGGAGGCCA 900 GGCATGGGGG TCGCAGAGTT GTCTACGTCA GGGCTTGTCT ATCCCTAGTT GCCCACATCC 960 TGGTCCCTGT GGGCGCAGGG CTGGGAATGG GGCTGCCTGG CCAGGTGATA CTGTGGAGGA 1020 GGGGTTGGGG CCTTGCCCCT TCCTCCTTCT GTTTGCCACG ATGCCTATTG TGATGAGGAT 1080 GGGGGGCAGG CGGGGCTTCC TCCCTGTGGT TCCATCTCTT CCTGGCTGTA ACCCCCCAAC 1140 CCAGTTCTGT ACCCTGCTCT CTCCACCAAT CCTGGAGCCC TCACCACAGA TCCAGGTCAT 1200 TTTACACAGC AATATCTGCC TCTCACTCCC CCACCTCCCC TGAGTCTCAC AGCCCTGCCC 1260 TCCCTACATA ATAGGCTTTC CTGGGCACCC CAAATTGGGA GAAGCAGAAC GGGGAAGGAG 1320 AAGAAGAGTG GCCACTTTGC AGCCAGCCCA GATGCTGACT TTCCGCTGCC ACTTCTGAAC 1380 TGAGTGACTG AGAAAGATCA GTGTCCCTTC TCAGCCTCCA TGTACTCATC TAAGAGGTGG 1440 GGGCAGTGAT ACTCCCTGCT GAGAGTGGTG GAAAGATAGT GTGCTCCTGT GAACAGGAGT 1500 CCTGAACTCT TGAACTCTAG GGTCTAGGAA AGAACTCCAT GAAAGGGGAG 1550
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