Tag | Content |
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EnhancerAtlas ID | HS095-07809 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:110707190-110709030 |
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) |
ZNF263 | MA0528.1 | chr12:110708725-110708746 | GAAGGAGGGCAATGGAGGAGA | + | 6.03 | ZNF263 | MA0528.1 | chr12:110707279-110707300 | GGGGGAGGACAGGAAGGTGAA | + | 6.13 | mix-a | MA0621.1 | chr12:110708970-110708981 | ACTAATTAATT | - | 6.62 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_28268 | chr12:110707552-110708298 | Fetal_Intestine | SE_29946 | chr12:110706983-110709211 | Fetal_Muscle | SE_40866 | chr12:110707047-110708878 | Left_Ventricle | SE_42743 | chr12:110707132-110708928 | Lung | SE_48901 | chr12:110707169-110708859 | Right_Atrium | SE_53187 | chr12:110707473-110708854 | Small_Intestine |
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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 |
GH12I110269 | chr12 | 110706930 | 110709064 |
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Enhancer Sequence | CTTTTATGTA CCAATGAAAT CAAGCCTTGC TGGAATGGTC GGTTGTCTAC CCCTAGTTTT 60 ATACTGGGAG GCTACTAAGA AGAACGGTTG GGGGAGGACA GGAAGGTGAA GGCGCTTTCT 120 GGAAAAGACC CATCCTAATG ATACATGTGC TATGACTGCA GCCCCCTCTC TCCCCTCAGG 180 TCAGAGAATC CTCTTAGAGG CTGTTCTGTG GTCTCAGAAT GCTCCCTGCC CCCAAGTTGC 240 CATGTCAGAT GTTTGAGGGA AATCTGATTT CTGAGGACAG AGCTCTAGGT GTGGGTTGTT 300 TTATTTTGGG GATGGGGTGG GGGTAGGAGT TGGCCATGGG TTTGCTGCAT TCCAGGAAGA 360 GGGAGGACTG CTCTCCTCCG ATGAGTCATG GAAGAGAAAC GTCTAATGTT TGCAAACGTC 420 TCCAGCCAAG CCTCTGCTTT CTTAGACTCC TCCCATCCCC CATCCATGCA GATTGGACCC 480 CCGTGAGAAG ATTTAAATGT TAAGGTTGAA GGCCAAAGAG GCCATGGCTC TACTGGTTGA 540 GATGGGAAGC AGCTAACAGA ACGGGAACGA TTGTCCAGTA CCTCTAGACT CCAGCTTGCA 600 AGACACGGGA CAGGACCTTA TAATAGGTGT ATCTGTCTCC CAAATCAGGA CATACTCTGG 660 GTGGTGCAGG AGGATCAGGT GAAAGAACTG GATTTTCACA GGGGCCCTGC CATCTGCAGA 720 GGGCCTCCAA TCAACACGGC ATCTGCAGAG GGCTGGGAGA TCAGAGAAGC CACAGTTGGA 780 GAAGAAGCAG AGGCGATTGC AGAAAAGGCC AGGGCATAGG GAGTCAGGGG AGGTCTTGCA 840 AATGACAGAA GCTGTGATCT GTTTCTTTCA GGGGAAGATG AAGGATAAGC GGGCTTGAGA 900 GGGATGGAGC TAGTGGGGGT GTGCTGGGAG CCCACGGCTG CCTCAGCCTC AGCCTTAGCC 960 AGACTGCTGG AGCCAGATGG GGTTCATGAT GCATCTTCCC AGATGGAACG GATCAGGCAT 1020 GTCAGACAAG CTTCTCTTAG GATACATGGT GTCCTCCTCC CTCCCCCTAT TTGAAATCAG 1080 GAGAGAATCA CAAGGTAACT TGGGAGGGCT GCCAACCTCC TGGGATCTTT TGTGAACTAT 1140 CAGGTAACTA CAGCAGGATC ACAATGGGAG ACCTAAACAT GCCTCCACCA ACACCCCCCC 1200 CCCTTTTTTT TTCTATTGTG GGACATCAAG GGAGCAAGCT GGTCAGCTTG GGAACAAAGA 1260 TCCTATTCTA GGAATTTGTC CACAGCAACC CTATCTGCTG TGTGCACTGT CCTTGGATTT 1320 CTGCCAGACT GAAACCCAAC CTGCTTGGGG CTGCTACCAC TACTGTGAGA GCAACACCCT 1380 GGCACCCGGC AGGGAAGGGA GAATCAGAGA ACTCATCCTA TAAAATTAAA ATTGCATTTA 1440 ATCACTCTTC TTTCTTCTAC CAGGCTCAGG AGGCCAGGCC ATCTCTGCAT TTTAAGTATT 1500 TCACCATTTA AAGTCTAAGC ACCTTGGGGG GTGAGGAAGG AGGGCAATGG AGGAGAACTT 1560 TTGAAATCTT TCCACAAAAA TCAAAGAACA AACCAACTAG AGGGAAAAAT AGCTGCTATA 1620 TTTAAACTAC ATTATCCCAT CAGGGAGCTA TGGTTTTGAG AACCATTCCA CAGTACTTTG 1680 TTTGGCACTG CTATATGGGT TTCTTTTCTT TCTTTTTTTT AAGATGGCAA GATTTTTTTT 1740 TTTCTTCAGA GCAGTAATTG CAAAGGAAGC AAAGGTCTTC ACTAATTAAT TTGGTAGATA 1800 TTCACTGAGC ATCTGCTATG TGCCTGGCAC TACACTGGTC 1840
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