Tag | Content |
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EnhancerAtlas ID | HS098-01357 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:33829240-33832320 |
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) |
Stat6 | MA0520.1 | chr1:33831048-33831063 | GGTTCTCAGGAAGGC | - | 6.03 | Stat6 | MA0520.1 | chr1:33830914-33830929 | GTTTTCTTGAGAACT | + | 6.37 | ZNF263 | MA0528.1 | chr1:33830290-33830311 | AGAGGAAGGGGTGGGAGAGAG | + | 6 | ZNF263 | MA0528.1 | chr1:33829595-33829616 | CCCTCCCCCACCTGCTCCCCC | - | 7.16 | ZNF263 | MA0528.1 | chr1:33829592-33829613 | CTCCCCTCCCCCACCTGCTCC | - | 7.1 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_03193 | chr1:33827954-33833250 | Brain_Angular_Gyrus | SE_03931 | chr1:33826399-33836016 | Brain_Anterior_Caudate | SE_04902 | chr1:33822310-33834277 | Brain_Cingulate_Gyrus | SE_05882 | chr1:33826050-33834668 | Brain_Hippocampus_Middle | SE_06849 | chr1:33827014-33834415 | Brain_Hippocampus_Middle_150 | SE_07821 | chr1:33822496-33836906 | Brain_Inferior_Temporal_Lobe | SE_09073 | chr1:33829143-33829607 | Brain_Mid_Frontal_Lobe | SE_09073 | chr1:33829652-33830555 | Brain_Mid_Frontal_Lobe | SE_25917 | chr1:33827240-33832198 | Duodenum_Smooth_Muscle | SE_30304 | chr1:33828568-33832324 | Fetal_Muscle | SE_33616 | chr1:33827075-33832653 | H2171 | SE_37317 | chr1:33828525-33832018 | HSMMtube | SE_40689 | chr1:33826435-33834223 | Left_Ventricle | SE_42268 | chr1:33828744-33834073 | Lung | SE_48345 | chr1:33828927-33831644 | Psoas_Muscle | SE_48345 | chr1:33831744-33833799 | Psoas_Muscle | SE_48801 | chr1:33828750-33834003 | Right_Atrium | SE_50397 | chr1:33828866-33831857 | Sigmoid_Colon | SE_51341 | chr1:33826598-33833990 | Skeletal_Muscle | SE_53534 | chr1:33828984-33831733 | Spleen | SE_53534 | chr1:33831914-33833591 | Spleen | SE_54994 | chr1:33827948-33834036 | Stomach_Smooth_Muscle |
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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 |
GH01I033361 | chr1 | 33826803 | 33833802 |
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Enhancer Sequence | AGGCCCAACT GGGTGAAAGG GCCCTGGCTT TTCAACAACC CGACAGTTCC CTTTTATCAC 60 AGCATATCCC TCCCAGTCAG CAACTTTCTC CTCACCTTTG GGCCTGAGTG TGCACCCAAA 120 GCCTGGAGTT TATCCACTAG AATGAGGACT CCAAGAACCA AGTCTCCTAT CTGGGGCTGT 180 GGCCCACTCC CTTAGGACTC GGCTTCCCTG AAGGCCAGGC CCAAGGGACC CCTGCTGCCT 240 GCCTCTCTTC TGCCCTCCAT TGCTCAGTCC TCATGTCAGT GAGAAGGGCA AGCCAGGCCC 300 TTCTCCTTCC CCTCCAAAGC CCAACCTCTT AGGCTCTGTT CTCCGCCCCT TACTCCCCTC 360 CCCCACCTGC TCCCCCACCC CTATTCTCGG CATAAGGGAC CTTTTCTATT TGCAGAGCCT 420 GAAGAAGCCG GTTGCCAAGG TGACAGGAGC AGGAACAGCA GGGAGCTTGC CATGGGGGAG 480 GGGCTTTGCC CCCAAACAGC TGTCAGTGGG AGCAGTCCCA GCTGGGACTG GAGGGTCTGC 540 CTGCTCTGGG AGGAAACAGC CCCCAGGAGA ACACATTCCT CACTGCCATA CCCCCTCCTA 600 CTGGCCCACT GCAAGTCTCC ACTGGTTACT TTCCCTGGGG GCAGCCAGCC AGCCAGCTCA 660 AAAAATGCTC CAATAACAAA CAAAAAATGT GTGCGCGCTC GCTTGCTTTC TCTCTCCCAG 720 ACACACACAC ACACACACAC ACACTTGCTT TCACACACAC ACACACACAC ACACACACAC 780 ACACACGCTC AAGCACGCTC TTCTCTCCTG CTCTCAGATC CCTTGGTTCA TTGACAGTGG 840 GTTGGCTGGG CAGGAGGCCA GAAGTCACCT CTGCCCAGGG AACTGTATAG CCCAAGACAG 900 GTGCTGCTCC TGGCTGCCGT GCACTAGGTC CTAAGAATGA TTTCAGTCTT TTTGTCCAGA 960 GGCCCTGAGA GGACCTTCCC CTACTAAAAC TCCCCAGCTG CCTTCCATAT GGGAGGTGGG 1020 AGTGGGGCAG CGCCATCTCT GGGCTTACAG AGAGGAAGGG GTGGGAGAGA GGAAGAATGA 1080 ACAGGATGGT GGGAGGCAGG AACAATGCAG GCCCACTGCT TTGTGTCTCT GGGGAGAGGT 1140 TCTTTGTGGA GCTGCAGCTC ACAGCTGCTC CATAGAAAGT TCTGTGGAGC CACTGGTCTC 1200 TGTACTGCAT TCTAGCCAGG CACTGTTAGC CTTAGGCCCT CGGGCCTCAA GCCTGTCACC 1260 TGCTGGTGTT TACCTTTACA TGGGGTCTCC ACCAGACTCT GCAAACCCTC AATAGGCTTA 1320 GACCCCCCAG ATACTTTCAG CTTTGGGTCA GAAACAGGAA AGGCTGAGGA GGCCCCAGAT 1380 TACTGTAAGA ACTGAGAGGG ACGATCTGGC TTGAGATGAA GAACAGTGTT TGACTCAGCC 1440 AGCTATGGCC CCCAGTCCTG CCACTTACTA CTTAGGTGAC TTTGAGTGCG TGACGGATGT 1500 GGTAAGCTCC TGGAGAACCT CTCTGAGCTT CAGTTTGCTC ATCTGTAAAA TGGATAAAGA 1560 CAGCTACCGG ACAGGGATCT TTCCAGGGTT TAAAGAAGCG TGATGCATAC AATGCAGGGC 1620 ACGTTATCTA GCACACGACG GACGTCCTGT GAGTGCTGGT CCCGTTTCTG TCCAGTTTTC 1680 TTGAGAACTG AGTTGCCTAG CAGCCTTAGG AGGAACCCAA GAACTAGTCT TTCTTTTGAA 1740 CAGTGTTAGA ACTTGGGGGG CTGGCTTAGA TTTAGAGAGA GGTTACATTT CGGCCTGGGC 1800 TGGAAGGGGG TTCTCAGGAA GGCCTGAGAC GCAGATGGTC CGCCAGGGCA TGCGGATTGA 1860 ATGAGAAACT AGAAGAAGTG CTCATCTGGG GTCTCAGCTG TAGTCCAAGC TGCTTTCAAC 1920 GCATTGAAAG AGCCCCCAGT CTACCCTTCT GAGCCTCACT TTCTTTTTCC ATAAAAGGAA 1980 GAGGCTGGGC CACTTTCTGG AGAAAGCCAT GCCAGACAGT GAGAAACATC TGAAGCCACA 2040 GGGCCGTGAG GCCTCCGTGG GGAGGTGCCT TTCTTGGCTC AGCGGTGACC ACTGGAATGC 2100 AGCGACTGAC CCTTTGCCCC TGGGTGACTT CTGAAGCCTC AAGAAGGTGA ATGAGGGATT 2160 TTGACCCCGT TTCCTCCTAA CTCAGTGCCA TGTGCGCTGC TTTGCTTTTC TCTGCCTGGG 2220 AACCTTCCCC ACTCTGTCTG TCAGGTCACA TGCTCGTGCC GCAAGGCTCA TGTGCCATGT 2280 CCTCTGAAGG ACGGCATCTC TGACCCATTC TGCCTGACAG GCAGCTGACC ATCTGTGCCC 2340 ACACTGTACC TGGTACTTAG TCCTAAAATA GAATTTATGA AGTGGAATGG ATTTGCTTCT 2400 ATATCTGGTT CCCTTCTTTT GACTGCACAC TCTAGGGAAA AATAAAAATC CTATCTTATT 2460 TTGACAAAGA TGTATTGAGA TATATTCTTG ATGTATTTTC TCAAGAAAAA ACCCCACAGA 2520 TTAGATTGGA TGGTAAAATG GTTTGAGAGA GGACTGAGGT TAGTGGTTGT CTCAGGGATG 2580 CGATCAGCGT GACCCTCTCT TTAATGCAAA GCCATGTGCT TCGCCACTCT ATTTATTTCT 2640 ATGGTAAAAC AGGGTGGTCT TGTTACCTAG ATCGATAGGC CTGGCTTCTT GGGCTCTTGG 2700 CAGATTTTCC CATTAAAGAT TGCCTACAAT GGGCAGCACA GGGAGAGTTT TAGTAGGCAG 2760 GGAAAGGGGT CTAGCAGGGC ATGTGGATTC ATCGGACCTG CCTCACAAGC AAGCTCCTAG 2820 ATTTATTCTC AAGTGTTACC CTCACTAGCA AGCCTTTCCT AGCTCCTCTC CTCAAGCCAC 2880 ATAGCTCTTC TGTTCTGACA GTGTTCAGAG CTTAGATCTA TTATGGCATA TGCACTGCAC 2940 TCTCTGTCTC CCCAGCTACA CTGTGGAGGG CAGGACCTGA GTCTCATTTA TCTCTGCACA 3000 CCTAGAATTG GCAACATGAT TGGCAAATAC TAATCAACAA ATGCTTGCTG AATGATGAGA 3060 AAAATAAACT TCCTACATTC 3080
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