Tag | Content |
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EnhancerAtlas ID | HS046-08523 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr12:58257400-58259800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr12:58257626-58257641 | CATCGTGTGTGGCCT | - | 6.18 | MIXL1 | MA0662.1 | chr12:58258300-58258310 | TCTAATTAAC | + | 6.02 | YY1 | MA0095.2 | chr12:58257744-58257756 | GCAGCCATTTTG | - | 6.52 | Zfx | MA0146.2 | chr12:58259063-58259077 | GGGGGCCCGGCCTG | + | 6.02 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_01602 | chr12:58256570-58259604 | Aorta | SE_03465 | chr12:58257834-58258487 | Brain_Angular_Gyrus | SE_03465 | chr12:58259275-58259770 | Brain_Angular_Gyrus | SE_04181 | chr12:58257981-58260008 | Brain_Anterior_Caudate | SE_05429 | chr12:58257885-58259940 | Brain_Cingulate_Gyrus | SE_06149 | chr12:58257645-58260324 | Brain_Hippocampus_Middle | SE_07273 | chr12:58257882-58259989 | Brain_Hippocampus_Middle_150 | SE_23544 | chr12:58258735-58259659 | Colon_Crypt_1 | SE_24094 | chr12:58258859-58259582 | Colon_Crypt_2 | SE_26211 | chr12:58257419-58260149 | Duodenum_Smooth_Muscle | SE_26717 | chr12:58257432-58259746 | Esophagus | SE_29576 | chr12:58257727-58259951 | Fetal_Muscle | SE_31793 | chr12:58257929-58259661 | Gastric | SE_42147 | chr12:58257909-58259832 | Lung | SE_46841 | chr12:58257423-58257783 | Ovary | SE_46841 | chr12:58257937-58258614 | Ovary | SE_46841 | chr12:58258713-58259581 | Ovary | SE_48108 | chr12:58257427-58260981 | Psoas_Muscle | SE_48620 | chr12:58257506-58259733 | Right_Atrium | SE_49678 | chr12:58258733-58259603 | Right_Ventricle | SE_50105 | chr12:58257312-58259665 | Sigmoid_Colon | SE_51099 | chr12:58257569-58261177 | Skeletal_Muscle | SE_52596 | chr12:58257931-58259626 | Small_Intestine | SE_53450 | chr12:58257930-58259691 | Spleen | SE_65570 | chr12:58257981-58259970 | Pancreatic_islets |
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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 |
GH12I057863 | chr12 | 58257413 | 58259989 |
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Enhancer Sequence | ATCAGTAGAA AATCAAGGAC ATTCAACAGA GGTATAGACC ATGGGTGGCC ATCACAAGCC 60 ACCTATGGTA CACAGTGCAC TGGTTTATAT ACCATCTACT GCATTAGTCC CAGCCTCCCA 120 AACTGGCACC AACAGTCCTC TTCTCCTTGC CCACTACTCC CTTCTTCCCT CCAAGATCCC 180 TTTGGAGGTG ATCCATCAAG TTGGAGCCTG ACACATAATT TCTGCTCATC GTGTGTGGCC 240 TTCCTCCAGT TTCCTGGGGA TGTGAAGGAG GAGGGAGGGA CCTGTCAGCT GGATGGAGAC 300 TTCTTTGCCC AAAGTTGATA GTACCACAGT GGGGCTCTTC ACAGGCAGCC ATTTTGAGAC 360 CTGTCCAGCA CAAGGTTCTA GTTTTGGGGG TCCTGTCACT TAAATAAGAA AATATTGAGT 420 GCTTGCCTTG TGCCAGTGTC TGTTTGAAGA GGCAGACCAC TGTCACTTTT CTTGTATTAT 480 CTAATTCAGT CCACACAACA ATTGCCTTTG GTGGGAATTT TAATTATTCC ATTTTACAGT 540 TGGAGAAACT AAGGTACAGA AAGATAAAGT CACTTATCCT TATCAAACAA CTAGTAAGTA 600 GTGGAGCCAC GATTTGAACC CAAGCAGACT GCCTGCAGCA TCCCTGGTCG GCACCCCTGT 660 GCACACTGCC AAATTGTCTT ATTCTAGGAA TTTCCCTTCC CTGCGCCATG ACATATTAAA 720 AACTCAGCTA GAGGTCATTT TGAGCAAGGA ACCCTTCTCC ACCCTGCCTT TCCATGAGAG 780 GGAGTTGGGA TCCCAGAGAA GAGGAATTCC AGAAGAGGCA CTGCCACTTT GGCTATTTTT 840 CCTGCATGTT CCCCAGGCAG GGAGCGCCAG CTTTTGATTT GCCAGGTGTC TCTCTGTTCT 900 TCTAATTAAC ACCAGATCCA GCCTTTAGCC AGAGCCCTGC CTATAGCTGG AATCCACCAC 960 CATGCGGCTC AGGGGCCAGT TCGCTGTGAC TGCCACAGAG GACAAAGCAA GTGCTAACTC 1020 GGGGTGGAGT CTTCTGTAAT GATGCTCCCT TTGCCTCATC CATAAAAAGC TCCACTCAGA 1080 TCTACCTCGT TTGTGGTGGA GGCCAGGGTG GCAGAGTGTG CAGGAGAAGG CAGAATCAGG 1140 CTGAAACAGC TCCTCTTTGC CTCCCTGGAT TCTTTTCCAA AATGCTGTCA GCACTGCCAG 1200 TTGGAAAATA TTTTTCTCCC TCCCTTTGTC TTCTTTCTTA TTAAGAAAAA AAAAAAAGCC 1260 ATCTGGTGTC AAATTCACTC CTGGCACATC ATAAAGGGTA GCACTAAAAA TGTCCCCGAA 1320 AAACTAAAAG CAAAACCACA GTAGTACACA TGGGATTTAA TCTCAGCATC CTAGAATTTC 1380 AGAGTTGATA GGGCCCTCTG AGATCAAACC CTTCCTGTAG ACGGGAGGAA ACTGAGGCCG 1440 GGAGGGATTA TGTTATTCTT TCAAAAATGT TTACTGAGCG CCTACTATGT TCAAGACACT 1500 CTTCAGGCGC CGCAGATGAA TCACGAACAC AACAGTGAGG CAGAAATCCC CGCCTCCTTG 1560 GAGCTTTCCG TGGGAGGTTC TTGCCTCGGC CCTCGGGCCT GCGTCTGCCG CCGTTTTTAA 1620 ACGGCCCCGA AGTTGGGAGC TCTGGCTGGG CCACCTCCGG GCTGGGGGCC CGGCCTGGGG 1680 CCGCCCCTCT TTTCCCGCCC GGAGCCGCAG TGTCCAGAGG GGCGAAGTTT GCGGCCACCG 1740 CCGGCCGTGC AGTCTCCCGC GCTTCCCCCG CCGGAGCGCC GGCCCCGCAT TCCTCCGGGT 1800 TGAGCAACAG CTTTTCCTCC GAGGGCGGCT GGCCGGGCAA GGCGGGGCCG CCAGCGCTGG 1860 GGCCCTCGCG GGGCGCGGCC CGAGTGTCCG GGGCCTCTGG CAGCGCCCCG GGTTTAAGTG 1920 GAGCGCGGCC GCCAGACCCT CCCCGGGGAG CCGAGCTCGG AGAGGGGGGC CGCAGAGCCC 1980 AGGCCCCAGC CTGCCCTTCC TGCAGCGCCG GCGGGATTGC CGAAAGACCA AGCGGGTGCC 2040 AGGCCTCACC CGACCTTGAT GTTGGCGTTA GTCCGGGTTG ACCGCCCACT CTGACGCTCT 2100 ATACAGAGAG CTCCTTTGCT TCCATTTTTA CTCCAATCCT GGAAATTCTT TGTCGATGAA 2160 AAGGGGACAG TTTATAGTGA ACTCCAAAAG AGGGGTCCTA ACCTAACCCA GCTCTTTGAA 2220 TTTAAACACT TACAATAATC ATATGTGTGT GTGTGTATGT GTGTGTATAT ATATATGTAC 2280 ACATACATCT GTGTACACAG ACGTATGTGT ATACATACAT ATATATGTAT GCATACATGT 2340 ATGTATGCAT ACATGTATGT ATGCATAGAT GTATGTGTAT ATATGTATGT ATACATATAT 2400
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