Tag | Content |
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EnhancerAtlas ID | HS139-28576 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:43132450-43137020 |
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) |
Atoh1 | MA0461.2 | chr2:43135174-43135184 | AACATATGTT | + | 6.02 | Atoh1 | MA0461.2 | chr2:43135174-43135184 | AACATATGTT | - | 6.02 | KLF5 | MA0599.1 | chr2:43133714-43133724 | GGGGCGGGGC | - | 6.02 | MEF2A | MA0052.3 | chr2:43135897-43135909 | GCTATTTTTAGC | - | 6.44 | MEF2B | MA0660.1 | chr2:43135897-43135909 | GCTATTTTTAGC | - | 6.92 | MEF2C | MA0497.1 | chr2:43135896-43135911 | TGCTATTTTTAGCCG | - | 6.69 | MEF2C | MA0497.1 | chr2:43135818-43135833 | TGCTATTTTTGGTTT | - | 6.82 | ZNF263 | MA0528.1 | chr2:43134007-43134028 | CCTCTTTTCTCCTCCTGCCCC | - | 6.28 | ZNF263 | MA0528.1 | chr2:43134023-43134044 | GCCCCCACCACTCCCTCCTTC | - | 6.39 | ZNF263 | MA0528.1 | chr2:43136893-43136914 | GGAGGAAGAAGGTGAGGAAAG | + | 7.23 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_00249 | chr2:43130206-43136208 | Adipose_Nuclei | SE_01603 | chr2:43129820-43136561 | Aorta | SE_13340 | chr2:43132971-43133878 | CD34_Primary_RO01536 | SE_26101 | chr2:43132837-43136480 | Duodenum_Smooth_Muscle | SE_26918 | chr2:43132509-43136380 | Esophagus | SE_29610 | chr2:43132087-43135929 | Fetal_Muscle | SE_31955 | chr2:43132608-43134821 | Gastric | SE_41001 | chr2:43130030-43136021 | Left_Ventricle | SE_42438 | chr2:43130331-43135877 | Lung | SE_46653 | chr2:43132449-43133922 | Ovary | SE_46653 | chr2:43133956-43135367 | Ovary | SE_48653 | chr2:43130245-43135329 | Right_Atrium | SE_49917 | chr2:43132964-43135285 | RPMI-8402 | SE_50379 | chr2:43130409-43136502 | Sigmoid_Colon | SE_52706 | chr2:43130385-43136477 | Small_Intestine | SE_53684 | chr2:43132408-43135384 | Spleen | SE_54955 | chr2:43132503-43136373 | Stomach_Smooth_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr2 | 43132657 | 43133201 | chr2 | 43133463 | 43133626 | chr2 | 43135640 | 43136093 | chr2 | 43132685 | 43134800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I042905 | chr2 | 43132340 | 43136304 |
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Enhancer Sequence | AGTCCAGTGC TCTTTTCTTG ACCCATATTA CCCTTTTCTG TGCGGAGCCT TCAGGGGACA 60 CTAAGTTAAG AGACGATGGC TGTGCTTTTG CCTTCTCGGG GCCACCCCAT TTCCAGTGCG 120 CTCCCACTTG GCTATGGCTT GACTTCCTGG AATGAGAGTG AAAGATCAGT GCCCTGAGAA 180 CCCCCCACTG TGCAGCTCAG CCCCACGGCT TTCACATGAC CTCTTCCCTG TTTGGAAGAG 240 CTGGCTCCGG TTTGCACAGT CCTTTTTCCC AGCTACGAGT CCTTGCGTTC AGCAGGGCTG 300 CTGGGTGGGT GCTCCTCCGT CACCAGCACC ATGGCTTGCA CCTGCGCAGG ATGGACGCCT 360 GACCCATCAG CCCTGCCTGG GTAGGCCAGG TGCCGCTCTG GATCTAGGAG GCCATCCCCT 420 GGGGCCAAGG TGGTCGCTTC TCCCAAGCGG TCATGTGGTT CAACGCTCTG ATTTCTGTGG 480 CCCCGGACGG CGGGTGGAGG ACGGGGTGTG AAAGGGTTAA TGTAATTTTG GCTGTGATTC 540 CATTTTGGCA TCTGCAAGTC AACTTAATAG GCTCTCAGTT TTCCTGTTGC CTCACCGATG 600 AAACAGAAAC CAGACCACAA GGGGGTCTGG AGATGTTTAA CCGGCGATGC CTCCTGGTGG 660 GCAGCAGGGT CTCCTCCGAG ATAGCACCAG AAATGACTGC TAGAAACTCG GCCGTGCTGG 720 GCTTCTGGGT CACCAGGACA AGGGAAGGGG CAGGGAACTG GGGTGCCCTG GAAAGTCCAG 780 CTCTAGGCAG AGGGGAAAGA AGGTGGGTGC AGGGTCCACA GATTCATGCT GGGATCCTGG 840 CTCCCCGACC TTGAGATCTT TGATCCTTAG CCTGCCAGGG GTTTCTGCCT CTCAGGATTC 900 AGTACCTACG AGAGCACTGA GCTTGGCACA GAGTATGTCC AGCTCAATAA CTGCCAGCCC 960 TGCTGAACTT CTGGCTTCTC TCTCTCCTGC TCTCCTTCTC CCTGGGCCTT TGCAATGCCT 1020 GTGCTCTCGT CCTGAAGCCC CATTGCTTCT GTTCATTTCC TGACCAGCTC CTACTCATTC 1080 TTCAGATCTC AGTTTGAATG TCACTTCCTC CAGGAAGACC TCTGCAACTG GACTAGGGAT 1140 CCTACCTTGG GCCCCATGTA AACCTCTGGG TGTCCTGAAC ATTCCCTTTC AGCCTTGTCC 1200 CCACCGCATC CCTTAGTCCC TTGCCCTCAC CCCCATTACA TTTCCCTGGT CTTCCTGTGC 1260 CTGTGGGGCG GGGCTGGAAT GTGGCTCAAA GCCCGAGCAG AGGTTCTGCA GAAGGGCTAC 1320 CCGTTCACTA CCTTGAATGT GGCCAGGAAA TGATTGGGGG GTGGAGGGCA GGTCACCAGT 1380 GCCCTGACCC ACCCAGGTGC CCTCTGGTTG CTGTGAGCAA GGGGATTTAG GCAATCCCAA 1440 TGTCGGGACT CTCCTGCCAG GATCGCTTTT CTCTCCGAGG TGGTTTTCAT TATTTTTCAT 1500 TCCCAGACTA TTTTGGAAGC TGGCTGCCAT GGGAACTGAG TCTTTGGAAA GCCCTGGCCT 1560 CTTTTCTCCT CCTGCCCCCA CCACTCCCTC CTTCCATCTC CATTCCCTCT TAATTGGTTT 1620 TTAGTTCCCT GGCTTTCAGG CCTGTCTGTT TATTTTGATT GCAACTCCAC AGAACAAATC 1680 TTTAATGAAC CAGCTTGCGG GGAGAGCCAT TAGCAGCCGC CTGCCTCGAG GGAGTGGGGG 1740 AGGTGCCTGG CCAGGCTACA GTCTCGGCTG CCCCAGGGAG GAGGCGGTGG CCAGGCATGG 1800 GGTAGCAGCC CGTGTTTTGG TTTCAGTCTT CCTTCGGGTA CAGTCTGGAG GTAAAGGAAC 1860 AGAGTTTGCC TTCCCTAAGC TGTCTGGAAC CTCAGCCAAG ATGACCTCAA AGTCTTTTAA 1920 ACAACCCAGG GGCCTTCAAA GTGTTCCCCG GTCCTCCCAT TGGCCCCAAG AGGGATGTCC 1980 TCTGAGTAAC CTCACTACAG AGGAGGGGAG TGAGGCTCAG AGAAATTGAG AAGCTCAAGT 2040 CACCCAGCCA GCAACCCGTG GCTCAATAAA CCCTGACCAG GGGCTTCCCC ATCATGCCTA 2100 GGATAAAGGT ACCCCCAGTT TCCCAGGAGT GTCACTTGTC CTTAGGCCAA ATTGGCAGCT 2160 GATAGTCCAG GCTAGGCTCT ACCAGGCCCT AGTTTTCTGG AGCAAATACC TCCTTGTCTT 2220 GTGCCTTGGT TTCCCCATCT CTAAAATAAA GACATATGGG CCTCACACTA TTTATAGGAC 2280 TTCTTCTTAG ACTGGATGAG ATTGTATGTG TCCAAGATCC TGGAAAGCAG AAAACATATG 2340 TGCGTGTGCG TGTTGTTATT ATTAAGAGCA GAGTACAGAC AATCCATGCA GTTCCCTTAC 2400 CTATAGCAGG CCTATTGATT GGCCCCATCT TCAGGGCAAC CTCAGTAGAT GTGGTTAGTT 2460 TTCCTTTTCA TATTGACCCT ATTCTGCCAG AGCCACTAAT CTTAGAAGCA TAGGGTAGTA 2520 GAGCAGGGAG GTGTCTCAGA GATCAAGCCC AGCAGTTTTG GAACTTCTGT GACTGGGACC 2580 TTGAGGAATC CAGGGGTGGG CTCCAGTCTC CTCCCCATCT TCAGTCCAAA GGGCTCTGCT 2640 TTTCTCTGCT CTCTGTCATG GGGGCGTGTG GTATTTCTTT AGAAAGGAAG CCTCCTTTGC 2700 TGTCCTGGTC CTGGTTGGCT CTCCAACATA TGTTCACACC AGGCAGTGAT CTCACTTTCC 2760 TGGTCAGTGA TTGGTTTAGG AATAGGCACT TCTGGCCAGT ATAGGTAAGG AGAAGTCTGC 2820 TGGGGGCTCA TGGGAAAGGT TTCTTGCTCT TAAAAATGGC ACACAGGCCA GGCTTGGTGG 2880 CTTACACTTG TAATCCCAGC ACTTTGGGAG GCCAAGGTGG GAGGATGGCT TGAGCCCAGG 2940 AGTTCAAGAC CAGCCTAGGC AACATGGTGA GACCTTGTCT CTACAGAAAT CTTAAAAATT 3000 AGCCAGGTGT GGTGGTTCAG CCCTGAGGAG CTGTGGTCCC ACCTACTCAG GCAGCTGAGG 3060 TGAGAGAATC ACTTGAGCCC AGGAGGTTGA GGCTGCAGTG AGCTGTGTTC ATACCACTCT 3120 GGCTTGGGCA ATGGTGTGAG ACCCTGTTTC TGAAAAAAGG AACACAAGAA AGATGGATTC 3180 TCTTCTTCCT TGACTGCTAT TGTGCCTGGC ACTGTGGAAG CCAGCCTGTG CCCATGAAGG 3240 AAGCTAGAAT CCATGGAGAA CTGCAGAGTG CCTGATGACC TTGGGAAGCA GCTACCAAAC 3300 CATTTCCGAA GTGTCTCTGG ACTTCTTGTT ACCCCCAATG ACACATTTCT TTGTTGTTTA 3360 AACTATTATG CTATTTTTGG TTTTTGTTTC TCTCTGTGTG TCCTTTTATG GTTTTGGCTG 3420 TTTATTTTTG TCTGCCCGCT TGATTTTGCT ATTTTTAGCC GAATGCAAAC TAATTTATAT 3480 AGTTTGAAAA TTGCAGACCT AGCTAAATCT CCTCTTTTCA AAGACGGGGT GACTGAAACC 3540 TAGGGGGATG GAGAATGACT GGATTGAGGT CATGCCCTGA TTCACGGCAG AGATGGGTTG 3600 GGATCCCAGG ATTCCTGACT GCTGGCCCAG CACCCTTCTC TTAGATTCAC AGCCTGGGAT 3660 CTTATATGCT AGGTTATCTC AGCTAGCATT GTCCCCTGGT CCCAGGAGGA TCCAGACAAG 3720 CCAGGGAGGC CCTGCAAGGC TGAGGGAGTT GGGACCAAGG TGGGAACAAC AAACCGAGGG 3780 CCTCTTCCAC TGTTCTTGTG GGCAACTTCT GAAAAGCACA TAGCAGGTGC ATAACCTGTT 3840 CCTGCACCAG CTGTGGGCTC ATGGAAAGAA GAAGAAAACT GAGGGGTTCA AGGTTTCCAT 3900 GTAAATCAGT TAGGAGTTAC ATTTGGCTAC TTAAGAGAAA CCTTAAACAA GTAAGGGGTT 3960 ATTTTTGTCC CATAGTTGGA AGCCTGGGTA TAGGCAGTCC AATTGGGTGC AGATGCTCAT 4020 TAAGAATCAA GACTCAGCCA GGCGCAGTGG CTCATGCCTG TAATCCCAGT ACTTTGGGAG 4080 GCCGAGGCAG GTGGATCACC TGAGGTCGGG AGTTCGAGAC CAGCCTGACC AACATGGTGA 4140 AACCCTGTCT CTACTAAAAG TACAAAATTA GCTGGGTGTG GTGGCGTGTG CCTGCAATCC 4200 CAGCTACTCG GGAGGCTGAG GCATGAGGGC CGCTGGAACC TAGGAGGCGG AGGTTGCTGT 4260 GGGCCGAGAT TGCAGCATTG TACTCCAGCC TGGGCAACAA GAGTGAAACT CCATCTCAAT 4320 TAAAAAAAAA AAAAATCAAG ACTCTTGCTA TCTCCCTGTT CTGCCATTCT TGACTTATAG 4380 CTTTTGTTCT CATGGTTACA AATGGCTGCA TCACTTTCAG GCATCATATC TGAGTTCCAG 4440 GCTGGAGGAA GAAGGTGAGG AAAGAAGTCT GGGCCGGCCC GTTCTGTCTT TTTATACAGA 4500 AAACAAGACC TTTCCAGAAG CCCCACTGTA AAATTCTTTA TACACCTCAT TGGCCAGAAA 4560 TGTGTTACAT 4570
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