Tag | Content |
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EnhancerAtlas ID | HS051-23918 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr6:111872720-111875580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr6:111873723-111873735 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr6:111873723-111873735 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr6:111873721-111873736 | GGACTAAAAATAGAA | + | 6.89 | RARA(var.2) | MA0730.1 | chr6:111873908-111873925 | AGGTCAGGCAAGGGACA | + | 6.21 | RFX5 | MA0510.2 | chr6:111873324-111873340 | AGTTGCCATGGCAAAC | - | 6.03 | RFX5 | MA0510.2 | chr6:111873324-111873340 | AGTTGCCATGGCAAAC | + | 6.34 | ZNF263 | MA0528.1 | chr6:111873842-111873863 | TCCCTCTCCCCTCTCTCCCCA | - | 6.15 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_00043 | chr6:111872754-111874669 | Adipose_Nuclei | SE_01892 | chr6:111872775-111874783 | Aorta | SE_25836 | chr6:111872420-111874786 | Duodenum_Smooth_Muscle | SE_26930 | chr6:111872756-111874615 | Esophagus | SE_31696 | chr6:111871948-111874935 | Gastric | SE_33474 | chr6:111869902-111875281 | H2171 | SE_33474 | chr6:111875283-111877144 | H2171 | SE_36956 | chr6:111871448-111878954 | HSMMtube | SE_41014 | chr6:111872539-111874578 | Left_Ventricle | SE_42404 | chr6:111872683-111874769 | Lung | SE_44157 | chr6:111871850-111874875 | NHDF-Ad | SE_44783 | chr6:111872522-111874865 | NHLF | SE_45702 | chr6:111872417-111874783 | Osteoblasts | SE_47224 | chr6:111870720-111877244 | Panc1 | SE_48418 | chr6:111872659-111874652 | Psoas_Muscle | SE_50264 | chr6:111871896-111874877 | Sigmoid_Colon | SE_51251 | chr6:111871765-111874852 | Skeletal_Muscle | SE_52559 | chr6:111872727-111874660 | Small_Intestine | SE_55947 | chr6:111872981-111874360 | u87 | SE_66964 | chr6:111869902-111875281 | H2171 | SE_66964 | chr6:111875283-111877144 | H2171 | SE_67791 | chr6:111872981-111874360 | u87 |
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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 |
GH06I111550 | chr6 | 111871688 | 111877634 |
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Enhancer Sequence | GAACCCATCT GAGAGGAATT TAAATCTCAG GAAAGTAGCA GCTTTCTTCA AGTTTCTGAG 60 TAACTGAACC TTGTAGATAA CAACAGATTG GAAGATAGAA TCAGTTAATC CCTGAACTCA 120 AGGAACCCTT GGCCCATAGC CCAGACAATA CAGCATGCTG AAAATTGGTC TGGTCCCAGC 180 CTCACGTAAA CCTGTTTCTC CTCTCCTGAG AAGAATGCAG CTTTTGACCA CTGCCCAGTG 240 TGAGAGCCCG GCCTCACTGT TAACACCTCA GTGAAGGCAA GAACAAGTGG TTTGCAGTGG 300 AGGGCATCGC CTGGAAGGTG GCAAAGGCCA GGCAGGTACC TGCGGCCCAG CTGCTGCTCG 360 ACGATGAGGC TGGCAGCCAA GTCTAGCGCC AGCCTTTTCA AAAGCAGCCC TTTTGATAAC 420 ACTGATTACA TTTCCCTCAC CGGAGCCTTG GGTTAATTGA GCAACAGCCA ACTTCTCTGG 480 GTAACAAAGA GGAGGGGAAA GTAATCCAAA CACAGGTTTT ATTATAAAAA CCAGGGAGTG 540 AGAGAAGTGT GTTTATTCTG TAAGATAACA CACCTGCTCG GTGCCGGGGA GGCTCATTTC 600 CATCAGTTGC CATGGCAAAC TCGTTATACT TCAAGGCCAT GTGGCTTTGT TTCCTTTTGG 660 GATCTGGTCC TTGTCCTACC TTTTCTAACA ACTCCAACAC AATGACATGG AAGCCTGCGA 720 CAGCATAATT GATTTCTCCT TCCCTCTATC AACGGTTCAC ATTTGTTCAG CACAGGACTG 780 AGTCTGCCTT CTCCTTTGAA CTCCTTGCTA AGCATGAAGG CATGCTTCAG AGAGCCACCC 840 TCATTAACAT TCCAGGTCCC TCTTCCCTGT CAGCAATAAA CAAGCCCTGC ATCAATGGCC 900 TCCTGCCTTC CACTTTTACA AATGAGTGGC TCAGTTCCAT GTTTTGCTGC TGATCCAGGT 960 GCCCAGGCGC ATACAACGCG AGCCTAAGAA GCACGCGGGA GGGACTAAAA ATAGAACAGC 1020 AGTTTTGGAT GCATACCAGA GCAGCTACTT CATCTCAACT TGCTTTGCAC GCTAAGCCTA 1080 ATGGGATCCA TCAGGCATGA GTTCTCTCGC GCGCTAGCTC CCTCCCTCTC CCCTCTCTCC 1140 CCAGCTGCCG ATTTCCATCA GCCCCTTCCT GGTGAAGGGA GCAAAGGGAG GTCAGGCAAG 1200 GGACAAGAAA TGTGTGCCCT TATGGTTTTC GTTTACAAGC CCTGGGAGAT CTGGGGGCTG 1260 CAGTTACTCC TTCCATAAGA GAGTTTCTAG AAAAAAAGCA GGCAGGCCCA GAACATGGTC 1320 ACCTCTGCCC AGGTACACTT TGGTCCAAGA CTTTCATTGT TTAGCAAAGC CTCAAATATC 1380 ACTTCCTAAT CACCCAATAC CTATAACCTG GACCCATGCT CCTATATTCC TTGAAAAGTT 1440 AAGTAGAAAA CTAAAGTACA CTGAGTGTTC CTCTTACAGA TCCCACCTGC TTGCTTGAGG 1500 CTAAGAATTT GGGAGCAAAT GCACAGTGAG TTGGCAACAT GTGACTGCCA GGGTCTGCAA 1560 AAGCCACCCA CCTGCCGCCA AGTACCCTAT CCAAAAGTGA TCCTATCCTA AAGCATTTTC 1620 CAATAGAAAA TGGAAGAAGT CATATGCAGT TAGGAACATG CTATCCTGCC TGGGCACAAT 1680 ACCTCCCAGC ATGCCAGCTG TGTTGACTGA GCGAGGCTCC TTTGTATGCT AAAGTGCCTC 1740 GTGCAGCCTC CCTCAAAAGG CGAGCCAGCA TGACCATACG TTTCTCATGT CTACATCCAA 1800 AAGGTAATGC AGATGTTCCA AACAGCTAAG TATTATTCCA AGAAGTGCCA TTTTTGTGGA 1860 ATCAGAATTG TGATAGGACG GGCTGGACGC AGTGGCTCAT ACCCGTAATC CCAGCACTTT 1920 GGGAGGCTGA GGCGGGCAGA TCACTTGAGG TCAGGAGTTA GGAGTTCGAG ACCAGCCTGG 1980 CCAATGTGGT GAAATGCAGT CTATACTAAA AACGCAAAAA TTAGCTGGGC TTGTGGTGGG 2040 TGCCTGTAGT CCCAGCTACT AGGAAGGCTG AGGCAGGAGA ATCGTTTGAA CATGGGAGGC 2100 AGAGGCTGCA GTGAGCTGAG ATCATGGCAC TATTGTACTC CAGCCTGGGC GATAGAGTGA 2160 GACTGTCTCA AAAAAAAAAA AAAAAAGAAT GGTGACAGGA AGATGAATAT CACAGTATTT 2220 AAAAATCTTT TTCATTGTTG ATGTTTTGGA GATTGGCCAG ATACAACTAA AAGAAACTGA 2280 TCTGGGCCAG GTGAGGTGGC TCACGCCTGC AATCCTAGTA CTTTGGGAAA CCAAGGTGGG 2340 AGGATTGTTT GAGCTAGGGG GGTCAAGACA AGCCTGGGTT GAACATAATG AGACCCTGTC 2400 TCTACAAAAA AAAAAAAATT TTTTTTATTT TGAGACGAAG TCCTGCTCTG TTGCCCAGGC 2460 TGGAGTGCAG TAGTGCTATC TCTGCTCACT GCAACCTCCA CCTCCCTGGC TCAAGCAATT 2520 CCCCTGCCTC AGCCTCCCAA GTAGCTGGCA TTACAGGCAT GTGCCACCAT GCCCAGATAA 2580 TTTTTTTTGT ATTTTTAGTA GAGACGGGAT TTCACTGGTC TCAAACTCCT GACCTCAGGC 2640 AACCTGCCCA CCCTGGCCTC CCAAAGTGCT GGGATTACAG GTGTGAGCCA CTGTGCCCAG 2700 CCAAAATTTT TAAAAAATAA ACTGGGCGTG GTGGCATGCA CCTTTGGTCC TAGCTACTCA 2760 GGAGGCTGAG GTGGGGGGAT CGCTTGAGCC CGGGAGGTTG AGGCTTCAGT AAGCCGTGAT 2820 CATGCCACTG CACTCCAGCC TGGGTGGCAG AGCAAGACCA 2860
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