Tag | Content |
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EnhancerAtlas ID | HS105-68319 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr6:26340920-26343290 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr6:26341591-26341604 | AAATTAATTAATA | + | 6.37 | NKX2-5 | MA0063.2 | chr6:26343061-26343071 | CTCAAGTGGT | - | 6.02 | POU6F1 | MA0628.1 | chr6:26341593-26341603 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr6:26341593-26341603 | ATTAATTAAT | - | 6.02 | ZNF263 | MA0528.1 | chr6:26342309-26342330 | GAAGGAGGAGAAGAGTGGAGT | + | 6.05 | ZNF263 | MA0528.1 | chr6:26342175-26342196 | AGAGAAGGAGGGAGGGAGAGG | + | 6.18 | ZNF263 | MA0528.1 | chr6:26342283-26342304 | GAGGGAGAGGAGAGAGGGAGG | + | 6.23 | ZNF263 | MA0528.1 | chr6:26342299-26342320 | GGAGGAACGGGAAGGAGGAGA | + | 6.23 | ZNF263 | MA0528.1 | chr6:26342152-26342173 | GAAGGAGGGATGGAGAGGAAG | + | 6.24 | ZNF263 | MA0528.1 | chr6:26342267-26342288 | AGGTGAGGAGTGGGAGGAGGG | + | 6.24 | ZNF263 | MA0528.1 | chr6:26342359-26342380 | AAAGGAGCAGGGGAGGAGGGA | + | 6.29 | ZNF263 | MA0528.1 | chr6:26342139-26342160 | AGAGGAAGAGAGAGAAGGAGG | + | 6.32 | ZNF263 | MA0528.1 | chr6:26342165-26342186 | AGAGGAAGAGAGAGAAGGAGG | + | 6.32 | ZNF263 | MA0528.1 | chr6:26342130-26342151 | GAGGGATGGAGAGGAAGAGAG | + | 6.54 | ZNF263 | MA0528.1 | chr6:26342156-26342177 | GAGGGATGGAGAGGAAGAGAG | + | 6.54 | ZNF263 | MA0528.1 | chr6:26342182-26342203 | GAGGGAGGGAGAGGAAGAGAT | + | 6.59 | ZNF263 | MA0528.1 | chr6:26342296-26342317 | GAGGGAGGAACGGGAAGGAGG | + | 6.65 | ZNF263 | MA0528.1 | chr6:26342340-26342361 | GAAGGAGGAATGAGAGGTGAA | + | 6.68 | ZNF263 | MA0528.1 | chr6:26342362-26342383 | GGAGCAGGGGAGGAGGGAAAG | + | 6.82 | ZNF263 | MA0528.1 | chr6:26342270-26342291 | TGAGGAGTGGGAGGAGGGAGA | + | 7.06 | ZNF263 | MA0528.1 | chr6:26342178-26342199 | GAAGGAGGGAGGGAGAGGAAG | + | 7.17 | ZNF263 | MA0528.1 | chr6:26342279-26342300 | GGAGGAGGGAGAGGAGAGAGG | + | 8.91 | Zfx | MA0146.2 | chr6:26341819-26341833 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_43581 | chr6:26339710-26344501 | MM1S | SE_66505 | chr6:26342011-26342675 | Jurkat | SE_67190 | chr6:26339710-26344501 | MM1S |
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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 |
GH06I026341 | chr6 | 26341629 | 26343207 |
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Enhancer Sequence | TTACTCTTCC AAAGAAAATG ACTTCCCCAT TTCCATCCCC AAGTAACTAA AATGTCTACA 60 TTTCCTATAG AAACAATGGC ATATTTCAGC AACTACCATA TGCTGATCAC TGTTTAGGAA 120 TGCAAAAAAT ATATCATTCT TGTAGAAGAT GTTTATTTTC AGTCTTTAAA TGAAATCTCT 180 CTTAATAGCA GGCTCAATTC AAAATCATCT TCTAGTTTTT AAAAATTCGT AGATACGTGG 240 ACTTTTGGAA CATGTTTTCT AAAAGGACCC CAACCACCTT TTTATGGATT CAGTTTTGTG 300 TCCCCCAAAA TTCATATGTT GAAATCCTAA TCCTAGTACC TCAGAATGTA ACCTTATTTG 360 GATATAGCTT TGGGAGGACC TGAGGCAGAG CTGTAGGGTG TAGGGGAAGC TGTGGATGCT 420 TCCTGGTTCC TCTGGGTGTG AATGTGGCTG ACGGGTTCAG AGGCTGAGGA TACCTCGCCA 480 GGATGCTGAG GAAAGAAGCC AGGATTTTAG TGGTTCTGCA CTCAGAAACC AGGGCACAAG 540 AACGCAGAGG CAGATGCCCT AGTGGACAGA CGACCAGGGA GGGCCAGCGG TTCTTCTCCA 600 TGCGTGGACA CAGGAGCGGT CTTCTCTTCA TGTCCAAACT GAGATACCAT CTGAGGAAAA 660 GGAGAGGCCC AAAATTAATT AATAAAGCCC TGAATTGACT AGGACGAAGA CCATTATTGA 720 CTCAGGAGTA GCCTGGTTTG ACTAAGATGA AGGATATGCC ATTAAGCGGG AAGGGGCAGA 780 GGATGGAAAT AAAGCTCAGT TTGCATTCAT ATAAACGTAC AGGCGCGCAC CATCATGCCC 840 GGCTAATTTT TGTGTTTTTA TTGGTCAGGC TGATCTCGAA CTCCTGAGCT CGCGATCAGC 900 CCGCCTCGGC CTCCCAAAGT GTTGGGATTA CAGGCGTGAG CCACCACGCC TGGCAACGCC 960 TCTAGGAGCA AAACGTGCAT TTCAGCTTTT GAGGTTCCCT GCTGTGCACA GCCCTCAGCT 1020 TGCCATCTAT AGGCCGCTCC ATTGACAGGG GTTGAGAGGG TGAGACTTTC TCAGGCCCAC 1080 GGCACAGGCA GTGATGCATA TCCGCCATGA GGGGGCGGCG AAGCCTAGAG AAAGAGAGAG 1140 ACACCTGAGA CGAGTTCGAA GAGGCGGGAG GAGGGAAAAA GCTGGGGCGG GAGGAAAGGG 1200 GACGGGCAGG GAGGGATGGA GAGGAAGAGA GAGAAGGAGG GATGGAGAGG AAGAGAGAGA 1260 AGGAGGGAGG GAGAGGAAGA GATGATAGAG TGAGGGAACG AGGAGGAGAC GAGGAGGACT 1320 TGTGGGAGGA AAGAGAGAGC AGAGAAAAGG TGAGGAGTGG GAGGAGGGAG AGGAGAGAGG 1380 GAGGAACGGG AAGGAGGAGA AGAGTGGAGT ACGAGGGAAA GAAGGAGGAA TGAGAGGTGA 1440 AAGGAGCAGG GGAGGAGGGA AAGCAAGTTA CTGAAGGGGA AAAACAGTTC TCTGGACAGC 1500 AGTTAGCGAC AGTTGTAGAG TACTTTACAT TTTACAGTGT GTCACAGATA CTGGCTCATG 1560 TTTCCCTCAC AGTAACAACC CAATTAAGCG GTAAGCAGTA ATTGCTGTCC ACGTATTATT 1620 TTCAACCTGA AATGTTATTT TTAACAAAAC ATACTTTATA TATGACAAAA TAAAGAGAAA 1680 CATTGGGGCA AGTGTACAGA CTAATGAACA TTTACTACGT TTTAGTTTAG TGGTTTTTTG 1740 TTTTGTTTTG GTTTGGTTTT GACACAGAGT TTCACTCCTG TCACCCAGGC TGAAGTGCAA 1800 TGGTGCTGTC TTGGCTCACT GTAACCTCTG CCTCCCCAGT TCAAGCGATT CTCGTGCCTC 1860 AGCCTCCTAA GTAGCTGGGA TTGCAAGCAT GCGTCACCAT GCCTGGCTAA TTTTTTATAT 1920 TTTTAGTAAA GACAGGGTTT CACCATGTTG GCCAAGTTGG TCTTGAACTC CTGGCCTCAA 1980 GTGATCCAGC CACCTCGGTC CCTCAAAGTG CTGGGATTAC AGGCATGAGC CACCAAGCCC 2040 GGCCTTGTTT TTTGAGACAG AGTCTCAAAA ACCAAGGCTC TGTTGCCCAG GCTGGAATGC 2100 GGTGACACAA TCACAGCTCA CTGCAGCTCC AACCTCCCGG GCTCAAGTGG TTCCTCCCAC 2160 CTCAGCCTCT ATAGTAGCTG GGACTACAGG CATGAGCCAC CATGTGTGAG CTACATTTCA 2220 TGGTCTCTTT AAATCCATTT CTATGTTAAT TCTCAGATCT CTGAATAGCA TGTCACCAAA 2280 AAGCATGCTG TCTGAGCATG TCAGAGCTCA GACACAGAGG CAAAGGGACA GAGCAGCACA 2340 CAAAACTTAA CAGAAGTGCG TTCTCAAGGA 2370
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