Tag | Content |
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EnhancerAtlas ID | HS101-00669 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:22281520-22285380 |
Target genes | Number: 12 | Name | Ensembl ID |
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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) |
E2F6 | MA0471.1 | chr1:22283664-22283675 | GCTTCCCGCCC | - | 6.02 | EWSR1-FLI1 | MA0149.1 | chr1:22283831-22283849 | GGAAGGTAGGACGGCAAG | + | 6.16 | EWSR1-FLI1 | MA0149.1 | chr1:22284265-22284283 | CCTTTCAACCTTCCTTCC | - | 6.53 | Foxd3 | MA0041.1 | chr1:22285219-22285231 | AAACAAACAAAC | - | 6.32 | HES2 | MA0616.2 | chr1:22284333-22284343 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:22284333-22284343 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:22284410-22284425 | TGAACTCGTGACCTC | - | 6.12 | STAT3 | MA0144.2 | chr1:22282028-22282039 | CTTCCCAGAAA | - | 6.02 | TFAP2A | MA0003.3 | chr1:22283357-22283368 | AGCCTCAGGCA | + | 6.32 | Zfx | MA0146.2 | chr1:22284435-22284449 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
SE_00032 | chr1:22280798-22286056 | Adipose_Nuclei | SE_01556 | chr1:22281528-22284380 | Aorta | SE_25801 | chr1:22281815-22284310 | Duodenum_Smooth_Muscle | SE_26605 | chr1:22281524-22284310 | Esophagus | SE_29681 | chr1:22281484-22283021 | Fetal_Muscle | SE_29681 | chr1:22284382-22285187 | Fetal_Muscle | SE_37945 | chr1:22282670-22286119 | HUVEC | SE_40620 | chr1:22281477-22285092 | Left_Ventricle | SE_42167 | chr1:22281597-22285044 | Lung | SE_47476 | chr1:22282432-22282926 | Pancreas | SE_47476 | chr1:22282944-22284257 | Pancreas | SE_48565 | chr1:22281500-22284373 | Right_Atrium | SE_53700 | chr1:22281497-22284094 | Spleen | SE_53700 | chr1:22284246-22285468 | Spleen | SE_54522 | chr1:22281743-22283438 | Stomach_Smooth_Muscle | SE_65890 | chr1:22281595-22285391 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 22283005 | 22284245 | chr1 | 22281632 | 22282689 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I021958 | chr1 | 22285241 | 22285390 | GH01I021955 | chr1 | 22281644 | 22285107 |
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Enhancer Sequence | TCACCATGTT GGTCAGGCTG GTCTCGAACC CCTGACCTTG TGATCCACCT GCCTTGTCCT 60 CCCAAAGTGC TGGGATTATA GGCGTGAGCC ACCGCGCCCG GCCATACGAA GTTCTTTAGC 120 AATAGAAACT CCTGTGCGGG CCCGTCACAA TCCACAGTCC ACAGTCACTA GGAGTCTTTT 180 GCCTGGGTTG GGTAGTTTCA GCTGCTGAAA CAGGGAGCCA GGAGGAGGGA TCAGAAGGGC 240 GGCCCGCAGC CAGCGGAAGA GGAGTGCGAG GGAGCTCGGT GGACCAGGGA AGCGGTGTCC 300 ACAGTTCCCT TGTGGGGCCT GAGCCAGGGC TTGGTTCAGC TCTGGGTGGG GGGGCCGGGT 360 GGGCAGGCAC CCAGCAAGAG GGCTGGGCCT CTCTAGGATG CTTGTCCCGA AGGTCCCAGG 420 CATCGAGATC ACTACCCATT TCTGGCCTAA GAGGCACTGG AAATAGCTCT AGGACAATTA 480 TTTCAGGAAG AATGTGCTAT TCCTCCATCT TCCCAGAAAG CCAGGCTGTG TCCTAGATCA 540 GGACAGTCCC TCTGCAGCCT CCCACCTCAG GGGAACCTCC AGCCCCACTG AAGGCCCCAG 600 AGGCCTTCAG AGCCAGAAGG GGCTGGGAGT CAAGAGTGGG AAGTGAGAGG CCCCTTTCCT 660 GGTGGGGGAG GGGAAGTTCT GGCCTTCGAT CCTGGGCTCT TAGGGCCCAG GCTGGAGTTA 720 GGCTGGGCCG GCTGGAGTCC AGCTGACTCC AAGCCCGGGG CGCATGATGG GAAGGATATG 780 GGGAAGAGGT CTGCCCCACC TCTTTCCTAG GCTCAACCCT GGGAAGCTGA TATTTGTGAG 840 GCATATATCA TGTGCCATAG AACATGATAT TGTGGGTCCC AGGCCCTTCT CAGCCTCCTT 900 CCCTCCCATT TAATCCTCAC AGCACCCCTA AGAGGTATTT TGTTTTCCAG ATGAGGTAAT 960 CGAGGCTCAG AGAAGGCTAG AGACTTGCCC AAGCTTGCCC AGGAGGCTTG AGTGAGAACC 1020 TGGCCTTCTT AAGTGCAAAA GAGGGTAGGC TGTCCCTCCC ACTCGGTGAG GACTCAGGAA 1080 GTGGCCCTGT GAACTGAGTA GCACTGGGAG GGGTCTAGTC TGGAGACCCA GGATGTTGGA 1140 CAGCAACAGT CCCATCCCCC ACTCGCCCCA TTCTCCACTC CCCAGCCAAG CCCAGCTGCC 1200 CCCGCTTCCA GCGCTGCAGA GAAGATGCAG AGTCTCAGAA GGTCCTGGGT GGTGGGGTGC 1260 CCTGTCCTGC CATCTCCAGC CACAGTGGTA CCCGCTGCCC CACCTGGCCC CTCTCCACCA 1320 CCTCCAGCAT TGGATCCTTG GCTTCATTGC CAAGGATAAA CTGGCTGAAA AGTAGCTCTG 1380 CATCATCCGT TGCCCTCCCC CTGCACCCAC CCCCAACCGG CTCTCCTCAT TCTCACCTAT 1440 CCCCCCTCCC ACCCACCAAG GGCCACAGTC CCACCAACAT CCTCTGCCCA TCCTGTGCTC 1500 ACCAAGAACA CTAGGGGCCC TTCCCCAACC CCAAGCACAG AAGTTCCAAG GCATCTCATT 1560 CTCTGTGCTC CCCTGGGTAG GGGGAGCAGC TCCCTTCTCC AGAGACCTGA GGACCCTGAC 1620 CCATTAGCAC AGGTGCTGCC CATTAAGCCT TCACCTGCCG CTCAGCAGTT TCTCTCCTTC 1680 CCTGGGGCCT GAGAGAGTGG GAAGTGCCCC CTTATCCCTT CAGCCACATG GCTCTTATAA 1740 GCCCAGCTCA GCAGCCACAT GTTTGTGACA CCCAGGTCAG TTCAGGGGAC AGCTAGAGCC 1800 AAGAGCCCTC CACCCTGCCC GAAGGGCATC TGTGTCCAGC CTCAGGCAAC TGTTGGCACT 1860 GTGTCCTGAG CCTATACCTG GCCTTGAGCC AACTTGCCTG CCAGACTGGA AAATCTCTCC 1920 TGGGCCTGGA CCTGGCCCTC CCCCGGCTGC AGCCTTATAC CCACCAGAGC ACAATGAGTC 1980 ACGCGTCCTC CTCACCTAAC ACCCTCAAGG ATATGGGGCC CCTGCTCACC CACTGCCAAA 2040 AACAGCACTT CCCCAAGTCC ACATGTGGCA GGCACAAGCC AGGGCAGATC TGAGCTCAGG 2100 AGCACTGGGC AGGAGTGTCT TGGCAGGAGT CCCTGCCAGG GAGAGCTTCC CGCCCGCCAA 2160 GCTACCTGAG GGCTTTGCAG GTAGAGCAGC CAATCTGGGA GGCAGCAGGG CTCCCATCTT 2220 GATGGGGCCC GGGAAAGTCC CTGTAAGGAG GGTGCAGGAG GACGGTCACA GGCAGGCTTA 2280 TGTACAACCT TGCTGAGAGA ACAGCGCCCA CGGAAGGTAG GACGGCAAGT AAGAGGCTTG 2340 TGCTGTGACC TGGGGCAAAC AGGTGAACTT CTCCAAACCT CAATCTCCTG TTCTGTGAAG 2400 TGGAGGTGGG GAGGGGACTT CCGGAACACT GTTGACTTGA CTGGCTCGCA ATCACAGCGA 2460 GTGTTCACAA CGTGCTCCCC GTGTCCCAGG CACACTTCCG AGTGCTTGAT TACCTTACGA 2520 GTGGCTGCAG CCGTGTGCTG GCCCACAAGA GCCAACTGTT AAATGTTCTG AAATGTGGTG 2580 AATGGTTGTT AAAACACAGG TAGCTTGAAA TCAGCCATAA GGAAAATATT TGGACGACAG 2640 GAATTGGCAG ATATGACACA TTAGGACTTG TTGCTGTTGT TGTTGTTGTT TTGAGACCGA 2700 GTCTCCCAGG CTGGAGTGCA GTGGTGCAAT CTCGGCTCAC TTCAGCCTTT CAACCTTCCT 2760 TCCCAGGTTC AAGTGATTCT CCTCCCTCAG CCTCCCGAGT AGCTGGGATT ACAGGCACGT 2820 GCCACCACAC CCAGCTAACT TTTGTATTTT TGGTAGAGAT GGGGTTTCAC CATGTTGACC 2880 AGGCTGGTCT TGAACTCGTG ACCTCAAATG ATCCGCCCGC CTCGGCCTCC CAAAGTGCTG 2940 GGTTTACAGG CATGAGCCAC CGCGCCCAGC CCCTTTCCTT TAATCGTCAG ATATAATGGC 3000 TCAAGTCTCC ATCCCGCGGG CTGTGGGAAG TCCAGAGCCT TCCCTGCTAT TTTTCAAGGA 3060 GCCCAGAAGG CTGTTATGGC CTTTTGTCAC CCCTCACTCG GAATCTCTGC TTCTGGGTCA 3120 GTGTTCAGCC CCTCTTGCTG CCCCACCTTC TGTGACTGTC ATGTTCTGTC AGCAAAGTCG 3180 CAGCCCCTGC CACACTGCTC TGTGACTGCT ACTCCACAGG AGACCTTTCT CCAGCTTCTC 3240 TCTTCCGCCT GCCCCTGTTG CGTGGCTCCC ACTGCCCCCG TAGTCCTCCC ACCCTCTGGC 3300 TGCTGAGCCT GAAAAATGGA TGGCTTTCAG CTGTTGACTA GAAAAGCCAA TATTCCCTGT 3360 TCTTTCTTGT ACCCAGCAGA GTGGCTCCTG GCAATCTTGA TTCTCAGCTG GGGTGGGGGG 3420 TGGGGGGTTT CCTTGACAAA TGAGCAGACT TCCTTCTGCC AACCCCACTA AGATGTGGGA 3480 GCAACAGATG ACAACTTCTT CCTTCCTGCA AATATGCTTT AGATGACAAC ATCCTTTCAA 3540 TAACATTGTG AGGTAAAAGC CATTTCTCCC AGGAGGCTGA GGTGGGAGGA TCGCTTGAGC 3600 CCAGGAGGTG GAGGCTACGG TGAGCTGGGA TCACGTCAGC TGGGTGACAG AGCACGACTC 3660 TGTCTCTAGC CTGGGTGACA GAGCAAGACT CTGTCTCAAA AACAAACAAA CAAAAAAGAG 3720 TCATTTTCCC AAGAGAGGAA TTTGGCAGTG AGGTTCTTCT TTGTACCAGT TGTACCAGCT 3780 GGGTTACCTT GGGTAAGTTA TTTCTCTTTT CTGAGACTCA AATTCCTCAC CTGAGATAAT 3840 ATCTGCTCCA CCAGGTTTAT 3860
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