Tag | Content |
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EnhancerAtlas ID | HS108-00355 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:11799600-11802710 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:11802500-11802518 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr1:11800180-11800198 | GGTTCCTTCCCTGCTTCC | - | 6.03 | EWSR1-FLI1 | MA0149.1 | chr1:11802484-11802502 | TTTCCCTTCCTTCGTTCC | - | 6.21 | EWSR1-FLI1 | MA0149.1 | chr1:11802582-11802600 | CTTTCTTTCCTTACTTTC | - | 6.24 | EWSR1-FLI1 | MA0149.1 | chr1:11802516-11802534 | CCTTCTTTCCTTCCTTTT | - | 6.61 | EWSR1-FLI1 | MA0149.1 | chr1:11802492-11802510 | CCTTCGTTCCTTCCTTCC | - | 9.09 | EWSR1-FLI1 | MA0149.1 | chr1:11802504-11802522 | CCTTCCTTCCTTCCTTCT | - | 9.09 | EWSR1-FLI1 | MA0149.1 | chr1:11802488-11802506 | CCTTCCTTCGTTCCTTCC | - | 9.17 | EWSR1-FLI1 | MA0149.1 | chr1:11802512-11802530 | CCTTCCTTCTTTCCTTCC | - | 9.17 | EWSR1-FLI1 | MA0149.1 | chr1:11802496-11802514 | CGTTCCTTCCTTCCTTCC | - | 9.45 | EWSR1-FLI1 | MA0149.1 | chr1:11802508-11802526 | CCTTCCTTCCTTCTTTCC | - | 9.47 | IRF1 | MA0050.2 | chr1:11802529-11802550 | CTTTTCTTTCTTTTTCTTTCT | + | 6.3 | RARA(var.2) | MA0730.1 | chr1:11802337-11802354 | AGGTCCAGATAAGGTCA | + | 6.17 | ZNF263 | MA0528.1 | chr1:11802512-11802533 | CCTTCCTTCTTTCCTTCCTTT | - | 6.15 | ZNF263 | MA0528.1 | chr1:11802476-11802497 | TTCCCTTCTTTCCCTTCCTTC | - | 6.37 | ZNF263 | MA0528.1 | chr1:11801251-11801272 | TCTTCTTCCCCCTCAGCCTCC | - | 6.68 | ZNF263 | MA0528.1 | chr1:11801116-11801137 | CTTCCTGTCCCTCCCTCCTCC | - | 6.76 | ZNF263 | MA0528.1 | chr1:11802500-11802521 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr1:11801254-11801275 | TCTTCCCCCTCAGCCTCCCCC | - | 6.97 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_06667 | chr1:11794426-11801891 | Brain_Hippocampus_Middle | SE_09715 | chr1:11795125-11803395 | CD14 | SE_53973 | chr1:11799645-11801794 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 11800736 | 11801236 | chr1 | 11800774 | 11801662 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I011739 | chr1 | 11800003 | 11801680 |
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Enhancer Sequence | TCTGTCTCAA AAAAACAAAC AAAAACTCTG GCTGGATAGA TTGATTCTGA CATTTGTGTC 60 TGGGCTCTGT TGTTTGTAAG CTTTATGAAT TGGGCCAATT TACTTAATCT CTCAGAGCCT 120 CAGTTCTACC CCATACAGTT ACACGGATGA CATGAGTTAG GGGCAGTGCA GTGTAGATGC 180 ATGGCAGGCT GGTGCTTGTC AGTAGCAGGA GTTGCTGCTG TCGTTGATGA TGCAGGATCC 240 CTGCCCCACA TAGGTATTTA ACAGTTAGTA AACGGATACT TACAGTGACC GTCCAGATAG 300 ATGCTTGTCT CTGGCAGTTG AGGCACCCCC GTGGGACAAA TGGGTACTGC CTCCGTTTCG 360 CAGAAAGGAG CCTGAGGCCT TGGCGCCTGG ACCAGCACCC AGGTTTCCTG TTCCAGCATA 420 GCATCCTGGG ACCCTCTGCT GCCTTGGTCC ATTGACCCCT GTCTGGGAAA GAGCTGGGCG 480 GCCTCCCCTG GGCTGAGCAC TGTAGTGAGA GTCCAGGGGC TCAGGTCCGT CCTTCCTGCC 540 CAGCTGGGAA AGGTCCTGGC CCTGCCACCC GTTTAGCTCA GGTTCCTTCC CTGCTTCCAG 600 CTCCTCTTTC AGGCCATACC TGAGAATCCT GTGTCTCTTT GGCTACCAGG AAGCTCCCCC 660 AGGGCCAAAA GACAGTGGTT TTGTCCTGAC AGTTACTGGC CCCTCTTTCC CTGGGCTGCC 720 AGGAAGTGCA GGGCCCGTTT GGCTCAGTTT CTCCCTGGAG TCTTCCTGCA CATTAAGGCC 780 TCTCTGGGTG TCCTCCTGTT ACACAGATGA AGAAACTGAG GCAGGGGAGG CTTAGGCTTC 840 TGGACGTTTC TTTTCCCAGG GGCTTAAGAG GAGCAACTGG TGCTAACTTT GTTCATATTT 900 ATCAAACCAA AGTGACGTCA CGCAGAGGAG ACTGTGTGTG TGCTAAGGAT CTGCAGTATT 960 TCCAGGTTAC GTTGTTTTCT TCCCTAACAG AGATGGCAGA GGTGTGGGCC CAGCTGGGTG 1020 CTCACTCTGT ATTACAGGCC CTTCCAGCGC TAGGAAAAGC CTTTACCTCA TAGGTTGTAA 1080 GCATGACCCT TAGGGTATCC TGCGGATCAG AGGCCCCCCT GGGACTCAGC CTTTCATGCT 1140 AACTGCCATT CTTTCCGGAA TAATCCAGGG CTCTGCAGGG CCCATTTATT AAAGACCTAC 1200 TCTGTGTACA GTCTAGGCAT AGGAGCGAGA GCATTGAAAA TGAAGATCAT TTCCAAAACA 1260 AGCCCAGAGT GGGAAGAGTT AGGTGTCGAT TTTGGGGAGG AAAGGGGTGA TGGGAGCTAC 1320 CTTCCCTCTG TCTCTTTCCT CGGTGTCTTC TTTAAAAGCT GGATGTTGGG ACCACTGTGG 1380 CTGACTCTGC GGTGTGGCCC TGAGCAAGTT CCTTCCTGTC TGTGGTCCAG GGTTTACTAT 1440 CAGATGGAGG GGACAGTGGT TAGCTCTGAA GATAAAGATC AGAATCGTCC TCATGCCCAG 1500 CCCTGCCTGC CCCCAACTTC CTGTCCCTCC CTCCTCCACT CCCCTCACCT TCCACTCCAG 1560 CCACACTGGC TTCTGTTCAG TTTCCAGAAA GTTCCACGCC CCCCTTCTGC CACAGAGCCT 1620 TTGTGAGTGC CGCCCCTCCT GCTCAAAATG CTCTTCTTCC CCCTCAGCCT CCCCCATCCC 1680 TTCCTCAGAG AAGCCCCTGA CCACCCCAAC CCTCCCAGCC TCCCTGCTGT TCAATCAGGT 1740 GCCCTTTCCC TTGCTTTCCT TCAGGATGCT TTCCTTCAAT CAGGTGCTTT CCTTCGGGAT 1800 GAGGGTTCAC TGCACCTCCA TTCCTAGGGC AGAGTACCTG GTTAGCGAGG TCAGTACTGA 1860 GAGCGCAGCT CCGAATCTGC TCTGCACACC TCTGACTCCC CAGGGTGAAT GAAAAGCAGG 1920 TGCCAGTGAT GCTGGGTGAC ACTAAATGTT TAAGAAACTT AACACCGTTT ATCACTTCAA 1980 GCCCCTGGGG ATTGAAATCC ATGGAAGACT ACACCTCTCT TGCCTCAGTT TCCCCATCTT 2040 TGTAATGGGG AGAGGCCTAA TGGCTGGACA GCACAGCCTG GGTTTGAGTC CTGGCTCTGC 2100 CACTGGCCTG CTCTGTGACC TTGGGCAAGT TACTTCCTTC TGAGCCTCAG TTTTCTCAGC 2160 TGTAAAATGG GGATAATAAG ACCTCAGAGG ATTGTAAGGA TTTAGTGCAT TTATATACAG 2220 AAAGCACTTA GAATGGCACC TAGCACATAG GAAGCGCTCA ATAGTAGACG AAGGTAGGTG 2280 AGGTGATGGC GAAGATTCCT TCTAGAGCTA GACTTCTGTA ACACACTACT CAGCCTGGTC 2340 AGAGTCTCGA GATCTTAAAG TTGGGTGCAT CGGTCCTTAC AGAATTATTT TCCTAGTCTC 2400 TTGGAGCTGA GAAAGGAATT TCTTTTGGGC CACAGAGCCA GGCCCCTTGT GGTTCACTCT 2460 GGCCCTGGGC CCTGGAGGTA AAGGTGAAGT ATCTCAGCCA CCAGCTCTGG ATTCCATCTG 2520 CCCCCATGTG TGGACCTTTC TCACAAGCCC AAACAGTTCC CAGCTGAAGG CCTGCGCCCC 2580 CAGCGGGGAG GTTGGGTGCA CTGGTTTTGG AGGCGAGTTT GAAATTTAAT TCCAGTTTTG 2640 CCACTTGCTA CCTGTGGAGT CTTGATCAAC ATAATTTATC TCTGAGTCTG GTTTTCTCAT 2700 CTGTGAAATG GGAATAATAG TACCAGAGGC TGCTGTGAGG TCCAGATAAG GTCATGTGAG 2760 ACGGTTGGCA TAGGGCCTGG CACATAGTTG GTGTGTGGTC AAGAGTAACT CTTCTAGAAA 2820 TGCTTTTTCC TCTGCTGCCA GAGTGAGTTT GTCTGTCTTT CTTTTCTGTC CTTTCTTTCC 2880 CTTCTTTCCC TTCCTTCGTT CCTTCCTTCC TTCCTTCCTT CTTTCCTTCC TTTTCTTTCT 2940 TTTTCTTTCT TTCTTCCTTC TCTTTCTCTC TTTCTTTCTT TTCTTTCTTT CCTTACTTTC 3000 TCTTTCTGGC AGGATCTTGC TCTGTCCCCC AGGCTGTAGT GCAGTGGCAT GATCTTGGCT 3060 CACTGTACAC TTGACCTCAC TGGCTCAAGT GATTCTCCCA CCTCAGCCTC 3110
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