Tag | Content |
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EnhancerAtlas ID | HS076-04109 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:156629470-156632400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:156629896-156629915 | CGGCCAGCAGAGGGCGCCG | + | 8.39 | EWSR1-FLI1 | MA0149.1 | chr1:156629488-156629506 | GGAATGAAGGAAGGCACA | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr1:156631742-156631760 | TCCAGCTTCCTTCCTTCC | - | 6.42 | EWSR1-FLI1 | MA0149.1 | chr1:156632207-156632225 | GGAAAAAAGGAAGGAAAA | + | 6.45 | EWSR1-FLI1 | MA0149.1 | chr1:156632199-156632217 | GAAAGGAAGGAAAAAAGG | + | 6.63 | EWSR1-FLI1 | MA0149.1 | chr1:156632203-156632221 | GGAAGGAAAAAAGGAAGG | + | 7.74 | FOSL2 | MA0478.1 | chr1:156631302-156631313 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr1:156631302-156631313 | GGGTGACTCAG | + | 6.02 | Myod1 | MA0499.1 | chr1:156629513-156629526 | GGGGACAGCTGGA | - | 6.02 | RELA | MA0107.1 | chr1:156632258-156632268 | GGAAATTCCC | - | 6.02 | RREB1 | MA0073.1 | chr1:156631796-156631816 | CCCCACACCCCCAACTCCCA | + | 6.03 | ZNF263 | MA0528.1 | chr1:156630027-156630048 | TGAGGAGGCGGGAGGGGAAGG | + | 6.97 | ZNF263 | MA0528.1 | chr1:156630030-156630051 | GGAGGCGGGAGGGGAAGGGGG | + | 7.39 |
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| Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
SE_29621 | chr1:156629384-156648365 | Fetal_Muscle | SE_35297 | chr1:156628792-156632773 | HeLa | SE_37066 | chr1:156627097-156648542 | HSMMtube | SE_39956 | chr1:156627225-156633960 | K562 | SE_40945 | chr1:156629243-156641635 | Left_Ventricle | SE_42863 | chr1:156629223-156641275 | Lung | SE_48663 | chr1:156629109-156641547 | Right_Atrium | SE_51411 | chr1:156629535-156641784 | Skeletal_Muscle | SE_54003 | chr1:156629212-156641500 | Spleen | SE_57133 | chr1:156628958-156629933 | VACO_400 | SE_57133 | chr1:156630106-156631879 | VACO_400 | SE_64001 | chr1:156630092-156635889 | HSMM | SE_68702 | chr1:156629456-156635165 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 156629760 | 156630406 | chr1 | 156630113 | 156630600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I156656 | chr1 | 156626377 | 156641724 |
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Enhancer Sequence | CTGCCAGGAA GTACTTATGG AATGAAGGAA GGCACAGGGG TTGGGGGACA GCTGGAGTGA 60 TGCAGCATGT TTGCAAAGAG ATGGAGTGCC CTGAGTGCCT AAGAGTCAAG TGAACGTCAA 120 TGAGTTCTGT CCTGGGAGGG AGAAGGGCTG GGGTCCCAGA GAGGAAGGCA GAGGTTGGTG 180 CCTTGGTGTC CCAGTTCTGA GCTTCCGGAA GGGCCGGCCT TCCCTCATGG GGGTGTGAGA 240 GTGAGGGTGA TGGGAGAGCT CCGCTGGCAC TGCAGCATGT CTGGGGGTTA GGCCGCAGGA 300 AGGTTTACGT CCAGCAGAGG AGGCAGAGAT GCAAGAAATA GGGAAACAAA CTAAGGGCCA 360 AGGGGAGGTT CCCAGCCCTG CGGTGGACTG GGCTTCGGGG AACGAACTGG GGGCCCGCAC 420 AGGCAGCGGC CAGCAGAGGG CGCCGCGGAC CCAGCACGGT GCTCTGAGAG TGCCGTGTAC 480 GCGTGCGCCG GTGGAGACGG GCAGAGGGGT GCGAGGAGCC CCAGGATCCC GCTAGGGGGC 540 GCCGCGGACT TGCGTCCTGA GGAGGCGGGA GGGGAAGGGG GGTGGCTGGC TATGTGGGGG 600 GGTTAGACTT CCGGCCAGGC TGATCTGGCC CTGGGGGCTG TGAGTCAGCG GAGGTTGAGA 660 GGATGAGGTC ACTCAGAGAA CTGGAGAGTG ACCCAGCGCC CGCGTGTGCC TGTGTGTGTG 720 TGTGTGTGTA CGCGTGCGTG TGTGTACGCG CATGCGTGTG TGTGAGTGTG CACCCTTCTC 780 CCAGTGCACA GAATTGTTGG TGAAGTGCAT GTCAGGATGC AGTCTGTCCT CATGATGAGG 840 ATGAATCATT GCTGCAGATC CTCAGGCACA CACGGTCACA CATAGGCACA CACGTGCACA 900 CTGTCGTGTG TACACACTCC TGCATGTGCC CACTTAGTTA CAGCACATCA CCCACATGGG 960 CAATACTTAT TCCTTCTCTG AAGCCAGTAA AATCCAGAGA CAGGGAGACA GATCCGGAGG 1020 AGCAAAGGCT GATAGTAATA CGGGGAGACC CAGAGATAGT GGGCAAGACA GGCAGACACA 1080 AGTTCAATAC AGCTCTGTGT TGGTGGGAGC TGGGGCTCTC CTAGGCCATC CCTGCCCAGC 1140 TCCTGGGCCT TCCCCACCCT ATTTCTAAAC TTGAAACCAG CTGGTCTCTG ATATACCAGT 1200 GTGACCTCCC ACACCCACCT ACCACCACAT TCCTCCCTCA CCCCAGGCCT CACCTCCCCC 1260 ACCTTCTGCC CCCCACACAA CTCTGCCCTG CGTGGCTAGG GAGCAGGGGC TTCTGTTTCT 1320 TAAGGAGCTA TAGGGAAGAG GATGATTCTG GGGCCAGAGT AGATCCTCAC TGTATCCTGT 1380 ATTACCCTGT GATTGTCCAG TCAATGCATT TTTAGGGCTC TCGGGGGCAT TTAGGTGGAA 1440 CTGTGAGTGG ATGAAGATCA AGGTGGGCCT TTGAAAGTAG GGCCTGAAGA GGAGAAGGCT 1500 GGGGAGGGGC AGTGTCTGTC CCTGGGCTCT TACGGGAGGT TCCCTGAGGT GGAGTTTAGA 1560 TAGTATATTG GATTCCCCAG AGAGCCCATG GTGGTGAGCT GGAAGGGGCT TTGGTTTCCC 1620 ATCAAGGCAT TCTCACCAAC TCTCCCCAAG AGCGGCAGGA GGGCTCCATC ATCTTCTCTG 1680 ATGTATTGAT CAGGAGAGCT CCAGAGGTAG ACAGGCTGAA GCTGGAATAC TGCCCTGTCC 1740 CTGACACCTG CTGGGGTGTT CTGGCGGGGC CCGGAAACGG AAGCCCTCTC CTGGCTTTGT 1800 TGGGTTTCCT GGGGAAGGCG GAGCTGGTCC ACGGGTGACT CAGCGTCCTG CACAGAGTCC 1860 AACCCCTGGC CCAGTCCGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTCCTATCC 1920 TGGCCTTGGG CAGGAGGAAT TGGCCCCTCA TAGAGTGTCA GCCCCATCTC TGGGGATGTG 1980 GAGTAGGGGC CACATCTGTG TCTGCCTCTG CCTCCAGGGC ACAGCACTAA TCTAACGATG 2040 TGCTCGCCCC TGCCAAGCCC CTGCATGTGT GGTTAAGCTC TCAGCCTCCT TCCCACGTCT 2100 AAACAGGGGT CCCTTCGCAG AGTTTTCAGT TTCCTGGGAA TGAAGGAGAT CAGAATGTGT 2160 ATGGAGGGAA GAGACGCAGC CTGGGTGAGA TTTAGGGGCT TGAACATTGC CGAGGGGCTT 2220 GGCAGCCTGA TGAGATGGCC TTCCAGAGAG CCCCAACTTA TCTGCCAGGG TCTCCAGCTT 2280 CCTTCCTTCC AGGCTGCTCT ACCACACACC TACCTCCCCA TTCCTCCCCC ACACCCCCAA 2340 CTCCCACAGC ACTGTCCTGA CCTCACTGGG GCCTTTGTCC CAGCCGTGAG GCCCTGTCTG 2400 TGGGCCTGTC TCCTGCACAG GGAAAGAAAG AGCCCCATTG TTCTGGCTGC CTGCTGTGAC 2460 ACAGCAGCTC CCAAAGACTT CCAAAAATGC TCAGCCCGTC AGGCTCCCGT GGGTGAGTGG 2520 ACTTTCCCTG GGGGCTGCAG GCAGATCTCT GCCTGGAATG AGGGCCCAGG TGCTGTCTCT 2580 CCCAGCTGTG CAAGAGTTCT TTCAATCTGC AGACTGGAGG TCCTTCCTGA GATCTGACTT 2640 CCGCTCTGCA TGCTGCAAAG CAGCCTACTT CCTCCCGAGA AGGGAGAACT GAAAAAGGCA 2700 GGGACAGAGC ATGAGGAACG AAAGGAAAGG AAAGGAAGGA AAAAAGGAAG GAAAAAGAAA 2760 AGAAAGCAGG AGAAAAGGAA GAATGCGAGG AAATTCCCCC CACTGAGAGA CTCTAGACTA 2820 GTTAATTGTC TGAGTGGGTG GATCTTGTGG CTTCTGTGTT TATTCCCGGA TGCTTCTTCC 2880 TTAGTATTTA GAGAGCTTGC TAATGGGGAG GCTGTTGACC ACAGGACTGG 2930
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