Tag | Content |
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EnhancerAtlas ID | HS104-39638 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr3:14946710-14949140 |
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) |
Gata4 | MA0482.1 | chr3:14949084-14949095 | AGGAGATAAGA | - | 6.14 | RREB1 | MA0073.1 | chr3:14946851-14946871 | TCTGTGTGTGTGTGTTGTGG | - | 6.27 | RREB1 | MA0073.1 | chr3:14946853-14946873 | TGTGTGTGTGTGTTGTGGGG | - | 7.01 | SP2 | MA0516.2 | chr3:14948031-14948048 | AAGTGGGCAGGGCTTTG | - | 6.04 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_25472 | chr3:14946513-14950052 | DND41 | SE_39502 | chr3:14947450-14949151 | Jurkat | SE_66419 | chr3:14947450-14949151 | Jurkat |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I014905 | chr3 | 14946514 | 14950052 |
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Enhancer Sequence | TCTTCTGGTG TACATCGTTT CTGGTGGAAA GTCTGCTGTG ATACTCATGA GTATCTGTCT 60 TTGTGTAATG TGTCCCTTTT CTCTGGCTGC CTTTAAGATC TTCTCTTTTG ATTTGATTTT 120 GGGAAGTTTG GCTGTGATGC GTCTGTGTGT GTGTGTTGTG GGGGATGGGG TGCTCTTTAT 180 CCAGTTGTGA TTCTTGAGCT TCTTGGATCT GTGGTTTGTT GTCATTCACT AATTTTGGGA 240 AATCCTCTTG GATGCTCTGT TCTTTTTCCC TGCTCTTTGT GTTTCAGTAT GGATCATCTC 300 CACTGATCTG TCTTCAAGCT CATGGAGTCT TTCCTCAGCT GTGTTCCGTT TGCTGCTAAA 360 CCTGTCAAAG GAATTCTTTG TTTCTGATAC TGATTTTTTA CTTTCAAAAT TTCCATTGGA 420 CGCTCACGTA TGGTTTCCAT CTCTGCCAAA ATCCTCCATC TGCTTGCGGG TGGTGTTCAC 480 CTTTCCCACC AGGTCCTTTT ACCCACCAAT CAGAGCTACT TCAAGGTCTG ATGGCTCAGA 540 CACCTGTGTC CCTTCTCACT GTGGTTTGAT GGAATGCTTT CTCCTCTTGA AAATGAGTTG 600 GGGTTGGGGA GTTTTTTGCT TGCATTTTTG TGTTCCTCAT AACTTGTTAT TGGAGGCCAG 660 GCATTATGTG TAGAAGCACT GTAGAGACTG AGGTAAATCG TATTTACCCC TCAAGGTGGG 720 GTAAGCCTCT TTTTTGGTCA TGGCTGTTCA CGGTAGGGTA CAGGGCAGTC GGGTCAGTCC 780 AGTCGGCACC TGATCTGGGT TTGGGTTTTG CTGCCGTGTC ATCAACCTTC AGTGACTGCC 840 AGGCTTCATG CTTCTCCCGT GGGTGCTGCT GTGACCTGTG GGGTAGGTCA GAGAGCTTTT 900 CTTTCATTCT TGCTCCATAT TCAGCTTTTA GCCCTCCCTG CACCACAGGA AGGCCCTCTC 960 CCCATGTTCT TGCTCTTCTC AGAGGCAGGC TACTGCCCTG TGTTACTCAG TGCTGGACTT 1020 ATGGTGGGCA CATGCCTACA TCTGAAGCAG GGCCTGTGAG CCGGGCTCTC ACAGCATTCC 1080 TGTCCCTCCC CTCCATGGCG GCTGAGCTCT GTGGCTCTGT GGCTGGCCTT AGACAGGTTT 1140 CTGGCCATCC CCCAGCAAGG TATTGGTGCA CAGTACTGGG TCCAAGGGGT TATCGCCCCC 1200 GTCCTAGGGT GCAGCTTTCC TCTCTTTCCC TAGAGGAGCA GACCTTTGCC TGGGCTGTGG 1260 GGGTGGGAGG TCTCCTGGCC TCCTCCTGGA ACTGAAGCCT TGCATGAGAG AAGGCCTGAG 1320 GAAGTGGGCA GGGCTTTGCA TGTGGCCCCA CCTTGCCCCT GCCTTTCTCG TGGGCACGTG 1380 GCAGAGACTC GTGGATGAGA GCTTGCAAGT GAGGACAGAT TCCCTCGCGT CTGCAGCTCC 1440 CCATTACTCT AAACTGGCAC CAGCCCACAC CTGTCCTTTG AGAATTCATT AACATTTTCG 1500 CTGCTTTCTT CTTACCTTCC TTTACACCAG CCACCTCTGC CTCCTGTGTG TCACCAAAGG 1560 TGCGGCAGTT CCTGCATCTC ATTCCTTTGT GGACGGGCTT GCCAGGTGGA ACCCAGTTCA 1620 CTCGGTTGCC TTGTGACCCC AGCTCTCCCA CAGGCTGAAG CATAGTTATG ATTTTGAAGG 1680 TTATCTGGCT TTTTCACACT ACAATGAGAA CAGTGTTCTC TTGTACTTCC TACATCTTAA 1740 ATGGAAATGG AACCACAATT ACTCATTTTT TACTACATAG GATTTTATGC CCAAAACCAT 1800 AGATAATGGA AAGGACTTTT CAGGGCAAAT TCTCTACCCA CAATGTTCAC CTTACAACTT 1860 TAGAACCTGC CCTGTGTAAG GTTCAAGGGG CACCTGCCCA CAGGGTGGGC GCTTGTTGTA 1920 TCTAGGATTG TGGGGTGCTG TGCAGAGGAG ACAGGGGGCT GTTACTTTAC ATTTTGTGGC 1980 TAACCCAGTG AAGTACTGAC AAGGCACACT TATTTTTCTA ACCACGAGGC TCCACAGAGT 2040 GTGGATCCAG TTTCCTCTGC AGGTGCTGTG TTTCATGGGC TACAAGCCAG GAGGGCCTGA 2100 GGCCAGCCTT GGGTCCGATG AAGTCCCCAT GCTCCAGACC TCATGAGAGA CATAGGCTTA 2160 GAGAGCGTAG GAGCAGTTGT CCAGAGAAAC ACAGGGATGC TGGACAGCAC AGTGAGGCCA 2220 GGCAGCCGGC TCCACAGCAC ATAGAGCCAT GGTGGTGGCT CCCTGCAGAC CCAGGCTCGG 2280 ATCCCAGTCC TGCCTTGTAC AGGAGGTTGG ATTTGGGGCA GGCCTTTCCG GGCTTCATTT 2340 TTGTCTGAAA CAGAAGCAAC GCCATGCCTT ACAGAGGAGA TAAGACGCCT GGTAGGGGCC 2400 CTGACCATCT CTCCCTCACC CCATTCCCAC 2430
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