Tag | Content |
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EnhancerAtlas ID | HS087-13413 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr21:16576120-16577820 |
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) |
TCF3 | MA0522.2 | chr21:16577757-16577767 | AACACCTGCT | + | 6.02 | TFAP2A | MA0003.3 | chr21:16576610-16576621 | TGCCTGAGGCT | - | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_43477 | chr21:16574727-16578159 | MCF-7 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I015203 | chr21 | 16575435 | 16578201 |
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Enhancer Sequence | AGAAGAATTC TACCCATCTC TCTGTTTCTG TCAGTTGTAG GTTGGATGGG AAATTAAAAG 60 TTAATTTTGT CTTTGTCCTT TTGTCTTTTT CTTATCAGCA GTGCCTGGGA GGCATGGTAA 120 ATAAAGTGTG CTCAAAGTGA CCTTCAGTTA ACTCATATCG TCTTGACACA AGTAAGCCAG 180 GCTCTACCCT TGTAATCTTC ATTGTCAGCT ACATGAAGAG GAGCTTCTTT CAGTAGGAAG 240 TGCGCATCAT CCAAAAATAT ATAGGTATTT TATTCATTTC ATGTGATTGT TTAAAGGAGA 300 CTGCAAGAGT AGAGAATCAA TAGAGAAGGC AATGCGTGAA GGAGAAAAAA TTACAGGCCA 360 AACTGCTGCC ACGCAGAGGG TGAAGTAATT TACCCAAGGT TAGTAGCAGA ACTTCCATTT 420 AGGGACACAG TCAAAATTAG AACCCGTGGG TCCTAGCTTT AGGTGCAGAA TGCCTTCCTC 480 TTCTCCATCC TGCCTGAGGC TGTGGAAAGG CAAACGAGCT GCCCTTCTCA TATGGGGTTA 540 GATGACTGGT TAGGCACTGC ACAGCCACAT GTCTGCGTGG CATGTTGTTT CTTTACCTCT 600 GCCCTATTCA CATTTCTGTC TCTCTCTACC GAAGTCAGAA GTTGAAACTT CTAGTTGTAA 660 GGGCACAAAG TGGCTCCATG TCAACTTTCC CCCGTAAATT ATTTTTATGG GCATACCAAC 720 CAAGGGCATA TCTCAAACGC ATGATTGCTT TTGGCATCGT ACCAATGCTT CTCCCCCCAC 780 CCCTGTTTTA TGGATAAAAA AGGCCTTTTC TGGTTATTCT TCTCAGATGG GGCCCTTGAA 840 ACTTCTGTAA TGCATAATGT TAATAAATCA ACTAGCAAAG GAAAAAAAAT AAGTCGCCTG 900 ATAAAAGTAG GCATTTGAGA GTTCAGGCTC CTGAAATCTA TACCCATTTC TTAGTTATAT 960 GGAACACATG ACTTCAGGCT ATTCCTGTAT CCCTTTTCAC TCCTCAGTAA AAAGCTGATT 1020 TTAGATGAGT GTTCTGATTA GAAGTTGCTG CATTAAGAAT GTTAGAACTA CAGGTCTCCT 1080 GCATCTACGG CCGAATAGAT AGGTGGGGCT GCTAATGACG TTGAGTGTTC CACGAAGAGT 1140 GATATGTAAA GATCTTCACT TGGATGTACT GAGTGACCAC TGTGTGTTCA GTAACCACAG 1200 GGCAGGATAT CTGAATTCTG CAAAGGACAC AGCGCTGCAG TGTGTGCCCT TGAGAGTCTC 1260 CTTTACAAAC ACGCCAGAGC AGAGATAGTG ACCTCATGCT TCCCAGAGAA CATCTTCGCT 1320 GGGCTGTCCT GAGGTCACCT CACACTCAAC ACACCCAAAA TAGAAACACA ATCCTCCTCA 1380 CACTTGTGTG GGGCCACATC ATTCCCCCAT TTGCTAGAAC TAGCAATCGC ATTTTTATGC 1440 CAATGACAAA TTGGTTCTGT GTCTGTACAG TCTCCTATAG CTACACCTTC CATGGCTCTC 1500 CTGCCACCAC TACCTTGATG CAGGCTTGTC ATTACCCTTC ACTGCCACTC TTGCCATGAC 1560 TTTCCTGATG GGCTCTGAAA CTGCAGATTC TCCCTCGCCA GTCCATCTTC TGTGCTGCTA 1620 ATGGGACTGC TTACTAAAAC ACCTGCTCAG GCCCACCACC TTACCCAAAA CCTACAATTG 1680 TTCCTTGCTG CCTACAGAAT 1700
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