Tag | Content |
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EnhancerAtlas ID | HS183-07164 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr6:12294630-12296190 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr6:12294636-12294654 | GGTAAGAGGGAAGGAAGA | + | 6.17 | RARA | MA0729.1 | chr6:12295967-12295985 | ACTTGACCATATGACCCC | - | 6.93 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_27736 | chr6:12287984-12298413 | Fetal_Intestine | SE_28655 | chr6:12288450-12297846 | Fetal_Intestine_Large | SE_38275 | chr6:12288335-12299813 | HUVEC | SE_47299 | chr6:12287161-12297248 | Panc1 | SE_64480 | chr6:12295928-12297406 | NHEK |
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Enhancer Sequence | AAACCAGGTA AGAGGGAAGG AAGAAAAATT AGGTAAGAGG TTCACAAGAA CAACTAGCCC 60 CAGTCAGTGA TGCCAGCAGC CTGTTCCTCC AGCCCTTCTT ACCCGGGCAG GTGAAAGACT 120 TAGAAAACAG TAGCAGAGGA GATCTATGCA TCCTATAGAT TAAAAGGAGC AAAAGAATCC 180 CTCTTAAATA TTTCCATGAA GCTCTGGAAT GCAAACCGAT GTCCTCTGTA CTTTTAGCAC 240 ATACCATTTC ATCTACAGGT AGATTTCCCA ACCAAAATAT ATCCAGAGAT GCCTTTGTCA 300 TTGGGTTATA TACAGCCTTT GCCTCTCTGA GTCAATGTAT TTACCACTTT CCCTGAGAAA 360 TCGAAAATCA TTTTGGGGAG CGGACATTTA GAAAAAGAAT CAAAGTGTCA TGGATAATCA 420 AATTCTTCAA TAAGTTGCAG TTATTCAGAT GGCCAAAGGA AAAATAAAGT CATTAGATAG 480 GGTTGGTAGA ATTTAGAACA TGCTGTTTTT CAGGTTTATG GTCTTTTTTT TTTTTTTTTT 540 TTTAAATAGG GAAATGTGTT TGGTGCAGAG CCAATGTCAT TCCAAAAAGC TCTCTCTTTT 600 CCTGGTCAGT CATGTGCTGG GACAGAGAAG GGATCTGGAT TAGGCAACAT CATAGAGTTG 660 CTCTGAGCTG CTCTTTGGTG ATAACCCTTC CAAATCCTAA ACTTTTTGGA ATTCACAAGC 720 TCAAAGGAGG AAACCTACTC TCTGATCTAC CACATGTTCT GCATTTTTCT ATCATGGTCT 780 ATGGAAACTT CTCTTAGAAA TCCAGTGGCA AGAAGTTCTA TGATTAAAGT GTTCTGAGCT 840 CAGGCCAGGC AGTCATGAAC TACTTCTGAG TTATTTACTA CTGATTTGTG GGGCAGCCTC 900 AGCTATCGGT TTCTTCACAC CTGCTTATGA GAGTATCCAT ATTTATGGTC GCAGGCCAGT 960 AATGCTCCCC ACGAGATCAG TTTCTGAACT AACCTGGAAT TTTTTATGGG TTTTTATTAT 1020 GCCAACTATT AAATCAACAT TACAGTTCTT CCCTCTGTAT TTCTCCTGTA AAACATTAGG 1080 CCTGCAAAAA AAAAAAATCT TTTTAAAAAT AATTGCCATA AAGTATTTGC TCTGGGCCTA 1140 CTGTATGCTT CTTTTCTTTT TCTCTCTTTT CAACTAAGTC ACCGTCAATT TATTAAGATG 1200 GCCATAACTA TTCAAAACCT ATGCTGAGTT CCTCAAGGCA GGGTCACATA GTGATGAAGG 1260 TTGGGATGGG GCTACGGAAG AAACCAGAAC AACTCTAGTT TATTTAAAAC CTGTATTTAC 1320 TGCCCACTTC CCCTTAGACT TGACCATATG ACCCCTCGCT CCCATTCTAA GCATAGGGGC 1380 AGGCTTTATT TTTACAATGG TAATAGATAT CACTTGAGGT TTTATCAAAG AGTTGCGGCG 1440 GGTGGTGAAA GTTCACAACC AGATTCAGGT TTTGTTTGTG CCAGATTCTA ATTTTACATG 1500 TTTCTTTTGC CAAAGGGTGA TTTTTTTAAA ATAACATTTG TTTTCTCTTA TCTTGCTTTA 1560
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