Tag | Content |
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EnhancerAtlas ID | HS184-00344 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:23076760-23078190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mafb | MA0117.2 | chr1:23077933-23077945 | AGTCAGCATTTT | - | 7.22 | NKX2-3 | MA0672.1 | chr1:23077570-23077580 | TTCAAGTGGT | - | 6.02 | ZNF263 | MA0528.1 | chr1:23077009-23077030 | GTTCCCCTTCCCTTCTCCTCC | - | 6.06 | ZNF263 | MA0528.1 | chr1:23076791-23076812 | GGGGCAGGGGGAGCAGGAGAG | + | 6.75 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_24067 | chr1:23076440-23077194 | Colon_Crypt_2 | SE_24067 | chr1:23077244-23077520 | Colon_Crypt_2 | SE_24067 | chr1:23077543-23078203 | Colon_Crypt_2 | SE_38845 | chr1:23075377-23078524 | HUVEC |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I022749 | chr1 | 23075723 | 23078402 |
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Enhancer Sequence | CTGGGGCAGT AGAAGGATTT TCAGCAGGCA AGGGGCAGGG GGAGCAGGAG AGATGGGCTG 60 GGATGGGTGC TGAGGCCCGG ACCCTTCTGT GGCATCAGAG CTTTGCTCTC TTCTCTTTCT 120 GGAGTCCTGG GTCACCAGAG CCAGACTTCT GATGTGCTTT AGTCCTGTGT TTACATGAGT 180 GTCAGACGGA GCAGGCTCCA GGGGAACACG GAAATGGCAT TAAATAACGC TGAATCACAC 240 AGTAAGAAAG TTCCCCTTCC CTTCTCCTCC GTGCCTGCTG ATTACTCATG GAGAAAGTCT 300 CTGTTTCCTG CCAGCATGTC TCTAACACCT CTCTGACAGC CCCTAATCTC CCTTTTCAAT 360 TGGGAAAAGC AGACTTCAAG CTCAGAACCT GCTAGGGAGC TGGAATGCCA GGACATCATC 420 TTGTTTTCAT CATGAATAGT TTAGCTTATA TATTTTTATT TAACAAACAT ACAAATGGCA 480 CTTTCTAAGT GCTTTGCAAA TATTACAAAT ATTTCATCCC CATTACGACT TTATGAGACA 540 GGTGCTATTA TCCACCTTCC AGATGAGTAA GCTGATACAC AGAGAGGTTG AGTAACCTGC 600 CTGGGTCACA CCTCCAGAGT GTCAGAGCAA GGACTAGGAA TCCAGGCAGC AGGCCCCAGA 660 GCCCATGCTC TTAAGCATCT CCCCAGACTA CCTCTGATTC TCAGAATTGG TGCTGGCTCT 720 CTTCTAGTTC CAGCAGTAGC CTGATTTTTT CCTTTACTGA TGAATTTATT TCCATGAAAA 780 TAGGTGAGCC AATTTAAAAG TAAAGTGGAG TTCAAGTGGT TGTGTGGAAA TAGCCAAAGT 840 CCTAACAGTA GTTCAAGGGC TACTGAAGTT TGAAGAACAC TGGTCAGTCC AAGCCCTTCA 900 TTTGGTGGAG GGGGATGCTC TGAAGAACAG AGAGGGGATG GGACCTAGCA GAGGTCACAC 960 AGCGAGTGAG CCTGGAGGCT GCCAGGACAG ATGGGAGCGC TCACCTGCCA CCCACGCCCA 1020 TCTGCTTCCT GCACGCAGGA CTGATGGGGC GCCAGGTGGC AGGAGCACAG AGGTGTGCTC 1080 ACCTGCCCAG AAGTGTCCCG GTGCTGTAAC AGGATCCCTG TTATCTCTGC TGTTCTGGGA 1140 ACAGGCAGAT CTGAGCCCCA AGGCCCAAGC CCAAGTCAGC ATTTTGGCCA CTGCTGAGCT 1200 GACATCTGTT GTATGTCTTT ACCTTGTCTT CCAAGTCTCA ACAGAGCCTG AGTGGGGAGC 1260 TCTGTCCTCA GCCTGCTGGT CAGGGCTCAC CTTCCCTACC TTTACGCCTT TCCAGAAGCT 1320 TTCACAGCCT CTGCCTTGAG AGATGCGAGC TGACCCTGGG TTCAAGTCCT GGTTCTGCCG 1380 TATACCCACT ATGTGGCTTT CTTTAGGATG CTTAGCCCCT GCAAGCTGTG 1430
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