Tag | Content |
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EnhancerAtlas ID | HS193-26897 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr4:182570700-182572250 |
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) |
HSF1 | MA0486.2 | chr4:182571859-182571872 | GAACTTTCTAGAA | - | 6.41 | NFE2L1 | MA0089.2 | chr4:182571380-182571395 | ACATGAGTCAGCAAA | + | 6.34 | Nfe2l2 | MA0150.2 | chr4:182571378-182571393 | CTACATGAGTCAGCA | + | 6 | RFX1 | MA0509.2 | chr4:182571686-182571702 | AGTTGTCATGGCTACA | + | 6.45 | RFX1 | MA0509.2 | chr4:182571686-182571702 | AGTTGTCATGGCTACA | - | 6.45 | RFX2 | MA0600.2 | chr4:182571686-182571702 | AGTTGTCATGGCTACA | + | 6.03 | RFX2 | MA0600.2 | chr4:182571686-182571702 | AGTTGTCATGGCTACA | - | 6.21 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_56494 | chr4:182570450-182572466 | u87 | SE_67735 | chr4:182570450-182572466 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I181649 | chr4 | 182570451 | 182572466 |
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Enhancer Sequence | CTTCAGGAAC TGCTAATGAA GAGTGTGGGA CAGTTGGGTG TCATTATGGG AACCCAAATG 60 GAAGGGATGT GTTCGTGTGT TTTGACTTAT AAAAGGAAGG GAAAGACCTA AGAGAATCCG 120 TGATTTGTTT GTTTTAAACT AGCACAAGTT TAGTTGATCG TGAAAAATGT ATTTCGGTAC 180 CACTTGGAAA ATTTCATTCA TTTTCCATCA CCTGGGGATA AATAATGTTT GACAGTGCAG 240 AAACGGGGTG ATATTTTATA ACAATATTGT CTACAGTCTC TGTGAAGTAG AGCTGTCGTG 300 GTACAGAGAT AATGTGTCAT TCCAGTCAAC TTGGATCAGG AGTGGATTGT GGGTCCTTAA 360 AAAGTTGTAC CCGGAAGGAA GCGGTAGCTG AAATTGATGG AGTTCTGGTA GGAGTGATTA 420 TCACTGGCTG AGGAATTTTG ACAGCAGAGA CAAACTTTGT TTTGAGGAAG TCACTCATTA 480 GACAAGTCAG GTATGGTTTT TCAGAGCATA TGTGCTTCTG ATTATAAGAA TCTGAGAAGG 540 TTTGATAGTA GGAAAGGAAC ACCTGTCACT CAAAGATTAT GCATAATAGC CTCAAACTGG 600 CGTATCACTC TGGCTGTTCT TAAATTCCCA GGATACTGCA TTTTCTGAAA CGGATTTACT 660 AACAGTTACA CCCAAGACCT ACATGAGTCA GCAAACTTGC CTTTGTAATC CTACTCACTA 720 GAATTTCTTA GACTTCTGTT TCAGATTGGG GTGTTCAGAA CACAAATTAA AGGACAGAGC 780 ATAAACAAAG CATGTAGAAA GCCAGTATAC AGACACATAC CATGTGCATT GTCAATTAAT 840 ACACTTGTCT GCTACATGGG GGTCATGTAG GGCTTGTTAG ACCTTTTCCA CTTGCCTAGA 900 AGCTTGTACT TAGGAACACT CTTCACCCTC AACCTTATCA TTTGGAGACG GGGTGTTCAT 960 CATCCGCTTC TCTTTCTTCC TATCTTAGTT GTCATGGCTA CAATCACTTT GTTTCCTTGT 1020 CACCTGTAAT TCTGCAGATC CCTATTAGGA GTACTTAGAT AATTCTGGCT TAACATGCAC 1080 AGGAAAATAT GCAGTGACTC AAAGAAGCTT GCAAACCCCA GATGTCATTT CATACAATTA 1140 ATTGAATAAC AGGAATCTAG AACTTTCTAG AAGAGCTACA GCAGTAGAAT GAGGTGTAAG 1200 AGACATTTTA GAAAAAAATA CCAGCACATT TAATGCTGTT CAAGAGCAAA TGCCTCATTC 1260 CTATTTTTAA AACAAAATGT TACAGAGTAT TTGGAAAGTG AAAGAACAGT TGTTTTCTTT 1320 ATCTTCCCTT TGAGTCCTGT TCGAATTAAA ATGTATGTTT TACAAGCATT CAAAAAGGTA 1380 ATGGATTGTT TCACAAGTAA AGTCCTAAGT GTTCAGCTAT TTCAGCTCTT CTTTGCCATT 1440 TGGGGCTTCT TACTTGTTAG GTGATTTCTC CGGCCTTCTA TCAAGCATGA TGTGTGTCTT 1500 CCTGTCCATA ATGCCAGAAA GGTTACTGAA ATTTTGGGAA TAAAAAGCAT 1550
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