Tag | Content |
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EnhancerAtlas ID | HS193-07863 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr12:53954790-53956120 |
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) |
FOXA1 | MA0148.4 | chr12:53954895-53954911 | TTTTGTTTACTTTAGA | - | 6.69 | FOXP2 | MA0593.1 | chr12:53954896-53954907 | TTTGTTTACTT | - | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09913 | chr12:53955277-53956313 | CD14 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I053560 | chr12 | 53953948 | 53956664 |
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Enhancer Sequence | GTGATCTTAG ATCACTGTAA CCTCAAACTC TTAGACTCAA GCAATCTTCC CACCTCAGCC 60 TACCAAGTAG CTGGGACTAC AGGTTCGCAC CACCATGGGC TATTGTTTTG TTTACTTTAG 120 AGATGGGGTG TTGCTATGTT GCCCAGGCTG ACTGCAAACT CTTGGCCTCA AGTGATCATC 180 CCACCTCAGC CTTCCAAAGA GCTGGGTTTA TCTGCACCCA TATACTTGGG GGCGTATTTT 240 GATGAAAGGA AATAGTATGA AAAAGTCACA GAAGACAGCA CCACTGCACT CCAGCCTGGT 300 CAACAGAGTA AGACTGTCTC TTTAAAAAAA AAAAAAAAAA AAGTCATAGA AAACTTGAGA 360 AAAACTATGA GGAGTAAGTT CTAGAATAGT GATGCTGGTG CTGAGCAGGT GAAGGAAGAA 420 ATAACTGATC TTTTTTTTGA ACACTATTTA ATTAATCACT TCAAGTGATC ACATATTCTG 480 AAAGAAGAAA CTGGAAGATC TGTAAAAGTC TTGACAAGGC TTCTTGCCCT CACTGCAGTG 540 CTTCTGTTCC CAATGTCAGA CATCATTTAA GTTTGGGAAA GCAGGGAAAG GGAGAAGAAG 600 GAAGGGATTA AATACACACA TACTTCAAAC CAAACATAAC TTTCATTTCT ACCTTGGTCA 660 ATCCTAGGCT CCTGCTCTCT ACTTCAAGAT GTTTAGCCAA TGATGGGAAA TAAATAAATA 720 AAAGGAAAAA AAAGATGCTA CTGTTTGCTA TGTGAGTCAC ACATCCTGCT TTGAATGTTT 780 CATGGCTCTT AAATGAATCA TTTCAAAGTA CAGGATTGTT CAACAAATAA AATACAACCA 840 CAGCAACAGT AGCTCATATG CTGCATGTGT GAGCGACATA ATTTATAGAG GAAAAACAAG 900 AACAGAAAAC TTTCCCCCAA AATACTCAAA GATAAAATGT TGTCAGGGGA ATGAAGGAGG 960 ACAAACTAAA CAGAGGAGCG GGGACAACCC ACCAAACTGT ACCTAAGGTA AATTCATTTG 1020 TCTATGGATT GAGGAATTTT CTGTTTTGGG AAGGCTGTTG GAATATCTTA AAGATTCTGG 1080 CAGCTTAACA AATAAGTCCA CTGTATAAAG AAAAGGAATT TTGAAAGCAG AGATATTATT 1140 TGATAGTTGG TCTAGCTGCC ATGCTGCTGC TACAATGTAA GCTCCTCAAG AACAAGGATC 1200 TCTCCATTTG CTTGTTCATG GACAAATCCC AAGCACCTAG AACGGTATCT GTACACAGTA 1260 GGTGCTTAAT ATTTGTTGAA TAAATGCCAA CTAGCACGTC TCACTAAAGT GCTACAAAGC 1320 AACCCCAACC 1330
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