Tag | Content |
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EnhancerAtlas ID | HS129-00929 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:40422890-40424330 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr1:40423209-40423226 | TGGCACACTGTGTTCCT | + | 6.38 | Ar | MA0007.3 | chr1:40423209-40423226 | TGGCACACTGTGTTCCT | - | 6.63 | NR3C1 | MA0113.3 | chr1:40423209-40423226 | TGGCACACTGTGTTCCT | - | 6.09 | NR3C2 | MA0727.1 | chr1:40423209-40423226 | TGGCACACTGTGTTCCT | + | 6 | NR3C2 | MA0727.1 | chr1:40423209-40423226 | TGGCACACTGTGTTCCT | - | 6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34178 | chr1:40424054-40425010 | HCC1954 | SE_64654 | chr1:40419968-40423814 | NHEK |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I039956 | chr1 | 40422618 | 40423686 | GH01I039958 | chr1 | 40424055 | 40425010 |
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Enhancer Sequence | CAGGTGAGTG GTCTAAGCCT TCGAGGGCTC CTTCAGCATC CTGAGGTGGG AAAGACTATG 60 CACCCCTGGG TCAGTTCGCT CAGTTTTCCC CATCTGTGAA ATGGGACCCC AAATCACTAC 120 TTTGCTGCCT CTGAGTCAGT GAGCAAGAAA TGAGAAGACC CTGGAAAGTA TCCAGTAAAG 180 GAGTGTCTCC ACTCCAGGAG TCTTTGCTGG AAAGGTCTGG CAACTCCTCC TTGCCTGGCA 240 TGAGCAACAG AGCCTGAAGG GGTAGGCGGT AGAATGAGGG AGAATGGGGC CTGCTGGGGA 300 TGCTGTTCTT AGAAGAGACT GGCACACTGT GTTCCTGGCT GGGAGATAGT CAGCTGGCTT 360 GACTCAGGGG TTGGTGGCTG TTGCCAGGCT TGTGGATGAG ATGCATCCCA CCTTTACCTG 420 AGGAGCAGAA GGGCACTTAG GTGCCAGGCT AAGTTAGAAT GCCCCAGTAC ACAGGGTCTT 480 TGACTGGGAG GGGTACTTAG GGTGAAACAG GACTATTCTG TGCATTGAGA AGCCTTGGCC 540 AGAAGCCTGG CATCCTGAGA ATTCACCCTG TCTGGATGGG AGAGTGGGAG GCAGAATAGC 600 CATGACTACC GGGGCTCCTG CACCAGCTGT CTTCTCTGTG TAGCATCTAA CTTGGCAAGC 660 ATCGCATCTT AGTTGTATCC ATTTACAGAG GGGGAACACT GAACTCCAGA AGGAACAAAA 720 AACTTCAGCA GCTAATTTTT GAGTAACTCC CATGGGCTGG GCCTTGGGTG GGGTGTAAAT 780 ATGAGGAACC TGCAGTCAAA GTGTAAACCT GTTGTAGTGG GTGTTAGAGC TGGGGTTGGG 840 GGGTTAGACT AGGGAGACTA TGGTATGGGG AAGAATACCC ACTCCCCAGA GAAATAGCAA 900 TAGCAGGGCT TTGATGGATA AGGAGGAGTC TGGAGAGTCT GTATTTAGGG CCTGGGGGGT 960 TTTGGGGCGG GGAGGGGGAT AACTTGAGTG GGTAGTGACA AGTCCCTTTT TAAAAAGCAT 1020 CTATAGGCTC CTTTTTCCAC ATCCAAGATA GAGCTTGAAC CTGTAAGGTA GAGCTCATAA 1080 CTCCCATTAT ACAGATGGGA ACACTGAAGC ACACTGTGTT CACCCCGTGA ATGCTCATTC 1140 TGATATCAGG TGGTCAGGAG CTCAGGGCTG AGAGAGGGAG GGAAGGAAAT GTTTGTGGAT 1200 TCATTTGAAT TGATGGGAAT GTTTTCAAGG GCAGTGGAGG GAAGCAATTA AGGAGACAGA 1260 GCTGGGAAAG CTTCTAAGGA GGCACCCAGT GCTACTGTTA TTGGAGAAAT GCTATTGTCA 1320 TTATTAACAA GGCAAGTGAA GATGTGTAAG GTCCATGTGG GAGCAGCTCA GGGTCACAAG 1380 ATCCTGGCTG AGATAGGGAG GGAGCCTCTG CTTCTGCCTA CCAGTGAGAG TTGAGGCGAG 1440
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