Tag | Content |
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EnhancerAtlas ID | HS094-08436 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr11:130729320-130730730 |
Target genes | |
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) |
Ar | MA0007.3 | chr11:130730478-130730495 | GGGTACACTGTGTGCTC | + | 6.84 | Ar | MA0007.3 | chr11:130730478-130730495 | GGGTACACTGTGTGCTC | - | 6.97 | NR3C1 | MA0113.3 | chr11:130730478-130730495 | GGGTACACTGTGTGCTC | + | 6.15 | NR3C1 | MA0113.3 | chr11:130730478-130730495 | GGGTACACTGTGTGCTC | - | 6.16 | NR3C2 | MA0727.1 | chr11:130730478-130730495 | GGGTACACTGTGTGCTC | + | 6.11 | NR3C2 | MA0727.1 | chr11:130730478-130730495 | GGGTACACTGTGTGCTC | - | 6.24 |
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Enhancer Sequence | AGGCTGCCTG GGTTTGAATC CCAGCTCTGA CCTTTACTAA CTGGATAAGT GGGGTGAATT 60 ACTTCTCTCT CTAAGCTTCA ACTCCTCCAT CTGTACATGG GGGTGGGGAT CCTCATACTT 120 CATGCAATCT TTGGGAGAAT TAAGTGAGTT AATCCACATA GAGCACGGAA ACCAGGCCTT 180 GACATGTTGT GAGCCCTCTC TGATGTTAGC TATTGCTATT AGAGCAAGTT ATTTCCCCTT 240 TTTGGGATTT CATACTGTTG TCCAGCGATT GTGAGCTTTG GAGGCATGGT CTCTTTAGCT 300 TCTCTCAGGA AGTCTGAGGC TAATTTATAT GTTATTCTGT GGACCATTTG CTTGTCATTT 360 GTTCTCTCCT CAGGAATTGT GTTTTTTCAC AGTCCTCTTG CTGGATTTAG CTTCTTTCCA 420 GTGAAGTTGA GCATGGGATC TTTCATTTGT CTTTGCTAGA CTTCCATTTC TCTCTGCCTC 480 ACTGGTGGGC TTTATTCCTT CCTGGAACTT TGCACACTAC TTCAGTACAT TTTGTTGATT 540 AAAAACATTC TCTCTACAAA CTTCAATACA CTGGCAAAGG ATCTCTGTAG CAGAAACTTT 600 AAAACATGAA ACTGCAGGCT GCTTTCTGTT TGGAGACCAA GCATCTGGGA AAGATGCCAT 660 TTGAACTAAG GGTGCACCAA GTCATAGACG CTCTTGGATG GCCCTTCCTG CAACATAGTC 720 ACAAATGCCA ACAAGCATCT TACTGCTGTA GCCATGTGCT CTGGTTGCTA ATCATATAAA 780 GTAGTGCATT TGAGAACCCA TCCTATCCTT GGTCTGAACA TTTGTCTCCA TCCAAAATTG 840 ACAGATTAAA ATCCTCAACA CCAAGGTGAT GATACCAGGA GGCGGAGCCT TCGGAAGGTG 900 ACTTGGTCTT GAGGGTAGAG GCCACACGCA TGGGATGAGT GCCCTCATAA GAGGGGCCTA 960 AGGGAGCTTG TTTGTCCCTT CTGACATGTG AAGTTACAGT GAGAAGATAG GGTCTATGAG 1020 GAAACAGGCC ATCATTTGAC ACTGAACCTT GCTCTCTGGA CTGTGAGAAA TGTGTTTTGT 1080 TTTGTTTTTT TTTGTCAGCT ACCTGATATG GTATTCTGTT ATGGCAGCTC AGACACAGTC 1140 CTGCGTCTTT AGAACTCAGG GTACACTGTG TGCTCCGTCA ATGCTCATGA CCATTTGGTA 1200 CTCACGCTGG AGTGTGGGGG TTCGGAATGA ACACTGAGAC CAGCCATGCA GCATCTGTCC 1260 TCTCTTTCTG TGAAAAGTGC CATTCTGTAT GTGACATGGA CCCCTAGCTT TAGACCCTAC 1320 AGATCACAGT GCAGTGTCTT TCACAGAGTG AGTGTGCTGG GTACTAGTGA TACTAAGCTG 1380 GGTGATAAAC CCTGCTAGAG AGGTGCGGCC 1410
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