Tag | Content |
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EnhancerAtlas ID | HS133-28192 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:29129710-29132130 |
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) |
Foxq1 | MA0040.1 | chr7:29130751-29130762 | TATAAACAATA | - | 6.32 | MEF2A | MA0052.3 | chr7:29131708-29131720 | GCTAAAAATAGC | + | 6.44 | MEF2B | MA0660.1 | chr7:29131708-29131720 | GCTAAAAATAGC | + | 6.92 | MEF2C | MA0497.1 | chr7:29131706-29131721 | ATGCTAAAAATAGCA | + | 8.07 | MEOX2 | MA0706.1 | chr7:29131502-29131512 | AGTAATTAAC | + | 6.02 | REST | MA0138.2 | chr7:29130203-29130224 | ACCAGCACCAAGAACAGCAGC | + | 6.8 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I029090 | chr7 | 29130122 | 29131615 |
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Enhancer Sequence | TCAGGTGATC TGCCTGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGTGT GAGCCACCAC 60 ACCTGGCCAC CCTTGAATTC TTTCCTGGGC AAATCCAAAA CCCCTCACAG GCTAAGCCCC 120 ACTTTGGGGC TCATCTGCCT TGCACTGGAC CGATACAAGC TCAGCAACAG GAATCCTGGC 180 AGTGCTGCTC TGTTGGAACC CGTGAAGGGA GCCTCTTCTG CATTCACTCT ACATCTAGCA 240 AGGCTGAGCC ATGATCCTCT CCACCTGGCA CAGGACACAG AGTTTTCTCA TTTAATATAG 300 GAAGCCTGCT TCCTAGCTGC ATTGCTATGA AGCTTTGTTT AGCAACACTA CATATCATTT 360 CCCATTGCAA ACCAACATGT AGGAGAAAAC TATAGCAGCA CTTCCATTTG GCTGCTAAGA 420 AAATAACTAT AGGTCCACCA CTAGACTGAG CACCAGGAGG GCAGGGGGTT TGAGGACTGC 480 TTACTACTGT CTCACCAGCA CCAAGAACAG CAGCTGGCAC ATAATAGGCA ATTGGTAAAC 540 AATGGCAGAA GGAGATTGGC ACCAGCTAGT GTACTCCAAA TCAAAGTTAA TACATTTCAT 600 AATTTGTTTT AAACCAGAGA GGCATTGTGA CTAAATAGCA TATTCCAAAT AAGAAAAGTG 660 GGAGAGTATT TTAACATCTT GTTCGTGAAA AAGTTTTATT TCCAAACACA AAAGCAGCAA 720 AACTGTGAAC GGTAAATGTC TCCTTACAGC CATGCACTAT TAATAGTCAA AAAGAATGAG 780 ATTTTCTGAA AAAAGAAAGT TGGTTTTCAA AGGGAGAAAA TGAAAGCTCC ACTCTTTAAA 840 CCTGTAGTAG CCCATTTGCA GGTTTTGAAG CGACCCTCTT ATTCCAAACA CCCATCTGGA 900 GAGCTGGAGA GAAGAATGTG GTCACAAAGG GAAATGAATA GTGTAAACTA TAAAGGAAAC 960 AGCTGAAATC AGTTTTCTGC ACCACCCTTG ATTAGCTATT TTCCAGTTCT AAGAGCCCGA 1020 AGCAAAAAGA ACTACAACAG CTATAAACAA TAGATGCTTT GAAATAGGTT CCCTTTACAT 1080 GTCAGGAAAG AGGAGATGGA CCACATGTCA GCAGTCGACA TCCCCATATG GAGGGGCAAC 1140 TGGAAGCTGT AACTGTCTTT GGGGGAGGGG AAGGAAAGAC AGAAACGGCT TGGCAGTGAT 1200 GCTCTGTCTT AGAGGGGGCC CGATGCATCT CTTCAATACA GAACCTCTGC CCTCAGGGTG 1260 TTTGCTAGTT AACCACTGAG CTTGTTTGGA TTTAAACCAA AGAGGGATGG GAGGTGGGGG 1320 CGGGGAGTAG GTTTCTAATC TGAAGAAAGA GAGCACACAG TGCCAAGAGA GCCCTGGCCC 1380 TGGCTCTGAA GAAGCCTGTG AGGAGGACTG CCGTCCGTTA CGTCTGTGGA GGGAAGGGGA 1440 GGAGGTGCTG GGGGGAACAC CCCGTCAGCA TCTTGGCAAA TATGTCCCTA GGACCCCACT 1500 GTATGTGGAA GCAGAAGTGT GGGGCCCTGG GCATCCCCCT AGAAACTGAA TAGAAGTGAT 1560 CGAATCATGG AACATGTGAA AAACAAACAA AAGTGGAGAA GACAACAGCC ATATTCTTTT 1620 CTGGGTGGGC AGAGGGAGAG ATCTTTGGGA AAGGGGCTTG GAAGTAGTTC TTTCTTCTCT 1680 CCCCCCGGCC ACCTATCTGC CTCAGAGAGA AAGAAAAGTA AAACGGAAAG CTTTTGTCAG 1740 AGATCAGCAA ACTCTGACTC CTATTAGATG CACTTTCGCT TTGAGGATTG GTAGTAATTA 1800 ACAGAGTGCT TGGTGGAGGT GTGGGGTAGG GAGCTAGTTA ACTCCTTCTG GCCACTAGGG 1860 TTCTTTTAGT AAATTATTAT AATACATAAA GCGGTGCCCT AGTGACCAGA AAGAATCTAG 1920 GACTTGGTCT CTAGTAATAA TTTGTAGACT GGAAAAATCT GACCAAATAA GAAAGGTCAC 1980 TTGCTTTTTT TTAAAAATGC TAAAAATAGC AATGATTAAT ATGAGTGAAA AAAGGGAGAA 2040 ATTATATGGA CACTGTTTGG CCAGACTTAC AACTTTACAT TTTTCCTTTT TTTTTTTTTT 2100 TTAAGCAAAA CAAAACTTTC ATAAGAAGAA GAGAGAATAC TAGAGACTAA CAAGCTAAGT 2160 TTTCAGCCTG GAAAAGTCAT GAAATAGAAG CAAAAAGTAA AAAATTGCAT CCAAAAGCCA 2220 CGAAAAGAAG AATCCTGAGA AACAAACAAA TATCTGAAAA GATGTTGTCT CCCTGCAAAT 2280 GCAAAGTTAA ATACAAATTT GGAAAACAAG TAGAAACCTT TCAGATGTCT GGTTGAAAGG 2340 TTTAAAAAAT AATCTTTAAT TGAAAAATTC TGCTCTGTGT GTGTGGATGT GAAAATATCC 2400 TTAAATTATC TTCAGGAATT 2420
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