Tag | Content |
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EnhancerAtlas ID | HS133-13014 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:59281730-59284300 |
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) |
ESRRB | MA0141.3 | chr17:59282921-59282932 | ATTGACCTTGA | - | 6.02 | IRF1 | MA0050.2 | chr17:59282515-59282536 | AGGTTGAAACTGAAAGAAAAA | - | 6.65 | NFKB1 | MA0105.4 | chr17:59284197-59284210 | GGGGGAATCCCCT | + | 6.78 | NFKB1 | MA0105.4 | chr17:59284197-59284210 | GGGGGAATCCCCT | - | 6.92 |
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| Number: 2 | ID | Chromosome | Start | End |
GH17I061199 | chr17 | 59277353 | 59283261 | GH17I061206 | chr17 | 59283421 | 59283570 |
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Enhancer Sequence | ACCTTTACAT TTAGTTCACT ATTTTTTGAA AATAATATTC TATGTTTGGA TTTGTCTTTT 60 TTTCCCACAT TCATATTTGA CTGCGCATTA TGTGAAAAAT TGAATTTGGG AAACATTGAG 120 TGGAATATTT TTTAAGCTGA AATACCCATG TTAAAAATAA CAAAATGTGT TGTTGCTTCA 180 TCATTGTAAC TTTCTTAAAA ACAGAATTTA TAGCCCCTTT ATTAAATATT TCTAGAATAT 240 AATTGCCTCT GAAAACACAG TACCAGGGTT TTTTTGTTTT CGTTTTTCTT TAAATCTCAT 300 TCCCATTAAT TGCTCAGTCT TTACCTTGGC GGAGAATGAA AAACTGCCTT GGAACTTATT 360 AATAAGCATT TAGAAAAACT CGACAAAAAA TTAAAGAATT GGCCTGGCAT GGTGGCTCAT 420 GTCTGTAATC CAAGCACTTT AGGAGGCTGA GGCACGCAGA TCAGTTGAGG CCAGGAGTTC 480 GAGACCAGCC TGGGCAACAG GGCAAAACAC CTTCTCAACA AAAAATATAG AAATTAGCCT 540 GGCGTGGCGG CACATACCTG TAGTCCCAGC TACTCAGGAG GCTGAAGTGG AAGGATCACC 600 TGAGCCCAGA GAGGTTGAGG CTGCAGTGAG CCATGATTGT GCCAGAGTGA GACCTTGTCT 660 CAAAAAAAAT TAAAGAATGA CAGGATAAAA ATTTAGGGAG GCCGATTCCA TCTGCAATCA 720 AAAGCTAACT TTTGGTCCAC ACTAAGTAAG AAGTATTATT TTTCTCATTT CTACCTATGA 780 AAAAAAGGTT GAAACTGAAA GAAAAAAAAA GGCATTATTT ATTTTCCTCC TTTTCTGTCT 840 TCTAGAGCCA GAACAGACAG AATATATCCT AAATTGGATA CAGCCAGAGA ATAGTTTACT 900 GATAAAATAT GTTTTAGGAA GGAAAACTGG TTACATTTCA GCATATACAG CTGGACTTCC 960 TGGTGGGCCT CCCACATTGT CAACATCAGT ACCATTTATT TGTTGACCAA CAGAAGACCA 1020 CCAGAATGAG GTATTTTCAT TTCTGCATAC TTCTAATTCT ACAAGAAAGA TAGCTGTTGA 1080 GAGAGCTAAT ATCAAGGAAA TGGCAAACAA ACACCTTAGG TGATCCTGTG TGACATTCAG 1140 GAACTATTGC AGACTTCCAG GACTCAAGAC AGTCTCCTCA GCCATAATGT CATTGACCTT 1200 GACATACTCA GAACAAATTG GTCTGTGTGA TTGCTACCAC ATGCTGTAGC GCCTCCTAAC 1260 CCTGCCGTTG GTCTGGAGTG AAGCAGAGCA GGAGAAAGGG CTCCTCATCA GAGGATATGC 1320 TTCTTTTATG TTCCTTAGAC TCTTGCCCAG CATGCTTTTC CCACTCTATT TAGTCTTAAA 1380 ATGGCTAATT TAAAGTTTCT GAAGCTTTGT AGGAGCCGCA GAGTGTACCT AGTTTTGCCA 1440 GGCAAGGACT GAATAGGTGA ATAGTCATTG TATTCTTAGG GTGTGAAACT GTTTCGGGAG 1500 CAAAAGATAA GGCAAACACA ACCAAAAAGA CAGCCCTTTT GCTTAGTTAG GAAGATAATT 1560 TATGTCCCCA AAGCTCTTTC AGTGATCTGT ACCCATCAGA CCAGTAGAAT TTGAACTTTT 1620 TTCCCAACTG AAGAGTCAAC TGAGATGAGT AATAAGCACA CTCCTCACTT CTGGTTTTCT 1680 TTTACGTCTG TAGGTTTTTT TCATTTATAT GGAGAACACA AGTCGTAGCC AGTGAAAGTT 1740 TGTATAGGCC CCTCTGTTTC TTGCACTCTA GTTATAGGCA CTTGCTAAAT GTTTCTTGAG 1800 TGGATGAATG AATAAGTGAA TCCTGGACAG ATTGAGATGT ATGGGGTGAG TCATAATCCT 1860 GGCAAAACCC TAATTAAACA CAGTGGAACC ATTGCCTTAT GCACAGGGCA ACCTCAGGCA 1920 TTCTGCGTTC ATCGTGTCTG CAGTGTTCTC CAAATTCTGA AGCAGAGATG TCTAGATGCT 1980 TGTTTAGTGC GGAGGGTCAC TTTCTTTATA TTTTAAAATC AGTAAGGTCA TACTTAACTT 2040 CGTTTGTACA TATTAATATA TCCATAAATG TTGGTAGTTC CTTTGGGTAC TATGAGTGAC 2100 TATAATATTA ACTAAACTGC ATTTTTAGAT TAGAAAATTG TGAGGGGGGA CCAAGCACAG 2160 TGGCTCACAC CTGTAATCCC AGCACTTTGG GAGGCCAAGG CGGATGGATC ACCCGAGGTC 2220 AGGAGTTCGA GACCAGCCTG ATCAACGTGG TGAAACCCCC GTCTCTACTA AACTTACAGA 2280 AATTAGCCGG GCATGGTTGT GCACACCTGT AATCTCAGCT ACTCGGGAGG CTGAAGCAGG 2340 AGAATCGCTT GAACCTGGGA GGCAGAGGTT GACGTGAGCC AAGATCTCGC CATTGCACTT 2400 CAGCCTGGGC AACAAGAGCG AAACTCTGTC TCAAAAAAAA AAAAAAAAAA AAAAAAAAAA 2460 TTGTGAAGGG GGAATCCCCT ATGAATGTAC CAGTTTTTAC TTTGATCCAA TCAAGTTGTT 2520 TTGTATGGTT TGTTGTTTGT TTTTTGGTTT TTGGTGTTTT TTTTTTTAAT 2570
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