Tag | Content |
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EnhancerAtlas ID | HS133-00985 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:29076610-29079080 |
Target genes | Number: 22 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr1:29077024-29077035 | AAGAGGATTAG | + | 6.62 | FOSL1 | MA0477.1 | chr1:29077332-29077343 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr1:29077332-29077343 | GGTGACTCATG | + | 6.02 | MAFK | MA0496.2 | chr1:29077030-29077049 | ATTAGCTGACTCAGGATAA | + | 6.33 | MAFK | MA0496.2 | chr1:29077030-29077049 | ATTAGCTGACTCAGGATAA | - | 6.65 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I028750 | chr1 | 29077313 | 29077512 | GH01I028751 | chr1 | 29077713 | 29078249 |
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Enhancer Sequence | TCCTGCCTCA GCCTCCCAAG TAGCTGGGAG TACAGGCAGC TACCACCATG CCCGGCTAAT 60 TTTTGTATTT TTAGTAGAGA CAGGGTTTCA CCATGTTGGG CAGGCTGGTC TTGAACCCTT 120 GACTTTGTGA TCCGCCTGGC TTGGCCTCCC AAAGTGCTGG GTTTACAGGC ATGAGCCACC 180 ATGCCCAGCC CAAATTTTTT TAAGACTAGA TTCTTCATGT CAAAAGACAA AGCTAGAACG 240 AATGGATAGA GGTTATATGG AGAAATATTT TTGTAGATGG AAAACTTGCT AAAAACGAAG 300 TTCTTAGTCA CAGAATTTCA AGAAACTAAA AGAGATGTTA TAGAAACTAA ACTAGGGATG 360 TTGTAGAGGG GGTTCATACA TAGGGTAGTC TGGACTAGAG AAACCAAGGG ATAAAAGAGG 420 ATTAGCTGAC TCAGGATAAC ATTTCAGGTT TGTGAAGATG AATTTGTCCT TTGAAACAGA 480 TCTTTTTAGA AAGGTTGTTT CATAATTTCT GACCGAAGTA TTTGTTACAC GTAAAATAAG 540 TAAGAACGGA CTGAGGCCAG AAAGCTGTGG ATGACAGAAG GGATTGGTGC ATTCTCAGTG 600 AATTTTGATA CAAATTAAGT ATGTGGGTAG TTTTTAAATA CATTTACTAT ATATATATAT 660 TAATGAAAAA TTGTTTCCTA AACTGTGAAA AGGCTTATTA AAGAAATTTA GAGGCTGGAT 720 GCGGTGACTC ATGCCTGTAA TTCCAGCATT TTGGGAGGCT GAGATGAGCA CATCACTTGA 780 GCCTAGGAGT TCAAGACCAT CCTGGGCAAC ATGGTGAAAC CCTGTCTCTA CAACAAATAA 840 AAAAATTAGC CAGGCGTGGT GGCTCGTGCC TGTAATACCA GCTAGTTAGG AGGCTGAGGT 900 ATAAGAATCG CTTGAACTTG GGAGATGGAG GTTGCTGTGA GCTGAGATTG TGCCACTGCA 960 TTCCAGCCTT TGTGACAGAG CGAGACTGTC TCAAAAAAAA AAAAAAAAAA AAGGCTGGGC 1020 GTGGTGGTGC ACGCTAGTAA TCCCAGCTAC TCAGGAGGCT GAGGCAGGAG AATCTCTTGA 1080 ACCCAGGAGG TGGAGGTTGC AGTGAGCAGA GATTTTACCA CTGCACTCCA GCCTGGGTGA 1140 CAGAGCGAGA CTGTCTCAAA AAAAATTCAA GTTTCTGTGA TATAAAAGAG GAAAACATCC 1200 TCACTTGAGC TAAATATATT AAATCCTTAG GAAGTAAATA ACCATGTGAT ACTGTTGGCT 1260 CCCATTTAGT ATCTTACCAC CCCACCACTG TTTTATTGAC TCTTCAGATC TAGTGAGTGG 1320 GCATCCTGTT TTAAACCAGG ATGACAAACA TGAGCATTTT TTGTAAAATC CTAAGGCCAT 1380 CTATGTCTAT TTTTGTCTTG CAGATAAATA TACTTGTTTA TCTGCCAAAA GGGTTAAGGA 1440 AATTTTATTT GTATTACTCA TCACCTTCCT TGCTTTGTGA ATAGATAAAA CGCCTCTTTC 1500 TGCAGCCTCC TTAAAGGAGG ACTAGAAGAG AATAGATAAC ATTGAATTTG TATCTCTGAA 1560 CCATGCCCCT TGTATCTATC TTTCAACAAA CGTTTGTGTT AATTGCTGGG ATGGAACAGA 1620 GAAACAAGGC ACCATCTTTG CCTTAGAAGC AGAGGGTTTT AGGAGGACAG CAAAATGGAT 1680 AAAATATGGG ATAAGAGCTG TAATAGAGGA ATGAATACAT TTTTGGCATT CTGGAGAAGT 1740 GATTAATTAC TTGGGGGAAA TTAAGAATTC ATGGAGGCAA TAACATTGGA ACCCTGCCAA 1800 ATAAGTAATA ATAGAATGAT AAGCACTCAA ATGGCAGCAC AGTGCTTGGC ACATAGTACA 1860 CACAGAAGCT TAGCTATCTT ATCTAACACT GTAATTCTCA TATTTCAGAT AAAGGAAGAG 1920 GCTCAGAGGT TATTTATCCA AAGTCTCATA GCTAGTAAGT GTTGGAGTTG GTCTTTAACA 1980 GAAGTCTCTC CAGCGATGTG TTGGAGCTGG CTAGTTGGAG CCAGCTGTTT AGCTTTCAAG 2040 AATACCTTTC TGTACATTAA ATTACATTAT AATTACCATC GTATTAGGTA ATATTCAAAT 2100 TCCTTACTCT TGAGGTTATT TACAGCTGTT GTATCAATAT ATAATATGCT GTTGCACACT 2160 GATAACACAT TGGTAATCTG AAATCAGCTG TGGTGTTTTT GTTGTTGTTG TTGTTTTTGA 2220 GACGGAGTCT CACTTGTTGC CCAGGCTGGA GTGCAGTGCA GTGGCATGAT CTCAACTCAC 2280 TGTGTCCTCC ACCTCCCGGG TTCAGGGCTG CCTCAGCCTC CCAAGTAGCT GGGACTACAG 2340 GTGCTTGCCA CCACTCCCGG CTAATTTTTG TATTTTTAGT AGAAGCGAGG TTTCACCATA 2400 TTGGTCAGGC TGGTCTCGAA CCCCTGACCT TGTGATCTGC CTGCCTCGGC CTCCCAAAGT 2460 GCTGGGATTA 2470
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