Tag | Content |
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EnhancerAtlas ID | HS133-03658 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:224895030-224897550 |
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) |
NKX2-3 | MA0672.1 | chr1:224895283-224895293 | TTCAAGTGGT | - | 6.02 | NR2C2 | MA0504.1 | chr1:224896345-224896360 | TCCCCTTTGACCTCT | - | 6.16 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_55814 | chr1:224894789-224898222 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I224707 | chr1 | 224895241 | 224896954 |
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Enhancer Sequence | CAAATCTATT GGATGAAAAG CAACAAGCCC AAAACACACT TCAACCACCC TCAACCTCAA 60 ATAACGAATT CTGTACTGCT TTGAAACAGC ATGGAGAGAC ACCCCCCGCC CCACCCCGCC 120 CCACCCTCAA TTGGTGTGGA TGATTGAGAG TTAACCACAA AGTTCACAGA AGCAGCTTTT 180 CTTCTCTCTC TACTCCACTG TGGGCTTGGC CAATGAGCAA TGTGGGTCCT GGGACGGTCC 240 GAGAATATTG CTATTCAAGT GGTCCATGAC TTGAATAGCA TAGTGAACCA GCAGCTTTGG 300 CATCACCTGG GAGCTTGTTA TAAAGGCAGA ATCTCATGCC CCACCCAGAT CTGTGGGATC 360 ATAATCTGCA TTTTAACAAG ATCCTTGTAT GCACATTATT TTGAGCAACA TGGCCGAGAA 420 CCCCGGCTGT CAAGTTCAGA CCTGGCAGGC TGTACCCGCT TTTCAGCACT TACTGGGCAT 480 CCACCTTGTG TGGCCTTTTT AGATGGCACC AAATAAATGA ACATCCTGCC CTCATTGTTA 540 TCTTGTTGTT ATTGACATAC CTTTCCCACC TCATCAGTTT CATTCCTCTG GGTGTGTCCC 600 TGGTGCTGCT GAGACCCTCT CTGTCCACTA GAATTCCCAC CATCTCACTG TTGCAGGGTC 660 CTCCTGCCAT GCAACTATCC TCTGACTCAC CCCATCCTGC TCCCTGTCTC TGGTCACGCT 720 GCCTCCATGG GCAGCTCTGG TTTTCCCTAC CTTCCTTAAG TTCCCCAGCA ATCCTGCCAT 780 CCCTCAACCC CTTCTCTCTC AGCCATGGAT GCTCTTGAGT AAGTGGAGGT TGTTGATGCT 840 GAGTTCCCTA TTTCCCCCTC CACTTCCTGT CCTCACCTCT CCAATCCTCC TCTCCCATCT 900 CAGGGCCTCT CTCCTCTCAG GGCCCCATTT TAATGCTGCC TCATGATTCA GTCCCCCTCT 960 GACTCACTCT GGAGCATATC CAGATCAGCT CCCTCTTTTG AGTACCTTCT CTCTCTCATT 1020 GTTATCCAGC TCCTTTTTTC CCCTGTCTTA AAACACATTT CGTCTTCCTT GTTCTAAAAA 1080 GTTGCATTGG CCTTAGTAAC CCTTCATGCT ACCAACCCAC ACATTTCTTT TTTCATATGT 1140 TGCCCAATTC TGGAAAGAGT CCCTTGCACT CCCCGCCTGC GCTTCCTGAC TCCTACGCAT 1200 CTCAGAATCC CTTGCAGTCC GGCAGATGTG CCTCTCCTTC TATTGAAACT GCTGATTGAA 1260 GGTCACCAAT GACGTCCCAG TTGCCAAATC TAATAGACTG ACTTGTTTGT CCTGTTCCCC 1320 TTTGACCTCT CTGTAGTATG ACATGACTAG TCTCCTGCTC CTCTTTGGCT TCCTGGCATG 1380 AGACCATCTT AGTTTTCCTC CTGTCTTGTG CACACGCATG TCTCTCCTTT TTCTCTCCTC 1440 CTTTCTCACA CCCCAAATAC AGGTGTTCAT GCGCCTTCTG CCCTTGTTTT CCTCTTGCTC 1500 TGTACTAAGA GTTGCTATTG GCAGCCTGTG GATCAGAGAT GTCCTGCAAA TTTGTTTTCA 1560 TTTGACTCAT TTAATATTTT AGGAACCTGA AAACCCCACA CAAAAATCTG GGTTTCAAGC 1620 TGCTTTTGAA AAAAACAAAA CAAAACAGAA CACAGGACCT GGAAATAGTG GATTCGTATT 1680 CTTCAGGACA ACAATCAGCT GGAGTGGGTA GCTGATTAAC CCTTTAGATG GGGTGTCTGC 1740 CCTCAGATCA CTTCCGTGAC CACCACGCGC GTCTGTCTAG CACCACATGG TTTTGAGTGT 1800 GAGCCACTTG TGCTCCTGAG TAAGTGTGGG CTCTCCCCTA AGTGTGGGCC CTCCCCAGGG 1860 CTCATCTCCT CCAACGCTGA AGCATCTATC ATCGTTCATC TTCTAGCGGC TCCAAATCTA 1920 TGCATCTTCT CCTGCTCTCT CTCTCTCTCT TGAATTCCAG GAATGTGCTT CTAACCATCT 1980 TGGGCATCTT TACCTGGTTT TACTCATTGT ACCTCAAACT CAGTCTTGGG GTTAGGAGTG 2040 CTTATGTATC ACACTTACCC ACCTCTCTGA GTTTTGAATC AATTGAGAAC AGACATAAGA 2100 GTCTAGATGA GAGCCGAAGA ACCATGTGGT ATCCAGCCAG CTGCATGGAA GGGCATGGCA 2160 GGACTCCAGC ACCTTCAAGT GTAGGAGAGA GAGAGTATTG AAGAGGGGTG GGCTGGCTTC 2220 AGGCTTGTGT TGCCAAGGAG GCAGTCTCTG GACCTGACCA CATAAACCTA CCACATGCTT 2280 GCAGGAGTAG AGAAAGAGGA TGCCTGCAGT TTAAGGGCAG GCAAGTCCAG GAGCAAGAGA 2340 AGCCAGGCCA CAGGCTTCCT CCCTAATACT TCCCCAAGAT GTGGAAAAGT TGGTGGAAAT 2400 TCCTATTTTA TGGGTTGAAG CAGGAATACA GAAAGAGGAA GAGAAGGGTT CAGGGTTCTC 2460 TCTTCCTTCA ACCTGCCATC TACTCATTAC AGTAGTACCC CCTTATCCAT GGGGCATATG 2520
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