Tag | Content |
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EnhancerAtlas ID | HS082-03251 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:224895040-224897570 |
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 | GGATGAAAAG CAACAAGCCC AAAACACACT TCAACCACCC TCAACCTCAA ATAACGAATT 60 CTGTACTGCT TTGAAACAGC ATGGAGAGAC ACCCCCCGCC CCACCCCGCC CCACCCTCAA 120 TTGGTGTGGA TGATTGAGAG TTAACCACAA AGTTCACAGA AGCAGCTTTT CTTCTCTCTC 180 TACTCCACTG TGGGCTTGGC CAATGAGCAA TGTGGGTCCT GGGACGGTCC GAGAATATTG 240 CTATTCAAGT GGTCCATGAC TTGAATAGCA TAGTGAACCA GCAGCTTTGG CATCACCTGG 300 GAGCTTGTTA TAAAGGCAGA ATCTCATGCC CCACCCAGAT CTGTGGGATC ATAATCTGCA 360 TTTTAACAAG ATCCTTGTAT GCACATTATT TTGAGCAACA TGGCCGAGAA CCCCGGCTGT 420 CAAGTTCAGA CCTGGCAGGC TGTACCCGCT TTTCAGCACT TACTGGGCAT CCACCTTGTG 480 TGGCCTTTTT AGATGGCACC AAATAAATGA ACATCCTGCC CTCATTGTTA TCTTGTTGTT 540 ATTGACATAC CTTTCCCACC TCATCAGTTT CATTCCTCTG GGTGTGTCCC TGGTGCTGCT 600 GAGACCCTCT CTGTCCACTA GAATTCCCAC CATCTCACTG TTGCAGGGTC CTCCTGCCAT 660 GCAACTATCC TCTGACTCAC CCCATCCTGC TCCCTGTCTC TGGTCACGCT GCCTCCATGG 720 GCAGCTCTGG TTTTCCCTAC CTTCCTTAAG TTCCCCAGCA ATCCTGCCAT CCCTCAACCC 780 CTTCTCTCTC AGCCATGGAT GCTCTTGAGT AAGTGGAGGT TGTTGATGCT GAGTTCCCTA 840 TTTCCCCCTC CACTTCCTGT CCTCACCTCT CCAATCCTCC TCTCCCATCT CAGGGCCTCT 900 CTCCTCTCAG GGCCCCATTT TAATGCTGCC TCATGATTCA GTCCCCCTCT GACTCACTCT 960 GGAGCATATC CAGATCAGCT CCCTCTTTTG AGTACCTTCT CTCTCTCATT GTTATCCAGC 1020 TCCTTTTTTC CCCTGTCTTA AAACACATTT CGTCTTCCTT GTTCTAAAAA GTTGCATTGG 1080 CCTTAGTAAC CCTTCATGCT ACCAACCCAC ACATTTCTTT TTTCATATGT TGCCCAATTC 1140 TGGAAAGAGT CCCTTGCACT CCCCGCCTGC GCTTCCTGAC TCCTACGCAT CTCAGAATCC 1200 CTTGCAGTCC GGCAGATGTG CCTCTCCTTC TATTGAAACT GCTGATTGAA GGTCACCAAT 1260 GACGTCCCAG TTGCCAAATC TAATAGACTG ACTTGTTTGT CCTGTTCCCC TTTGACCTCT 1320 CTGTAGTATG ACATGACTAG TCTCCTGCTC CTCTTTGGCT TCCTGGCATG AGACCATCTT 1380 AGTTTTCCTC CTGTCTTGTG CACACGCATG TCTCTCCTTT TTCTCTCCTC CTTTCTCACA 1440 CCCCAAATAC AGGTGTTCAT GCGCCTTCTG CCCTTGTTTT CCTCTTGCTC TGTACTAAGA 1500 GTTGCTATTG GCAGCCTGTG GATCAGAGAT GTCCTGCAAA TTTGTTTTCA TTTGACTCAT 1560 TTAATATTTT AGGAACCTGA AAACCCCACA CAAAAATCTG GGTTTCAAGC TGCTTTTGAA 1620 AAAAACAAAA CAAAACAGAA CACAGGACCT GGAAATAGTG GATTCGTATT CTTCAGGACA 1680 ACAATCAGCT GGAGTGGGTA GCTGATTAAC CCTTTAGATG GGGTGTCTGC CCTCAGATCA 1740 CTTCCGTGAC CACCACGCGC GTCTGTCTAG CACCACATGG TTTTGAGTGT GAGCCACTTG 1800 TGCTCCTGAG TAAGTGTGGG CTCTCCCCTA AGTGTGGGCC CTCCCCAGGG CTCATCTCCT 1860 CCAACGCTGA AGCATCTATC ATCGTTCATC TTCTAGCGGC TCCAAATCTA TGCATCTTCT 1920 CCTGCTCTCT CTCTCTCTCT TGAATTCCAG GAATGTGCTT CTAACCATCT TGGGCATCTT 1980 TACCTGGTTT TACTCATTGT ACCTCAAACT CAGTCTTGGG GTTAGGAGTG CTTATGTATC 2040 ACACTTACCC ACCTCTCTGA GTTTTGAATC AATTGAGAAC AGACATAAGA GTCTAGATGA 2100 GAGCCGAAGA ACCATGTGGT ATCCAGCCAG CTGCATGGAA GGGCATGGCA GGACTCCAGC 2160 ACCTTCAAGT GTAGGAGAGA GAGAGTATTG AAGAGGGGTG GGCTGGCTTC AGGCTTGTGT 2220 TGCCAAGGAG GCAGTCTCTG GACCTGACCA CATAAACCTA CCACATGCTT GCAGGAGTAG 2280 AGAAAGAGGA TGCCTGCAGT TTAAGGGCAG GCAAGTCCAG GAGCAAGAGA AGCCAGGCCA 2340 CAGGCTTCCT CCCTAATACT TCCCCAAGAT GTGGAAAAGT TGGTGGAAAT TCCTATTTTA 2400 TGGGTTGAAG CAGGAATACA GAAAGAGGAA GAGAAGGGTT CAGGGTTCTC TCTTCCTTCA 2460 ACCTGCCATC TACTCATTAC AGTAGTACCC CCTTATCCAT GGGGCATATG TTCTGAGATC 2520 CCTGGTGGAG 2530
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