Tag | Content |
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EnhancerAtlas ID | HS062-07760 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr18:56751080-56753950 |
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) |
CTCF | MA0139.1 | chr18:56751585-56751604 | TGACCACGAGAGGGCAGCA | + | 7.04 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_44101 | chr18:56750991-56757190 | MM1S | SE_59425 | chr18:56738668-56763214 | Ly3 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I059084 | chr18 | 56751501 | 56751670 |
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Enhancer Sequence | GGATGGGAAG GGACTTTAGA GATAATCTAT TCAAGGACAT CATTTTGTAG TGAGGCAACT 60 GTGTTGTCTC CTGCCCGAGT TCACCCACCT GCTCTTCCTA CCAGACCACG TGGGCAGTGC 120 ACTGGAACAA AATCTCTCTA TCAGATTATC TCTCCTCTGT TTGTCTCCCT CTCCACCTCT 180 GTGTTCATAT GCATAACACA CACACACACA CACACACACA CACACACACA CACACACACA 240 CACACACACG TTTTCTTTCC AAATTTCCTC TTAACAAAGT CTAAAGAATA ATCACTGTTT 300 CTTGCCTCTA TGATTTTTTT TGACCTCCTC TGAACCCCAC ACATTGACGA AGTGCCAGCC 360 ATAGCAATAG TTTCAGACCC GTGGAGTCAG CTGTGCTGTT GCCAACCTCC ATCACCTGTC 420 CGCCTTTATC CTGGGCTCTG TTCCTGTGGA TTTGAACAAA TAGATGAGCG GCATCGGAAG 480 AAAGCTTTAG CTGCATGTGT TTGGGTGACC ACGAGAGGGC AGCACGTAAG AGACCAGTGT 540 CGGCCCCGCT GCCTTCTTGA ACACACCGGA AGCCTCCTAG GAAAACTGCA GATTTTGTCA 600 GACTGTGAAG TAGAAGAGTC AAAGAGCCTT CATTGCTTCC TTTTAAATGA CCAGCCTACT 660 AAGGAATTTA GAATGCCCAA GTAAGGTTTT CACTTAATCC TTTAAGAAAT ACATCTAATA 720 TTTCTAATCT AATCTATCAT TTTCAATGGA AAACAGTATT TTTTTTTTCA GTGATTCTCA 780 CTGCTTTCTT TCTGAGGAAC TTGAAATGAA TCTTATGTTT TATTTATTTT TCAATTTCTA 840 AGGTAAGGAC TGCTGGTCAG ACTGGACTTC AAAATTCCTG GATCCTTAAG ACCCAATGCA 900 TCAGACAAAT GTCCTGCTGG ATCCTCCCAC CGTCAGCTAA GGGACAGTGC TAGCTCTCTG 960 GTGAGGGAGA TCCGTGTGGA GGTCTCTGGC ATTCCTGGGT CAGTGGATGG CTGGGAGAAC 1020 TGCTCAGCTC CAGGTTCCAG GGCCTCTGAT CAAAGCCAAC CCTGGGGGCC AGCCAGAGAT 1080 ATCGCAAACC TAAGGACTAA CGTGGAATCT ACACCTGCCT TGGGAGTAAA GAACAAGCAG 1140 GGTGCTTTCC GGGATGGCTT TGGGATGAGA TGCCCAAGAC TTAGTGCCCC TGGCATTGCT 1200 CAGCTCTCAA GCTGACTTCC ACAGCACCCC CATGGAAGCT TCATTGGTGC ATCTTTGGGT 1260 CTTGAATGCA GTGCTACAAT ATTGACGAGG AAAGTCTCCT TGGAACCACA GGAAGACAAA 1320 AGTGCAGAGT GATTTGCTGG CCTTGGCTAG GACAGGGTCC AGGGTGCAGC CAAGGGAGGG 1380 TGATCTAAGC CAGCCATTCT CCTAGTGTGG CTCCTGGACT ATGCGCAACA GCATCACCTG 1440 GGAGCTTGTT AGAAACACTG GTTCTCAGTT CCCATGCAGA CGTCTTGCAT CAGAAAATCT 1500 GGGGCTGGGG CCCAGCAATC AGTGTCTCCA AAGGCCCTGA GATCATTCTA TTCAAGTTTG 1560 GGAACCAGCA ACACAGCATT TAAGTGGAAA TGTTTATAGT TGCAAAGCCA GGTGAAGCTT 1620 GAAATGCATC ATAGAGGAAA TGAGGACAAG AATGTAGAAA AAGAGTAAAA ACAGAGAGGA 1680 AAAAAATTTA CAAGCCATCA TAGAGTGAAA GAGCTTCCCC TGCTGCCTGG GGGTGTGGGA 1740 AATGAGAGTT GCACCTGCTC ACAAGTATGA CCAGCAATTT AATATCTATC TAGAGCTTTC 1800 AACCCTGCCA TGTCAAATTT ATTTAGCTAA AAACAACTCT TGTGGTGGTG ACCTTTTATT 1860 CAGCTAATAT TACTCCCCTC AATGCCTCCA AAGCACACAG AGAAATTGGA GGGCTGATGA 1920 AAATCTTTAA AGTCTACTAA ATACTAAAGC CTTCCCAAAC ACTGTGTACT TTTCAGAGAG 1980 AGTTTCTTTT TATTGGAATT TCAGATTATT GAAAGGTTAT CTGTCTCCTG TTCCTAGAGG 2040 GATTAAAATA AAACAAAAGC AAGAAGAACA CATTGTGATG TGTGCTTTCC TCGCTGAACT 2100 GGTGGTGCTT ATCTGACTGC AGTGATGGGC AGCCAGTGGG AAGATGCCAA AGTCCTTCCA 2160 GAGAATTTCC CCAGGAACTT GGGAGGCTGA ATCACCAGAA TGAGAAAGTT CTCTGGCATT 2220 CTGGGGATGC ATTTCCTTCC ACATTGCTGC ATCCCTGTAT GCTGGAGTTG CATGTGACTG 2280 CCCCATGCCT CAGTTTCCTT TTCTGGAAAA TGACAGCTTC AGGCTCTTCA TGCTTCTGGC 2340 AGCCATGATT CCCCTCTGCC TAGCTCTATT CTTTTTCTCT CATTACCTTC CTGGCTCTTT 2400 TCTGTGTTAC ATCGCCATTC CTTGGGTTTC TTTTCTCTGA TCTATATATT TTGTTCTGTT 2460 TCATAATTTT ACATTAATTT TTATTTAATG CCACAAGCCG CTTACCTGCT TTGAGCTCCA 2520 CAAAACCTAT ACTTTGAGGT AGAGTAGAAT TGGAAGTTAG AAAACCAGAT TCTGAATCTT 2580 TAAGCAAATC ACTTTAGTTG AACCTCAGTT TTCCTACCTG TAAAGTGCTT GCCATGTGCC 2640 AAACAGAATT GTTTCATTTA ATACACAAAA CTCATAGAAA TAGATACTAA ACAATCTTTC 2700 CAAGTAGATA TTGTTAGTAT CCCATTTTAT AGTTGAGAAA AATGAGGCTC AGAGGGGTTG 2760 AGTTCCCCAA GATCACACAG CTCATAAATG GCAGAGCTGA GATTTCAATC AGGCAGTCTG 2820 ACCCCAGAGG CTGCACCCTG ACTACTTATT ATTAACAGTG TCTGTCCCTG 2870
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