Tag | Content |
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EnhancerAtlas ID | HS138-00316 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:18203720-18206240 |
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) |
EBF1 | MA0154.3 | chr1:18204182-18204196 | ACTCCCAGGGGACT | + | 6.22 | ESR2 | MA0258.2 | chr1:18205615-18205630 | AGGACAGTGTGACCT | - | 7.22 | ZNF263 | MA0528.1 | chr1:18204680-18204701 | AAGGGAGGAGGGAGGGGGGGG | + | 7.28 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_56008 | chr1:18198118-18206961 | u87 | SE_67868 | chr1:18198118-18206961 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I017876 | chr1 | 18203445 | 18206264 |
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Enhancer Sequence | CTCAGATTTC CTTACTGCTG GAACATCATG GAATTGGCTC ATTTAGGCCT TGGGTTGACT 60 CTCCCAGCTG AGCATTTTCT CTCTCCTCCA TCCTTTTGTT CTCCCTCACA TCCATGCAGG 120 GCACTTTCTG GAAGGATATC AATGTCTGGA CCCAAAGTGT GCGGTTTTGA ACATCACTCA 180 CTCAGCCTCG CCCGCTGCCA GCACTCCAGT TGGTTCCGCT GCCATCCCTG ATCCTTTGAT 240 CCAAGAGAAG TGCTGAGAGC CTCTTTCTCC CCTCAGAGGC AGTGGGTTTC AAACCTTGAG 300 GCAGCGTTTT CATGTCCTCA CCCACATTGC CGGTCCAGTC TTGCCTAGTG GGAACGTGAT 360 CCACGAGGCC CTTCATGTGG CAGATAATGA GGTGGATGGC TCTTTCAAAC ACCTCCTCCC 420 AGAGGCCCTC CAGACTGCTG CAGTCCACAA GGTGCTCTCT GAACTCCCAG GGGACTTCTG 480 CTTCAACACC TAATTGTAGC TTGTCCTCTA AACGAACAGC TTCCTACTTC TCTGTCTTGC 540 GTAAAGCCCT TCAGGACAAG AATACATTTT CTCCTTCTCT TATGTTCTCT GTGGGTCCTT 600 GGGTGGAACT GAACACAAAA TCCAGCAAAT GAAATAAAAT CAAGGTGAGA TTTATTTAAC 660 CTGGACTGTC AGACACCCCA CCAGGCGTGT TTGCATCCAA GCTTTCATTT GGTTCCCACC 720 AACAGCCCTG TGAATTGGAT ATTCGGACAC ATACTTTTAC ACACAAAGAA ACTGACACTT 780 AAGACAGACT GTGTCACACG CCCAAGGTCA CATAAAGAGC GAAAGAAGGG CTGTTGATGC 840 AACTGCCAGG CTTTCATTCC TTTGGTATTT ACCAAGTGTC TTCCATGCGC CAGGCTGTGG 900 GCTCAGCTCC CCAGGGAAAA TACTGAACTG AACAGGAGGA ATCTCTGCAA CTTAATGATT 960 AAGGGAGGAG GGAGGGGGGG GTCTCTGGAA TTGGCCTTTT TGGGTTCAAA TCCTGCCTTG 1020 ATAGCTTTTG AGCTGTGCCC CCGTGGAGCA GGCGTTTCTT CTCTCCAGAC CCAGGTGTCT 1080 GTGTGTGGGT GCATGGTAGG ATGTCCAGGG CCTGTGTTCA TACCACTGCC CCACACTGCC 1140 TCATTTATCA AAGCCCTTAT GGAGCACTTA TTTAGCACTT ACTATACGCC TGAAAAGACT 1200 TTAAGTGCTT TATAATTTTT TTTTTTTGAA GGTGGAATCT CACTCTGTCA CAGAGGCTGG 1260 AGTGCAGTGC GTGATCTCAG CTCACTGCAA CCTCCGCCTC CTGGGTTCAA GTGATTCTCC 1320 TGCCTCAGCC TCCTGAGTAG CTGGGACTAC AGGTGTGTGC CACCACATCT GGCTAATTTT 1380 GTATTTTTTA GTAGAGGCGG GGTTTTGCCA TGTTGGCCAG GCTGGTCTCA AACTCCTGAC 1440 CTCAGGTGAT CTGCCCACCT TGGCCTCCCA AAGTGCTAGG ACTACAGGTG TGAGCCACCA 1500 TGCCCAGCCA AGTGGTTTAC AGTTGTTAAC TAATTTCATG CTCATGCCGT CCTGTGAAGT 1560 AAGTGCTATT ACCCTTCCTA TTTTACAGAT GAGGAAACTG AGGCTCAGAG AGGCTAAGTG 1620 ACTAGTCCAA GCATTGCAGC TAGGATTCAA ACCCAGTCCA CCTGGCTCCA CAGTCCGTCT 1680 TCTTAGCTTC CATGTTTTGC TGTCTGTTCA CTTAATAAAC AGTGGTTGAA TTGGATTGAA 1740 TTAAATCACC CACATGATTT TTGCCAGGCC TACTTGGGGC TGAGTTTTCG TGAGTGCCTG 1800 AGGGGCTGAG TCAACCACAT CCATCTTTCT TTTGGACTCT GATTCAGGGA GTGAAGTCAC 1860 ACTCCCATGA AGGCACGGTT ACCAGCCCTG TAGGCAGGAC AGTGTGACCT CCATGAGCTG 1920 CCCTGACCTG GCCCTGGAGG CTGGGCTGCC CAGCAGTGGT TCAGAGGCTC TGAAGAGGGG 1980 TGCCCTGCTC AGACCTGGCT TAGTGGTACC AGGAGCTGCC AACTCCCCTC TCCGGGCTGG 2040 ACATGCCCTC CCCTAGCACT CTTGGGACCC CATTCTCTCC ATCATCTCAG AATCTACAAG 2100 GAAAATGCTC CAACTTCGAG GCAGCCACCA GCTCATGCTC TGGTGCCTGC ACTCCAAGGC 2160 TTCCCGTTTG AAAACAGCAG TTTTCAAAGG AGTCTTGTTT GATCTTGTGG GTCTTTTTTC 2220 CCCTCTACTT GACTGGAAGC TGATGGCAGC GATCAGATGT GGCTTCTGAC AAACCTCAGG 2280 GCTACTGAAC AGTCCCTGGC ATGGCCGATG CTGGCCGCCA AGGCAGGAGA AACAAATCTG 2340 CCAGCTGATG GTGGCAGGAC CTGGTGACAG ATCCAAATGT GCCTTCTTCC CGTGGGCCTT 2400 TCCTTTCCTG TGTGGCTCTG TCTGTTTGAG ATTCCAGTTG CCCTTTGAGG ATGGCTCTGT 2460 GCTCCCAAAG GCGCTGTTGT CTGGGGAGAG CACAGATGTA CCCAGGGCAG AACTTCGCAG 2520
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