Tag | Content |
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EnhancerAtlas ID | HS138-07896 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr11:100609340-100611890 |
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) |
BCL6 | MA0463.2 | chr11:100611341-100611357 | AGTTCTTGGAAAGCAG | - | 6 | MAFK | MA0496.2 | chr11:100611056-100611075 | ATTTGCTGAGTAAACACTT | - | 6.03 | MAFK | MA0496.2 | chr11:100611056-100611075 | ATTTGCTGAGTAAACACTT | + | 6.22 | MNX1 | MA0707.1 | chr11:100609989-100609999 | GGTAATTAAA | + | 6.02 | TEAD1 | MA0090.2 | chr11:100611322-100611332 | ATGGAATGTG | - | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I100738 | chr11 | 100609169 | 100613145 |
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Enhancer Sequence | TTCATCAGTG AGGGTAATAT ATGTAAAACT TGCAAACAAT TTATTCCTCT AAATAAAGTA 60 AAAAACTATG TTGCTAGAGA AGTACTATTG CTGCTGACTA CTAAAGGTAG TTAAGAAGTC 120 AAAGTGTTTT ATTATAATAC AAATAAAGTG AACATGTAGA AATCTGTTTA TTATTACGTT 180 TCAAGTTTGA ATATTTTGTT TTCTTTTTAA GAAGAAGCAG GGCAAAACAA ACTGTGCCCG 240 TTGCATTCCT TGCCAAGGTC AATGCTCCAT ATTTTGTCTG ACTGTTTAAT TTAATAGCAT 300 TCAAGCACAG AAGCAATCAG GAGGCCACTC CTATTGGTAA ATCCATGCTT ATAAAGAAAG 360 CATGTATTTC AGAACTTAGG AAAAAAGCTG TTTGTTAAGC CCAGACCTAG TTTGAGATCT 420 TTTTGAAAAG TGCTTATAAT TTTCCAGAAT TCTAGGATTA ACTCAAGGAA ATGCACAACA 480 GAAATATGTA GATTTGACAG TGGCTTTTTT CTTCTGTTCA AGTTATCTTA GAGTCTTTTT 540 TTTTGTTTTT GTTTTTGTTT TAAATGAAGC AGTTTTGAGA TTCATTAACT GGTTATCTTT 600 TGTCTGAGTT TTACCAAAGT GATCAAAAAA TAAGGAACTA TTGACTTTTG GTAATTAAAA 660 TACTCTTGGA TTTTTTTTTT TTAGTTAAAG TTCAGGACCA TTCACTTGGT TCTTAAACAA 720 TCTTGTTTTA ACCTGAAGAA CTCTTGATTT GAAACTTTGA AATCCTGAGA AACATTTTTT 780 CTATGACTCT CAAAAATAAC TTCAGATTGC AATTTGTTCT AAAGAGGATA AAGTAGATAT 840 ACCATGCTTG TTTTCTTTTC CTTAATTGAG TTTCATTTAT GTGATTAACT TAGATAAAAA 900 TACTCTAATT TGATTTACTG AAGCAGTCAG GATGAAATAT TTTGCATAGT GAAGTGTGCT 960 AAATCTTTAA AACTATTTCT AGAGTTTTTA AAGAAAGAAT TTTAAAATGT AATGTACGAA 1020 GGTATAATTC TGTGTATCTA TACTTTGTTT CTCCCTCCCC TCTGCATCTA ATAAGCCCCT 1080 CTTTTCTTGT TCCTTTTGTA AACATGAGTT GCTTATGGCT TGTGTACTGA AAATGCTGCC 1140 AGGAAGTAGG GTGAGCATAA CTTCTTTTCC CATGACCCTC AGTCTAATGT TGTTCCAAGG 1200 GTTCCTTACT TAGAAATGCC TTGATAACCG CATTCATTCC TGACATACCC CACCCCCAAC 1260 ACACACAACT GCTGAGTGCC ATCTGACCCA CAGTCCAGCT GCAGCTTTTA AAAATACTAG 1320 TGGCAAAGGC TTTTACCTAG AACGGTGACT ATCTGTGAAA AAATTTTGTG TGTGATTTGT 1380 TTTTTGCGTG TTGAAATATT ATTTTTTAAA GAAAGTTACT TGGTGTCAGC CTGCAAGTTA 1440 AAGGGTTATT AGTACAATTT TTTTTTTTTT TTTTAATTTT CAACTCACTA AAGCTTGCCT 1500 GTGTATGTTC ATCCTTTTTG TATGATTTCT GGAAGTTTTC CTGTTGACAG TGAAGTCTAA 1560 AATGCTAAGA CCTTTAGATT CTCTTGTTTC ATGACTTTTA TTATGAACAT AAAACTTTTA 1620 AAAAAGACCT GGTCATGCTA TGGCCTCTCC CTTCTCCCAA ATTTTATATG ATACCCTCAG 1680 TTTTTTTTCC TTTGGTGCAC AAGGGAAGAA AAACGTATTT GCTGAGTAAA CACTTGGGCA 1740 CTGAATTTAT TTCTCCCATC TTCTAAAAAC TGTGAAGTGA GCACTAGCGT TCTTTTATAT 1800 GTAGAAAATT GAGAGTGCAA AACAGGTTAA CTAATTTGCT CCAGGAACAA AAGCTAGTCA 1860 GTCATGGAAC TAAGATTTGA ACCTGTCTGT CTGATACTAA AGTGCTATTC TTTGCCATTT 1920 GAAGGCAGTA TCATTCATGC CATGAACATT AGCCAGAAGC TTTATGGTAT AGGGGGAGGA 1980 GAATGGAATG TGTAGAGGAA AAGTTCTTGG AAAGCAGAGT TTGATGTAGA ATGGTTCCTG 2040 AAAGTGAAGG GGATGGTGCC AGCAGTTGCA AGATAAAGCG ATGGGGTAGG TACATTGCTC 2100 CTGGCAGCTG CTCCTTCTGC CTCTCCTGTT GTTGAGTGTC AGATTTTGCT GCTCCAGGGA 2160 AGATTCAACC ACTGTTAAAG TTTGGCACAG GGTTGATGAA GCTTTGGAAC GTTACTTACT 2220 GGATTATTTA AAAAAAATAT GTCTATCAAG AGAAGAATAA AGAGGGTATC TGTGGTTATA 2280 CTTTAATTAG TTATTCCTGG AGAGGGGACA TGTGGCCTTA TTCTAGTCCC ATGGGCTTGA 2340 GGGGGAAAGC AGACAGATTT ATTTGACTGA CTGTAAGGCT CCTTTGCAGA TTACATAAAG 2400 AGAGAAAATA AGAAATTTTA TTTATTTATT TCTTTTTTTG AGATGAAATC TCACGCTGTC 2460 TCCAAGGCTG GAGTGCAGTG GCAAGATCTC AGCTCACTTC AGCCTCCATC TCCTGGGTTC 2520 AAGCGATTCT CCTGCCTCAG CCTCCTGAGT 2550
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