Tag | Content |
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EnhancerAtlas ID | HS017-28438 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr6:39185770-39188050 |
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 | chr6:39186839-39186855 | AGTTCCTTGAAAGCAA | - | 6.25 | Nr2f6(var.2) | MA0728.1 | chr6:39186065-39186080 | TGAACTCCTGACCTT | - | 6.04 | Zfx | MA0146.2 | chr6:39186088-39186102 | CCCGCCTAGGCCTC | + | 6.24 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_23358 | chr6:39186069-39187289 | Colon_Crypt_1 | SE_24296 | chr6:39186138-39186794 | Colon_Crypt_2 | SE_27719 | chr6:39184801-39187893 | Fetal_Intestine | SE_28608 | chr6:39184011-39187590 | Fetal_Intestine_Large | SE_31742 | chr6:39186062-39188216 | Gastric | SE_40245 | chr6:39186089-39187952 | K562 | SE_50547 | chr6:39184883-39186009 | Sigmoid_Colon | SE_50547 | chr6:39186021-39188234 | Sigmoid_Colon | SE_52394 | chr6:39184868-39187982 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I039217 | chr6 | 39184915 | 39188030 |
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Enhancer Sequence | AGGTAGGTCA GTTTAGTGTA AGTAGAAGGA GTCTGCACCC CAAAATACCA TCAAGAGCTT 60 TTTTGACTTA CAGGCCTTTT TTTTTTTTTT TTTTGAGATG GAGTCTAGCT TTGTCACCCA 120 AGCTGGAGTG TAGAGGCGCG ATTTTGGCTC ACTGCCACCT CCGCCTCCCA GGTTCAAGCG 180 ATTCTCCTGC CTCAGCCTCC TGAGTAGCTG GGAGTACAGG TGCCCACCAC CACGTCCAGC 240 TAATTTTTGT ATTTTTAGTA GAGAGAGGGT TTCACTGTGT TGGCCAGGCT GGTCTTGAAC 300 TCCTGACCTT GTGATCCACC CGCCTAGGCC TCCCGAAGTG GTGGGATTAT AAGCATGAGC 360 CACCACGCCC AGCCTATGGG CCATTTTAAA AGGGATTAGA AATAAAGTGA GAATGACCCA 420 GAGAAGAAAG GCCTGGATCT GGGTAGGCCG TGTTGTTAGA GTAATCTGAA CTTGGTTCTA 480 GAGACTGTTC TGCCCCCAGC TAATCCTCAC CAGGCCTTGG TGTCCCCATC TAGTGAATGG 540 GATGGCATCC ATTTGGCTGC CAGACCTCCC AGAGTCAGGC CCACAAAAGT CATAGAAGGG 600 AGGTCTCAGA AGAATGGGTC CGCAGAGACC CATGGTAAGG GCAGGTTGGG ATGCACACGA 660 GCACAGTCTG TGTAGCTGCA AGCCTCTTAG AGGACTGGGT GGTGTACCTG GTGCTGCTGG 720 CAACACCCTG CAAATACTTC TGCTCCTTCC CCCTGGAGTG GTGCAGGCTC CAGTCATGCC 780 AAAGGTGCCC CCAGCTAGGG AACTGCCCTT CTCCACTGCA AACAGTGTGG GCCTCCCCGC 840 CAACTGCACT TCTCAGAAGC CTCTGAAAAT TAAAGAAGTC TTCACAAGGA AGGGTCAAGG 900 GGATGTTTTT CTCCTGCCCC AGCTCGTCCA ACTTGCCCTC TTGGTTTCCA CAGAGAGGCA 960 GGGACCAGGG CTGATTCTCT TGCAGCAGTC CTTGAACAGG TCTGGACACA CAGTATGTGC 1020 TTAGTAAAAT ATCTGCTGAA TGAGGAGCTG GATGGTTTGC TCTGTCTCAA GTTCCTTGAA 1080 AGCAAAAACC ACGGCTGCCC TCCAGCACCA AGGGCAGACC TGCTCAGTGT ACTCTTGCTG 1140 ACCTCTGCTG CCTGGGCCTT ATTTCACAGG GGAAAGGAAT TCGGGAAAAG TTGATGGAAC 1200 AAGGGATGGG GGATAGGGGA AGAAGAAGAG GGGGCTCCTG GAGATAAACA GACTCAGGCA 1260 GGGAGAGCAG TTTATTCTGT AAAGTCCCTC CCTCAAAGGG GAGAGGATAA CAATAAGCTG 1320 GTCTTGAAGG CTGCCTCGAG CTGGAAGCTG CACTGAGTGA GCTTTACAGG CATTTCCTCT 1380 TGCGAGGGGG GTATAATTAG TTCCATTTTC AGATGATGCA ATGTGCTCAA GGCCTCACAA 1440 TTTGTAAAGG CAGAGAGGTG GTATTAAATC CCAGGTGTGA CTTGAATACC TGTCCTTAAC 1500 CAGGTTCCAC TCCAGCCTGG GCAACAGAGT GAGACTCTGT TTCAAAAAAT AATAATAATA 1560 AAAATAAAAT AATGGCACCC CTACCCCTTC CATGACTTAG AGCCTGTGAG ACCAAGGACC 1620 AGAGTCTGGG CCTGGGGCAC CTGGCTTCAT TCACTCTGCT GTGACCTTGC AAGAGGCTTG 1680 GCTGCACTGA CTAGACTTCC AACCAAAAGG GCCACACAGC TTTTGGCATC CCCCTGAGCT 1740 GAGCACAGTG CTGGACAGAC GGACACAACA AACTGAGCAA GACTGAAATC CACACACTCA 1800 CTGAGCATCC TGAGAGCTAG GCCTGGCAAC ACAGGCCCAG GGCTGGGAAG ACATGGCCAC 1860 TGCCCACGAA GGTTGCAAAT GGTCTAGCTG GACCTAACTA GCACTCCAAG CCTTTCTGAA 1920 TGAATGGACG AGTCCAGAGA GGGAAAATAT GGCCAGGGGC ACACAGCATA AACCGGAGTA 1980 CAGGTAAAAG TAGAACACAG GTTAGAATCA GTTTTCTGCT ACACAGTAGT TCAGATGAGG 2040 GTTCCTCATC CCTAGCCCCA AGCACAGAAG CACTCAGACA AATGGAAGGG GGCTCTGCTG 2100 TGTCCTCCCC ACCCAGTGTG GCCAACAAGG CCCCTGGCAG CCCTGCAGGA CTGGAGACTA 2160 CACCGTTGAA CAAAGGGGGT CCTGCTACCA GCTGCACAGC TTCTCTCCCA GACTCAGGGG 2220 GCAAGCATCC CCGCTCATAG CAGGGGCCCA GCTAAGCAGC TGCAGCCAGA TTACAGTGGG 2280
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