Tag | Content |
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EnhancerAtlas ID | HS138-03619 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:222059460-222061360 |
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 | chr1:222061242-222061258 | CATTCCTCAAAAGCAC | - | 6.35 | FOSL2 | MA0478.1 | chr1:222060687-222060698 | GGATGACTCAG | + | 6.32 | JUNB | MA0490.1 | chr1:222060687-222060698 | GGATGACTCAG | + | 6.14 | RREB1 | MA0073.1 | chr1:222060325-222060345 | GGGAAGGGGTGGGTTGGGGG | - | 6.22 | RREB1 | MA0073.1 | chr1:222060324-222060344 | TGGGAAGGGGTGGGTTGGGG | - | 7.16 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_36705 | chr1:222058928-222062088 | HMEC | SE_55946 | chr1:222059265-222061847 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I221886 | chr1 | 222059486 | 222061718 |
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Enhancer Sequence | CACATACACA AGTTATTAGA ATTGATCACC ATTCTCAGAT TCAGAAGCTA CTGGTAGTGT 60 TCTCCCTACC CCCAAGATTG GGAGAGCATT AGCCTTTATA GCTAACATTA GGCAACAGAA 120 TGGCTTACTA TTGGAGCTGG CAACCTGCAT GCTTCTACAC ACAGACCACT GAGACAGGCA 180 ACCTCCACAC CTTCTACCAA CTGCTGATGG GCTGTTGCTT AGACAACCCC ACATCCTGGA 240 CCCAAGCTCC TAAACAGACC AAGAAGAATA GCAGTGCACT GAAGGTGGAG TAGACAGAGG 300 GAGAAAGAAC AAGCAGACCA CCTAAAATGA TGACCCTAAA GAAATGGAGT GCCTGAACGA 360 ATGGGACTGA TGTCAATTTG GAAAAGGGGT AGGGAAAGAG AGGGGGAGAG AAAAAGGGGG 420 AGAAGGGGGT GTGAAAGAGA GGGAAGGAGG GAGGAATAAA AAGAATATGA GAATTTAGGA 480 GATTCACATA CATATTTGAG ACTCAAAGTA GTGACATGGA AGATCAAGTT GAAGGAATAT 540 TCTAAAGCCT ACGACAAATA TCCATATCTC ACCATTGTTA GTACAAGGGG CCTGAAATAA 600 AATTCCCTTG GGGTAAGATT GCACACAGGA GGCTACATCT GCTGTGCAGC TCCCCAAAAC 660 TTTAGCCACT CTGACTCATC CCAAGGGGAA GAATTTTGGC CACCTGAGTT CCTGACTTGG 720 ATTCTGACTG TGGCTTTTAG CCTTTGCATC ATCCTGCATC TTAAGGATTG CTCTGTCTGT 780 CTCTCCTTCT CTGTCCTGGG TGAGCAAGCT GCTGGCATCT CCTGTCGGCC ACAGGAGGTG 840 TGTTGACAAG GGCCAGGAAA TATGTGGGAA GGGGTGGGTT GGGGGGAGTT TCCTAGGCAG 900 CGTTCCTCTA GGAACTTTCT TCTCTAGGAA TTCTCTTAGA TCAGCATCCA TTGCCTGTCC 960 ACTGGGTCAT AAGCTTTCCT TATGCACGTT CAGTTGTTAA ATCTACAACA CCTCTCGCCC 1020 CCACACAGAC TTTCACTCCC GCTCAAGAGA GGGGTCAGGG TGTGTGTGTG TGTTGTGAGC 1080 AAACTCCTTC ATTGCCATGG ACCTGGCAGA GGCACAAGCC AGCCCCATTC CAGGACCATG 1140 TGACACTGGC TGGGTTACTC ACTTGTTTGC CCTCCAGCAG GGGCAGCCGG GGACACCTCC 1200 CTAGAGTGAC TACAGCGTTT ATCCCTGGGA TGACTCAGCC CAAGCCTCCC TCTGCCCAAA 1260 AAGGGAATCT GAGGCTGGGG CTGGAGATGG GGCCTGTTGA TTAGCCGCAT CTATGGTTGG 1320 GAGAGCATAG AAACTACCTC TCACCTGGGA AACATGAGGG ACAGAGTGAG TAATGCTCAG 1380 ATCAGTGGCT CAGGAACTCA GCGTGAAACA TAAGTTTATT TGAGAAGCTC AAGTGACAGG 1440 TGGAGCTTTG CTTCCAGAAC CCCAAGGAAG ATCCTACTCA GCCACCTAAT GATAACATTT 1500 TCATTTCAGA TTTCCATTCA TTTCATCTCA CTGACTTCAC TCTCACCTTT ATTTTGTTTT 1560 CGTCATTTCT GGAGTGGGTC AATTACTTAA CCCTGAATAG AGATGTGATA TAGCAGAGTC 1620 TTAGGGTGGG TTCTGGCTGA TTCCTCATCA AGAATAAGAT TCTATTTCCT TTGTCCTGAA 1680 CAGGATAATC TCTTCAGATT ACAAAGCTGT ACCTACCTAG TATTGTTTGT TGATGTTTCT 1740 GTTGTTTATA AACACTGGTC TCATCTCTCC AAGAGCATAA TACATTCCTC AAAAGCACTC 1800 GCTTCCCTTA TAGTTCTAAT TCCTCATGGC ACTCTCTGAG AAGCACATGT GGATACTTAA 1860 CACTTGTTAC TTGATTGTTC TCAATCTTAA ATACCTGGAA 1900
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