Tag | Content |
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EnhancerAtlas ID | HS138-29604 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr4:26049810-26051440 |
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) |
IRF1 | MA0050.2 | chr4:26050594-26050615 | TTCAACTTTCTTTTTCTCTCT | + | 6.2 | SPI1 | MA0080.4 | chr4:26049913-26049927 | TTCTTCCTCTTTTT | - | 6.14 | SPIC | MA0687.1 | chr4:26049913-26049927 | TTCTTCCTCTTTTT | - | 7.01 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_30137 | chr4:26049180-26052472 | Fetal_Muscle | SE_59332 | chr4:26050417-26092107 | Ly3 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I026047 | chr4 | 26049396 | 26052582 |
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Enhancer Sequence | AGACTAGGAA GAGAGCCATT GGAAACAGTG CGTAGAGCAG AGTTGTGGGG GTGTCACAGA 60 CAAAGGGGGG CAGGGGGTCA AGAGAAGTTT GGGGCTTTTT GATTTCTTCC TCTTTTTGCT 120 TTAAGATTGG AAAAGAGATG GCCAGTCCAT AACGTTGATG GGACTGAGTG AGTCAATGAA 180 GGAGCGCATG AGGGAGTGAG TGACTGAGGG CAGATACAGG GTCAAGCGAA GTTTCCGCCA 240 TCTGAGAGAG GTCTGAGCAG GAGTCCCAGG ACATGGGAGA TTGCCCTGGA GAGTGGATTC 300 ACAGAGACGG GTGGGGGTGC TGTCTGTCCG CAGTCGTTGC CTTGAGGGGC CCTTTGTTTG 360 CTACCCTCTT GTTGAATCTG GCTGTCCCCA CAGCTACTTT GCCTGGGGCC CAACTAGGGC 420 AGAGATACAA ATACGCCAGG CCATGGCCCC ATAAAGTCTG GCCTCAAGGC TGCAGCCCAT 480 TTGGAAAACG TTTTAATTTC ACTTGCGTGT TTTTTCAATT TGATTATTAA GTGCCGTTTA 540 CACATGGACG GGGAAAGCCT GTTTTCATTC GCTGATTCCC CTTCCTCCCT GGCCTGCGTG 600 CCTCCCTGGT GAGTAATGGG GAGGCTGCTT TTCTGGAACA CAAGGGAAAA CTTCCAGCAA 660 ATTGCAAAAG CATGTTCCTT CCTTGAAAAA TCCTTTCACA CTTGTTTTTT ACTCCGTTTG 720 TAAAGTTCAT GAAAAGCCTC CATAAAAGTG CTTTAAAAAA CCTAAACTTT CTTTGTTCTC 780 CACGTTCAAC TTTCTTTTTC TCTCTTAAGA GGGTATATAA TTTCAAGGGA TAACAAACAA 840 AACATCAAAC CTAGGGAGCA AGTGGCGAGA TGAAGGAATG AAGCAAACTT TAGAAATGTC 900 GGAGGATCAC AGGTTGGAGG TGCCAGTGAG GGGGAAATTT CCACATGTGT TTTCAGAAGA 960 TGAGAATCCG GCACTCCCCG ACTGGCCCCA TCATCGCTCA GATTTGTTTC TGAAGTTATT 1020 AACATTTCAC GCAAGGCTGG GGCAGCTGGG CAGACAGAAA GACTGAAATA ATAAAGGCTC 1080 AGGAAGAGCG ACACATCCTT TTAGGTACAT TTCAGCAGCC TCAACTATCA GGGGTGCAGG 1140 AGATGGGAGC ATAGGAAACG GTGCTGCCAA GAATTTGCAA AGAAGGTTTC CCTCCTGAAG 1200 GCCAGAGTGG GGTCATCCGA TCAGAGAAAT ACAGAAGGTT CTTAAAGGGG ATGGAGGCCA 1260 TATAAGGAGT TTCCCTCTGC AGAGACAGAC TCCATTCTGG TTTGGGTTTG ATGAGACAGC 1320 TAGAAAAGAG CTGAGAGGAT GGGGTTCCCA CCAGCCTCGA GGGACTGTCC TGGAGAGCCT 1380 CATGGGGGTA GCCAGGGGAA GTGCCGTGGG GTTCTGTGGG CAATGTTTGG GGACTGGGTG 1440 GCATGCCTTA GCCAGCTATT GATCTAATTC TGGTCACTGT CCTGGTGTCT GAGTCCATCT 1500 AGGGCTGCAT GTCTGGTGTA TCTGTCCCTA GCCCTCTGGG CTCCAACGTT GGCAAAGTAA 1560 CACTGGTGGG CTCCCCTCCC CACTCCCATT TCTCTCTCTG CAGCACCTGC TTCCCCCCTG 1620 CATACCCCCT 1630
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