Tag | Content |
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EnhancerAtlas ID | HS092-04604 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:212090660-212092120 |
Target genes | |
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) |
DUX4 | MA0468.1 | chr1:212090805-212090816 | TGATTGAATTA | - | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27820 | chr1:212088149-212095215 | Fetal_Intestine | SE_28649 | chr1:212087848-212099385 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I211914 | chr1 | 212088252 | 212094992 |
|
Enhancer Sequence | TGTGGAAGGT GCTAATTTCT AGATGCTACT TTAGAGTATG ACTTTGATTG ATTACTTGCA 60 AAAGTAGACC TATGCTTGTT AGTTATGCCT CTTTCACCTG CTACTCCTCC ACAGTTGGTC 120 AAGACCAAGC CCTAGTCATC CTTATTGATT GAATTAGGAG CAAAATCTAG GTTCTAGTCC 180 TCCTAATTCT ACTACTTACA AGTTGCCTCA CCTTAGGAAC GCCATTTAAC TGCTGTCTCC 240 TTATTTTCCC AGTCTGGCCT TGTCCTCACC GTTGTGGGGT ATCAGGCAAG ATAAAGCACA 300 CAAAGTCTCT CTGCATGCCG GAGAGCATTT TGCAGCATGA GGAGATGTTT TCTGCCCCAC 360 CTATGTACTA GAATCCTCCA AGGAGCCCGT AATGTGAGTG TAGGGGTCAG GGGCAGGCTG 420 GTGACTGGAT GCTTTTGTTT AAGTTCCACC AGTGATTTTG ATGCACATCC AAATGTGGAA 480 ACCACTGACA AAGTACAAAA GACAAACAGG AGAAGAGAAA TAAATTGTGA GCTAAAGATG 540 CAGGCATGTT TTAAGCTCTC TTTAGAGTGG ATAACTAAGG GCCAACTTAG AGAACAATTA 600 AATTGCCCAT CTTTTTCAAG GTACCTGAAA CCCTAATCTC AAGTCCCTTT TTTCTTCCTG 660 GAAAAGATGT ATATGACTTC AATTACATTA CTTTTCTTAC CTAGCAATCT AAACACACAC 720 TGAAGATTTC ACACGCACAC ACACACACAC ACACACACAC ACACACACAC ACTTCGTGAA 780 TCATCTCTGC CTGGTTGCAT GCTGAAGTCA GATTCCGAGT AATGTCTGTT ATTCTTTAAC 840 CTCTGAGTAA TCACTCTGGC CCTGGTCTGC TCTTTATCGT CCAGGAAAAC AATCTGATCA 900 AGCCTTGGAT GATGGATTCA TAGTTGCTCA AGTCTCCAGA GTGCTGTATA AACCAGACTA 960 TTAATTTATT CCATGGGGAT ATTCTGTGAA AGTCCTACTT CTCCTTTTTA ATAATTGAGT 1020 GGCCTCGAGC AAGTCACTCA ATCTCTCTAG GTCTCTAAGA TGATTATGAT CACTAAGCAT 1080 CACTCTTTAC AAAGTATTTC CTTCTTTGTG ACATCTCTCT TTAAAATGTC AGTTGAATGT 1140 TCTCAGAAAC TTGTTGCAGT GGGCATAACA TTAAAGAAAA TGGGTAAGAA TGAGAACAAT 1200 GAATTTAAGG AACATTTCAT TCAGTCCATG GGACACCAGA GTGGACAGCT GTGACTTGTG 1260 TCTGCTCAGC ACTTCTTCTG CTCTTCAGGG GACAGAACTT CCTTCCATGG GGGAACTGCT 1320 CCTTTCTTCT TCCACCTGGT TGTGAGGAGG CTGCTGATCA AAGGACCCTG GCCTCCTCTT 1380 CTTCGGCCAC AGGGGTGGGC ATGTGACCCT GATTCAACCG TAATAACAAC CTACTCACCT 1440 AGCCACAGTG ATTGATCTGG 1460
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