Tag | Content |
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EnhancerAtlas ID | HS180-04454 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:212090750-212092130 |
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 |
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Enhancer Sequence | CTTTCACCTG CTACTCCTCC ACAGTTGGTC AAGACCAAGC CCTAGTCATC CTTATTGATT 60 GAATTAGGAG CAAAATCTAG GTTCTAGTCC TCCTAATTCT ACTACTTACA AGTTGCCTCA 120 CCTTAGGAAC GCCATTTAAC TGCTGTCTCC TTATTTTCCC AGTCTGGCCT TGTCCTCACC 180 GTTGTGGGGT ATCAGGCAAG ATAAAGCACA CAAAGTCTCT CTGCATGCCG GAGAGCATTT 240 TGCAGCATGA GGAGATGTTT TCTGCCCCAC CTATGTACTA GAATCCTCCA AGGAGCCCGT 300 AATGTGAGTG TAGGGGTCAG GGGCAGGCTG GTGACTGGAT GCTTTTGTTT AAGTTCCACC 360 AGTGATTTTG ATGCACATCC AAATGTGGAA ACCACTGACA AAGTACAAAA GACAAACAGG 420 AGAAGAGAAA TAAATTGTGA GCTAAAGATG CAGGCATGTT TTAAGCTCTC TTTAGAGTGG 480 ATAACTAAGG GCCAACTTAG AGAACAATTA AATTGCCCAT CTTTTTCAAG GTACCTGAAA 540 CCCTAATCTC AAGTCCCTTT TTTCTTCCTG GAAAAGATGT ATATGACTTC AATTACATTA 600 CTTTTCTTAC CTAGCAATCT AAACACACAC TGAAGATTTC ACACGCACAC ACACACACAC 660 ACACACACAC ACACACACAC ACTTCGTGAA TCATCTCTGC CTGGTTGCAT GCTGAAGTCA 720 GATTCCGAGT AATGTCTGTT ATTCTTTAAC CTCTGAGTAA TCACTCTGGC CCTGGTCTGC 780 TCTTTATCGT CCAGGAAAAC AATCTGATCA AGCCTTGGAT GATGGATTCA TAGTTGCTCA 840 AGTCTCCAGA GTGCTGTATA AACCAGACTA TTAATTTATT CCATGGGGAT ATTCTGTGAA 900 AGTCCTACTT CTCCTTTTTA ATAATTGAGT GGCCTCGAGC AAGTCACTCA ATCTCTCTAG 960 GTCTCTAAGA TGATTATGAT CACTAAGCAT CACTCTTTAC AAAGTATTTC CTTCTTTGTG 1020 ACATCTCTCT TTAAAATGTC AGTTGAATGT TCTCAGAAAC TTGTTGCAGT GGGCATAACA 1080 TTAAAGAAAA TGGGTAAGAA TGAGAACAAT GAATTTAAGG AACATTTCAT TCAGTCCATG 1140 GGACACCAGA GTGGACAGCT GTGACTTGTG TCTGCTCAGC ACTTCTTCTG CTCTTCAGGG 1200 GACAGAACTT CCTTCCATGG GGGAACTGCT CCTTTCTTCT TCCACCTGGT TGTGAGGAGG 1260 CTGCTGATCA AAGGACCCTG GCCTCCTCTT CTTCGGCCAC AGGGGTGGGC ATGTGACCCT 1320 GATTCAACCG TAATAACAAC CTACTCACCT AGCCACAGTG ATTGATCTGG GAATTCATCC 1380
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