Tag | Content |
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EnhancerAtlas ID | HS098-07736 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr10:88161980-88163150 |
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) |
Klf1 | MA0493.1 | chr10:88162746-88162757 | TGGGTGTGGCT | - | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28526 | chr10:88159172-88163228 | Fetal_Intestine | SE_60459 | chr10:88136635-88177911 | DHL6 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I086399 | chr10 | 88159201 | 88163119 |
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Enhancer Sequence | GAAAAGGCGT TGTCCTGGAG GGGATCCCTG AGAAATGGGG GCGCCTGCCC TGCCCAGAAC 60 CCTTTTAAGG AAAGCATATG GGCAAAGCTT CCACAGACTG GGAGGAACAG CAATCAGCAG 120 AGAGCTCAGG TGCTGGCAGG GGCTTCTAAA GAAAGGAGGG AGGGCGGTGG CAGGAGGAGG 180 CGTTCGGTGC AGCAGGAACA GCCTAGGCAG AGGGCACGGG CGGTGGGAAT GGCAGCACCA 240 TGGCAGGAAA TCCGAGGACT AGTCACCACC GCTGAGATGT GTTCTGATGT CCCTGAGTCT 300 CCATCCCTAA GAGACCTGAG AAAGTCGTCC TTCCGTGCAG CCTGGGAGGA CTTCATAGAG 360 CGAAGAGCAG AGGCAAAGGC TGGTGCGGAG AGTGACACAG CAGGGTCCAA AGCAGGACAG 420 TTTGCTTGCA GGCTGGGTTG CCTGTAGCCA AAAAGAGACA TAACTCTGAG AGGCAGTGAG 480 ACTGAATCAC GTGGGTCCTT GAATGCCAGG ATGAGATGGT CAGACTTCCA AGGGGCGCTG 540 GCAGCTGAGG CGGGGTGATC CAAAGGGCAG GGGCGGTTTT GGAGCTGGGC TGCAGAAAGC 600 CACATTTGTG TCTGGAGAAG GTGATTTTCC TAAAGGCAAG CCAGAGACTG ATTTGCCAAG 660 AGCAGGAGAC GCCTCGTGCT GCACGATAAG GACCTGAATG TGGTGATGGG GATGGAAAAG 720 CAGAGGTCAA TGGGACAGGT GGTATGCAAG CCAGTGCCAG GGGATATGGG TGTGGCTCCT 780 TTAATCACGT GGGGAAGCCC ACTCAGTCTG CCTGGAGGAA GGGGGAGTTT CCTTAAGGGC 840 AGAGATGAAG CCCAGCCAGG TCTTACAGAA ACGAGGCTGA GAGCTGGGAA TCATTAAGAT 900 TGGAGAAAGC TCCTCTTTCC ATGTATGTGT GTCTCTCCTT TCTGCGACTC TACCCTGTCC 960 TCTGTGGCTC CGGTTTCTGT TCCCTGTGAC TTCATCCTGC ACTGGTCTTC CGTTGCCCTG 1020 GAGCCAATTC TGACCTCTCA TCTCTGTGAC CTGGAAGCTC CTGTGTTCCA CACTTCTGCT 1080 CACAGTTAAG GATCTTGACA TTAAAATAAC TGGCCGGCAC TGGGCCATGA ATACACTGGA 1140 TCATGTGTCC ACTCTTGGGT GAGGTCACCC 1170
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