Tag | Content |
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EnhancerAtlas ID | HS095-08605 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr13:99095250-99096560 |
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) |
EWSR1-FLI1 | MA0149.1 | chr13:99096131-99096149 | GGAAGGAGGGAAGGGACA | + | 6.04 | IRF1 | MA0050.2 | chr13:99095387-99095408 | AATGGGTTTCACTTTTTTTTA | + | 6.21 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_32401 | chr13:99095360-99096258 | Gastric | SE_37511 | chr13:99094873-99096932 | HSMMtube | SE_45616 | chr13:99094612-99099363 | Osteoblasts | SE_65772 | chr13:99095332-99096284 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I098442 | chr13 | 99095039 | 99098865 |
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Enhancer Sequence | CCCAGCTTTT TTGGATAACA AATCTACACG GTCGCAGCCT TCCGTGTGCA TGATCAGGTC 60 AAGGCACTGA GTCAGGGGCA CGCTGGCCCC CAGCCAGATC TAGCCCCGGC CTGGTGGCTT 120 ACAGCCTGCG AACCAAGAAT GGGTTTCACT TTTTTTTAAT GGCTGCTACA TAATGTCTTC 180 AGTTTTGCCC CTTGGCCTGC AAAGCCTGAA ATATCTGCCG TCTGCCTTTT GAGGAAAAGT 240 TTGCTGACCC TAGTAGAGAG CAGGAGAGTG AGCCACTGGC CAGTGGGGTT TGAAGGTGGC 300 AGTGACCACC TAGTACAGTC AGGGACCTGG GCTGCTCTAT CACTTTGCAG ATGTCCCTCC 360 TTGCCAGAAA GCCCCCTCCC AAGGCACGTG GCATCAATCT TGTGTCGGTG GCAGGCAGCC 420 CTCATGTGCC AGACGCCAAA TGCTCGCTGA CTCGCAGATG AGCCATCCCC AGGGCCTCCT 480 CCCTGCATGA CAGGACAAAG CAGCTCCATC TCCTCCTGAC TCAACAGCCT CCTCTCCCCA 540 GTCCCGTGCC CAGCCTCTCC CAGTTCCCAC TCCCGTCTGA CTCGTGTAGG CACACTTGAG 600 GAAGGGGCGT ATCTGGGGAC CGTGTGGCCT CACTGGCCTC TGCTAAAAGT TGTGGGCAAG 660 CCGGCAGGCC TGGGGGCTCC CACTAGAGGT GGGGTCAGAT GTTGGGATGG CCAGAGGGCT 720 GCCCAGCCTG TGGGCACTAG AGCCAGTGAA GGGCCAGAGG CAAAGCAATG CAAGTTGTCT 780 TTTAAGGCTG GAGTGGCGAG ACGGGACAGC AGGGAAGTTG TTCAGCAGAC AGAGCGCAGA 840 CAGGACTGGG AGGAGGGAAG GGACGGGGTG CAGACAGGAC CGGAAGGAGG GAAGGGACAG 900 TGAGGCCAGG GAGTGGCGGG CACGGGGGTT ATATTTGTTC CCCGTGGCGT CACTCGGCAC 960 CAACCTCAGA CTGGGTGAGG CCACAGAAAC ATCTCCCACA GTGCGGGAAG CCGGAAGTCC 1020 AAAATCAAGC TGCTGGCAGG TGGGTTCCTT TGGGAGGCCT TGAGGGAAAA TGTCCCCACC 1080 TGACAGCATC TGGTGGCTGC GGCAGTCTTC TTCTCGGGGG GTCCCCGACT CCACCCATGT 1140 TGCAGGGCTC CGGTCTGCCG TGTCACCAGC TGTCCTCCCT GTATCTGCAC TCTAATATCC 1200 TCTTCTAAGG ACACGGCTCG TGCTGGGCTT AGGGCTCGTC CTAGTGACCT TACCTTGACT 1260 CGATCGCATC TGCAGAGACC CTGTGTCCAT GTGAGGTCAC CATTGTAGGC 1310
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