Tag | Content |
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EnhancerAtlas ID | HS051-23607 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr6:43780570-43781790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:43780976-43780997 | TAAGTGAAAGGGAAAGTATTT | - | 6.26 | Nr5a2 | MA0505.1 | chr6:43780765-43780780 | GCTGGCCTTGAACTC | - | 8.25 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_24400 | chr6:43780623-43781013 | Colon_Crypt_2 | SE_24400 | chr6:43781249-43781662 | Colon_Crypt_2 | SE_27752 | chr6:43776723-43783445 | Fetal_Intestine | SE_28697 | chr6:43777090-43783195 | Fetal_Intestine_Large | SE_31486 | chr6:43780506-43781743 | Gastric | SE_33438 | chr6:43773463-43786777 | H2171 | SE_52639 | chr6:43780397-43783312 | Small_Intestine | SE_57095 | chr6:43780635-43780956 | VACO_400 | SE_65246 | chr6:43780829-43781742 | Pancreatic_islets | SE_67049 | chr6:43773463-43786777 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I043810 | chr6 | 43777444 | 43783218 |
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Enhancer Sequence | TTATTTAAGA GACAGAGTCT TGCCCTGTTT CCCAGGCTGG AGTGCAGTGG TATGATCATA 60 GCTCACTGCA GCCTCCTGGG CTCAGTGGAC CCTCCTGTCT CAGCCTCCCA AGGCTGGGAC 120 TATAGGCACA CACCACTGTG CCTGGCTAAT TTTTTGGTAT TTTTTGTAGA GATGGGGTCT 180 TGCTATATTG CCCAGGCTGG CCTTGAACTC CTGCCTCAAG CGATCCCCCC ACTTCAGCCC 240 CTCAAAGTGC TGAGCCATTG GCTTCGGCAC TCTGTTCACG AAGAGGCATG AGCCACTGCA 300 CCTGGCAAGG GCAGGGATTT TGTCTGTCTT GTTCATGATT GTCTTCCCAA GACATGACCT 360 AGAATAATGC CTGGCATTAG AAGGTGCTGA ATAAATATTT TTAGTATAAG TGAAAGGGAA 420 AGTATTTCTG AGAAAATGGC ATTTAAGTAG AGGCCTGCAG GATGAGTAGG CGTTAACGAG 480 CCAGGAAGGG GTGAGGACTG TGCTAAGCTG CAGGGACAGT GTGTACAAAG GTCCTGAAGT 540 GCGAAGGAGC AGAGTGCATT CTGAGGAACT GACAGGTGGC GGGTGCAGCT GTGTATGTGT 600 GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT ATGGCTTTCT CAGTCATTCG AAGGAGGTTT 660 GAAAGTTGCC AGAGAGTTTT AAGCAAAGGA GTGACATGAT TACAGTCATG TTTTAAAACA 720 TCCCTCTTGC TGCTGGAGGA GGCTGGATTC TGGGGCGGGG GTGAGAGTGA AAGCAGCAGG 780 GCCAGGTAGG GATCTCAGGC GAGAGAGGGT GATGGCTTGG TCCAGGGCAG CTTCTATGAG 840 GCTGGAGCTC CAAGGATAAT CAGGAGTTTT TCAGCAGGAG ACTTGGCAGG GTTTTGGTGA 900 TGGGCGAGGT GTAGAAGGAG TTCGGAAGGG AAGGAGAGGG AGCTGCTGGG GATGATTCCG 960 AGATTTCTGA GTTGCTTAAT TGGCTGGATG GTGAGACCAT TTATGGGAAT GGAGAATTGA 1020 TACTTGCTAA CGACAGGCAC TTTACTGGCT GCTTCGCTCG CCCGGTAATC TTCACGGTCC 1080 TCTGAGGTGG GGCAGATGAA AATCCACAAG GAAACAGGGG CTCAGTGATA AAGCCTTTGC 1140 TGCAGGACTT ACAATTGGTG CGGTGAGGCC CTCCTATCCA ATACCATCAA GGCTTGTAGT 1200 TGGTTAGTTT GACAAATGAT 1220
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