Tag | Content |
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EnhancerAtlas ID | HS048-30283 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr5:141739560-141740800 |
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) |
Foxo1 | MA0480.1 | chr5:141740134-141740145 | TGTAAACAAGA | - | 6.02 | SOX10 | MA0442.2 | chr5:141740187-141740198 | TCCTTTGTTTT | - | 6.32 | Sox3 | MA0514.1 | chr5:141740188-141740198 | CCTTTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr5:141740172-141740193 | CCCTCTGTCTCCCCCTCCTTT | - | 6.59 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34287 | chr5:141734813-141741679 | HCT-116 | SE_35588 | chr5:141738937-141741441 | HepG2 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I142355 | chr5 | 141735231 | 141745153 |
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Enhancer Sequence | GTGATGGGAG GGCTACTATT TTATTTAGGG TGAGGAAGGC TCACTGATAA GGTAGAAGGG 60 AAGGAGTGAA CCAGGCAGCT TCCTGGGAGA AGCTTACTGT AGGTATTTGA AATGGCAGAG 120 ATAAAGACTG GAGATGGGAC TGTGTTGCAT AGCACTTGCT GTGTGTTGAG CACTGTGCTA 180 AGTGCTTTGT AGTCTTATAT GTTTAATCCT GCTTATCACT GTTTTGTTTT CTTTGAAGTG 240 TGAGACTCAG GTTAAATGAT TTACCCAAGG CCACACAGCT AGTATGTAGC GAAGGTGATA 300 TTCAAATGCT AGTTTTAATC ATCATGCTGC TTCCCACTAG GGACTCTCCT TTTTGAGCTG 360 GACCTGGCAT TTCATTCATG ACCTGGTTCT TTTGATTTCT TGGGGATTAA ACAGCAACAG 420 TGGCCAAGGT GACACCTGGC AACTGAGTTG CATGGTTGAC AACAGCTTAG GGCCTGAAGT 480 TCCTTTTTGT GAGTGGAGGA AGGTGATAAG TTTAATACTG GAAAACCCCA TGTTGTGTTT 540 ATGGCAGAAG GGGGGAGAAA CACCTTTGGA TTATTGTAAA CAAGAGAAAC GGGAGAACGG 600 GGTAGCCTGA ATCCCTCTGT CTCCCCCTCC TTTGTTTTAA TTTCCCTAAG ATAGTCCCAG 660 CACAGCATGT TGTATTATAC AGCGATAATT AAAACACTTG GATTTGTGAA CTGAGATTTA 720 TAGGGCAAAC AGGAGCCAGA GGAGAAAACG ACAGTCATCT CTTTTATTTG CAGGCAGATA 780 TCCAAATTGC CACTTGCTTG CTTTTTCTTC CCGACACTAT CACCTACTCT GCTTAATTAG 840 ATCCTTTCTT TTCCATATCA TTTCCAACTG CCCGCTCTCC CTGCTGCACT GCAGTTTGTG 900 AAGCCACACA CTGAACACTT TCCCACAGCC CAGGGAAGAT GTGAGTCAGA AACGCAGCAG 960 CAAACAAGAG CGGAGGAGGG CACCTTTGCA TCGATCGATC GGGCTGTCCC GCCTGCCTGT 1020 CCATCAGCCT CAGGGAGCAG GGACGGGAGG AACCTAACCG AGGGATAAGA TGAGAAAGTG 1080 CTAGACATTT TCCAGCCTTC CTAAGACAGT TTTCTACTGA GTGCCCATTT GTTGTGGGGA 1140 GTGGAGAGGA GAATGAATTC CCCAAACAGC AGGCCACCCC CAAATCACAT TGCAGTATCA 1200 AATAATATTT TGCTATGTTC AAAACTGTCA TTCTAAACTT 1240
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