Tag | Content |
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EnhancerAtlas ID | HS055-00804 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr1:228996300-228998560 |
Target genes | |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr1:228998007-228998018 | AATTTAATTAA | + | 6.32 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23450 | chr1:228996189-228997694 | Colon_Crypt_1 | SE_27943 | chr1:228995103-228998116 | Fetal_Intestine | SE_28861 | chr1:228994670-228998359 | Fetal_Intestine_Large | SE_49948 | chr1:228997517-229000847 | RPMI-8402 | SE_52925 | chr1:228994663-228998395 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I228859 | chr1 | 228994940 | 228998147 |
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Enhancer Sequence | CTCTAAGAGG GCTGACCCAG GTATGAGTCA TTCAGTCAGC CTGAGGGTCC AAGGGCTGCT 60 CCATGGTGAG GCAGACATCC AGAAGGGTCC AGAGGGAGAA TCTATGGCAA GAGACAGCAG 120 TCTAGAGGGA TGGAAGTGGT GGCAGAAAAG CTGGCTTTTA AAAGGCAAGT TTTTATTCTA 180 GGCTGACTTT CTCTTATGTA AAATGTAGAT TTGCTGAGTG CCAGTGAATT TATAATTTTA 240 GAAACCCATC AGGGAGTTTC TAGATGAGTT TCTAAGAAGT CTAAGAAATG TCCAGGAAGG 300 CCCTTAGCCA CCTCGTGGAA ATTGGGAGAG AAGAAATGTG TGCAGAGAAA AGAGGGATTT 360 TTGATGCAGA GAAAAAGAAC AGGTGTGTCC CGGCTGCTGG CTCTGAGTAA CCCGTCTAAT 420 CTCACTGTAC AGAACGTACC TGCACTTTAT ACTAACAATG AGTGCCATTC AGCGTGCCAT 480 TTATGATGTT CACAGTGGCC TTCCTTGGTG TGGTCCCTGA AGCCCTGCAA AGCAGGGACT 540 GTGCGGTCTG AACCAAACAG GGGCCCCTGG GAATAGGGTA GCGTGTTCTG ATACCTGAGC 600 TGGTAGTAGA GTCAGAGCAA GAACAAAAGC CCCAGCGAGC AATCTGGGTT CAACCCCTGT 660 CACCTTAGCT CACGTGCCTG CATTGTGAAG TTCACGGTAA TAGCTTGACT GCATTCTCGC 720 CATGGTTCTG GGTCAATAAA TCAGTCAGTA AGCACTGGGT GAGTAAGTAG TGCAGAGCAA 780 AGTCTGAGCT TGGTGCCACA AGTGGATAAA AAAGAAATAG ATGACTCAAC CTCTGCTTAT 840 AGGGAGGCTC TGATCTAGCT GAGATAGCAC AGAAATATTT GGAGAATGAC TCTAGTGCAG 900 AACTGAAGGT GCAGAATGAC TCTGAAACGT TGCTGCACAG CAGGGTCCAA GAAAGGAGAG 960 GGCAGTGCCA GCTGGGTATG CCAGGAAGGC TTTTGGGAGA AAAATACTGG CCAGGGTCTG 1020 GGAGAATCAG CAAACATGCC TGAGGGTAGA AAACCAGTGT CCCAGGACAG GGACCCTGTG 1080 CAGCCCTGGG GTGGGCTGGG TGGGACCGAG CCGGCAGTGC CTGCAGGGAT GATGGGCACC 1140 AGAGCACAGC TCTCAGCCTA TGTGTCCCGG AGCTCTGGGC GCTCCCAGGT GTCCTCACTG 1200 CACCGTGGTA GCTCCTGTCT CATGGAGCCA CCTGTCCTAG CACAACAGCT CCAATCACTG 1260 CTATTAGAAC AGATCCAAGG GGCAGGCTGG GAGGGTGTTA GGTTCAAAAA GGAGCACTAT 1320 GTAGAAGCAA GAAAAGAGAT GAAAGTTTTG CTCCTATCTG CATCTGGCCA GAGAGCAGAC 1380 TTTGATTTGC AACACCGTGT GGTCTCTGCA GGATTACGAA AGGGAAGAGG GGGTGGGCGG 1440 AAGGCTCTCC TCCCCAGTGC ATCATTTTCA GTTTTGTCTT TTACTTTCAA AGAAAGCTGT 1500 CTTTCTGACA CTGCATTCTG CCCTTTCTGA CCCATGTCCC ATATTTAAAG GCTTCACATA 1560 GACTATATAA TCCAAGTTAT CCCTCTGTGG AGAAAGTGGC TATGAGAATT AGAGAGACAA 1620 AGGGTGTGCT TGTGGGAATG GGATGTAACG TCAGAGCAGG TTCAACCTTA CAGCTGTGCA 1680 GTCCAGTTAG TCAAATATTA ATGAGTCAAT TTAATTAAAG ATTAGGTCCT CTGTTGCACT 1740 AGCCATCCTG CAAAGTCACA TGTGGCGAGT GTTTTCATAC TGGATAGCAC CACAGAAAGT 1800 TCTGTTGGGC ATCATTGCCA CTTGGACCAA GGGATCAACT GCTTTCTGGG TGGGAGAACT 1860 GAGGCACAGG GAACCACGGC TTGGACTCCA AACTTAGTGC TCTGATCAGT GTGTTGTCCA 1920 AAGCTTCCAG CAGACAAGGA TTCAGACCAC ACAATTCAGG AGCAATAAGA TGGCTGGAGT 1980 GAACAACAAG TTTCCCTTGA CTTTAGAAGA AAAAGATCTC TAAATCCTGG AGATGATTAC 2040 ATGCTTTTCC TGAGGGCTGA GGAAAGAGGA GAAGCAGTTG GTTTGTTTTC AATTAGCCAC 2100 CCTCCTCCTT TTTCTAAGAA GAGGAAAGTC ACTGCCAGGT CACAGGGCTC GGAGCCAGGG 2160 TCAGCAGAGG GGCTGGTCGG AGCACCTGAG CCAAGTGGGC TGAGACTCTG ATCCTCGTGA 2220 GTGTCACCTG CCACCAAATG CTCTCTCCTG GGCTCTGCCA 2260
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