Tag | Content |
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EnhancerAtlas ID | HS050-06213 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:228995870-228997420 |
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) |
Foxd3 | MA0041.1 | chr1:228995926-228995938 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr1:228995930-228995942 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr1:228995934-228995946 | GTTTGTTTGTTT | + | 6.32 | Nr2f6(var.2) | MA0728.1 | chr1:228996186-228996201 | TGAACTCCTGACCTC | - | 6.22 | RREB1 | MA0073.1 | chr1:228995967-228995987 | GGGGGTGGGGTGGGGTGTGG | - | 7.06 | RREB1 | MA0073.1 | chr1:228995962-228995982 | TTTTGGGGGGTGGGGTGGGG | - | 7.13 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23450 | chr1:228995808-228996099 | Colon_Crypt_1 | SE_23450 | chr1:228996189-228997694 | Colon_Crypt_1 | SE_27943 | chr1:228995103-228998116 | Fetal_Intestine | SE_28861 | chr1:228994670-228998359 | Fetal_Intestine_Large | 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 | GAGATTTTAT TTTCCTTTCA CAGGCCTTTC CACTGTGGTG TTTTCTTCTG TTTTTTGTTT 60 GTTTGTTTGT TTGTTTTTTG CTTTTTGGGT TTTTTTGGGG GGTGGGGTGG GGTGTGGGAC 120 AGAGTCTCAT TATGTCCCCT GGGCTAGAGT GCAATGGTAC GATGTCAGCT CACTGCAACC 180 TCTGCCTCCC AGGTTCAAGC GATTCTCCTG CCTCAGCCTC CTGAGTAGCT GAGATTATAG 240 GCACATGCCA CTACACCTGG CTGATTTTTG TATTTTTAGT AGAGATGAGG TTTCACCATG 300 TTGGCCAATC TGGTCTTGAA CTCCTGACCT CGTGATCCAC CCACCTCAGC CTCCCAAAGT 360 GCTGGGATTA CAGGTGTGAG CCACCACGCC CGACCTTTTC TTCTGTTTAT GCAGTGGCAT 420 GGAGCAGTCC CTCTAAGAGG GCTGACCCAG GTATGAGTCA TTCAGTCAGC CTGAGGGTCC 480 AAGGGCTGCT CCATGGTGAG GCAGACATCC AGAAGGGTCC AGAGGGAGAA TCTATGGCAA 540 GAGACAGCAG TCTAGAGGGA TGGAAGTGGT GGCAGAAAAG CTGGCTTTTA AAAGGCAAGT 600 TTTTATTCTA GGCTGACTTT CTCTTATGTA AAATGTAGAT TTGCTGAGTG CCAGTGAATT 660 TATAATTTTA GAAACCCATC AGGGAGTTTC TAGATGAGTT TCTAAGAAGT CTAAGAAATG 720 TCCAGGAAGG CCCTTAGCCA CCTCGTGGAA ATTGGGAGAG AAGAAATGTG TGCAGAGAAA 780 AGAGGGATTT TTGATGCAGA GAAAAAGAAC AGGTGTGTCC CGGCTGCTGG CTCTGAGTAA 840 CCCGTCTAAT CTCACTGTAC AGAACGTACC TGCACTTTAT ACTAACAATG AGTGCCATTC 900 AGCGTGCCAT TTATGATGTT CACAGTGGCC TTCCTTGGTG TGGTCCCTGA AGCCCTGCAA 960 AGCAGGGACT GTGCGGTCTG AACCAAACAG GGGCCCCTGG GAATAGGGTA GCGTGTTCTG 1020 ATACCTGAGC TGGTAGTAGA GTCAGAGCAA GAACAAAAGC CCCAGCGAGC AATCTGGGTT 1080 CAACCCCTGT CACCTTAGCT CACGTGCCTG CATTGTGAAG TTCACGGTAA TAGCTTGACT 1140 GCATTCTCGC CATGGTTCTG GGTCAATAAA TCAGTCAGTA AGCACTGGGT GAGTAAGTAG 1200 TGCAGAGCAA AGTCTGAGCT TGGTGCCACA AGTGGATAAA AAAGAAATAG ATGACTCAAC 1260 CTCTGCTTAT AGGGAGGCTC TGATCTAGCT GAGATAGCAC AGAAATATTT GGAGAATGAC 1320 TCTAGTGCAG AACTGAAGGT GCAGAATGAC TCTGAAACGT TGCTGCACAG CAGGGTCCAA 1380 GAAAGGAGAG GGCAGTGCCA GCTGGGTATG CCAGGAAGGC TTTTGGGAGA AAAATACTGG 1440 CCAGGGTCTG GGAGAATCAG CAAACATGCC TGAGGGTAGA AAACCAGTGT CCCAGGACAG 1500 GGACCCTGTG CAGCCCTGGG GTGGGCTGGG TGGGACCGAG CCGGCAGTGC 1550
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