Tag | Content |
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EnhancerAtlas ID | HS050-06263 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:229825040-229826160 |
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 | chr1:229826083-229826095 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr1:229826087-229826099 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr1:229826091-229826103 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr1:229826095-229826107 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr1:229826099-229826111 | GTTTGTTTGTTT | + | 6.32 | JUN | MA0488.1 | chr1:229825720-229825733 | GAAATGATGTAAT | + | 6.07 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_25523 | chr1:229824555-229832857 | DND41 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I229689 | chr1 | 229825145 | 229826053 |
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Enhancer Sequence | GGTGCTGGGA TTTGGGCCAG GTAAAGCTGT GGAAGAACCA GAAGTGAACC AGCCTCTGGG 60 TCTCTGCTCA GGGGAAGAGT GAGGAGTGCA GCTTGGGGCT GACTGGGCTG ATGCAGGCTG 120 CCTCTCTTCT CTTGTTCTCT CTCCACTCTG TAGCTTTAGT TGGTGGAGCA CTTCCGCCAC 180 TCGAAGGTAC TTGGTCTCCT CTGCGGTGAG GCCCTTGTGT GGTGTGTAGC CAGCACCTCT 240 CAACCCTGCC TGTCGCCCAA AATGCTGAGT ACTTTCCTGG GTCTGTTTTG TGAACAGAGA 300 ATTCATGATG ATATGGGTAG CTTTAGACTT CACCACTGGG ACTGTGTCAC ACTGTCAATG 360 ACAGGGTCAT GGCAGGGGCG GGTAGGCTGG TCTCTCCTTC CTCCTCCTTG GTGAGGCACT 420 GATACTTGCA CTCTGGAATC ACTGGCTTCC AGTGGACGCT GCCCGTGTCC GATGGAGGAG 480 TCATGGGCAC AGGGTCCTCG AGGGCATCAT CATAGCTGGA TGCCCAGCAG TTTATCCTGA 540 TGGGCAGGGA CATCTTTCCT AGAAGCCCAC CCAGCCTCAA GAGCAGGCAC TTCTGGTTGT 600 GTTGAAGCCA GTGAAAGACT GGGACCCAGG TGCTTTTTCC ATATATATAG AATTCTGAGC 660 TGAGTCCCTC CCACCACAGT GAAATGATGT AATGACTAAG CTGACAGATG TTAATGAGGA 720 ACACAGTGCA GCAGCTGCAA ATTAGCAAAG CTTCCCAGGA AGAGTGCATC CAGAGGTTCT 780 GCTATCCTGC TGCTGCTGCT GCTGGGCTGC CTGCGGCCTG GAGTCCAGCG CTAAAGAGGT 840 TCTGAGGGCC CACGTCTCCC GAGAGGCTGT GACGCAGTCT GGACTGAAGG CATGGTGAGA 900 GCAGTGGCAA CACCGAAGGT CTCCAGGACC CAGCAGACAA CACTGCCCCC CTGCTATGGT 960 TTTGAAGTGT CTTTTTCTGT ACTCAGCCCT TACGTGGTTG CTATAAACAT TAGACTATTT 1020 TTTAAAGTAG TTACAAATGG TTGGTTTGTT TGTTTGTTTG TTTGTTTGTT TTTTGAGACG 1080 GAGTCTCGCT CTGTCGCCCA GGCTGGAGTG CAATGGTACG 1120
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