Tag | Content |
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EnhancerAtlas ID | HS050-39917 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:217928990-217930020 |
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) |
IRF1 | MA0050.2 | chr2:217929512-217929533 | ATCCTGTTTCTCTTTCTTCTT | + | 6.14 | ZNF263 | MA0528.1 | chr2:217929536-217929557 | TCTTTCTCCCTCTCCTTCACC | - | 6.21 | ZNF263 | MA0528.1 | chr2:217929533-217929554 | TACTCTTTCTCCCTCTCCTTC | - | 6.2 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_56359 | chr2:217928754-217930082 | u87 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I217063 | chr2 | 217928333 | 217930056 |
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Enhancer Sequence | TTCGGCCTGT GGCTAAGGCC CATCTGCCCA TGGTTCCTTC TTGAAGTAAT TGCTGTAAGA 60 ATTTGTCATT CACAAAAGGA AGTCTCTATT GTCTCTTTTC GGATGTCATG TAACCAATGC 120 GTGTTAAAGG TCAGTTGCAT CAGTTCTCTT AAATGGCAAT TAAGCTATTG TCTGAGCAAA 180 CCAGAGGCAT CCGGAGTGCA AGCTTCGCTC AAACCTAGGG ACCTGGGAAA GGCTGGGAAC 240 AGAGGAGCAA GTAGGACACC ACAGGGGAGG GCCGTGGCTT CAGGAAACGT GGGGAACACC 300 CTGAACTGTA AAAGCAGATG CGTCAGCAGA CAAAGGGGGT CATTTCACTA AAGCCTCAGT 360 GAAGCAGAGA AATTCCAGAC TTTGCCCATC ACCTACTGGC AGGCTCTCCC TCCCTCTGTC 420 CCCTCCCCAC CCTCTCCTCA CCCTTGTCTT TCTCTGCTTC ATTATCTCAC GCTCTCTCTT 480 TCTCTCCCGC AGTTTCTCTG TCTCTCAGTC TCGATTTCTC ACATCCTGTT TCTCTTTCTT 540 CTTTACTCTT TCTCCCTCTC CTTCACCTCT CCTGGCTTCA CTCCACTCCC CCCACCCACT 600 CTGTTCCCTC TCACATTCTC ATTTGGGGAT GGGGGGCGGC TGACAAACCG GATTGGGGGG 660 GTCTGACAAA CTGGATTTAA ATTTCAGCTC CGCAGCGTTC TCAGCTCTTG GTCTTGGAAA 720 TGTTCCCTGA GCTTCGGTTT TTCTCATCTG AAAATGAAAA AAATAATACC TAGCTCCAAG 780 TATTGAGCTT GTTGTGAGGA ATCAAACAGA TAACGTTTCT AAAATTCCAA ACACAGTGCC 840 TGGTCCACGG CAGATGCTTG ACTGGTGACA GCTTCCTTTC CCAGTGAGGC CCAGGGAAGT 900 AGGCACAGTG CTTGGCACCC TGCAAGCATG CGACACAGCT TCACAAAATA CCCACAGGGA 960 GCCAGGAGCA CCGCTTGAAT TTTATGGATG ACAAAATTGT GGTTCAAGGA AGGTAAAAGT 1020 ACCCTGGTAG 1030
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