Tag | Content |
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EnhancerAtlas ID | HS101-42013 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr8:8284830-8286200 |
Target genes | |
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 | chr8:8284844-8284856 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr8:8284848-8284860 | AAACAAACAAAC | - | 6.32 | IRF1 | MA0050.2 | chr8:8285194-8285215 | TTTTTCTTTCTCTTTTTCTTT | + | 7.4 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I008427 | chr8 | 8284686 | 8287708 |
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Enhancer Sequence | TCTCCATCTC AGACAAACAA ACAAACAAAC AAAAACAAAA CAAAACAAAA CTATTTCAAA 60 CATTTTAAGC TAATGGCAGC CCATAAGTGC CACATCTCCC TTTTGACCTC TTCCCATAGG 120 CCCTGGAGTC TGTGCACTCC CAGGCACACA TACCCTGTTG TCTCTCAAGC ATCCGCAGTG 180 CAGGTGGGGG ACTTACGTTC TTACAATCCT AAAACCTTTG ATTATAACCC ACACTAAAAT 240 AAGAAAGGTA ATCAAATGTG TGGGTGGAAG CTTGCCAGAC ATTTGTAGAG TTCCATACCG 300 TTCATAAAGT GCTTAAAAAT GCTTAATTTC ATTTGAATAA CACTTGCTGT TGTAGCTATG 360 TAGATTTTTC TTTCTCTTTT TCTTTTTTAA AAAGCAAAGG TATATACAAC AGCTCATTTA 420 AAAAGACTAG ACAGACCCTA GCTCCAACTA ATTCTCTAGA TTGAGCACGT GAGAGAACTA 480 TGTTCCATTT CCTTTTTTGG TATCGCAGGC CTTGATCTCC AAACAAACAC ATGAAGTAAG 540 TGTCTAAACT CTGGGTGGAA GTAAGCTAAT CATTGACATT CAAAACACTC TGCTACTTGA 600 CACACTTAAA CAATAAATGC CCAGCTGGCT AAAATTCTAT TGCTACAAAT CATTATCTCT 660 TTAAGGGGCC CACATAAATC TATGCAGGTG TTTGGAAGAC TATAACCTGT CTGCGACTTT 720 TTTTTGCATC TCTAGGAGTG TTCAGCTCAC AGACTGGCAC AAAGGAATGA TGACTGTGCC 780 TTTGTGGGAG GAGGAGAGAT TAGGTCATTG CCACCGAGGG AACACTTGCT CTGACCCAGG 840 TGGCTGTCAA GAAGCGACAG ATTGAATCCC TCTAACTCAT GTGGCAAATA GATTATTCTC 900 ATTTCACAGA TGAAGAAACT GAGGCTCAGA GAGGTTAACT TGTTTAATTT CATAAAGCAT 960 GAGAGTGGGA AGATGAGATT TGAACCCGAG TTCCTCAGAA TTGTATAATA TCTTGCTGTT 1020 TACTCTTTCT TTTCTCTCTC TCTCTCTTTT TTTTTTTTTT TTTTGTTGTT GTTGTTGTTG 1080 AGGCAGGGTC TCGCTCCATC ACTCAAGCTG GAATGCAGCA GCACGATCGT GGCTCACTGC 1140 AACCTGCACC TCCCGGGCTC AAGAGATCCT CCCACCTCAC ATCCTGAGTA GCTGGGACTA 1200 CAGGCACACA CCATCATGCC TGGCTAATAT TTGTATTTTT TGTAGAGATG GAGTTTCCCC 1260 ATGTTGGCCA GGCTGTTCTC AAACTTCTGG ACTCAAGCAA TTCACCCACC TGTGCCTTCC 1320 AAAGTGCTGC AATTACAGGC ATGAGCCATC ATGCTTGGCT TACTCTTTTT 1370
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