Tag | Content |
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EnhancerAtlas ID | HS050-69039 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:89020060-89021670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr9:89021508-89021519 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr9:89021508-89021519 | CTGAGTCACCC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 89020200 | 89020600 | chr9 | 89020840 | 89021025 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I086405 | chr9 | 89020124 | 89023330 |
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Enhancer Sequence | AAAACTGCTT TTTGAGACAG ATAGGATTGT GATTCCTGTA GCAATCTTGA AACTGGACTC 60 AGAGAGGGTA GGAAGTTTGT TCTAAGGCGC ACAGCTATGA CCAGCACAAC TGAATCTTAC 120 CTTAACTCAC ATCAAAGCCT CTGAGCTTAA ATATTAGGCT ATTTACCATG GCTGTGAGAG 180 ACGGGGAACA AAAAACAGTG TTTAGTTAAA TCAACAGCTA TGTTTACACT CTCTGTATAA 240 ACAGTGCAAT GTCCTCAAAG AAATCACACA AGAAGGAACA GTAACTCCTG CCAACACACT 300 GGTAAACTTG GCTCTGCCAA AACTATTAGC TCTTGTTTTC ACTCATCAAT GTCTTATGTT 360 TCTTTTGCCA TCATCTTTTT TTATTCATTA ACCCCAGAGC CTCAACTATC TCTCATTTAA 420 GATAATTGTT CTTATAGTTT TCCAGAAAAA CCCATTTCTC CTTTTACTTT TTCCTAGTAT 480 CTCTTCCCAT AAAAGGCAAT GCCCCTAAAT TTGTATCATT CCAGGCATTA GAGAACCAAG 540 CTCAGAAACA CTTATAAGAT TTTTAAGGTT ATCGTTCTCC CCCCAAAACA CATGCACATT 600 ACCTTTGCAG AGTTATTATT CAAAATATAG ACTTAGAAGC TCTCTGGGCT ATAGTCAGCT 660 GGTAATTAAT TATAATGACT TCAAGGTATG TTAAATTTGT ACGGGGGTGG GGAGAGGGTC 720 ACTTGCAGCC TCAAGAGGAC AGAGCACACC GTGAACCAGT TCTGGAACCT GCTTACAGAT 780 CTCAAAAGTT CCTGCAGCAG GAGGGCTAAT GACATTCTCC CTTCTAGAAA AGCAGAGTGA 840 CTCAGGATAC AGATGTTCCG CCTACCCTGC ATTTGTAATT ATGAGCTGGC TGTGGTACTT 900 CCCAGGGAGT CTTTGAATCA TCTGTTCTTG CAATTTATCT TGCCGCTGCT CTTTTTAGAA 960 CAATCTAGGA CATGTCAGCT GAAAACATGT ACCAGTTGCT TGCAAAGAAA AGAATGGCTT 1020 TTTGTGTGGG GGTGGGGGAC ACAGAGCGTT CTCTTCCTCC CTCTCTGCTG GGGAACATGG 1080 TAGGCAGAAT GAGCTAATAA TTCTCAGAGA AAAAAATATG AGCCCTGAAG AACCCCAATG 1140 CCTAGAGAGC ACGAAGTGAA GGTAGCTTAA TGTTAGTCCT GGTGTGTATA CAATGAGGGC 1200 CAGAGCTTCA GGAAGACGTG CTAATTTCAC TTTAATTAAC ACATACTAAT GCAAAGGAGA 1260 TGAACCAGAG AAACTTGAAT TTGCAGGCAG ACTCATGAAA CAAAAGTAAA CCTGGTACCT 1320 ATTGTGAAAT CATCTTTGGT GCAGTGTGGC TCAGGAATGT GCCACTCCTG ATACTTTTTT 1380 TCATCTGCAC GTGAGTGTCT GGACTCTGGA TTCAGAAAAA CAGATGGAAC TTTAGGTCAG 1440 ATGGGTTCCT GAGTCACCCC GACACAGGGG GCAGGCTGTA TTTTAAAAAT TTGTTGAGTA 1500 TTTATTTGTA CAAAGCATTC TGTAAGGCAC TAAACCGTAG TTTCTGCTCT AGTCTTCTTT 1560 CAATGACGGG TTCTGGGAGG GGTGATGGAA GCAGAAGTGA TAGTTATTTA 1610
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