Tag | Content |
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EnhancerAtlas ID | HS048-16273 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr17:48519780-48521460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr17:48520576-48520588 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr17:48520580-48520592 | GTTTGTTTGTTT | + | 6.32 |
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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 |
GH17I050443 | chr17 | 48520392 | 48521496 |
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Enhancer Sequence | CCAAAAGTGC TGGGATTACA GCCATGAGCC ACTACGCCTG GCCTTTTAGT TTAGTTTTGT 60 TTTAGAGACA GGGTCTTTCT CGGTCACCCA GGCTGGCATG CAGTGACACA TTCATGGCTC 120 ACTGCAGCCT TGACCTACTA GGCTCAATCA AACATCCTGC CTTAGCCTCC CAAGTAGCTG 180 GGACCACAGG TGCACACCAC CACACCTGGC TAATTTTTAA TTTTTTTGTA GAGACGGGGT 240 CTCAATATGT TGCTCAGGCT GGCCTGAGCT CCTGAATTCA AGCGATTTTC CTGCCTTGGC 300 ATCCCAAAGC GTTGGGATTA TAGGTCGTGA GCCATTTTGC CTGACCATGT CTTCATTTTT 360 TAATGGCAGT ATTGCATTGT ATATGCTCTC TAATTTAGTT ATCTAATCTC TTACTCATAG 420 GAATAATTTT TTTTTCCCAG TTCTTTGCTA AGTGGCAATT AATCATACCT TTAGGCATTT 480 TTTAGGTTTT ATTTCTTTTT TTTTTTTCTG AGACGGAGTC TCACTCTGTT CCCAGACTGG 540 AGTGCAGTGG CGCAATCTCG GCTCACTACA ACCTCCGCCT CCTGGGTTCA ACTGATTCTC 600 GTGCCTCAGC CTCCCGAATA GCTGGGACTA TGGGTGCACG CCACCATGCC CGGCTAATTT 660 TTGTATTTTT AGTACAGACA GGGTTTTACC ATGTTGGCCA GGATGGTCTC GATCTCCTGA 720 CCTTGTGATC CGTCCACCTC AGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCGC 780 GCCCGGCCAG GTTTTTGTTT GTTTGTTTGT TTGTTGTTGT TGTTTTTTAG AATAGATCCC 840 TAAAAGTAGA ATTGCCAGGA GGCCAAACAG CTTCTCCCCT TAGATTCTCC ATGGCAGACC 900 TGTTTCAAAA GGTATGCATA TTCAGAATGT TAGTAGATAT TACCAAATCA GAAGGAATCC 960 AGATTTACAG GTTTTGAAGC TAACACAGTT TGGGATGCCC TCTTTCTAAA CAAGAATAAA 1020 AAGCTCTTAA GTATCAGATT TTGTGCAAAC TGAAGATCGA TTTAGAATAA GAAAAGAATT 1080 TGCTACCAAT TGCTGCGAGC TTGAAGATTC TCTTTTGAGC TCTCTTTAAG CAATTTGTCA 1140 GAAATGCTGA CAGATAAATG CTTCTTGATT TGCAGCCAGC TTTCCCTCTC CAATTTCCAG 1200 GCACGCCCAG CACTAGGATG GTAGGGAGGG GCCAGGCTGG GGGGCATGCT AAAGTGTAAG 1260 TTTCTTAGGC TTCCTGCCTC TATACTTACC ATCTTCTAAA AATCTTATAC CAGTTTACAC 1320 TCTGGTATAT TTCTCCACAT CCTTGCCAAC ATTCCATATA ATCAATAACT CCTGTTTTTA 1380 TGTTGAAATT CATAGCCATT TTATTAATCT TCTCTACTTG GGGAGTTTTT TTTAGGCCCT 1440 ATTGAATGCA GCGTGATCAT CTAGTGCTCT AGCTTATCTT AAAATAACCT CTCCCACTGA 1500 TTGCATAAAG CCAGCAAGAA CATGAACCTA CTTGGGTTAC AAGGATTAAC TCTTATTTAG 1560 CTGCAACTGC TTTCTAGTAC TGCTTATGAA TATTCTTTGA CAAAAGTGCC TATCATGGAA 1620 ATTTGAAATT AAATATAGAC TCCTCTAGAA AGACAGCAAT CTTTGGTTTG GGTAGAGGAT 1680
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