Tag | Content |
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EnhancerAtlas ID | HS048-25520 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr3:48893060-48894350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr3:48893107-48893122 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr3:48894219-48894240 | TCCTCCTCCACCTCCTCCTGC | - | 6.24 | ZNF263 | MA0528.1 | chr3:48894213-48894234 | ACTTCCTCCTCCTCCACCTCC | - | 7.27 | ZNF263 | MA0528.1 | chr3:48894216-48894237 | TCCTCCTCCTCCACCTCCTCC | - | 9.35 | Zfx | MA0146.2 | chr3:48893132-48893146 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 48893682 | 48893813 | chr3 | 48893773 | 48894070 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I048855 | chr3 | 48893133 | 48894457 |
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Enhancer Sequence | GTATTTTGAG TAGAGATGGG GTTTCACCGT GTTGGCCAGG CTGGTCTTGA ACTCCTGACC 60 TCAAGTGATC CACCCGCCTC GGCCTCCCAA AGTGCTAGGA TTATAGGCGT GAGCCACTGT 120 GCCCGGCCAA AAATGTTATT TTCTCCTCGG CCATAATTCC TATCTGGTCA TTTAGAAACA 180 TATTCCAAGC TATAAAGCCT CCTTTAAAGT CCCAAGTCTT CAACTTCCTG CTGGGTTGAT 240 CACAGCCCCA ACTCCCAGAT AGGGGTGTGT CCCTTCCCTT CTTACCAGGT CTGATTCTGT 300 TGCCCAGGCT GGAGTGCAGT GATGCACACT CGGCTCACTG TGGCCTCAAC TTCTTGGGCT 360 CAAGTGATCC TCCTACCTTA GCGTCCTGAG TAGCTGGGAC TACAGGCACA CACCACCATG 420 TCTGACTAAT TTTTTAATTT TTAAAAAATT TTGTGTACAG ACAGAGTCTT ACTATATTGC 480 CCAGGCTGGT CTTGAACTCC TGGACTCAAG TGATCCTCCT TCCTTGGCTT CCCAACGTGT 540 TGGGATTACA AGCGTGGCAT GATCCAGTGC TCCCAGCTTT TTTTTTTTTT TTTTTTAACA 600 GTTCAAAACT AGAGACAGAG TGATGGTTCT AAAGCCAAAG TCCAGGAGTC TCTATGCAGC 660 TGCAGTGAGA CAGGAAGTGC CAGTGGAACT GTAACTGTAA CTGTGACCAC CAGATGGGAT 720 AATGCCAGAA AAGCCCAGCT CCAGTAGCTT CAGCAAGCTC TCCCCTCCAC CAGAAAGTAA 780 TAATCTAGCT TATGACTCTC CAACTCCCTC ACCTTTTCTG GACACACCTG GATAGCATAA 840 TCTGCCTGAT TAGTAAAGTT AAGCTAGCTA CCTCAGATCG CACAGCAACT CCAAAGCCCA 900 CATGAAAACC CGAGATTGCT TTTGTCCTTT TAGAACAACT GACTCTCCAT CTGTTAGCTC 960 AGACACCCAT GGTGCTCAGG GAAGAGAGGG GAATAAATGA AGGGATGGGT TGCAGGCTGG 1020 GCCTTGGGAG GGCCTGTCTG CCAGGCTTGC ATTGAGGCCT GTGTGAACAA TTACCAGTCG 1080 GGTCACACCA CCCCACACAC CCTCCCTAGA GCAGCCGGGG CTAGGGCAGT CAGAGAAGGC 1140 AGAGCCAGCC AAAACTTCCT CCTCCTCCAC CTCCTCCTGC TGGATCCCCA GCCTAAGGTT 1200 CCCAGGGAAG AATACTGGAT CCCTGAAAGC CTCCACCAAG GCTACAGGCT GCCTGCTGAA 1260 ATGTCCCAGA ATCAAAAGAA GAAAATATAA 1290
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