Tag | Content |
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EnhancerAtlas ID | HS101-00419 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:16390280-16392490 |
Target genes | Number: 27 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:16391695-16391716 | TCCACCTTCCCCCCATCCCCC | - | 6.7 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 16390918 | 16391006 | chr1 | 16391252 | 16391355 |
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Enhancer Sequence | GGGGTCCAGC CAGATGCCCT CCTGCCTGTG CCCCTCAGCG GGAATTACTG GCCTCATCTT 60 CTTTTTACTC CCTTTTCTCA GTTTCTAGCA CCCACACTCC AGCATGATTT TGGCCTCGTG 120 GAGATCTTTA ATCCATTTAC CCTCATATTT CCAGACTAGA TCCTCCCGTC CTCTTTTGCT 180 CCTGGCCCGG CTGACACCCT GGCATGGCCT CTGAGCTCTC TCTCACAGAC GCCCTTACCT 240 CTCACCCCGG TTTGGGTCTG ACCCTCCTGC CCTGTGCCTG GATCTGAGGA GCTGAATGTT 300 GCTGGAGAAA GTGACCGCTG CATGCGAGAT TGTAGCCCCA GCCTCCCGTG GGACGCTGCC 360 CGGATCCTTC TCTGTTTCTG CATTTCCTGC TGTCTTTGTT TCCTGCCAGG TTGACAGCTT 420 CACCCCATCC TTCCTTCTCA GACATGAAAC ACACCCCCTC CCCTACCCCA CACACTGCTG 480 GGGGCTTCTG CCCCTCCCTC ACTGGGTCCA GGATCCTTGG AAAGGTGTCA CCTGGATCTT 540 TCCACCCAAA TCACCAGAGC CTGCCTGCAC CTTTGCCCAC ATCATCGCCT TTCCCTCCTG 600 CAACAAAGGA AGAGCTGTTC CTGCTGCACC CAAGACCTTC TGGCCCATCC ACCCAGGGCT 660 GGGTCCTGCC CCTGCCCTCC CCCCAGAGGC TCTGCTCTCC CTCCTGCGGT GTCACTGTGC 720 CCTCTCCACT CTGTCCACTT TGAAGCATTC AGCCGGGATC TCATATGCTG CGATGTGTCT 780 TGGGCTCTGG ACCTTCTCCT GCATTCTCAC TCCTCTGTCC CCTTTACCAC TGGGTGGGGC 840 CGTCAGCATC CTGGCAACCC AAGCATCTCC TGTCTTCTCA GAAGCTTGTG ACCACTGTTT 900 CCTTCCAGCG ACTTGGCCGT TCCTCTGCTC CCTTCTCGCT GGACGTGCAG AGAGCTGTGT 960 CCCACATCTA CTTCCTCGTC CTCCACTTCT CCTCCACCCA TTCCAAGCAG GCTTTCATGA 1020 GGCAGCCCTT GCCAAGCTGC CAGGAAAATC CGTGGGGCCA ACTCCAATGG GGGCTGCTCC 1080 AGCCTCTTCT TGGAGCTGGA GCTGTGCAGC CTTCCTGCCC TCTTGAGCCT CGCTCTTATC 1140 CTGGCCTCTG GCCTCTCTGG CTGCTGTCCT GGGTCCCCTC TTTGGCTCCT CCCTGGCTCA 1200 CCCCTGCCCG TTGGCTGGCA CACTTCTGTC CTGGCCCTTC TCCACCCTCT CTCCCCAGGA 1260 GGTCTCACCT TCCTGTTTCC GCTGCCCGCT GCCCATGTGC ACACCTCCAG CCCTGACTCC 1320 TCACTTGAGC TCCCAACTGA GTTTCCAGCT CTCCACATGG ATGCCCAAGG GGCACCCCAA 1380 GCACACCTGG GCAAAAGAGG ATTCCCAATT CCAGGTCCAC CTTCCCCCCA TCCCCCACTG 1440 CACCAACTAC AACCCTGGGA GTTTCTCAGG GTCCTGCCTT CCCCCACTCT CCCCGGGGCC 1500 ACGCAGTCAA CCGGCAAATC CTGTTAGCCC TCTCTTAGGT CTATTCCAGG TCTCCCGGCT 1560 CCCTTCTCCC AGGGCTCCCC TGCTGCAGGC ATCCTCCCTC CCTGGAAGAC AATGGTCCCT 1620 GCGCTCACTC TCTGCCCGCC AGCGGAGGGA CTTAATGCTC TAGGCCAGAT TGTGTCACTG 1680 GGGTTAGGGG ACCATGTGGG TGCTGCCCCC AATTCCCCTG GATTCCTTTC TCCTGTTTTT 1740 GCCCTGGCGC CCTGCATGGC TTCTAAGAGG CACCACCTGT GGCTCTTTCT ACAGGGGCTG 1800 CCCTAGGTAA ATTTCTGTTG GCCCCACCCA GAGTGGCCCC AAGCCAATGA CTACCAGGTG 1860 CAGAACCCCA GCTCTTTTGT CTGGGATCCG AAAATTCCCC TTCACTTACC CTCCGGAGTA 1920 CCCTGCAGGA CCAGGCTGAG GCCAGGCCTG AGACCACCCC ACTGCCTGGC TGGCCTCCTC 1980 CATCCTCCTC TCGCTCCATT CCCTACTGGC TTCCTCTGGA AGGTTCACCT CATATCAGTT 2040 GTACCCAAAT CCTCATTTCA GGGGCAGCTG GCAGGGGGAA GGTAAGCATT CAGTTGGAGG 2100 TGAGATTAAG GTTTTCTTTT CTTTTTTTTT TGGAGACAGA ATCTCGCTCT GTCACCCAGG 2160 CTGGAGTACA GTGGCGTGAT CTCGACTCAC TCTAACCTCC GCCTCCCAGA 2210
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