Tag | Content |
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EnhancerAtlas ID | HS148-08128 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr18:43362710-43364190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr18:43362877-43362898 | AATGGAGGAGGGGAGGGAGAG | + | 6.56 | ZNF263 | MA0528.1 | chr18:43362880-43362901 | GGAGGAGGGGAGGGAGAGTGG | + | 7.23 |
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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 |
GH18I045782 | chr18 | 43362275 | 43364670 |
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Enhancer Sequence | CCAAACTCCT TTGCTACCTG GGTCTCAGAA ACAAGAGAAG GTACCAGCCC TCCCACTCAC 60 TGAGCAGACA GATGACCGGT GCCAGGGAAC TGTGTGTCTA TTTGTACTCA TAACAGCTCT 120 AGGGGACTCC CAGCCTCATA GCCCAACCTC CCATTTACAC ACTTGTAAAT GGAGGAGGGG 180 AGGGAGAGTG GGGTTTCTGG TCCTCCTGGT GCCAGTATGT TTCCAAGATG AAACTTAAGG 240 CCCCAGAGAG TCCCACCCTC TTCTGGAGGG CTCTTTCAGG TAAATAATAG GTGCCCTGTG 300 GGCCCAGATC CACTGTGGAT TTTTAATGCA TATCCTGGTA GGAGATGGTT CCTTGAAATC 360 TAATTGCTTC CAAGACCTTA ATATCAGCCA TTTTATTGTG TACAAAGAAT GCTCAGGAGA 420 GCAAATGTGA ACATGGGAAA GCCCATACCT CAAGGCATCT GGCTCAGTAA ACAGTGTGTT 480 CAGGAAACAG CAAAGGATTA AACAACCGTC AGGGCATCCA TAGCCAGGAC TCTTCGTCTG 540 TGGTCTGCTG TACTCCGATT CCTTATGATC CCCACTCCTA CTCCTCACTC AGCCCTGTTC 600 CTTTACCTCT TATCCAAACA CTTCCATAAG ATTTCCTATC AGTCACTGAC CCCTCAGTCT 660 AGTATAGCTC CAAGGGACTA GATTCTCCTA TCTCTGGTTC TAGAGAAAAA CTTTATCCTT 720 CCTAAAATGA GTTTTAGGCT CTGAGGCACA GGAGACGGTG AGACTTTGTA TAGTGCTTAT 780 GACAGTGCTT ACTTGAGGGA ATTCTTCCCT GGATTCCTGA GATTCCTGAG TATTACTGCC 840 TTCTTCACAG AAGCCCAACC CTGATTCTTT CAGATGGACT TATCCCTATT CCTCACATCC 900 AAGCAGTATC AGATCCGAGA GGCTAAATAA CTTGTTCTGG GCCAGGGAAC TAAGTGCCCA 960 AAACAGTAGT TCAATCCAGA CCTGCTCCAC CCTAGAGACG GAGACTGTAA TACTCCTAAA 1020 CTAGAGGAAT GGGAAGTAGC ACCAAAGGGC ACAAAAAATG TGCACGTGTA TGAAAATCTA 1080 TTAACCTGAA GAGGCTGTTA TTTCAGTGAG GGTATGAGCA AAAACGGAAA TGCGCTCATG 1140 CTAGAAATGC ACACACAAAC ACATCCACAG CCAGATCAAA AGCATGGGAT TCCTCCCTTA 1200 ATAGACCTCC TAAAATAAAT TTAGATGCAT CAAGCTGGCA GATGGAGATG GGAAAGGGGC 1260 CTCCCCAAGA AGTCAAGTTC TGCTAAAGCT GCAGTGCCTA ATAAGGTATT ATCTTGCCTC 1320 TCTGATCATT TAAGTTAGAA AAGGGAGGCA ATAACAAGAG GAAGTTGTAT GGTTTCTCAG 1380 TGTTTATATC TGAGTGAAAA GAAAGAACCA AACAGAGTCA TGAAAGTGAC ATCCTTGGGA 1440 GGCAGTGATT TCTCCCCTGC TGTTGAAAGT GGATTTTATT 1480
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