Tag | Content |
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EnhancerAtlas ID | HS060-07064 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:121198920-121200420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr11:121199965-121199985 | ACACACACCACACACACACA | + | 6.16 | ZNF263 | MA0528.1 | chr11:121199813-121199834 | TCCTCCCTCACCTCCTGCCTC | - | 6.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 121199600 | 121200200 | chr11 | 121200200 | 121200378 |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I121327 | chr11 | 121198557 | 121199652 | GH11I121329 | chr11 | 121199761 | 121199910 |
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Enhancer Sequence | CAAGCAATAT TCATTGAGCT CTTACTCAGT ACCAGACACT GCTGTGGTAC GGGGGATACA 60 GAAATGAGCA GAACAGATTT AAATCGCTAC TCTACTGGGG CAGGCGGAAA ATATACAAGG 120 TAAGTAAAAC ATGCAGTATT CAAGTCAGTA TCAAGTGCTG GGTAGAAAAC AAGGCAGAGA 180 AATGCAGAGG AAATGTCAGG GGAGCGAGCA GGAAGTGGTA AGATTTGATA GGCGGTCAGG 240 GATGCCTCAT GGGGACGGAG ACACCTGCGC AAAAGAGCTA AGGGTGGAAG AGAGTGAGGG 300 ATCTTGTCAT CTGGTGGAGA AGAATTCCAG GCAAGGGAAC ACAGTGCAAG CTCCTGAGGT 360 GGGCGTGAGC GCAGTACCCT AAGAAAGGGT GAGGACGCTG ATATAGTTGA GTAGAGGATG 420 GAGTCAGAGT TCACAGAGGC CAGATCACAC AGAGAACTGA CAGGATTTGA AAGGATTTTG 480 GCTTTCACGT GGAATGAGAT AGGAGCAGGC TACTGAGCAG AGGAGGGACG TGATGGACTT 540 ACACTGCAAC AGCATTGCTC TGGTGCAGGC TCAGGGGATG CGGCATGGGA AAGAGGCTGG 600 ATACTGGGAA AGTGAAGGCA GGCAGACCAT TGCCACTGTT AGGATTAGAC AGAATACCAA 660 GTTCCCTGCT CCCTCCATTT TCACCCAGCC TGCAGGATCC TCCCGTCTTT CCTCTCCCCT 720 CTAACCAGGC CAACTCTAGA GTAGATCACC GTTTCCTTGG CTGGCGTCTC CTCTCCCATT 780 CTGCCTGGTG CTCACACCAA GCCTTCACTC TTCTTCTTAA GTCACTCTGT CAGCACATGG 840 CCTAGCCTAT TTCATCATGA AAACCGAGGC CACCAGCATG AACTTCTTCT GCTTCCTCCC 900 TCACCTCCTG CCTCCATAAG AAAAACAGCA TCAACAACCA AGCAACCTCT ATCACACCTG 960 TAACCACCCT TCCCTCTTCT TCAGTCTCAG GGAAGAAGAT ACCACCTCCC ACCAGCCCAT 1020 TCTCTGTCAC ACACACACAC ACACCACACA CACCACACAC ACACACACAC ACACACACAC 1080 TCTTCTCCCC ACCCTCATAT CAGCTTTCAT TCATTATCTC CCTTCCCCTT TGGGACCTTG 1140 CTCCATGCAC AGTTTCCTTT CTTCTATAAA TTAACTCTCT TGCCTTTCAG TAGCTCACTG 1200 CCCTCAGCCT ATAAATACAT CAAAACTCAC CTATCGAGGA GCAAGGCTCT CTTGACCTCT 1260 CCTTTACTTC TCAGCCAAGC GTCTTGAAAA TAACACCTAT TTTGTAATGA TAAATACTTG 1320 GAGTCTTTAC TTCCTCACTT CTAAACTCAC TGCTGCCTGG CTTCTGACCT TACCACTCAA 1380 CTCAAACTGC TTTCAAAAGC ATCACCTCCA AATTGTCAAA GACACTGGAC ACTCCCAGTG 1440 TTATTCTAAC TGGGCTTTTC ATTTGAGACT GTTTCTTATC CAGACCTTTC CAAATTCTCT 1500
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