Tag | Content |
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EnhancerAtlas ID | HS118-18649 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr8:117068700-117071070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPB | MA0466.2 | chr8:117070662-117070672 | ATTGCGCAAT | + | 6.02 | CEBPB | MA0466.2 | chr8:117070662-117070672 | ATTGCGCAAT | - | 6.02 | PHOX2A | MA0713.1 | chr8:117068948-117068959 | TAATTGGATTA | - | 6.02 | Phox2b | MA0681.1 | chr8:117068948-117068959 | TAATTGGATTA | - | 6.02 | SPI1 | MA0080.4 | chr8:117070292-117070306 | TACTTCCCCTTTTT | - | 7.58 | SPIC | MA0687.1 | chr8:117070292-117070306 | TACTTCCCCTTTTT | - | 7.82 | ZNF263 | MA0528.1 | chr8:117070590-117070611 | TCCTCCTGCCTATTCTCCTCC | - | 6.83 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 117069192 | 117069529 | chr8 | 117070380 | 117070761 |
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| Number: 2 | ID | Chromosome | Start | End |
GH08I116056 | chr8 | 117069192 | 117069825 | GH08I116058 | chr8 | 117070226 | 117070826 |
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Enhancer Sequence | GAGGGAATAA ATTGGGCAAC ATCTATATAA CAAACTGCAT GAGTTACTTT GAGTGATTTC 60 AAAGCAATAT AAAATAACAT CCCCTGCCTC CAAGAATTAT ATGATTTACT CAGGAGACAA 120 GACTGTCACA TGTAGCAGTA AAGAATATAA ACTGTTTCAT TTAATCCTCA CAAGAAAAAA 180 TAACATACGC CATAAAAATA ACAATAGCAT CTGGCATTTA TTGAGAATCA ATTATATGTG 240 CATCACCTTA ATTGGATTAT TTCACTTAAT CCTCACAACA ATTATGAGTC ATTACTAAAG 300 CTATTTCCAT TCTATAAATG AGAAAATATG AACTTAAGAG TAGTTAAGCA ACTTGCTTGA 360 AGTCTTACAG TTGGTAGGTA GCTGAGCCAA GATATGAATC CAGGGTGTTC CATTCCAAAA 420 CCCATATTTT TAATCAGTAT AATAAAAAGA AGAGTGTCTA CTTTGTTCTA AGTGTCAAGC 480 ATCAAACATG TGCATGTGCG TGCACACACA CACACAGAGT CCCTGTTGGG TAAGCTCCCT 540 CAGTGGCCAC GTTTTGTAAC TTGCAGCACT TCTCCATCTG CCAAGATGAT TGCACCACTG 600 GTAGGTGTCT GATCCAAGAG CAGCCAATAA AGCAACTGGC TGGCATCTGC TGAGGTTGCC 660 TGATACCGGT GCTCTGCCCT CTATGACCAA TATTGATTAA GTGAATTAAT GAGAGTCCCT 720 CACGTGGTGG TAGTCATAAT AAGAGAGAGA GAGAGAGAGT GAGAGCTATT GGTAGAGAAG 780 AGTACAAATT AAAAGACTGA CAAAAGCAAG CAGCAAAGGC CTGTAGCCAG CACAATCAAT 840 GAGTAAGCAG AGGAAAGGGT GAGGTGGCTG GCTGGCACTG GGATTAGATT TGGAAAGACA 900 TTGAGAGAAA GGCACCAACA CAGAAAGACA AACTCATATT ATTGATAAGG AACAAGGTTA 960 TCTACAAAAT TCTTCTATAC CAAAGGCAAC AGATAAACCA ATACCTAGAG CTGGATCTCA 1020 AAGGACTTTT TAGTCACTGA AGAAACTGTT CTACATTCAA AACCCAGGGA GACTGGTCTT 1080 CTTGAGGCTG GGCCATCCCA TTGTTCTTGA GTTTCTATCA TGCCTGGATG TATGGCTTAG 1140 ATGCTTGCAG TCTTACTATT ACCTATATTG ATTTCCTATT GCTACTATAA ACTGTCATAA 1200 ACTTAGTGGC TTACATCAAC ACAAATTTAT TATCGTACAG TTCTGGAGAT CAGAAGTCAA 1260 AAATAGGCCT CAGTGGGCTA AAATTAAGGT GTTGGCAGAG TGTGTTCCAA CTGCAGCCTC 1320 TAGGAAATAA TTCATTTCCT TGGCTTTTGC AGTTTCCAGA GACAGCTCGC ATTTCTTGGC 1380 TCATGGCCTT TTGCATTTCT TTCAAGATAG TGGTGGAGCA TCTTCAAATC TCCTTCTGAC 1440 CAAGACAGTG ACTCTTCTCC CTCTCTCACT TGTCAGGACC CTTGTGATAA TGGGGGGGTC 1500 TATGCAGACA ACTCAGAACA ATCTCGCCAT CTCTAATTCA GCTGATTAGC AACCATAATT 1560 CCATTTAATT CTCTTTAATA AAGGGGCAAC CTTACTTCCC CTTTTTCATG CAACATTACA 1620 TATTTGCAGT TTTTGATGTT TAGGAACAGG ACTTCCTTAG GGGTCTTATT GTGCCTACCA 1680 CACCACCTAT ATTCCTAAAG TAATCTTTAT ATTACTTGAG AACACTTGAG TAAGTCTGCT 1740 TTTTGCAACC ACAAGAACTT GACTAACACA AAGATGCTAT TTGGCCAGTT TGAGTAGGGC 1800 TTCTGTTGCA ATTTTTAAAA AAATCTTGAC TCATAGGGTC CCAATTCCAC ATATTACTCA 1860 TATTATTCTC CTGTCTGGTT TGCCTTTCCT TCCTCCTGCC TATTCTCCTC CCACTTTCCT 1920 AATCTGCTGT TGTGAAAATC CAGCTCACGC AGGGCAAGTA CTATTGCGCA ATGCAGCATG 1980 AAGCAGGTTG TATATGAGAT AGGAGATAGA AACACAGAAT AATTGTTTAT ATAGGAAGTT 2040 CTTGGGAAGT TTCACAAAGA AGGAGATGGC ATGATTGCTA GGTTTGATTT AAGATCCTGC 2100 TTGACTATCC ATCCATATGG GGAAGATTCA GATCAGGCAG ACAGTTAACA ATAGAGCCAA 2160 GAATTGTACC AAGGTCTTCT GATTCCTATT CTGTTGTTCT TGATAAGTTT TTCCATATCT 2220 ATGATGGTTT GGGTATACCA GATGGCTATA ATGCATATTT GTTGAATGAA CAGAATGAAT 2280 AAATGAATGA AAAAATTAAA TAAATGGAAT GAGTAGGTAG GATGGAAGGC TCAAGGCAGA 2340 TGCAAAATAT GAATTAAAGC AGATTCACTC 2370
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