Tag | Content |
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EnhancerAtlas ID | HS182-20738 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr8:33437710-33440150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr8:33438046-33438057 | AATTTAATTAA | + | 6.32 | Nr2f6(var.2) | MA0728.1 | chr8:33439742-33439757 | TGAACTCCTGACCTC | - | 6.22 | PHOX2A | MA0713.1 | chr8:33438045-33438056 | TAATTTAATTA | + | 6.62 | PROP1 | MA0715.1 | chr8:33438045-33438056 | TAATTTAATTA | - | 6.32 | PROP1 | MA0715.1 | chr8:33438045-33438056 | TAATTTAATTA | + | 6.62 | Phox2b | MA0681.1 | chr8:33438045-33438056 | TAATTTAATTA | + | 6.62 | RARA | MA0729.1 | chr8:33439739-33439757 | GCTTGAACTCCTGACCTC | - | 6.52 |
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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 |
GH08I033580 | chr8 | 33438236 | 33439834 |
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Enhancer Sequence | CAGTCATTTT TAAAAAAAGA GATGTGGTCT CAACATGTTG TCCAGGCGGG AATGCAGTGG 60 CTATTCACAG GCATGATCCC ACTACTGATC AGTACAGGAG TTTTGACATG CTCCGTTTCT 120 GACCTGGGTG AGTTCATCCC TCTTTAGGCA ACCTTGATAG CCCTCAGCTC CTGGGAGGTC 180 ACCATATTGA TGCCAAATTC AGTGTAGACA TTTAACTGGC ATAGCGCACT GCAGCCTAGA 240 ATTCTTGGGC TCAAGCAATC CTCCCACCTC AGCCTCCTGA GTAGCTGGGA CACAAGTATG 300 GGCCACTGCA CCCGGCTCAT GTGCAGTAAT ATAGTTAATT TAATTAACTT ATTTAAATAT 360 TTAATTGAGG TGAAATGTAC AAACTGTATG TATAAAAAAT AAAAATATCC AGGCATGGTG 420 GCTCATGCCT GTAATCCCAG CACTTTGGGA GGTTGAGGCA GAAGGATGGC TTGAGCTAGG 480 AGTTTGAGAC CAGATTGGGC AACTTGGTGA GATCCCATCT CTACAAAAAT AAAAGCATTA 540 GCTGGGTTTG GTGGTGAGCA CCTGTAGTCC CAGCTCCTTG GCAGTCGGAG GCGGGAAGGT 600 TGCTTGAGCC AGGGAGGTCA AGGCTACAGT GAGCTTGGAT TATATCACTG CACTCCCATT 660 CCAGCCGAAG TGACAAAGTG AGACCCTGTC TCTAAAATAA TTTTAAAAAT ACAGTAAAAA 720 ATAAAAATAG ACCTGCTTTG TTTGAATCAC AGTAGGATTT CTCTCTCTGT CCCCATTCCA 780 CATCAGTGGC CCCTTTGAAA GTTATTTAAA ATACTAGGGC TCTGTCAAGC ACTGTCCAAA 840 AATCACCAAA CTAGAAGTTC TCCTGGATTC CTTCCAGTTC TGGTATTTTT GAGGTTGTGA 900 TCATTCACCT GTGTGCCCTG AACTGGGTTG GATCACAGGC TTGTCTTGCT TGGCTGCTGT 960 GAGCTTTTTG TACTTGGCCT GCATTGGCCG AGGAAAATGC TCTGGCTATC CAGACTCACG 1020 TCACTTCCTT TCACCCCTCA TGAGGAAGGG GCATACCTCT CCTTTCTCCT AATGCAAGCG 1080 ACGGTCCCCT TCCTTCCGGG ACCAGGGGCC AAAGTGCGGT GGGGCTGGGA TGGAGTGTTG 1140 TGGGTTGCTA GTATGCATCC CCCCACCGAC CTCTGCGCTG CACCTCTCTC CTGGTGTTGG 1200 ACTTGCAGAT TGTTGGAGCG GACTCTGCCT CTCTCCCCAG GTTAATGTTT TTACTCACCC 1260 TCTGGCCTTG TCCTCTTGTA GGCTGCCATT GGTTTGGACT GGAATCAAGA GCTCAGGCTC 1320 CGTCAAGGTT ATAGACTGAG GATATGAATT TACCCAGCCC AAACTCAGTT TGTGAGTAAA 1380 CTCCGGAGGC CAGAGAGGAG GGGCCTGAAT TCATCTTGGT ATCTCTCCAG AACACAAACT 1440 GCTTCAGGGA AAGTTACCCA GGAGGAGGGG GCATTCGGCC TTTTCCTGGG CAGACCTTCA 1500 GAAAGAAGCC TGCCTGGGAA CTGATAAACA CATCTCCCTC TCTGGTTCCC AAGGACAGGG 1560 CTTGGCCTCT ATCCACTTGT TTCCAAAGTT CCTTCCTGAG TGGCCTGCCT GTGTTAGCTA 1620 CCTTCTCCCA GCCTGGCTCC AGTTGCTGGG TGGGAATCCA GCTGGGGGCT TAAGTGTCTG 1680 CTGTATCAGG GAAAACAAAA TCTTAGGCCA TTCTGAAGTC CAGAAACCAC TGCCCAAAAA 1740 CTAAGAGCAT TCCTAGAATG GCTGGGAGAG GAGTGGGGAT TGGGAGAAGA TGAGAGAAGG 1800 TGAACTAGCC TGAGTTCCCT TTTTTCTTTT TGAGGTGGAG TCTCACTCCA TTGTCCAGGT 1860 TGGAGTGAAG TGGCGTGATT TCGGCTCACT GCAACCTCTG CCTCCTGGGT TCAGTTGATT 1920 CTCATGACTC AGCCTCCCAA GTAGCTGGGA CTACAGGTGT GTGCCACCAT GCCTGGATAA 1980 TTTTTGTATT TTTAGTAGAG ACGGGGTTTT GCCATGTTGG ACAGGCTGGG CTTGAACTCC 2040 TGACCTCAGG TGATCTGCCC ACCTTGGCCT CCCAAAGAGC TGGGATTACA GGGTGAGCCA 2100 CTTCACCTGG CCTAGCCTGA GTTCTTAAGA TGAAGAACTC AGATGAACTC TTAAGATGAA 2160 TAACTTTTTT TTTTGAGACA GGATCTTGCT TTGTCACCCA GCTTGGAGTG CAGAGGCTTG 2220 ATCACAGCTC ACTGCAACCT CCAACTCCTA GGCTTATGCC ATCCTCCTGC CTCAGATTCC 2280 CAAGTAGCTG GGACTACAGG CATGTGCCAC CGCGCCCGCT AATTTTTCTG TTTTTTGTAG 2340 AGACAAGAGT CTCTCTTTGT TTCCCAGGCT GGTATTGAAC TCCTGGCCTC AAGTGATCCT 2400 CTTGCCTTGG CCTCACAAAG TGCTGGGAGT ACAGGTATGA 2440
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