Tag | Content |
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EnhancerAtlas ID | HS182-21018 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr8:104089900-104092380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EHF | MA0598.2 | chr8:104090426-104090438 | AACCCGGAAGTG | + | 6.74 | ELF1 | MA0473.2 | chr8:104090426-104090438 | AACCCGGAAGTG | + | 7.22 | ELF3 | MA0640.1 | chr8:104090426-104090439 | AACCCGGAAGTGT | + | 6.57 | ELF4 | MA0641.1 | chr8:104090426-104090438 | AACCCGGAAGTG | + | 7.22 | ELF5 | MA0136.2 | chr8:104090427-104090438 | ACCCGGAAGTG | + | 6.32 | IRF1 | MA0050.2 | chr8:104090762-104090783 | TTCTGGTTTCCTTTTCATTTT | + | 6.54 |
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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 |
GH08I103077 | chr8 | 104090030 | 104092216 |
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Enhancer Sequence | AGCAGCCAAA TGAGAAAAAG GACTCTGTCC ACATGGAGCC TACCTGCTGG TGGACGATAC 60 ACAATAAACA TAGCGAACAA GGTAAGACTT TTCGCCCTCT GCACCTGTAA GGCCATTGAG 120 GACTAACCTG GCTGGGAATG GGTAGGAAGA GCTGCTTCAG AGGGGTGTCT AGATATACCC 180 CAGAGGATGC CAGCCATGTG AAGACCTAGG GGAAGGAAGT GTCTCATAGA GGTTGGGTAA 240 TAGAGGATCA GCGTGGCAAT AGCTGAGTGA GTGAGTGAAG GGTGTGGTAT GTGCAGCAGA 300 TGCACCTAGG TGGGGTCTTC AGAACATGGT GAAGAACTCA GACTTTTTTC TTCTAGCAAA 360 GGGAACCCAT TTTAGGGACT CATGTGCATG TTTCAAGGAT CACTGCAGCA GTGGTCATAC 420 TTGTGTGTTT GTAGCCCCTA TTTCTTACGT CGTGCTTGGC GCATTCATAG CAGGCACTGG 480 GTTCTGGTTC AGAACTGAAG TGGATGAATG CATGGAGAAT GTACTAAACC CGGAAGTGTG 540 CCAGACTCTG CACCCGAAAG TTCTCTGCAG CTTCTCCAAC TTTAAGAGTG TTCTGCAAAC 600 ACACTGAATG CTTTGCCTGG ATCTTCCTGT GAAGATCCAG GCAGAATTTA GTAATAGAAA 660 TTTGTAAAAT TTATTCTTAA ATTCTTTTGC AACTGTCTTG ATTTCTTCAC AAACATAGTC 720 ATCATCTGTT TATCAAATGG GCATTTTAAA TAATATTTGA CACATAACTG GCTGACTCCA 780 CAGCTCCAAA TTAGTCACAC GGTAGTCTTT TGATAATAGC CAACATGTGA CAACAGGGAT 840 TTTTTGCACG AGGTGGGGAG CATTCTGGTT TCCTTTTCAT TTTTCCAATA TGTCATATTT 900 CTCACTTCCA CTTTTCTTAG AGGGGAGGGT TGTCTTTTTG CTTCAAACTA TTATAGGCTT 960 TTACTGAGAG ACAAGAGGCT ATGAGCCCCA CTCAGTAGAA GAAGGGTTTA AGTCTATCAT 1020 ATAAATTATT GCCGCTCTAA CTTCTCTCTG TCCCTGCCTC TTAAGTCATT TACGGTATTT 1080 GTTTGGGTAG CTATATTGGA TTTCTTCCGT TTTTCCAGGG GAAATACAGC AACTTTGGAG 1140 AGACGTGAAC ATGGGAATAT ATGAATTGAT TGCTTGAGAA GTGTTAGTGT TAGTTCTGGA 1200 ATGAAGTCCT GTGTCATTAG GTGCTTACGT TGAAAGGAAA TGTAGAATTT TCCATAGTCG 1260 CAGCTTTCCA GATTTTAATT GGCTGCTTGC CCTCGTGTCA CTTTCTTTTC TAAAATAAAT 1320 GTTTTGGATG GCTCTTATCT TTACAACCAG GCACACAGCT TCATTTCCTC CTAACTAGGA 1380 AAGTTAACTC TTCAGCTACA TGGTGGTACA CAATGTTGTC CCTGCTCAGC AGCCCTTGAA 1440 CACTCATTAA ATCCCACATT AGAGCTGCAA GGAGATAGTA ACATTTATTA GGTGCCTCAT 1500 TTTTTTTTTT TTTCTCTGAG AGCGGATCTC GCTCTGTTGC CCAGGCTATA GTGCAGTGGT 1560 ACCATCAGGG CTCACTACAG CCTCAACCTC CCAGGCCCAA GTGGTCCTCC TGCCTCAGCC 1620 TCCTGAGTAG GTGGGACCAC AGGCACACTC AGATATTTTA AAAAATTTTT GTAGAGACTA 1680 TGTTGCCCGG GCTGCCATTG TTTATCCATT GATTTTTTAT TTTATTTACT TATTTTTCTT 1740 TTGTCTTTTT TGTTGCCTAG TTTCCCCCCT GTTCTTTGCT TCTTAATTTT GGTTGGTCAA 1800 AATCTTTCTT TTAACATTTT GTTTCCTCTT CAACCTTGGG AATTCTTCTG TTTCTATTCT 1860 TTCTTGCCTT TTCCTTGCTT CATTTCAGGA CTCCTTTCCA ATGAACCTGC CATTTTTTCC 1920 TGCAAAGATT GTAGTTTAAA AGAAAGCCCA CTGGCCTGAA ACTTTATGTA GCTAAGCAGC 1980 TATTTCAAAT TCTTTCTGAG GTTGAGGGCA ATAAATGATA AAATCACGCA GTCAGGCAGT 2040 GTGTTAGTTC TCTAAAGACA AGAGTTCAGA GTTCTGAGTT CTCCAAAGAC AAGAACTAGT 2100 ATATGAAGAG GTTTATTATA AGAAACTGGC TCACATGATT ACAGAGGCTG GCAACTCCAA 2160 AATCTGCTGA GTAGATGTCC TGGTTTGAGT CTGAAAGCTG GAAGCTGCTG TAGAACCCAG 2220 AAGAGCTGAT GTCCCAGTGC AAAGGCATCA GGCAGGAGAG TTCAGTCTTA CCAGGGTCAG 2280 TCTTTTATTC TATTCAGCCC TTCAACTGAT TGGGTGAGGC CCACCCACAT TATGTCTGCT 2340 TTACTCAAGA CAACTACTAA TTTAAATGTT AATTTCATGT AAAACACTGA TATGGCTGGG 2400 CTGTGACCCC ACCCAAATCT CATCTTGAAT TGTAGCTTCC ATAATTCCTT CGTGCTGTGG 2460 GAGGGACTCA GTGGGAGATA 2480
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