Tag | Content |
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EnhancerAtlas ID | HS182-01624 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:180983460-180984920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr1:180983868-180983879 | TTTTATTGCTT | - | 6.32 | ZNF263 | MA0528.1 | chr1:180984228-180984249 | TCTCCTTCCTCTTCCTCCACT | - | 7.12 | ZNF263 | MA0528.1 | chr1:180984225-180984246 | TTTTCTCCTTCCTCTTCCTCC | - | 7.24 |
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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 |
GH01I181014 | chr1 | 180983137 | 180985335 |
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Enhancer Sequence | CGAAGGTTGC AGTAAGCCGA GATTGCACCA CTGCACTCCA GCTTGGGAGA CAGAGCAAGA 60 CTCCATCTCA AAAAAAAAAA AGAAAAAAAA AGAAAGAAAA GCAACACAGG ACAGAACATT 120 TATTGGTGCA GCCATCAATG GAAAAAATAC AATCTGCCAC AACTCTTTTA TCTGGGACAG 180 CACCTACTCT GCAAGTCTTT ACAGAGGGAT CCCCATTTCA TCAATACAGT AAAAGAGGCT 240 AGTCAAGGCT GAAAGTTTCC ATTCTAGTAA TGAAACATGA AAAATTCAGG TTGAGTGAGC 300 CTCTGCAACA CATCAGACTC CCACTCCTCA CTCTTCTCCA ACTGGTTCCT GCCCCATACC 360 CCACAAACCT GGTTTCACCA CTCATCTCTC CAGAAAGAGA GGAACTCTTT TTATTGCTTG 420 ACTTCTACAT TCACATCGTT TGTATTTGAA AGGAAACACA TGCACACCCT TTACTTGACT 480 TTATTGCCAT TTCCAAATTC AACCACACTG TGACATATTT TGTAATTACT CTTGTGAAAA 540 TGAAACATCA TTTTTACTCA GTTACCTACA ATTATATACA ATTTTTGACC CTAACTTACT 600 GCTGCTTCCA CAACTCCACC AATGACACTG CAGGTCAAAG TCACGAGTGA ATTTAACTTG 660 TCCTCATTTT TGGTGCACTT GACACTATGG CCCATTATAT CTATTTGCTT GAAACTCTCA 720 CTTTCTCTGT CTCTGTGACA TTGTGCTGTT CTAGTTTTCT ACCAGTTTTC TCCTTCCTCT 780 TCCTCCACTG GATCCCAATG TTTCTCAGTA CTCTTTGTGG CCTCTATGTG CTCATCAGCA 840 TTCACAAGTT CAAAGCACCC CTCTTAAGCT GATGACTCCC CCACTATACT TCCAACCCTA 900 ACCACTCAGC CAGGCTTAAT TCCTATATTT TTAGCTGCCT ATAGGATCAT TCCATTTGCC 960 TAAAACCAAA TTAATCATAT CCTCCCTACA AAACATAATG TATTCAAAAC AAACAAAATA 1020 GAAAAATCTG CTTCCCTTTC TAGCTTCCTC ATTTTAGCCA ATAGTGCCAC CATTTTCCAA 1080 GTTTCAACAC TTGTCTAGAC AAGAGTCATT TTTGACTCCT CCTCCTCCTT ACCTTGCACA 1140 ACCTCTACTT AAATCCAATC ACTGAATTTT CAGATCTGGA AAGAACTTTC AAGATAATCT 1200 AGTTTGTGCT CCTTAAACAT AAATAAGAGA CCTTGGGGCT CAGACATATT GGCTGCTTGC 1260 CTCAAGTTCT TCCAACCCTG ATTATAAGAC ACTTTCTATT ACCAAGACTT ATTTAATTGC 1320 ATTTTTCCAA AACTTCCACA CAAATCTTTT TTTTTTTTTT TGAGAGGGAG TTTTGCACTG 1380 TCACCAGGGC TGGAGTGCAG TGGCGTGATC TCAGCTCACT GCAAAAGAGG GTTCAAGCAA 1440 TTCTCCTGCC TCAGCCTCCC 1460
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