Tag | Content |
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EnhancerAtlas ID | HS182-19454 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr7:427590-429210 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT1 | MA0137.3 | chr7:428011-428022 | TTTCCCAGAAA | - | 6.02 | STAT3 | MA0144.2 | chr7:428011-428022 | TTTCCCAGAAA | - | 6.32 | Stat4 | MA0518.1 | chr7:428008-428022 | CTGTTTCCCAGAAA | - | 6.14 | ZNF263 | MA0528.1 | chr7:428480-428501 | GGAGGAGGTTGGGGAGAAGCA | + | 6 | ZNF263 | MA0528.1 | chr7:428477-428498 | GGAGGAGGAGGTTGGGGAGAA | + | 7.74 | ZNF263 | MA0528.1 | chr7:428474-428495 | GGAGGAGGAGGAGGTTGGGGA | + | 8.47 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGGCTCCGT CCAGAATTCT GCCCAAGTTT TCCTCCGTTT CCCTGGTCCT GAGCCCTGGG 60 GAAAGTTGTG TCATTTTTCC TGTATTTCTT AATGCAATTT CGGCTCCTGG TGAAATTGTT 120 GCGGCTGTGC TGGACCCGGA CGTCCCTCCT GACAGCTCCG AGCCGTGGAT GGGGACAGAT 180 GGCTGAACTG CTGGGAACCT AGGCTGGGAG GCAGCCCCCT ACCTTCAAGG GCACCCCTGG 240 TTTGGGGTAG ACAGACAGTC GGCTCAGCTC CCAGCAGGGA CCGGCCACTT GTGGGAACAT 300 GGAAGACCCA GGGTGGCCAC ATCAGAGGGC TGCGGCGGTC TCTTGGCCTC ACCCTGACCT 360 GGGCTGGCCG TTCACTTCCA AAACACCCTG GCTGGGTTTG AATGGTACGT GGGATGTTCT 420 GTTTCCCAGA AACCAGCAAG ATGTGAAGCA AGATGGCAGA ATGTCAAGGT TTGGCCGAGC 480 TGCAGGGTGG GTGGAGGGGC CTCCACCATG TTCATCCTAG GTATGCGGGA TCCTCTCATT 540 CACCACATGT GGGGCCTCCT GGTTCCAGCT GCCCTGAAAT GGCCTCTCCA GCCACCGACT 600 TCCTTTCCTG TGTGTCTGGA CGCCCTGGGC AGGGAGCCGT TGCTAAACGT CCCTCGGCCT 660 CCAGATCTGA GCCTGTTGTG GAGATGGAGA TTCCGGGAGG AAGAGGGAAG GCTCATCCCC 720 TCCCCGTCCA CCTTCCTGCA AAGGAAGATT GGCTGGCAAC AGGGTAAGGG AAAGAAAGCG 780 GAGAGGGGCA GATTGGACCC ACATAACGAG GACCGAGAAG GGGACAGAGC TGGCTCTGGC 840 CACTGGGAGT GGAGGGGCAG GGCCCCGGCT CAACGCCCCG TGCGGGAGGA GGAGGAGGTT 900 GGGGAGAAGC ATCACCGGCC GCTGCTCTTC GCGGGAGAAG TGAGGGGATC CAGCTCACGA 960 GGCAGTTGCT GGCGTTTGGG CTGTGAGCTC TGACCAGGCC CCATCCTGAG GCTGGACGAC 1020 AGGGATACAG GAATCCCCAG GAACCCATGA ACCTCAGCGC ACGGCCCACA GAACACCACG 1080 TACTCCTCAG CGCCAGGCCT GCAGCCACAG GGAATCGCAG CAGCCCAGCC TATGCAGAGG 1140 CCATAGCAGG GCTGCCCCAT CCTGCCCCAT CGACCTTGCA GGCAGATGCC CCGCCTCCCT 1200 GTGAAGTGCT CTCCACCGCT CACTCCAGCC GGCTCCCGGG CAGGGAGCCA GGAGGGAGCC 1260 GGACACGGAG CGGCCCCGCT CTTCCACCCC CGGCCTGGCC TCTCAAATCC TGGCCTTTGG 1320 CTTCAGGACA GCGATGCTGC ATCCACATCA CCCAGAAGGT GAGGGCTGTG TCCGCCCAGG 1380 GAGCCGGGAT CAGCTGCTGG GTCTGGAGAT CTGAGAGGAA ACGGAAATGG CCCCTTCCAA 1440 AACGCACCAC GAGGGTAGAG CCTCCAGGCC TCTGGCATTG CCCTCGTCCG CACACCCCGT 1500 TTTCAAAGTA ATCACCCCAG AGAGCAAGGC TGCAGCTGCC GCCCGGGCGA GGGTCCACTC 1560 TGGATTTCCA GTCAGAACAG GAGCCACTGC GGTAGCTGCT CTTTCGATCC CCCAGCCTGG 1620
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