Tag | Content |
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EnhancerAtlas ID | HS018-13567 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr2:225306450-225307910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr2:225307302-225307314 | CACCCCCTGACA | - | 6.22 | NFKB1 | MA0105.4 | chr2:225307158-225307171 | GGGGGAATCCCCG | - | 6.36 | NFKB1 | MA0105.4 | chr2:225307158-225307171 | GGGGGAATCCCCG | + | 6.46 | ZNF263 | MA0528.1 | chr2:225307477-225307498 | GGAGGAGGGGAGCGCGAAGGA | + | 6.23 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 225306713 | 225307810 | chr2 | 225307433 | 225307612 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I224442 | chr2 | 225306718 | 225307917 |
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Enhancer Sequence | GAGTTCAAGA CCAGCCTGAC CAACATAGTG AAACCCCCCG TCCCTACTAA AAAAAGTACA 60 AAAAATTAGC CAGGCCTAGT GGTGCGTGCC TGTAATCCCA GATACTCGGG AGGCTGAGGC 120 AGGAGAATCG CTTAAGCCCA GGAGGCTGAG GTTGCAGTGA GCCGAGATCG CGCCACTGCA 180 CCCCAGCCTG GGCGACAGGG CGATACTCGT AAAAAGGAAA GAAAGAAAGA GAGAGAGAAA 240 AAAAAAAAGA AAAAATATAG TTTCCATGAC TTTTTGTTTG TGTAGGATGC AAAGTGACTG 300 CTGTGTGCTG TGAAAGATGG GACAAACGGC TTTGAGCTCA AGGGACATGG ATTTGGGAGG 360 AATTCAAAAT GTGAAGCCTA ACTCAGGATT CAGGAACCAG ACTAACAGAG GGCAATGAAA 420 CAAAACCAGA GAACTCAGGC CCAGAGCCAG CGAGGGAGAG GAAGGACGCC GAAGCGTAGC 480 GTCCCGCGCC GCCCCCCGCC AACCCGGGAG GACGCAGACC CCCCAGAGCC GGTGTCCAGC 540 CCCACCTCTC CGGGCGCCTG CAGGAGGGGA ACCGCGCGTC CCATCGCCCG GACCCCGGGC 600 CGGCGGCGCG GCCGAGTCCC GCTGCTTCCG CACTCGCCCC GGGACCCGGA CCCCCGCCCC 660 ACCGCGCCCC TCCACCTCCC CGCCGGCCGG TGCCACGTGT AACGCCGCGG GGGAATCCCC 720 GGGGACACAG GGCTGGCTGG ATTCGCCTCT CGGCCACAGC TCTGCGCTCC ACGAGCTGCT 780 CCTGCCCGGT CCCCGCAGGA CTCGAACCCG CGACACCTCT GCCGCGCCCT AGCCCTCGCG 840 CCCCGCCGGA GTCACCCCCT GACACTGCCA GGATCCCCGC CCGGCTGCGG GCACCACGTC 900 CCCCGGGCCT TCGCGGGGCC CCGAGGGCCA AGACCGAGGA CGCGCCGAGC CGAGGCTGCC 960 TGGGGACCTG GTCCATCCGG TTCTGATGGG GTCCGCAGGG AAAAGGCACT ATCCCGGAAA 1020 GCTTCCTGGA GGAGGGGAGC GCGAAGGACG AAACTGGGCC TCCCTCTAGG CGGAGCTTAG 1080 TGTTTAAAGC TGGCCGGCCT TTCTCCTTTT CATAGTAATT ATTCTCTCAC TAAGCTCAGG 1140 AAGCACGCCC TCCACCATCT CATTAAGCGA ACCGGCTGTG GCTGACTCTT CCCTCCTCTA 1200 ACAACTGTGG CTCCTCATAG CCGGCACAAT GACGTCCAAA GCTGTCGGCT CCCGCACGGG 1260 TTCCTCCCTT TGAGGCTTGT CTTTCGCACT CCTTCCACCT GCTCGGAGAA CTGCGCCCAG 1320 GTGGGTTCAG CAACTAGCAG GTGCCATGAA GAGACCCTCA GAGAAGCGGC CGGCCTACCT 1380 GGCGCCCGTT ACCCCTCTCG CCGCAAACCC ACTTCCCTGA ACTGTTTTGC AGTTCACAGC 1440 CTCTCTCCCC GCTCTAAAAA 1460
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