Tag | Content |
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EnhancerAtlas ID | HS019-12771 | Organism | Homo sapiens | Tissue/cell | CD20+ | Coordinate | chr5:42908230-42909370 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr5:42908664-42908675 | CCACACCCTGC | + | 6.62 | NRF1 | MA0506.1 | chr5:42909111-42909122 | GCGCATGCGCA | + | 6.32 | NRF1 | MA0506.1 | chr5:42909110-42909121 | TGCGCATGCGC | - | 6.32 | RREB1 | MA0073.1 | chr5:42909016-42909036 | GGTGTGGGGATGGTTTCGGG | - | 6.25 | SPI1 | MA0080.4 | chr5:42908347-42908361 | TGCTTCCTCTTTTT | - | 6.41 | SPIC | MA0687.1 | chr5:42908347-42908361 | TGCTTCCTCTTTTT | - | 6.59 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTAAGATACG GTTTTAAAAT AACAGATTGC AAGGTTGGAG ACACCTGGGG TACTTGATGT 60 CTTCCAACAT CCATTATCAT TTCTCTGTAA ATGATGCTGC TACTATCCGA GTTCTTATGC 120 TTCCTCTTTT TGAAGCCAGC AATTTCTCAA TCTTAACATG TAGTTTAAGT ATTACCCATT 180 CCAGTGCTTC TCAGCCTTTA TTAGCATTTG AAGATATTGT ACTTGTCTTC AGTTCTTCAA 240 GGTAACTGCT GAGGCTGATT CTTTTCACAA TGATTGTGGT TTCTTGAGTC AAAATAGTTT 300 TTTTTCTGGG TCCTGAAGAC TATGTTTTGG CTCTTGCTGC AACAGTAAGG GACTTGCAGT 360 TCCCACTCTG TGCAGAGAAG TCTGTGGCCT TGCAACTTTC CAGAGGGATC TATATATCCT 420 TCCAACACAT CAACCCACAC CCTGCTCAGG TTCGCAGGGC TTGGGTATTT GTGCATTGCA 480 GCTGTTGTAA CAGTTTCCCA CGGGTGGTGA AAGACGTGCT CTGCAGTCCA GATCTTGATG 540 GTGCAGGCAG TCTGCTAGAT GTCTGTGAAG CGCAGGGGAA AATGAGGTGA GGAGGCTACA 600 CCTGTCCCAC CCCGTCGGGG GCCCTTCAAC CAGCTTCGCT GTGCGCAGGT GCCGTCGGCT 660 CCAAGTGAGG CGGTCCTCCA CTCTTCGTTA CAATGTAACA TTTAAACCAT TTAAAGCAGA 720 GATCCGCAAC GTTTTTGGCA CCAGGGACCA GTTTAGTGGA ATACAATTTT TCTACGGATG 780 GAGAGGGGTG TGGGGATGGT TTCGGGATGA AGGTGTTAGA AATCAAATAA TCAGGCACGC 840 AATAGATTCT CAAAAGGAGA GCAAAAGCTA GTCTTGGTCC TGCGCATGCG CAGTTCACAA 900 TAGGGTTCGC ACTCCTGTGA GAATTTAATG CAGCAGATCT GACGCTAGGC GGAGCTCAGC 960 CAGTAATGCT CGCTTGCCCA CTGCTCAGCT CCTGCTTTGG GGCCGGGTTC CTAACCGGTC 1020 CGTGGTGGGG GGGATTGGGG ACCCCTGATT TAAAGAACAG TGCTAATGCC TGTTTTCTGC 1080 CTTTATTTGG AGGGCCACAG TCAGTTTCAA AGCAACTCCA GCATATGATC CACCCAGCTG 1140
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