Tag | Content |
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EnhancerAtlas ID | HS182-14499 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr21:42768340-42769530 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DBP | MA0639.1 | chr21:42768543-42768555 | GATTACGTAACA | + | 6.92 | EWSR1-FLI1 | MA0149.1 | chr21:42769335-42769353 | GAAAGGGAGGAGGGAAGG | + | 6.96 | EWSR1-FLI1 | MA0149.1 | chr21:42769339-42769357 | GGGAGGAGGGAAGGAAGC | + | 7.51 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr21 | 42768451 | 42769062 | chr21 | 42768428 | 42768800 | chr21 | 42768800 | 42769119 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I041396 | chr21 | 42768062 | 42769793 |
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Enhancer Sequence | CTGGAACTTG TTGTTCCTGA ATGATCCAGG AGCACAGAGG TCACTCCTGC TTGAAGGAGA 60 GCTAATGGGA AAACTGAATT TGGGCCGAGT AGGTCTACGG CTTGCTGACT ATGTGATCTT 120 ACAATATGGG CCACCTTCTC GGAATTTTGC CTTTCCCATC TTCTCCAGGG GATCCTACTA 180 CTGCCTCACA AGATTGTGGT TAGGATTACG TAACACGACA TACACAAAGG TCTTGAGCGC 240 CAACAGCCAG CACTCAGTAA ACACCACCCG GTTCCTTCTT TCTTCCTCTC TGCTCCTGCT 300 CTGAGTGGAT GAAACATACT GTTTCCAATA GCACTGGAGG ACATGAGGAG AAGAAAACTC 360 TCCTCCTTGA GCTGGGAGAA GATTTCAAAA TAATCAGGCC CATGGTTCTC CATGCTGAGT 420 GAGCAGCAGA CTCTCTGGAG AGTTCCTTAA AATTGTGCTA GCTCTGTCCT GCTCTGCCCT 480 GAGGCCGGGG GAGGTGCCCA AGACTTCCTG CTTCTAACAG GTTCCTCCTG GTTGAGGCTA 540 ATGTTGCCAG TCCAGGGACC TCCCTTTGCA AACCGCTTCT CAAGGTCTTT GGGAAATCTG 600 AAATCCTTGC ATGCCTGCTT GCTGGGAGCC GTCCCTTGCA GTAAGAGGCA CTGGCAGTGC 660 TGGGGAATAA TCCTGTGTGC TTCATCCTAA ATTCCTGCTA TTGGCAAACA TGCTGCAGCC 720 ACGCTGCCTG CTGTGTGGCT GCAGCAAGCA AATGCAGCAA GCTGCTTAAC CTTTCTGTGT 780 CTCAGCCTTT CTTGCTCTAA AGTGGGTTGT TAAATGACTA AATGTGTTAA TATTTATAAA 840 GCCCTTAGAT TGGTGCCTGG CACTTAGTAA GCACCATATA TACTTTTGTG ATGAGAAATA 900 AAATACTAAT CTGGGCAACT CACTTAATCT CCATGAGGCT GGGTTTGTTT TCCTGTAGCT 960 AAGATGACCT ACCTCATGAG TTTGTGGGGA TGATAGAAAG GGAGGAGGGA AGGAAGCTTC 1020 CTGGCCCACA GTTGCCTGGG TGCAGGCTGG TGGCAAGTGT CTTTCTTATG CACCACTTGG 1080 CTTTTCTGAT GGCACGTGTT GCCCCGGGGA GCTGGGCTCA CCTACCACGC ACAAAGTCCG 1140 GTACTAGCAA GATGGTACAC AAGTCCTTCC TGAATGCATG AATGTCTGTC 1190
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