Tag | Content |
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EnhancerAtlas ID | HS182-19526 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:2529320-2530500 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6 | MA0677.1 | chr7:2530086-2530100 | AAGGTCACAGGTCA | + | 6.47 | RREB1 | MA0073.1 | chr7:2529755-2529775 | CCCCCACCCACCCGCTATCC | + | 6.61 | Rxra | MA0512.2 | chr7:2530086-2530100 | AAGGTCACAGGTCA | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 2529641 | 2530385 | chr7 | 2530409 | 2530497 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I002489 | chr7 | 2529134 | 2530412 |
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Enhancer Sequence | AACCCTGGAG GGAGAGGCTG CAGTGAGCCG AGATTGTGCC ACCGCACTCC AGGCTGGGTG 60 ACAGAGTGAG ACTATCTCAA AAAGAAAAAG GAAAGAAAGA AAGGTGGGCT TGTGCGCCAG 120 GCTGGGAGCC AGGCAGAGGG TTCTGGGCGC TGACTGCCCA AGGAAAATGG TGTGAGAGGT 180 GCTGGCACAA GGCCTGGGAG GGGATGCTTG GATTTAGCAA CGAGAGGTCC TCAGAGGGCA 240 TGGAGTGAGT GGGCAGTGAG GAAACGGGGA CCCTTCCTCC CCCTTTCACC CCCCTTTCCT 300 GTCTCCCTCG GTCTCCACCC TCTCCACCCA CCATCCCAGG ACCCTGCGCT CTGGGGGCAG 360 AGCAGACACA AAGAGGGGCT CAGGGGCTGG AGTCTGGCTG CCACTCACCC TGGCCCCCAG 420 GGCCACCAGG GGCCACCCCC ACCCACCCGC TATCCCCGCT CCAACTGCTG CTCCCACTTC 480 CCTCGGCCGG GACGGGACAC AAGAGTCTTT CAAAAACATT TCCTTTGCAA AATAATCCTT 540 CCAAAAATGT TTTTGGAAAC GGACTCCTGA TCTGAACAGG AAGACGTTAA TTATGGTCCC 600 TCCCCAGAGG GGCAGGGGGA GGAAGCCTGG TGGTCGAAAC AGGAGCGGGG GCCAGGACAG 660 CCCCAGCCCA CACCCAGCCT CAGCCTCCTG CCCCCCAGGC CCCTGGGCCC AGCCCCTCCA 720 CCCACAATGG GGAGACAGAG ACTTAGGGAG GGCCAGCGAC ATGGCCAAGG TCACAGGTCA 780 GAAGCTGAGC AGGGTGGAGT CTTCTACTTC TGCTGCCACG TGGCATCCGT GCGAGAGCGT 840 GGCGAGGCGT TGTGCATTCG TGTGTCTCTG TGCCTTTGTG TGCAGGAGTG AAGGTGGGGC 900 GGGGGCAGGC AAGGAAGCTC CCAGGGTCCA CAGCCTCCCC AGGCCTGACT TCCTCCCCCA 960 GCAGGCCACT TTCCCCTGGT GCCCAGGTGT TGGCCGGACT CCGACTACAG CAAGGAGGAA 1020 GGAGACAGGG CTGAGGACCT CCCTTTCTGC TGCTGCTCTT AAGCGCCAAC CACCCTCCAA 1080 ACAAGTGCCA TCTGGGATCC CCCTGGGCCT AGATGAGGTC CCACCATAGA CGTTTTCTGA 1140 ATGTACCTAT GTCCATCTCA GTCAGCCCTG ATGCTTATGT 1180
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