Tag | Content |
---|
EnhancerAtlas ID | HS136-16379 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr5:177738970-177741190 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr5:177741177-177741188 | AAATCACAGCC | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr5 | 177739679 | 177740143 | chr5 | 177739725 | 177739871 | chr5 | 177739258 | 177739529 |
| | Number: 1 | ID | Chromosome | Start | End |
GH05I178312 | chr5 | 177739024 | 177740600 |
| Enhancer Sequence | ATCCACCTGC CTCGGCCTCC CAAAGTGCTG GGATTACAGG TGTGGGCTAC CGCGCCCGGC 60 CTGCGTAACT GGTTCTTATG AGTCCCCAGG TGGGTGAAGC TGGAGACACA GTGACTGCAC 120 CTCAGCAACA CTGCAGGCAG GTTCGAGGTG CTGAGACGCC GACGGAGCCC TTGACTGCAC 180 TTTGAGCAAA GTGCAAGGGC AGCCCCGTGG GAAGCCGGGA GCTTTCCCGT GTCCCTAATC 240 ACTGCCTGTC TGTGAACCTC TGGATGAGAA TGCAGAGGCT GAGCTCTTTG GGAATGAGGT 300 TTCTCAATGA AATTTCAGGG TGCCAGGTCT AGCACAGGCC AGCCAGGGCT CCAGCTCGTT 360 GCCCAATGAC TCTGGACGTC TGAGAGCAGC ATCAGCACAG TAAACAACTC CAGGGAGGCC 420 TACGGCTTTC TCAGCACTGT TGGAGGCCAG ACAAAAGGAA ACCATTTCTA ACTCATAAAA 480 ATCTCATCTC TGGTTGGGGT GGAGAACTCA CGCCGCTGAT CAACTCCAAA GGGGGGCCTC 540 GAACCCCAAC AGGCTTCCTC TGAGGCCTGA GCTGCAAGGA TTTGGCTCTC TAAGTGGCTC 600 CCCCCGCCCA GCCCTCCCGG CACCTCCCTC CCCAAGGACG TCCCCTCTAG CAATGCCCGT 660 CTTATCAAGG TCCCTTCACA AACCTGCAGC CACCCCACCT CAGCCGCACT GGGGACAGCC 720 TGCCCAGGCC TCTCCCTCTC ACCCTACTGG CCTGGCTGCT TCCTGTGGGC TCCTGACTGG 780 TTGCTCCGCC CTCAGCCCAA CCCTGATCCT CCCTTCAGCC AGCCCCTGAG GACAGGGGGT 840 TCATGGAATC CACACAACAG TCTGTGAAGT GCTTTCATTT CTCTCTACTC TTTTCTTCCT 900 ATAGATCAGG GGAACTGAGC CCCACAGAAG TCAAGAATTA CTACCAGGCG CAACAGCCAA 960 AAGGTGGAAG CAACCCAAAC GTCCACGGAC AGAAGAATGA GCAAACAGAA CGTGCACTGA 1020 TACAGCGGGA CGTGAGTCAG CCCTGGAGAG GAAGGAGTTC CTGCGCACGC TGCAGCATGA 1080 TGGGCCTGGA GGACGTCACG CGATGGGAAG TAAGCCAGAC ACAGAAAGAC AAATACGGAA 1140 GGATTCCACT TCTGGAGGCT CCTGCAGTCG CCAGATTCAC AGGGGCAGAA GGTGGAATAG 1200 GGGGTGCCAT CGGTGGGCTG GGCTAGGGGA GGCGAGACTG GGAAGTCGGT GGGCCCAGAG 1260 ACTCCGTTTT GCAACATGAA GAGTTCTGGA GAGGGATGGT GGTGGTGACG GGTGCGTGAC 1320 AATGTGAACA TACTGAATGC CACTCAAGTG TACACTTAAG GATGGTTAAG ACGGGAAATG 1380 TTATGGTATG TGTATTTTAT CACAATTAAA GAAAACAAAA CAAACACCCC AGGGGTCTCA 1440 GCTACCCCTG AGCGAGGCTG TGAGCCGGGC CGTCCTGATG GAGACTGTGG GGATGCTGCT 1500 GGCAGCCACA GCAGTGTCCC GTGTGAGGAG CCCGGCACTG TGGAGTCACA GAGGATGGCA 1560 TCCCCAAGGT CACACAGTGG AGAAATGGCG GAACTGGAAC TGGAACCCGG GTCTGTGTGA 1620 CTTCGGAGTC TGTCCCCTGA ACATCTGTGT GTGATTTCCA GTGTGACCAT GGCCAAGATT 1680 TTCTCATCCC ACCACGTGTC GAGTGTCCCT TCAGACCTGG TCCTTCTCAA CACCACTGGA 1740 AGCCCCTTTA TATGACCCTC TTCCCAGAAC TTTGGGAGGA AGTGGGGTGA GATGGCCTGA 1800 ATCCTCCCAG ACCTTCAGTC TGGAGCTCTA TGAGATTGCT GGGGCTTCAG GGCCATCAGG 1860 GGGTGCACCT TGAGCAGAGA AGGCAAGCGA GGTCCCTGGA AAAGAGCTTC CGAGACCAGA 1920 TCATTAAAAC ATCTCCCCAG ACCATTTCAT TTGTTTTACA AGTCTCAGAC CAACCTCAGA 1980 GCTGAAAACT GCCCAACAAG GGAGCATTCT CTCTGCACAT TCCCAGCTTG GCCTCACAAA 2040 GCCCTCTGTC CCTTGGAGGA GTGAAGGAGT AGGTGTGTCC CGGTGGGTGT CTCTAAGGTG 2100 GGCCTGGGGA CCCTACTGCT CCTGGAGGGG ACACTGAGAC CCGGAGAGGC TGGCCAGCTT 2160 GCTCTGGTTC AGCCAGTGCT GCGGGCACTG TGGTCCTCCA GGAATTAAAA TCACAGCCTC 2220
|
| |
|
|
|