Tag | Content |
---|
EnhancerAtlas ID | HS161-10790 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr22:43548230-43550230 |
Target genes | |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:43548994-43549012 | GCTTGCTTTCTTCCTTTC | - | 6.21 | EWSR1-FLI1 | MA0149.1 | chr22:43549135-43549153 | TTCCCCTTCCTTCCTTCC | - | 6.42 | EWSR1-FLI1 | MA0149.1 | chr22:43549143-43549161 | CCTTCCTTCCTTTCTTGT | - | 6.64 | EWSR1-FLI1 | MA0149.1 | chr22:43549002-43549020 | TCTTCCTTTCTTCCGTCC | - | 6.8 | EWSR1-FLI1 | MA0149.1 | chr22:43549081-43549099 | CTTTCTTTCTTTCCTTCC | - | 6.95 | EWSR1-FLI1 | MA0149.1 | chr22:43549022-43549040 | CCTTCCTCCCTCCCTCCC | - | 7.28 | EWSR1-FLI1 | MA0149.1 | chr22:43548998-43549016 | GCTTTCTTCCTTTCTTCC | - | 7.2 | EWSR1-FLI1 | MA0149.1 | chr22:43549006-43549024 | CCTTTCTTCCGTCCTTCC | - | 7.8 | EWSR1-FLI1 | MA0149.1 | chr22:43549014-43549032 | CCGTCCTTCCTTCCTCCC | - | 7.91 | EWSR1-FLI1 | MA0149.1 | chr22:43549097-43549115 | CCTTCCTTCTTTCCTTTC | - | 7.97 | EWSR1-FLI1 | MA0149.1 | chr22:43549010-43549028 | TCTTCCGTCCTTCCTTCC | - | 8.2 | EWSR1-FLI1 | MA0149.1 | chr22:43549018-43549036 | CCTTCCTTCCTCCCTCCC | - | 8.32 | EWSR1-FLI1 | MA0149.1 | chr22:43549085-43549103 | CTTTCTTTCCTTCCTTCC | - | 8.46 | EWSR1-FLI1 | MA0149.1 | chr22:43549089-43549107 | CTTTCCTTCCTTCCTTCT | - | 8.46 | EWSR1-FLI1 | MA0149.1 | chr22:43549093-43549111 | CCTTCCTTCCTTCTTTCC | - | 9.47 | EWSR1-FLI1 | MA0149.1 | chr22:43549139-43549157 | CCTTCCTTCCTTCCTTTC | - | 9.6 | Foxd3 | MA0041.1 | chr22:43549165-43549177 | GTTTGTTTGTTT | + | 6.32 | IRF1 | MA0050.2 | chr22:43549053-43549074 | CCCTTCTTTCTCTTTCTTCTT | + | 6.22 | IRF1 | MA0050.2 | chr22:43549111-43549132 | TTTCTCTTTCTCTTTTTTTCT | + | 6.3 | IRF1 | MA0050.2 | chr22:43549066-43549087 | TTCTTCTTTCTCTTTCTTTCT | + | 6.77 | IRF1 | MA0050.2 | chr22:43549105-43549126 | CTTTCCTTTCTCTTTCTCTTT | + | 7.67 | ZNF263 | MA0528.1 | chr22:43549081-43549102 | CTTTCTTTCTTTCCTTCCTTC | - | 6.02 | ZNF263 | MA0528.1 | chr22:43549127-43549148 | TTTCTTTCTTCCCCTTCCTTC | - | 6.02 | ZNF263 | MA0528.1 | chr22:43549085-43549106 | CTTTCTTTCCTTCCTTCCTTC | - | 6.03 | ZNF263 | MA0528.1 | chr22:43549002-43549023 | TCTTCCTTTCTTCCGTCCTTC | - | 6.32 | ZNF263 | MA0528.1 | chr22:43549010-43549031 | TCTTCCGTCCTTCCTTCCTCC | - | 6.37 | ZNF263 | MA0528.1 | chr22:43549017-43549038 | TCCTTCCTTCCTCCCTCCCTC | - | 6.86 | ZNF263 | MA0528.1 | chr22:43549021-43549042 | TCCTTCCTCCCTCCCTCCCCT | - | 6.9 | ZNF263 | MA0528.1 | chr22:43549026-43549047 | CCTCCCTCCCTCCCCTCCCCT | - | 7.32 | Zfx | MA0146.2 | chr22:43549600-43549614 | CCCGCCTCGGCCTC | + | 6.01 |
|
| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23668 | chr22:43546568-43549082 | Colon_Crypt_1 | SE_24969 | chr22:43546648-43549190 | Colon_Crypt_3 | SE_26727 | chr22:43546429-43549260 | Esophagus | SE_26727 | chr22:43549901-43550487 | Esophagus | SE_54378 | chr22:43546505-43549380 | Spleen |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr22 | 43549179 | 43549267 | chr22 | 43549976 | 43550230 | chr22 | 43549677 | 43549746 |
|
Enhancer Sequence | GAGAAGCGGG GGCTTCCTGC TGTGAACGCG CTGCTGGCCA GGGCAGCTGC CAGAGGCCAT 60 GGCCTGGCGT GGGCCTGGAG CCCCTCTGGC CAGCCTGCCA GGGGCCAGGG CTACGGGATA 120 CCAGCAGCGT GCCCTGGGCT GGATGGCAGG AGAGACAGGA CTTGAGGCTG TCCCAGAATG 180 GGCTCAGGCA GGGCGAGGAT ATCAGGGGAG GTGGTGTACA GGAAGCAGCC GCCCAGCTTG 240 CCTGGCACAC AGCAAGCCCT GCCCATGAAG GCCTACTGCC AGAACAGTGG GCGAGGCCCG 300 GCGTCTCTGT GGAGTCGGTG GGGCCCGGGA CAGGGCAGCC TGAGGCAGGT TTCCACTGGC 360 GGTGAAAGGG GCCGTGTGGC AAGGACAGGA GAGCCAGCCT CAGCCCAGCA GGGGAAGGCG 420 GCCCCTGAGT CTCCACCTGG CTGCTGGCAG CCCCACAGGG AGGTTCGGCG AAACTGAGGC 480 TTGCCAAAGA AGCCTTTGTC CAGAGTCACG CAGCTGGCGC GGTGGAGCCA GGGCCAGAAC 540 CCGTGCAGGC TGATCCCAGC CTGCCTTCTC CACTGTGCCC CGAGGACCAC TTTCTTTCCT 600 GGGAGTGTGT GTGTGCACAT GTGCTGTGTC CTGTCGTCTG TACACACTTG TGCCTGGCGT 660 GAGGCAGGAT GTCTGGCTGG ATCTACCAGA AAGTATTCAC AGCGGGTTCT CCAGCTGGGG 720 TGAGGGGCTT GGGCTCGCAG GGAGGGAGCC TACTTTTCAC TTTAGCTTGC TTTCTTCCTT 780 TCTTCCGTCC TTCCTTCCTC CCTCCCTCCC CTCCCCTTCC CACCCCTTCT TTCTCTTTCT 840 TCTTTCTCTT TCTTTCTTTC TTTCCTTCCT TCCTTCTTTC CTTTCTCTTT CTCTTTTTTT 900 CTTTCTTCCC CTTCCTTCCT TCCTTTCTTG TTTTTGTTTG TTTGTTTGAG ACAGGGTCTC 960 ACTCTGGTAT GCAGGCTGGA GTGCAGTGAT GCAATCATAG CTCACTGCAG TCTCCTGCAG 1020 AACTCCTGGG CTCAAGCGAT CCTCCCACCT CAGCCTCCCA AAGTGCTGGG ATTACAGGCA 1080 TGAGCCACTG TTCCTGGCTT ATTTGTGTTT TCTTTTTTTT TTTTTTTTTT TTTTTTTTGA 1140 GACGGAGTCT CGCTCTGTCG CCCAGGCCGG ACTGCGGACT GCAGTGGCGC AATCTCGGCT 1200 CACTGCAAGC TCCGCTTCCC GGGTTCACGC CATTCTCCTG CCTCAGCCTC CCGAGTAGCT 1260 GGGACTACAG GCGCCTGCCA CCGCGCCCGG CTAATTTTTT GTATTTTTAG TAGAGACGGG 1320 GTTTCACCTT GTTAGCCAGG ATGGTCTCGA TCTCCTGACC TCATGATCCA CCCGCCTCGG 1380 CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACCGCGC CCGGCTTATT TGTGTTTTCT 1440 TTACTTTTGA TGGTGCAAAC AATGCTTGGA TGTGCTCTCT GTTTAAAACG GTAGTCTTTT 1500 TTATTTTTTT TTTTAACCAC TAGACCACTA GGGAAGTCAT TCTTAATTTC TTATTTTTAT 1560 TTATATATAT ATTTTTTGAG ACGGTGTCTC GCTCCATTGC CCAGGCTGGA GTGCAGTGGC 1620 TCCAGCTGGG CTCACTGCAA CCTCCGCCTC CAGAGTTGAA GTGATTCTCC TGCCTCAGCC 1680 TGGCTAATTT TTATATTTTT AGTAGAGATG GGTTTCACCA TGTCGGCCAG GCTGTTTCTT 1740 TATTTTTTAC TAAAAAAAAG TTTAACCCCC GAACCTCGAA GGAAAGGGAA GTAGTCTTTC 1800 TTAACAGAAC CAATTCCCCC TGGATACCCC ACCCTCACCC TACCCTCTCC CAGGCCACTC 1860 GATGGCCAGG TTCGCTGTGG ATTTTTCCAG ACCTGTGGGC TGTTTCACTG GTTACTTTTG 1920 TAATGAAAAA TGCACACAAA GGTTACGATG AGGACGATTA GCCATGAATC ATTTTTAAAA 1980 AGCCTGAAAA CAAGTCCCTG 2000
|