Tag | Content |
---|
EnhancerAtlas ID | HS060-12814 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr16:29655410-29657820 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr16:29655451-29655461 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr16:29655451-29655461 | GGCACGTGCC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH16I029644 | chr16 | 29655562 | 29657567 |
| Enhancer Sequence | CCCCGTCTCT ACTAAAAATA CAAAAATTAG CTGGGCATGG TGGCACGTGC CTGTAGTCTC 60 AGCTACTTGG GAGGCTGAAG CAGGAGAATT GCTTGAACCA GGGAGGCAGA GGTTGCAGTG 120 AGCCAAGATC GTGCCACTAC CCTCCAGCCT GGTGACAGAG CAAGACTCTG TATCAAAAAA 180 AAAAAAAAAA AAAAAAAAAA AAGCTGGGCA TGATGGCACA CACCTGTGGT CCCAGCCACT 240 CAGGAGGCTA AGGTGGGAGG GTCGCTTCAG CCCAGAAGTT GGAGGCCGCA GTGAGCCATA 300 ATTGCACCAG TGTACTCCAG TCTGGGCCAC AGAATAAAAC TCTGTCTCTA GAAAACAGAA 360 CAAAACAAAG TTGAAGCTCT CTAAACTCTC CACACTGACT CAGAGTGAAA GTGCTAATAA 420 TGACCTAAAG CCGTGCCCTA TGGCCCCCTT TCCTCTTGAC TTCGCTTTTC ATGCACTCTG 480 CTCCAGCCAT ACTGGCCTCC TTGGGCTTCC CAGAACACGC GAAGCAGGAC CCAGGTTAGG 540 GCCTTTGAAC TGGCTTTGTT TGTCCGTGGG ATTCCCCATG AACATCTCAT GGCTGCTCCC 600 TCTCTTCCCT CAAGTCTCCC CTCAGATGTC CCCTTCTCAG AGACATCAGC CTGTAGAAAG 660 GAGCACTTCC TTCCCCCACT TTCCTGCGTG ATGTTTCTCC ATGATGCCTG CTTCCTACAT 720 ATGTAGAGTC TGTCTCACTC CGGAGAAGGC TACCTCCAAG AGGACAGGTG ACTGGCCCTT 780 GATTTCATTA ATTGTCACAA TCCTATGCCG GACACATGGT TGGTGTTCAA CAAATATTTG 840 CGGAATTAAA GAACAAATTA ATAATGTTGT GAGATAAATA CTCTGTGCCC ATTTTTCTTT 900 ACTTTTTAAT ATATTTTTTA AATCTAGAGA GACAGGGTCT CCCTATGGTC CCCAGGATGG 960 CCTCAAAACT CCTCCTGCCT TGGCCTCCTT GGCTGGGATT ACTGGACTAC TACTGTGCCA 1020 CCATGCCTGG CTCTTCTTTT CCTTTTACTA TGCCCATTTT AAAGGTGAGG AAAACTGAGA 1080 CTCAGAAATG TTCCCAAGGG CACACAGTGA GTGGTGGCTG CCTTCAGGTT GGTCTGACTC 1140 CAGTGCCCAA GCCTTTCTCA GGAGTGGTGT GTTGCCCATC AGCCATTATA TCCATGACAT 1200 CAACTGGCAT AAGATATGTT CTTATATGAA AATTAATTTT AGAAGTGAGT GTCACGAAAT 1260 ATTGACCTTC TCTAAGGAAC TAGTTCTTAT AGTCAAAAAG GAGGAACTTA TGTAAATTTT 1320 CCCTTTCAGG GCCAGCCCCA GGAAGTTCAG AGCCTAATGT GGTGTTCATT CTATTAATTT 1380 TTTCTTACCC TGGGACTTTT TTCTTTCTTT CATTTATGTT AACCTAATCA CCAGCTGCTT 1440 CCTGTTCCTT AGGAAATAGC TAAGTCGTAC ATGACACTTT TGGGGTTCCA GTGTGCCCGG 1500 CATGGGTTTT CTTTCATTGG GCAGGCACTA GGTGGGCTTT TCAGCCTGAA GACGCATGTT 1560 TCTCATCAGA GTGAGAATGA TCTCTGATCA TTCTCCTTCT TCCATTTCTT GGGTTCTCTC 1620 TTCCTGGCAC TCCTATTGGT TAGCTTTTGG GCCTCTTGGA TTGCCTGGCT GTGTCTCTGT 1680 GGCAAAGACT ACTCATTATC CAAAATCCAA TGAGCCCTTC TTCCCCAAGA ACATGGTGGA 1740 ACTGCATGTC CCAGCCTCCC TTGCAGTAGG CATGGTCATG TGACTAAGTT TCCACCAATA 1800 GAATGTGAGG AGGTGATGTA TGTGACTTCT GGTCTTTGGC CTTAGGAAGT AGGCCAGCTT 1860 CATACTCTCC ATTCCTGCTG GCTGGAGATC CCCACAACAG ATTCAAACGT GCAGGTGACA 1920 AACGGTGCCC TACCGATGGC AGAAAAGTGA TGAGGAAGGG CCCTTGGTCC CTGAGCAATG 1980 AGAGAAGCAG AGCTGCCTCC CTAACTACCA CCATTTCACT TGAACATGTC TCTTCTTTTG 2040 TTTATTTATT TATTTGTTTT TTGCAGACAC GTCTCTTCTT TTTTTTTTTT GAGATAGAGT 2100 CTCACTCTGT CCCAGGCTGG AGTGCTGTGG CACAATCTCG GCTCACTGCA ACCTCTGCCT 2160 TCTGGGTTCA AGTGATTCTC CTGCTTCAGC CTCCCAAGTA GCTGGGATTA CAGGCATGCG 2220 CCACCATGCC TGGCTAATTT TTGTATTTTT AGTAGAGACG GGGTTGGCCA GGATGGTCTC 2280 ACACTACTGA CCTCATGATC CACCCACCTT GGCCTCCCAA AGTGCTGGGA TTACAGGTGT 2340 GAGCAACTGC GCCCGGCCGA CACGTCTCTT CTTTAAGCCG CCACTTATTG GATCTCTATG 2400 TTAGAGCGGC 2410
|
| |
|
|
|