Tag | Content |
---|
EnhancerAtlas ID | HS026-19653 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr2:238440270-238441710 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr2:238441536-238441546 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr2:238441536-238441546 | GGCACGTGCC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr2 | 238440819 | 238441227 | chr2 | 238440392 | 238440595 | chr2 | 238441398 | 238441668 | chr2 | 238440863 | 238440971 |
| Enhancer Sequence | GAATTGTTTC TCTTTATTTA TTCCTATTAA CTTGTATTTA CTTTGCCAAC CCTAAATAAT 60 GAGATTCAGA AAATATAAAT AAGTATTAGT ATATCAAGTT TATCAGAACA AAAGCTTGAC 120 AGTGGCCACC CAGAAACACA GACTTCAAAC AAATGGGGCC CAAAGTGGAC TAGTGAAGTT 180 TTCACCTATG TAGAAATTGT AGCAGGATCA CAACCTTGCA AAGGAACAGT GACCTGGGGG 240 GCCCTTATCT CCAATCCTGT TTGGTCTTAA TTATTCACAG GGAAAAAAAA AGTAGAAGTT 300 TCAGCTGTGA AACATGTCCT CTCAAGACTC AGAATTTAAA GTTCCAACAG CTTTGTTTGA 360 ATTATTCAAT GTGACAACCT CAACTAATAT TTCACCTAGA TTGTTTCCCA TGCATCTTTA 420 TATGGAGGAA ATTAAGCAGC AGAAAGAAGC TCCAAATGCA GCAGCGATCC TGTACTTCAG 480 AGAAAACCCA GGCAGACTCT TAGAGGGGCC TTTGTGAAGT GGCTGTGGTG GGACCCCAGG 540 AGGAAGCACT CTCAATCTGC CCATCAACCC CAAGACTCCC AGCCATGCCC TCAGGGCCTG 600 AGCTTTCTCA GGAATCGTAT TTTATCACAG CTCATCTGAG GGGTCAGGCA GCTGTGCATT 660 GCCTGCCTTT GCATTTGTAT TGACAGTCAC AGCTTTCCCG ACGAGGGGTA AAGACTTCCT 720 GTAGATATTG TTCAAGCCCA GACAAGGCCC AAGATGGCAC AAGCATGTGG TAGGAAGGAA 780 GTTTCTAAGG GGCTGAGATG GGAGACGGGA GAGGAAACGG CCCTGGCACG CACCCTCCGC 840 CCCCTCACTC CCAAGGGCCG GCCCTGGGGC CATTCGTGTG TGCTCGGGCT ACAGACACTG 900 ACGGTTTCCC ATAAAAGTGT CACCAGTGAC ATATTTTGTT GGTTTGCTTT AATCCCTAGC 960 TAGTGTCTGT ATTGCATTTG TAAACTCTAA ACTTTGGTAT TGTCGCGAGT TGAAAGCTCA 1020 AGGGGTTCCT ACCTAGTATT CTGTCCGTAC ATATCTAAGT AATGTGATAA TCCTGATGAC 1080 TGGTGCCCAC ACAGGGTCAG ATGCCCACGT CTGAGTGATG CTACTCCCAC CAGAGCAGTT 1140 GTTACTGTTG GAGAAATATA ATTTTTAGAA AAACCCGAAA TCTTTTCATT ACCCAGAAAA 1200 TCTCTCCATA AGGGTAGCAG AGGAAGAAGA CAGATTTATT CTTGAACAAG CATCAAACCA 1260 GAATATGGCA CGTGCCCCAG GCAATCCGCT GAGAGATTGC AAAGACAGGA AGGCCTCTCA 1320 GCCCTTCTGC AGCCCGGCAG GCCCGGCCCA TTCCACACAG TTCTCAGCAC AAACCATCAC 1380 CAGTCCTTAC CAATGAGAGG AGCTGATGGT GCCTTTGATC ACAGTGTACA TCCTCACTCT 1440
|
| |
|
|
|