Tag | Content |
---|
EnhancerAtlas ID | HS044-04236 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr14:65047110-65048580 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROG2 | MA0669.1 | chr14:65048158-65048168 | GACATATGTT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTATAAACAA TTATACCATA ATTAGAGAAT TTATAATATT TTTTAGTTCT CGGCATAGAG 60 CCTCCACTGA AGTAATTATA CTTTTTCCAA GGCAATTTTT ACACAAACCT TTAAAGGAAC 120 ACATATGTTT GAAAGTAGAT GATGGCCTCT GGTTAGCACT AGCTCATTTC CAGATGGTGC 180 TGGTCATTTT TCCACTGTAT GCGACATAAC CCATGTTTCC TCTGCCTGCT GGATAGCAGT 240 TTATAGAAGA ATGAGCGCAG ATCTCACCAC CCACGTAACA AATTCCATAC AGGTCAAACG 300 CTGAACAAAG GACATAAAAG ACAGACTGGA ACAGGTTTTT GCCATGATTC GGAAGTTTAT 360 ATTGTTCTTT TGGTGGCTTT TATGCAGGAG AAGATGAGGA CAATGTTTTT GCCGGTTATA 420 AGTGATTAAC TCATTTTAAC ATTCCACTTC TTTCCGATTT CAGTAAGCTA ATATTTTCAT 480 GTGTATTTTC TGACTTTTCT CTTTCATATA TGTGTTACCG AAGTGAACTG GGGTCCGCTT 540 GCCTGATGCA GTCAGGTGAA ACATCCACAC CGTGGTTTGT AATATCAGGA GAAAGGAGGG 600 TATTTATTTG CAGGTTGGCA AGCAAGTAGA ATCAGGCAGC TCTCACTTAA GACCTGACCT 660 CTCTGATGGC TTGTAAGCAA GGGTTTTTAA AGGCAGGAGT ACATTTCAGG AAAGCAGAAG 720 TTACAGGCAA AGTTGTAAAT CAATACATAG AGGTTATATA TTGGTTTGGA CTAAAAAGGC 780 AGGATATTTT GAAGCGGGGC CTTACAGGTC ATAAGCAGAT TCCAAGATTT TCTGATTTGG 840 TTAAGGTAGA GCAGCTTTGT TTTAAAAACT TGGGGTCTGC AGAAAGATGT GTTAGGTCTG 900 GCTCATGTAC ATGACTTCTA GGCCTCTCAG GAAGAACTTT AGAACAATGA ATGCAGTTAG 960 AGTTCAGTCC TCAGTCTCCC CTTATCTGAG GTCTACATGC CAGTGGACCC ATTTGGTGGG 1020 GGTCTGAGTT TCTGAAAAAC AACGCAGGGA CATATGTTAA AATGTTATTT TTACTTTATA 1080 TAGGGAACCA AACATCTTGT GACTCTAACT TCCTTGGCTG TCTTTTAAGC TACTGTTATC 1140 TTCTTATCAA GTTGCTCATT TACTTCTCAG GGCTAGCTAG GTGCCTGGAA TTTCCCTTAC 1200 AAGAACTCAA GGCTTCCCTT TATTTCCATG TTTGGGGGTG GGGGTGGGGT GGCAGATCCC 1260 TAAGTGTGGG GGGTGGTCCC TGTTTTGTCT CATGTGCACA CTTAATATTT GACTACAACA 1320 CATTATGCTG CGTATCTCTA TGATTAAAGA TTTTAGTAGA ACCAGCAGTT TGGGTGCTGT 1380 TAATTTAGTG CTTTCATGTC TCTTGAGAAG TAGAAGGATG TGCCTTTAAA TGTCTGAGGA 1440 ACCCTGACAT CCTGAAAGCT TTGGCAGAAT 1470
|
| |
|
|
|