Tag | Content |
---|
EnhancerAtlas ID | HS044-11552 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr6:124150410-124151910 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr6:124151025-124151036 | TTCTTTGTTTT | - | 6.62 |
| | 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 |
GH06I123828 | chr6 | 124149684 | 124152104 |
| Enhancer Sequence | TTAAAATTTT CCACCCAGAG TTCTCCCTTG AGCTCTAGGT CTAATTATCT AATTGTCTAT 60 CTGACAGCAT CCTGTGGGTG TCTCAAAGGC TTATCAAACT CTGTGTGTTT GTTAGGATAT 120 TCCTAGCTGT TGTATCGGAC ATAGCCCCAA ATTCCATTGG TATAACATGA TAAAACTTGA 180 TTTCTTGCTC ATGTGACATC CTGATTCAGG GTTTCTAGTC AGCAAGCAGC TTCCTACATG 240 ATGAGTCAGG GAAGTTAATT CTCAACTTTA CTTTGTCTTA AGGCTTGTGG ACTTTTGCTT 300 GTAGACTGCT TATGCTTCCT GGCCCAGAAA TGCTACATAG TACTCTTGTC CATACTCCAT 360 TAGTGAGGAC CAACCACAGA GTCCCAGCTA AATGCAGAGG GGTGGGGAGG TTTGGGAAGT 420 ATAGTTATTG GTAGAACAGC TAATTTCTCA TAATGACTCT TCACTGTGAA AAGTCAAGCA 480 CTAATCCTTG GCTGATAACT AGTCATCTGT GACACATTCA ACGTAACGAA AAGTCAGCCA 540 GTTTCCCAAA ATAAGCAAAG TAACTAACTA ATCATGCAGA CAAACAGACC AGTAAACCCT 600 GGCCTTCTTT CAGTGTTCTT TGTTTTGGAT GATGCTACAC TTCTGCATAA GCTGGGGACA 660 TGTATATTGT TGTTGACATC CTCTTACCCT TAACCCTTAT ATCAAAGAAG TCTATAATTT 720 GCCTGGCTTC TTTAATTAAT GACTAAAATC TTGGAAATGA AACAACCTTA AATGTTAGGG 780 AAATGGGACT CAAAAGCCAA GGAATCATTC CTGACTTTTC TCTCGCCCCG TGTGCTGTCA 840 TTATTTGGTC TTGTGTAGTT TGCATCCTAA AAATTTATTG GCTGGGTTCA TCTCTTCTTA 900 GTGACAGTAA CACTGCCATC CTCCTTGCTT AGACCACTAA ATAGCCTAAC TTCACTTCCA 960 CATGTCCTCT GGCTCCCCTC TTGTCTTCTT TACACAGCAG CCAAAGTGAG CATTTAAAAT 1020 GCATTTTAAA TGCAGATCTA ATCGCATTAT TTCCCTGCTG TTAACACTTC AAAGCCTTCC 1080 TGTTGCTCTA GGCGTAAAGG CAAAACTCCT TAACATAATT TACAAGGACA TGCCTGGCCT 1140 AACCCCTTCC CTGTCTCACT CCCCTTTGCT AATAAATTTC CCCCTGTTTG AGCCTCACTG 1200 TCTTCTGGTA TTCTCCGTGC TACCCTCTGC CATATGGCCT CATCTGCAAA ATTATTTTCT 1260 CTTGTTCTCA CGTAGTTTAC ACTTACATAT CCTTGATATC AAAGTAAAAT AAGTTTCACT 1320 TTCTCAGGAA AGTTTTTGCT GACCCCCCTA GTCAGGTCAA CTTCACCCAC TGAAAAATTT 1380 AGAAACAACT TGTATTTCTC TTTTGTAGCA TTTATGATAA ATAAATTCTC ACATTTCTTT 1440 TGTGAATATT GAATAAATAA CTGTGTCTGC CACTGGATTT TGTATATTCA GTAAGCAGGG 1500
|
| |
|
|
|