Tag | Content |
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EnhancerAtlas ID | HS049-03877 | Organism | Homo sapiens | Tissue/cell | Fetal_spinal_cord | Coordinate | chr19:10589580-10590490 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr19:10590046-10590061 | CTTTTCCTGAGAATA | + | 6.01 |
| | 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 |
GH19I010478 | chr19 | 10589121 | 10590829 |
| Enhancer Sequence | TAAATCATCG AGGTAAATGC TCACAACAGC CCTATTAAGT AAGTACTATT ATTATAAAAA 60 GGGTCACAGG CATAGGCAGG GAAGGAGGTA GGGCTGGGAG TCGGAGCCCG TGAGCGCCCC 120 CTAGAGTAGG GCTAAGGGGC GGGGGGGCGG GCTACAGCAG AATAGGGACC CAGCGCACTC 180 GCAGAACGAG GGGGGAGGCG AGGCGAGAAC GAGCGGGAGT TTTTTTCCCG ACTACGATTG 240 GCTGGTGTAA TTGTCATCAC TTGAAAAGGC AGCCAATGAG AGGCGCGGTC GCCTCGCTGG 300 TGGAAGCCGA GAGCTGAGCG AAGTGAGGCG TGCGGAGCCA AAGGCGCTAG AGCGATAGCG 360 GGAGCCCCGG ACCCCGAAGC GGTTGAGGGG ATCCAGGCCT CACAACGTCT TGAGAGTGGC 420 CCCAGCGTCG TTCCTAGTCT CTTCGGCAGA CCCCAGCGTC GTCCTTCTTT TCCTGAGAAT 480 ATCCTGACAC CAGTCGCCCG TTCCAGAAGG GGACACTTGG CGTCATCCCT TTTTTTCTGA 540 GTGACCCCAG AGTCGTCCTC ACTTCCTGAG GGGGATCCTG GCGTCATCCG CCCTTCTTGA 600 GGGGACCCTG CTGTCACTAC CCTGTCCTGA TGGCCAGCAC CGCATTGTCC TTTCTTCCCG 660 CGGGAAACCC GGACATCATC CCCTCTTTCT GGCGGGGACC CCCATGCCAT TATCCCCTCC 720 TGAGGAGACC CCAGAGCCAG AGCCGTCCCC CCTTCCTCAA GGCTCCCCAG CGTTGTTTCT 780 TCTTCCCGAG AAGGGGCCTG GTGCTGTTCC CCGTTTCCAG AGTGTTTCCT ATCGTTGTCC 840 TCCCCACACT CAGAAGGCAT CTGTCATCCC CCCTTTTTCT GAGATCAGTC CCTTCCTCCT 900 TTCCAGTTTA 910
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