| Tag | Content |
|---|
EnhancerAtlas ID | HS118-07743 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr17:4567510-4569190 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr17:4567617-4567630 | AGGAGCAGCTGCT | - | 6.11 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 4568731 | 4568815 | | chr17 | 4568927 | 4568977 |
| Enhancer Sequence | AGCATCAAAC CTCTGCCTCT GTTGGGGTGG CCAGGGCCCA GAAGCCTGAG ATCTTGGAGC 60
TCTGCCTCTC TGTCCCTGCA GACTGAGAAG GAACCATAGA GAGGCTGAGG AGCAGCTGCT 120
CCCTGGCCGA CAGAAACCAT TCAAAGAACA TACCATTCAG GAACCAAGTA GGGCAGGCGC 180
CTGGGTTGCC ACAGTCCCTG TGCTGAGGTG TGAGTGGCGG CGGAGCAGGG CCGGCACCTC 240
ACCGCACCAT CTTCTCTCCT TCCTTCACGA GGTCTTACTC TTCCCCAGAT CCAATGGACA 300
TTTCTCAACA GCACGATGTT TTCTATGTTT TCTGCCTCCT GTTTGAAGTT CTTTTCTGGG 360
ACATGGCCTT CTCCAAGTCC TCTTCACGCT CCTTAAAGGG GCTCCTCTTG CCCCTAAAAT 420
GTGGTGTGAT GTGGTTCCAC TTAAGCCCAC GTCTCTTTCC ACTCCAGTCA TCCTCCCTGG 480
GTGACCTGCC CCCTCCCAAA TCTTCTCCAG CCCTGAACCC TGTCCTCAAC TACACACCTC 540
ACATATCCAG CTGCTTCTTA CCCCAGAGGT ACTGCTCATT CAAATGTTCT ACATTATTGT 600
CAGCATGTGA ATTCCCTTGG AGCAGCATCT TGGATAATAT GCATTTCCCC AATGCCTGGT 660
GCCCTGGCTT GTGCACCATA AGTATTCAAT AAATGCTTGT TTAAATCTTT CTTCCTTTCC 720
CTTTCCCAAC CCCAAACTAC TCCTATCTTG GCTACAGGCC CTTCATTTGG GGGATGATCT 780
TTAGTTTCCA GCTACCTACT CTCCCAAAGC CCCGTCTCTA GGGAAGCAGA AGCAACAAGG 840
ATACTGAGTG TGACGAGAGA AGGCTAAAGG CCGGGGCTAG GCAGCCGGTT CTTTCAGGGG 900
AAAAGCATGA AGACTGAGAG ACTGTTCAGT CCTGCCAGCC TTTGGCAAGA GTACCAGAAA 960
CCGAAGCACT CCTATGTGGC AGCCAAGCCC GGGACGACAG GCCAAAGGGC ACTCTGACAG 1020
GGCAGCACCA CCTCCCCATC CCTGCCCTTG GGTCCTAACC GAAGCCAGAC TGCACCAGCC 1080
TCCACGTGGA CCTGTGTAAA TCTCCTCTCT GCTCTCCCAG GTCCAACTCT CCTCCACAGC 1140
CTGCCAAAGC TGGTCAAAAA GAGGAGTCAC TTCCCTCAAG GATGAACTGT AAAGGAATGC 1200
CTGCCACTTA GAACACGGCC CAAGTTCCTG AGCACAGCTT TCGAGGCTCT CACCACCTGA 1260
CCCCCGTAAA CCTGGCCAGC CACATCCTCA TGCCTCCTTT CCTGCATCAC CTGCTCCAGC 1320
GAACTAAAGC AGCAAGGTGC CCTGAAGGTC TCCACCCATC TCTGAACCCC CCTATTTCTG 1380
CTAAGCCATT ATCTTTCTCC TGCACTTAAC ACAACTGAGG GGCTCAAAGA CAGAGCCATA 1440
GTCTATAAAC CCTGTGAAAT TTCACCATGC AACTTTTTGA AAATCCTTGT CAGACAATTC 1500
CAAATAGACG CTAGCCATCC AATTGTGTCC CATGCACCCG TGCAAATTTA ATAAACAGAT 1560
CTACACCCAA GCTACTTGCA GTGGTTTTTG GTTTTGAGAA TGGGTCTCCC GGTGTTGCCC 1620
ATGTTGGTCT CAAATTCCTG GGCTCAAGCG ATCCTCTTGC CTCAGCCTCC CAAGGATCTG 1680
|
| |
|
|
|
