| Tag | Content |
|---|
EnhancerAtlas ID | HS139-46669 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr6:27654930-27656320 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RAX | MA0718.1 | chr6:27654945-27654955 | GCCAATTAAC | + | 6.02 | | Sox3 | MA0514.1 | chr6:27656244-27656254 | AAAACAAAGG | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 27655000 | 27655243 | | chr6 | 27655152 | 27655475 | | chr6 | 27655751 | 27655869 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I027687 | chr6 | 27654780 | 27656741 |
|
Enhancer Sequence | TTAAAATGTA CATAGGCCAA TTAACTTTTG AAAATATTAC TACCCTTAAC TAACAGAAAC 60
AGTCGTGGTA GGAAGAGGGG GAAAGTAGAA ACTTGTCAAA AAACAGACAG TAAATCATGA 120
ATTAGCTGCT CCAGTGGCCC CTTCCTGGGT TGTCACCTGC CAGCAAGAGC ATCAGGCTCC 180
GTCTGGAAGC GGGGCACCTC TCAGGGGCAA ATGTTTCACG CCTGCTTCCT CTGAGTTGTC 240
GAATCCGGGC CTCGCCTCCT CCTCCCTTTT CAGATCATAG GATTTCTCTC CCCCGCAAAT 300
AATGGCCCTT ACTTCGTAAA CACGCTGGCT CCGTAATCCC TATTATTGTT TTGGGGGTTT 360
GGTTCTGTCC AGGGAGGAGG TGAGGGCAGA TGCTCAAGAG AGGCTGTCCC CACCGTCCTT 420
TTGTCTCAGC GAACCGCAGT CCGCGCCCGA GCGCCACTAG CTGTCCTGGG ACGGGAACTG 480
CAGCGGCAAG TGTGTGACTT TCTTGAGCCC GGAGCCACAG GCCTGGGAAG CGCCGCTGAG 540
ACTTCAGGGT CGTAGTGACA GAGGAACCAC CCGAGGCTAG GCGGGGAGAG GGTGCAGTTT 600
CCGGATCCCG AAGGCTTCGA GAAGAGCCGA CCTGTCTGGA AGGGTCTCCA AGAACAGAGA 660
GGACTCTGCA ACCATCACTC GGGAGCCGCG TCCTTTCATC CTTGAGACAG CTCCGTGGTC 720
CAACGGTTCC CCGATCCGCT GGCCGAGATC TCAAGCTTGG ATGCAACTTC GGATTCGCCC 780
CAGGCAGGAG GAAGGAAGCC CCGATTGGAA ACGTTGACTT GAATCTTCTC GGATCAGAAT 840
TAGCAGGTTA AGAAAAACTG TTTCCCCGTA AGAAGCAGGG TTCTTTGGTG TTCAATGTGG 900
AGCTCCGCCA CTCCCAGCCC GGGTGAAGGA AAACTGGGAA ACAGAATGAA TGTGATTATC 960
TATTCGAAGA TAAATTTCCA CAAAGCATGC CGTTTGATAG TAGCTTATAA TGTGGAAGTA 1020
AGGCATCCTG TCATCCGGCC GGTTAGCTCA GTTGGTTAGA GCGTGGTGCT AATAACGCCA 1080
AGGTCGCGGG TTCGATCCCC GTACTGGCCA AGTATTCTCT GTGGCTTTTA TCACCAGAAT 1140
GGATAGTAAC CCAGACATCG ATCTAAACGT GTACCTGTGT GTTTCTCCAG GCTTAACTTT 1200
GCCCCGAGAA AACGGATCTG TGAATTTGGT GCGCCCTCGC TTACTCGACA GCGGTTAATT 1260
TGAACGGGGA CGTTTCTTTC CGCTGCCTCC AAGGCATACC CACATCCTAC CCGTAAAACA 1320
AAGGGGCTAT AGGCACCTTA CAGTGACAGA GGTACGTTAC GGTTGGAGGC TTTTGTGATT 1380
TTTGTCCTCC 1390
|
