| Tag | Content |
|---|
EnhancerAtlas ID | HS118-04832 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr12:110016360-110017600 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEOX1 | MA0661.1 | chr12:110017255-110017265 | GTTAATTAGC | - | 6.02 | | MSC | MA0665.1 | chr12:110016432-110016442 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr12:110016432-110016442 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr12:110016432-110016442 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr12:110016432-110016442 | AACAGCTGTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGGTTACAC TTGTTGGTGA CACTGAAAGG ATTCAGACCC AGGTTTCTCC TAGCCCCAAA 60
GTCCAGGCTC TTAACAGCTG TTCCATCTCG ATTACAAAGC TCTGAAATAC CTGGGTTCTC 120
AATGATGCCA TGACTTGGCC ATTTGAGTAT ATCATTAATC CATTCAACAC ACATTTACCC 180
AGTACTTAAC CAGTGCCCGA AGTTTCCTAA CACACGCATG CCCAATTCCA TTTCCCAGTC 240
CCTTGAGAAT GTGACCTGAG GCTCAGCGAG TGATTTGTAA AGGTGAGCTG GCCAGAAAGG 300
CTCTGCCTTC TCAGTGTCTC AGAGGAAAGT GGCCCAGGTT CCTGTACATC CCTGGGAACA 360
ACCTGCCTCA CCTTCCCCTT CTGCCCAGGC ACCGCCTCGC ATTTACACTG TCCTATTCCT 420
GATGATTATC TTTTGGAGGA GGGAAATATT TTGGGGGTTA ACTTAACACT CTTTTGATTT 480
TGGTTTTATA CAATGGAAGG TGAAACCTAG GCCCTTGTGC GATTGAGCCA GCATTCTCTG 540
TGTGTGTCTG TGTGTCTGTG TGTGTTTGTT TTAAGACTAC AATTTTTTTT TTTTTTTTTT 600
TTGAGACAGG GTCTCACTCT GTTATGCAGC CTGGAGTACA GTGGTGCGAC CACAGCTCAC 660
TGTTTCTTCA ACCTCCTGGG CTCAAGCGAT CCTCCTGCCT CAGCCTTCTG AGTAGCTGGG 720
ACCACAGGTG TGCGCCACCA TGCCTGGCTA GTTTTTGTAC TTTCTGTAGA GTTGGGGTTT 780
CGCCATGTTA CCTAGGCTGG TCTCAAACTC CTAGGCACAA GTGATCTGCC CACCTTGGCC 840
TCCCAAAGTA CTGGGGTTAC AGGCATAAGC GCCTGCACCC AACCTTAAAA CTACTGTTAA 900
TTAGCACTTA CTACATGCCA GGTGCTGTGC TAAAAAGTTT ACACCCCTTA TTTAACTTTA 960
CGTTCCTGAC AACCGTAAGA AGAGGCACTG TTGTTATCCC TGTTTTACCA AGGTGGGAAA 1020
CAGGTTCAGG GAGGTTAAGT CACACGGCCA GTAAATGGCA CAGTTGGGAC TCAAACCCAA 1080
GTCTGCCTAA AGCCAATGAA CAGACTTGGG TGTGGGGTTC AGACCATAAA TTCGTGTCCA 1140
TCCATGTTCC AATTCCAGTG ACTAGTCGAT TTTCTGTGTT CTGTTGTTTA TAAAGCACCA 1200
AAGTCCCTCT CACCCACTTG TGTTTGCTTG TTTGCCTGTG 1240
|
