| Tag | Content |
|---|
EnhancerAtlas ID | HS139-14026 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr12:122948320-122949330 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr12:122949276-122949291 | AAGGTCAGGAGTTCA | + | 6.04 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27577 | chr12:122948145-122949851 | Esophagus |
|
| | 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 |
| GH12I122463 | chr12 | 122948038 | 122949938 |
|
Enhancer Sequence | CAACAAAATT TTTTTTTCTT AGGAGACAGG GTCTGTCTCT GACCCAGGCT GAAGTTCAAT 60
GTCACGATCA CAGTCCACTG CAGCCTCGAC CGTCCTCCTA TCTCAGCCTT CCGAGCAGTT 120
GGGACCACGG GTGTGTACCA CCACACCAAG CTAATTTTGT TTATTTTTTG TAGAGACAGG 180
TCTCGAACCT TGCTATGTTG CCAAGACTGG TCTCAAACTA CTGGCCTCAA CCTATCCTCT 240
TGTCTTGGCC TCCCAAAGCA TTGGGATTAC AGGCGTGAGC CACCACATCC AGCCCTGCTG 300
CAAGGTTCTT AACTGGGGGT CCACGGACCT TCTGGATAGA ATTCAGGGAA ATTTGACATT 360
TCCTTCAATT ATGACTGTAG GCAAACATTC TGTTTCTACC ACATGCCTGC TATGCCTGTC 420
CTAATCCTTG ACTCTCTAAA GTCATGAACC CTATTAGATT TCAACTACCC TCATATAGTA 480
GGTGTTCAGT ATTCCTCCAA ATGTTCTAAA TAAAAACTTA GTAGAATGGG CCAGTACAAT 540
GAACAGAGTT GTAATTGGTT TGAAGAATCC AAGATCAGGA CTGTGGTAGG AACAGAAGGA 600
AACTTGTTCC AAGTCTGTGA GAAATTTGCC CCAGGTCCAA TCCCACAACC TGTTCCAATC 660
CAGTTTCATT TGTCATTCTC ACTTATGACT AATGAATTTG CTTCCATGAC GGAAAACATT 720
AAGAAATCAC TCTGGCATGA GGTCACCCTA CAAAGGAGCA ATCTCAGCTG CCCGGAATGT 780
CAGCGTTCAG TAAGGGCCAC ACCCCTTGCC TTTTCAGTAA TTCCTCCTAT TACAAAATTC 840
CAAATGCAGC CATATTGTTG ATAGGAAATT TTGTTTAAAA AATACATTTC TTAGGCCGGG 900
CGCGGTAGCT CGTGCCTGTA ATCCCAGCAC TTTGGGAGGC TGAGGTGGCG GATCACAAGG 960
TCAGGAGTTC AAGACCAGCC TGGCCAACAT GGTGAAACCC CATCTCTACT 1010
|
