| Tag | Content |
|---|
EnhancerAtlas ID | HS098-14829 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:122948400-122949450 |
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 | CAGCCTCGAC CGTCCTCCTA TCTCAGCCTT CCGAGCAGTT GGGACCACGG GTGTGTACCA 60
CCACACCAAG CTAATTTTGT TTATTTTTTG TAGAGACAGG TCTCGAACCT TGCTATGTTG 120
CCAAGACTGG TCTCAAACTA CTGGCCTCAA CCTATCCTCT TGTCTTGGCC TCCCAAAGCA 180
TTGGGATTAC AGGCGTGAGC CACCACATCC AGCCCTGCTG CAAGGTTCTT AACTGGGGGT 240
CCACGGACCT TCTGGATAGA ATTCAGGGAA ATTTGACATT TCCTTCAATT ATGACTGTAG 300
GCAAACATTC TGTTTCTACC ACATGCCTGC TATGCCTGTC CTAATCCTTG ACTCTCTAAA 360
GTCATGAACC CTATTAGATT TCAACTACCC TCATATAGTA GGTGTTCAGT ATTCCTCCAA 420
ATGTTCTAAA TAAAAACTTA GTAGAATGGG CCAGTACAAT GAACAGAGTT GTAATTGGTT 480
TGAAGAATCC AAGATCAGGA CTGTGGTAGG AACAGAAGGA AACTTGTTCC AAGTCTGTGA 540
GAAATTTGCC CCAGGTCCAA TCCCACAACC TGTTCCAATC CAGTTTCATT TGTCATTCTC 600
ACTTATGACT AATGAATTTG CTTCCATGAC GGAAAACATT AAGAAATCAC TCTGGCATGA 660
GGTCACCCTA CAAAGGAGCA ATCTCAGCTG CCCGGAATGT CAGCGTTCAG TAAGGGCCAC 720
ACCCCTTGCC TTTTCAGTAA TTCCTCCTAT TACAAAATTC CAAATGCAGC CATATTGTTG 780
ATAGGAAATT TTGTTTAAAA AATACATTTC TTAGGCCGGG CGCGGTAGCT CGTGCCTGTA 840
ATCCCAGCAC TTTGGGAGGC TGAGGTGGCG GATCACAAGG TCAGGAGTTC AAGACCAGCC 900
TGGCCAACAT GGTGAAACCC CATCTCTACT AAAAATACAA AAAAATTATC CAGGCATGGT 960
GGCATGCACT TGCAGTCCCA GCTACTAGGG AGGCTGTGGC AGGAGAATCG CTTGAACCTG 1020
GGAGGCAGAG GTTGCAGTGA GCTGAGATTG 1050
|
