| Tag | Content |
|---|
EnhancerAtlas ID | HS176-10703 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr12:122948530-122949560 |
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 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I122463 | chr12 | 122948038 | 122949938 |
|
Enhancer Sequence | TCTCAAACTA CTGGCCTCAA CCTATCCTCT TGTCTTGGCC TCCCAAAGCA TTGGGATTAC 60
AGGCGTGAGC CACCACATCC AGCCCTGCTG CAAGGTTCTT AACTGGGGGT CCACGGACCT 120
TCTGGATAGA ATTCAGGGAA ATTTGACATT TCCTTCAATT ATGACTGTAG GCAAACATTC 180
TGTTTCTACC ACATGCCTGC TATGCCTGTC CTAATCCTTG ACTCTCTAAA GTCATGAACC 240
CTATTAGATT TCAACTACCC TCATATAGTA GGTGTTCAGT ATTCCTCCAA ATGTTCTAAA 300
TAAAAACTTA GTAGAATGGG CCAGTACAAT GAACAGAGTT GTAATTGGTT TGAAGAATCC 360
AAGATCAGGA CTGTGGTAGG AACAGAAGGA AACTTGTTCC AAGTCTGTGA GAAATTTGCC 420
CCAGGTCCAA TCCCACAACC TGTTCCAATC CAGTTTCATT TGTCATTCTC ACTTATGACT 480
AATGAATTTG CTTCCATGAC GGAAAACATT AAGAAATCAC TCTGGCATGA GGTCACCCTA 540
CAAAGGAGCA ATCTCAGCTG CCCGGAATGT CAGCGTTCAG TAAGGGCCAC ACCCCTTGCC 600
TTTTCAGTAA TTCCTCCTAT TACAAAATTC CAAATGCAGC CATATTGTTG ATAGGAAATT 660
TTGTTTAAAA AATACATTTC TTAGGCCGGG CGCGGTAGCT CGTGCCTGTA ATCCCAGCAC 720
TTTGGGAGGC TGAGGTGGCG GATCACAAGG TCAGGAGTTC AAGACCAGCC TGGCCAACAT 780
GGTGAAACCC CATCTCTACT AAAAATACAA AAAAATTATC CAGGCATGGT GGCATGCACT 840
TGCAGTCCCA GCTACTAGGG AGGCTGTGGC AGGAGAATCG CTTGAACCTG GGAGGCAGAG 900
GTTGCAGTGA GCTGAGATTG CGCCACTGAG ATTGCGCCAC TGCACTCCAG CCTGGGTGAC 960
GGAGCGAGAC TCCATCTCAT AAATAAATAA ATAAATAATT TTTTTGCGGA ACGTGGTGGT 1020
TCGTGGTTAT 1030
|
