| Tag | Content |
|---|
EnhancerAtlas ID | HS034-07734 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr12:122948600-122949620 |
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 | CACCACATCC AGCCCTGCTG CAAGGTTCTT AACTGGGGGT CCACGGACCT TCTGGATAGA 60
ATTCAGGGAA ATTTGACATT TCCTTCAATT ATGACTGTAG GCAAACATTC TGTTTCTACC 120
ACATGCCTGC TATGCCTGTC CTAATCCTTG ACTCTCTAAA GTCATGAACC CTATTAGATT 180
TCAACTACCC TCATATAGTA GGTGTTCAGT ATTCCTCCAA ATGTTCTAAA TAAAAACTTA 240
GTAGAATGGG CCAGTACAAT GAACAGAGTT GTAATTGGTT TGAAGAATCC AAGATCAGGA 300
CTGTGGTAGG AACAGAAGGA AACTTGTTCC AAGTCTGTGA GAAATTTGCC CCAGGTCCAA 360
TCCCACAACC TGTTCCAATC CAGTTTCATT TGTCATTCTC ACTTATGACT AATGAATTTG 420
CTTCCATGAC GGAAAACATT AAGAAATCAC TCTGGCATGA GGTCACCCTA CAAAGGAGCA 480
ATCTCAGCTG CCCGGAATGT CAGCGTTCAG TAAGGGCCAC ACCCCTTGCC TTTTCAGTAA 540
TTCCTCCTAT TACAAAATTC CAAATGCAGC CATATTGTTG ATAGGAAATT TTGTTTAAAA 600
AATACATTTC TTAGGCCGGG CGCGGTAGCT CGTGCCTGTA ATCCCAGCAC TTTGGGAGGC 660
TGAGGTGGCG GATCACAAGG TCAGGAGTTC AAGACCAGCC TGGCCAACAT GGTGAAACCC 720
CATCTCTACT AAAAATACAA AAAAATTATC CAGGCATGGT GGCATGCACT TGCAGTCCCA 780
GCTACTAGGG AGGCTGTGGC AGGAGAATCG CTTGAACCTG GGAGGCAGAG GTTGCAGTGA 840
GCTGAGATTG CGCCACTGAG ATTGCGCCAC TGCACTCCAG CCTGGGTGAC GGAGCGAGAC 900
TCCATCTCAT AAATAAATAA ATAAATAATT TTTTTGCGGA ACGTGGTGGT TCGTGGTTAT 960
AATTCTGACA CTGTGGGAGG CTAAGGCGGG TGGATCTCCT GAGCCCAGGA GTTAAAGACC 1020
|
