Tag | Content |
---|
EnhancerAtlas ID | HS158-14822 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr12:133009570-133011280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX5 | MA0510.2 | chr12:133010255-133010271 | GGTTGCCATGGCAAGC | - | 6.24 | RFX5 | MA0510.2 | chr12:133010255-133010271 | GGTTGCCATGGCAAGC | + | 6.57 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_10775 | chr12:133010030-133011047 | CD19_Primary |
|
| Number: 3 | ID | Chromosome | Start | End |
GH12I132434 | chr12 | 133010201 | 133010290 | GH12I132433 | chr12 | 133010311 | 133010350 | GH12I132426 | chr12 | 133002876 | 133010130 |
|
Enhancer Sequence | CAGCTGTTTG GAGCCTTTCT TCCAGTGCAC CACCTCCGCA TCTTCCCTCC ACCCCCGCCC 60 CTGCCGTGGG GAGCCCTGCC GACGGCGTTT AACTGACTGT GTAAGGCTGG GCCTCTTGCC 120 CTCCCACTCC TGTCCAGAAC AGTGAGGACC TGTTCCATCC ATCAGAAAGG CCTCCGCAGA 180 AGCCGCGAGC CGTGCCTTCG CGTGTGCACA CCTGAGAGCT CACGCGTGTC TGTGGGTACT 240 CAGGGTGCGA TGTGTACACA GATCTGAATG CAGACGCACG TGCCCATGAG CACGCACGTC 300 CAGAGAGACG CACGTCTGCT TATCCACAAG GTGCACGCGT GTCTGGATCC GCACAGGTGC 360 GCGTCTGCTC GTGGACACGC AGAGGCGGGT GGGGCTGTGC ACGTATGCCT GTCTGCACAG 420 GAGGCTGGAA ACATAACCGC ATGTGACTTG AGGGCCTGTG TGTGATGGTG TCGGGGTCTG 480 CGGCGTGCCT GGTAGGCATG TGTGTGTGTT TGCCAAGGTT ACATGTGCCT GTATGTTCAT 540 GCTTATCTTG GCGTGTCTGC ATGTTTGGTG TACAGAGTAG ATGTCTGTGT GCATGTGTGC 600 ATATGGTGGG TGCAGGGAAA GAATGTAAGA TCGGGGAGCT GGAAAGGACA CGCCCTCGCC 660 TGGCCAGCCG AGGATGCCTG TCCTTGGTTG CCATGGCAAG CCCTGGCATC TGCACGTGGC 720 CTCGGCACAG CCCCTCCCCC CGGGTCTGCT CCCAGGGCCC CAGGCAGGCG CTGCTTACCA 780 GGGCAGGTGC TTCCCCCGCG GGTGTGGCAG GCTGGGGTGG GAGCTCATGG GCCCCTGCAC 840 CTGCAGAGGG TCTCCCCATC ACCCTGGTCA GGTGCTGGAG GGACCCCTGA GCTGCCCCCG 900 TTGTCCTGGC CTGGGCAGAG GCAGTGGCAG GCAGACAGCC CTGGGCAGGG ACACACCTGG 960 AATCAGACCA AGGCTGCGGC ACAGCCCAGC AAGCAGGGCG TCGGCCTGTG GTTTCTGACT 1020 TGAGAGTCAC TGGGCGACAG TATCTCCGAG GCCAGAGCAG TCCCTGGAGA TGGAACGGGC 1080 ATTCTCCCAG GGTGCCCAGA GCCCAGGGAA AGACGGGGAC GGCAGAAGGA ACTGCAGGTG 1140 GCGCCCACAG GTGCGCAGCT GAGACCCCAT CACCACATCC CGGGGCCGTC AGGCATGAGT 1200 TGACCCTGAG GTGACGTCGG CGCCATGCCT GGGGTGACAT CGGCACCATG CCTGGGGTCA 1260 CCAGGGCCGT GCTGAGCCAA AGCGCCCTGG CAGCTGGCTG CGAAGCTCGT GCACCCACGG 1320 GTGCAGCCAC GGGGCTGGTT CTGACCCAGG CCACGCCCGC CCACTCTGCA GCCTCCGTCC 1380 TCATTGGTAC AACAGGGGCA ACGGGGCTCA GTTTGCGTGT CCTGTTCCAG AAAGTTCTAG 1440 AGATGGCCTG TGCCCTGTTG CTGCTGTCAC TGTTGCTGCT GTTTCATCTA CACTGAAGAT 1500 CTGCTGTGAG TGTAGCCGCC TTCATCCGTG ATCTCAGCTG GATCTTCCAT CGGGGAGCTG 1560 GACGTGCTGC CTCACCTGCA CTTCTGTGTG ATGGAGGTGG CTTCTGTCCC TAAACCTCAG 1620 GAAGCCACCT CTGCCAGCTG CCAGCTTTTC TTCTGGAGCT TCCTCACCTC TCTCAGCCTC 1680 CACAGAATTG AGGAGAGTTA CAGCCTTGGT 1710
|