| Tag | Content |
|---|
EnhancerAtlas ID | HS118-03604 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr11:69073160-69074620 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:69074103-69074121 | CCTTGCTCCCTCCATTCC | - | 6.1 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_59763 | chr11:69043247-69081064 | Ly4 | | SE_65857 | chr11:69073308-69074563 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I069305 | chr11 | 69073309 | 69074563 |
|
Enhancer Sequence | TCTGTCTCAA AAAAAAAAAA AAAAAAAAGA ATAAAACGAG CTAATATATG TGAGCTGATA 60
TAAATAAGCT AAGATCCTGG ATAGCTGCAG AACAGTGGGT GTAGTGGGAG AGCTTGAAAG 120
ATACCGGTTA TTTTATAAGG AAGCGGTCCT CTTGAAAGTC AAGGACAGCC AGGCCGCAAG 180
CAGAAGCTGC AGAAGACTTC TGCAGTTCCA CATAAAACAG AGCTCCACGA CGCTCAGGGC 240
AGAGACAGAG GCAGGATCAC ATCTAACAGA TGGGCAGGTG GAGGCATGGG GAGGCTCTGA 300
GGCGTGTGCA TAGTCACACG TGGGTGCAGG AGAGATCTCG AATGTTCTTG TTCCCAGCAC 360
TGCCCCCGGA GACCTCCCAG TGTGGACCTT GCCCAGAAGG ACACACGACC TTTTGAATTA 420
TGTTGGCTTG GCAGAAAGCT GGACTCTTGG CAGCATGCCC CCAGGGCCTT CTCAGTTCTC 480
ATAGATATTA GTCAATGTGG ACACTCTCTC CTTTCTGGAA TGCCCCCAAT AACAGGTGTT 540
GGAGACATCG AGGCCCTGAG TAGTAAGGGG CCTGACCCAC AGGCACAGAG TTGGGTGCTG 600
CGGGATGGCC AGGAGCTTGG GTCTCCTTCC TTCCCACCAC ACCAGTAGGA GCCGGATGCT 660
GGCAGGTGGC TTGGGGATGC CCCTTCACTT TGCTGCCGGG AAGTTGGCTG CAGAGTCCAG 720
GGCTCATAAA AGCAGCCAGT TGAGTGAGAA TGCACTGGTT CAGAAGCCAG TGGGCCCCTA 780
GCTCCTCACA GTGGGCCCCC TTGGCCAGGC CAACAGGCCA TGTCTCCTAG CCAACCTTGG 840
GTCTGGCCCC CAAAGATTCA TTTCTATCCG CAAAGTGCCT GCCCTCCACC TTGTTCAGCA 900
GCCTAAGCCC CAGTGACCAT TGGCCACCCG AGATAAGGGC CATCCTTGCT CCCTCCATTC 960
CCTAATACTC CTGAGGCCCT GTGCACCTGC CCCACGATGG GGGCTAGAGT CCCCAAGAAC 1020
AATAAGAACC TAGCTCTTGT CTTGGGAAAC CTGGCAGGAT TTCCCAAGTC ACCCGAATGC 1080
CCAAGCTATT AGAGACTATG TTTGCCCTGA AGAAGAAAGA ATCAGGCTGA AAACAGAGCA 1140
GGTAGCAGTG GGGGAGTGAA GACTGAGGTC CTTCCAGGAC CACCAATGCC CTCACGTCCT 1200
CCCGCTGGGG TCCAGTGTCC CCTCCCCTCC TCCTGTGCAG AAGCCACCTC CCTGGGCCTT 1260
GGTTCCATCC TTTGTGAAGT GCAGTGACCA GTGGTTGCCA TGCAGGGGAT GCTTGCTGAA 1320
GTGTGCCATG GTGCCCAGCA CAACACAGTG GGCAGAGGGC AGCCCATCAA TACCACTCGC 1380
TGCCTTTGCT GCTCACGGTG AGTCTTACCT AGGGCAGTGC AGCGCTCCCT CACATCACCC 1440
TTCCTTGGCC CCAACCTCAA 1460
|
