| Tag | Content |
|---|
EnhancerAtlas ID | HS059-15011 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr14:106764850-106766220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr14:106765465-106765484 | GAGCGCCACCTAGTGTCCT | - | 6.22 | | CTCF | MA0139.1 | chr14:106765171-106765190 | GAGCGCCCCCTGGTGACCT | - | 6.36 | | CTCF | MA0139.1 | chr14:106765228-106765247 | GAGCGCCCCCTTGTGGTTC | - | 6.42 | | CTCF | MA0139.1 | chr14:106765327-106765346 | GAGCGCCCCCTGGTGTCCT | - | 6.55 | | CTCF | MA0139.1 | chr14:106765386-106765405 | GAGCGCCCTCTGGTGGTTC | - | 6.85 | | CTCF | MA0139.1 | chr14:106765366-106765385 | GAGCGCCACCTGGTGGTTC | - | 6.92 | | CTCF | MA0139.1 | chr14:106765346-106765365 | GAGCGCCCCCTGGTGGTGC | - | 7.07 | | CTCF | MA0139.1 | chr14:106765406-106765425 | GAGCGCCCCCTGGTGGTTC | - | 7.14 | | Gfi1b | MA0483.1 | chr14:106765091-106765102 | AAATCACAGCC | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_25326 | chr14:106765092-106772880 | DND41 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH14I106308 | chr14 | 106765161 | 106765310 | | GH14I106309 | chr14 | 106765361 | 106765510 |
|
Enhancer Sequence | CTATTTTAAT AATAGTATTA TTTTTAATAA TTAAAATATA TAAATAACCT ATTTTAATAA 60
TTGTCCCGAG AGATCATTGC TAGTATTACT CAGAAAATAC GCAGCAATAA AAGTTGCATT 120
ACATCCCTGT TCTAAGTTAG TGTTTTGTAG GTAAAAGAAA TCATGGAATT AAAAGGAAAA 180
ATCAGACATC CTGGGGAAGA CTTTTGCTTG ACCAGGTCAG GAATTTCCAG GGTCTGAAAG 240
GAAATCACAG CCTCTGAAGC TCCTGATGTG CAGCTGCCTC CTAAGAGAAC CTGCATGTCC 300
TGAGCGTCCC CTGGTGGTTC TGAGCGCCCC CTGGTGACCT GAGCCCAGAA TTGTTGTCTT 360
TAGCACCACC TATGTCCTGA GCGCCCCCTT GTGGTTCTGA GCAACCATTG GTGGTCCTGA 420
GCGCCCCCTG TTGGTTCTGA GTACCCCCTC TTGTCCTGAG TGTCCCCGAG TGTTTCTGAG 480
CGCCCCCTGG TGTCCTGAGC GCCCCCTGGT GGTGCTGAGC GCCACCTGGT GGTTCTGAGC 540
GCCCTCTGGT GGTTCTGAGC GCCCCCTGGT GGTTCTGAGT ACCCCGTGGT GACATGAGTG 600
CAGCAGTGTT GTCTTGAGCG CCACCTAGTG TCCTGAGCGT CCCCTAGTGG TTCTGAGCAC 660
CCCCCTGGCG TCCTGAGCGC TCCCTAGAGG TCCTAAGCAC CCCTTGTTTC CTGGCCACCC 720
CATGGTGGTT CTGAGCAGCA TCTACCACGC AGTTCCCTCC TGTCTCTCTG CAGAGATTTT 780
TGTGTCTGGG CTCAGACAGA TCTTCCCTCC CCTGTGTCCC TCACTGTAAT ATACGGCCTT 840
GCCCTTGGCT TTCAGGTTGG TCCTTGTAAG GTAGACTGCA CTTGAAAGGG TGTCACTTGG 900
GAATGTTGAT TTATCTGTAC TCATGGAGAG TAACCCTTAG AACTCCCATA TGATCTCTCA 960
CTGTTGCTAC CCACACCAAT TCCTGTTGTG AAGCGTGCTG GACCAAGCTC ATGCTGCACC 1020
CAGTAAACCC GAAACCAGAG GCTTTGCAGG ACAGTCTCAG TGAACTGCTG GGCTGTTAAA 1080
TTTTTCTCCT TCTGACTCCA TCAGTAAACA TCACACAGGA CTTCTGTGAA TACAGAGGAA 1140
ACAGACTGAG AACAGCCACA GCTGGACCTG ATTCACAAGG CACACTAATA TTGAGGGGGA 1200
TGAGAAGGGA ATCCAGATCA GTGCAGACCC CATGGTGTGG ACACTAAGGA AGGGCAGAGA 1260
CATGGGGTGG CTCCATACCA GGGCCTGAAG GAAGAGGGCA TGAGCTGCCT TTCATGAGGA 1320
GGAGTGGGGA CACATTTCCA TGTCTTCATG TTTGTGGTCA TGGGTACACT 1370
|
