| Tag | Content |
|---|
EnhancerAtlas ID | HS112-12569 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr6:41553680-41554740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr6:41554725-41554739 | CCCCCTCGGGCCCC | - | 6.65 | | STAT3 | MA0144.2 | chr6:41553867-41553878 | CTTCCCAGAAG | - | 6.14 | | ZNF263 | MA0528.1 | chr6:41554465-41554486 | GAGGGAGGCGGGAGGAGGGAG | + | 6.04 | | ZNF263 | MA0528.1 | chr6:41554452-41554473 | GAAGCAGCGGAAGGAGGGAGG | + | 6.26 | | ZNF263 | MA0528.1 | chr6:41554461-41554482 | GAAGGAGGGAGGCGGGAGGAG | + | 6.3 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_27953 | chr6:41549879-41554533 | Fetal_Intestine | | SE_27953 | chr6:41554607-41555945 | Fetal_Intestine | | SE_28956 | chr6:41549728-41555676 | Fetal_Intestine_Large | | SE_31492 | chr6:41548891-41556560 | Gastric | | SE_65317 | chr6:41547965-41559615 | Pancreatic_islets | | SE_69040 | chr6:41551604-41553856 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I041580 | chr6 | 41548426 | 41555595 |
|
Enhancer Sequence | CCCAGCTTCT TCCCCTTCTT CTTATGACTT GCCCAGCCAC CCCTCGGTCT CCTCTCAGAG 60
CTCCCCAGCC TACATCCCCT ACCCCATCGG AGCTTCTATA CCAGGCCCTG GAGGCCCTTC 120
TCCCCTGGGT CCCAGACCTG TGCATCTCTC CTGCTGCCCA ACCGCAGCCC CAAGCTCTAA 180
GTTTCCTCTT CCCAGAAGGC TGCCCTGACA CCCAGGAATT CTCCAGCACC CCCAGTCTCC 240
CCCTCAGCAG TCTTGTAATT GCTGTGTTAT CAGCAGGTAA ATCTCTAGGC TAAGTTTATC 300
CTGTGTCTCT CTATTGAATA GCCAGCCCCC ACCCTACCCC ATGCTTCCCA CCCCCAGCAG 360
GCAGGCAGAG ACATCTCTGC CTCTCAACCC ACCCAGGACA TGCTTGGCTC ATGGGGCTCA 420
AGAGAGACTT GCTGACAGCC TGACTTGTCA GTGCCTGTGT GAAGAACTGA ATGGGTGGGG 480
GTAGGTAGAG TGGGTGAGCC AACGAGTACA GGGCGCCTGG GCAGTGGTGA TGTGACTGTT 540
CTCCGAGCCT GGGTCCCAGT GAGTCCCGTC AGACTCCTTG ATTCTCTGTA TCTAAAAAGC 600
AAGAGAGGAA AAGAGCTGGG GGAGAGAAAA CTCCCTCCCC AGAGCAGAAG GGGGCACCCC 660
GGGCATGTGG GAAGGGTGCC CTCCAGGCAG GAGTGGCCCC CAGAATCTGA CAGGCTCATC 720
GATCATTGTG ATGAGGCACC CCCAGGCGTG CACAGCTGCG GTGCAGGGAG CTGAAGCAGC 780
GGAAGGAGGG AGGCGGGAGG AGGGAGGGCG TCGTGCTGCG TGTCTGGGTC TGGCTGTGTG 840
TGTTTGCGCG CGTGCGTGCG TGCGTGCATG CGTGTGTTTA CTGCGAGGAG GCATGCAGCC 900
TTATGGAAGC TGGGCCGGGA GCAGAGACAC TGCAGCTGCA GACGCCACAA CGACAGCTCC 960
AGGGGCTGAC AGGCCCTGGG AGGGGGTGGC CGCGGGGTGG GGGCCAGATG GCATGCCTGA 1020
AGCTGATGGC ACCCCTCTCT GCCCGCCCCC TCGGGCCCCT 1060
|
