| Tag | Content |
|---|
EnhancerAtlas ID | HS108-35002 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:69470650-69471830 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr6:69471007-69471018 | GACAGCTGCTG | + | 6.14 | | NFAT5 | MA0606.1 | chr6:69471712-69471722 | AATGGAAAAT | - | 6.02 | | NFAT5 | MA0606.1 | chr6:69471719-69471729 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr6:69471712-69471722 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr6:69471719-69471729 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr6:69471712-69471722 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr6:69471719-69471729 | AATGGAAAAT | - | 6.02 | | NFIL3 | MA0025.1 | chr6:69471532-69471543 | ATGTTACATAA | - | 6.32 | | Tcf12 | MA0521.1 | chr6:69471007-69471018 | GACAGCTGCTG | + | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I068761 | chr6 | 69471294 | 69471734 |
|
Enhancer Sequence | AACGTCACTG GGTATGAATT CTAGCTAGAT TCAATGTCCA ATTACTGAGC CCACCACAGG 60
ACACTATAAT AGCAGCATGT CCAGTTCTCT GAATAAATTT GTCAGCTGCA TTCAACATGC 120
AATTTAGATA TGTGGCATAT AGTGGAAACC AAAAGGAAAT ATTCAAATAC TATAATTTTT 180
CCTTTTGCTA AACTTATAAT TTCTAAAATA CATTGGTATC ATTTTTAATG TTGTCTTCCA 240
GTTAAATGGC TTGGGTTATT TCCATGCTGG AAAAATTAAG TTGATTCTGT TGATATCCTT 300
TCCTGCTGCC TCCTCCAGCG GATGTTCTCA CTCCTCCCTG GTGATCCTAA GAAACAGGAC 360
AGCTGCTGAC GGTAGTAAAC AGCAGTACAA TTCCTGCAGT CCCAATTCGG ATCACATACC 420
CTGTTAAGGC AGGAACTCCC CACCTCCAAG TCTCCAGGTG AAAGGCAACA AGGAGAGAGG 480
GAGAAATAAT AGATAGTATG TAGACAGTGC CCTAAATATT TTCAAACAAG CACACTTGGA 540
TTTACATATT TATATAAATG ACCTAAACTT CTTTATTTGT CCCTTTCTTT TGACTCACCT 600
AGGTTTTCAG TTGGTAACTC CTTGCAGGCA GTCTCAGGCG TGACTAGTTA ATTCCATGGT 660
GCTACTTTGA ACCTAAATTA GGCTTCTACA GTTACTACAT ATTTCTTTGT ATGTGTCAGT 720
GTAGCACAGG TTGTGCTTTG GTGTCCTCTG CAGGCTTGTT CAGTGTCGAT GTGGTGCTTG 780
CTTGGTTGAC TTCAGTGAGT GCACAGAGTA TTATGCTGCT ACGTTCCAAA ATATGCAGGC 840
GCCAGACATG TATTTTCTCT TTTATTATAT AGGCTGTAGG TGATGTTACA TAAACCTGTT 900
TTCTCATGCC CCGTTTCTTT AGATTCTGCT TTTTTGTTGT TGTTGTTTCA AACTTGTTTG 960
TCCTCTGATC AAGTCTAAGG TTTTTAAACA GGACAATGCA AATATGTTTT ACTATTAGGT 1020
TTTCTACTCA TCATTACACT GTGTTCAAAA ATGGTAATTG AAAATGGAAA ATGGAAAATT 1080
GTTATGAGAC CAATTAGATA ATGTGCATGT CAAGTTCAAG TTTAACTGAG AAGTGTTGTA 1140
TGTGACCATT ATATTGTCTA GTATTTTCTA TAAGAATGGC 1180
|
