| Tag | Content |
|---|
EnhancerAtlas ID | HS108-00295 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:9926880-9928470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:9927706-9927725 | CAGCGCCACCTAGTGGGCA | - | 7.54 | | PLAG1 | MA0163.1 | chr1:9927319-9927333 | GGGGGCCACTGGGG | + | 6.13 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_60796 | chr1:9907685-9935747 | DHL6 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I009867 | chr1 | 9927381 | 9927530 | | GH01I009868 | chr1 | 9927621 | 9927830 |
|
Enhancer Sequence | AGACAAGAGT GAATATGGGC TCAGTCCAAG AGGGGGCTGG AAATGAGAGG GAGAGAATGA 60
AGCAGGTCTG GGGAGCCTTA GGATGGACTC AGTAACCCAT TAGGTTCCTG AGGAAGAGAG 120
GAGTCGAGGC TGAGTCCTCG GGCGCCGTGT ACTTGCTGGG CATTGGTCAG GGCAGAGCAC 180
AGGTGGAAAA TCCATGTCAG CTGGGCATGG GTGGCTGTGG TGATGCTGGC CAACAGTCAG 240
CTGGCTATGT TCTCTGTTGA GATCACAGCA CTGCGTGTGG AACAGGGAGA AGAGAGGGGG 300
CAACCCTGGA GGATGACAGC CCTGATTGAG GGAAGGGAGT GGGAAACAGC CAGTGAGGGG 360
TGACGTGAAG GACAAGGGAG GGAAAGGAGG CTGTCATTGG TGGTCTCAGC CCAGCAGAGG 420
CCAGGCAGGC TGGGAACTGG GGGGCCACTG GGGCCTCTGC TGGAACCACC TGGTGAGCCC 480
GTAAGGGGAG GCCCCCACCC CAGGGTCTCC AGCACCTGCC TGGCTCCCCA TAGATACTCA 540
ACAAATGTGA CCGAGGAAGG AATCGAAGGG TAGGGGGTAA AGGGGTGCCC ACGGCCCCCT 600
CCCTGGGCCT CAAGTAAGGG AGCAGTGCCC CAGGTACCAG ACCCATCCAG CCCTGGAGGG 660
GAAGCATGTG CAGGGCTAAA GGTGGCGGCC AGACCCTCAG GACCAAGGTC GGGTGCTGTC 720
CGTTGGAGGG TCTGCCTCAG ACCCCCTGCT AGAGGAGTCC CGGGGTAGAT GGAGCCTCCT 780
CTGGCTCAGG GAACACCTAA AGCAGCCTGG AGCATTTGCT GAGAGACAGC GCCACCTAGT 840
GGGCAGGAGG TGCACGCCAG GCCATTACCC ACAGGCTCCA GGCCTTTGGG GTTCATTATG 900
GCAGTCTCTG CACCCTGCTC TGGCCCCCGC ATCCTGCCCC AGTCCCTGGA GACAACAATC 960
CAGGGCTTCT TCCACCTAAG CAGTGTCTGA GCCTCTGACA GCAGGATCCT GCAGCATCAG 1020
CTGAGATTGG CTCTGCGATG GAGAAGGTGG GCAGGTGAGA TTTTAACAGA GATCCATTTG 1080
CCCACATGGC ACAGGCAGAT GCAGGGTCCT GCCCTCACAT GGGTAAGCCC AGTATGGGAC 1140
TGGGCTGATT GCAGTTCTGC TGTTATTGTT GTTGTGTTTG TTTGTGGTGT CGTTAGGCTC 1200
GCAAAGAAAA TAAATATGCT TATGAAACTC TTCCAGACAT GGCTGACCCC TCCCCTCTCC 1260
ACTCCCAGTC CACAGAATTC TCAGAACCTC CTGCAGCTCA GGTCTGTGTG GCTCAGGCCC 1320
CGGCAGCCAG GTTAGAGGTA TCTTTATGGA GGTAGGGGCA GTCCACAGGG CGCCCCAGCA 1380
GCAGGGAGTG ACTCCCACCA CCTATTCCGC AACGATTCCC TGGGGTCTTC CCTGGCTCCA 1440
GCTTCAGCTC CAGAAGACCC CTCCCCGGAG AAAGAAGTAG CTGTGGACAG ACACCACCCA 1500
CCCAGAAGGG CCTGGACTCC ACGGCCCACA CAGTTGGTCA CAGCTGCCAG CTTGCTCCTA 1560
CTGCTCAGCA GTTTCAGGGC AAGGTCAACA 1590
|
