| Tag | Content |
|---|
EnhancerAtlas ID | HS108-41597 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:131013220-131015370 |
Target genes | | Number: 42 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr9:131013904-131013924 | CCCCCAACCACCCCCTCCGC | + | 8.86 | | ZEB1 | MA0103.3 | chr9:131013457-131013468 | CCCACCTGCCC | + | 6.14 | | ZNF263 | MA0528.1 | chr9:131015192-131015213 | GGAGGTGGCGGGGAAGGAGGC | + | 6.04 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I128251 | chr9 | 131013948 | 131014210 |
|
Enhancer Sequence | TGAGTAGGGG CTGAATGCGG CTGGAGAGGC TGCCGGACGG GCGTGGCCGG GAGGGAAATG 60
GGGCTGGATT CCAGAGCATC GGACCTGGCC GCCAGAACCG GCCGTTTCTA TCCCAGGCAA 120
TCGGACTCTG GGTGCCGGAG CCACGCCACG TGTGGCCGAG GGCTGGCGGA GCCTGCCCCC 180
GAGGGAGCGC TGAGTCCCGG AGGTGGTCGT TTCTGGGGAG GGGGCTGTGG GGCTCGTCCC 240
ACCTGCCCCC TTCTTTCCAG CACTTGCATG GCGCTTCCCT CTATTTTCAC TCTTGGCGGC 300
CGCCCACACG TTGCATTCCT CCTCCTTTCT TCTTCTTGCT GTCCTCCATC CTCCATTCCG 360
TCCAATTCCT CTCCCAGCCC CTGGGGAGCC TACCTTAGGT CTGACTCTGA ACCCCGATCT 420
GCTCTGAGTG TGTGGATTTC CTTCAGCTAC CCTGATGTCC CCACTTCCCA GCCCTGACTC 480
CTTTGAGCCA TCCCAGGGGG TGTCCAGCCA CTGGCCCACA GGAGCAGAGG CCAGGCTGTG 540
ACTGTGTGAC TAGAAAGGTG TGTGATGTGT GTGTGGGCGT GCACACGAGT GTGAGAGTGT 600
AAGCATGGCA CCCAGGCCCG GGCTAGGACA GGAGCAGCTG GGGAAGCAGC CTGGGCCGTG 660
GGCAAACTGA TGGCTTTTTT CCTCCCCCCA ACCACCCCCT CCGCGACTTC TGGCCCTACC 720
CAGTCTAAAC CAATGTGGTA GGGGTGGCGG CAGGGGCAGG GATGGGAGTG CTTGAAGCCT 780
GCTTCATTCC CAAAGATTTC TAGGGAAAAG CTTTCTACTA CATCCTTTGG CTTGACCTTC 840
TTGACCCATG ACTCTCTTTC AAGGAAGTTC ACTCCAATTC CCAGTCTGCC CTGTTTCCAC 900
TGGCCACATT CTCTAAGGAA GAACACAGCA GAACAATAGC ATCTGTTTTG TTTCTGCATG 960
GCTGGAGGGT AGGGCTGTCG GTCTAGCACC CATAAACCAA AATGAGGCAG GGATTGGGGC 1020
TTGCCCTATG ATGCTCTGAT GACCAAAGCA GATGCGTAGA GGCAAGCAGC ATGGTATTGG 1080
GCAAGAGGAC TGGACTGGGA GTCCAGAGAT GCTGCTTCAC CCTGGGCCTT TAGACACGTC 1140
TCTTTCCCTC CCAGAGCCTC AGCATCCCTT CTATCAAATG ATGACATTCT GCCTTTTTCC 1200
CAGGGCGGTT GTGGGGATCG AGGGAGACAG TGGCTATAGG GATGCTGTGT TAACTGCAGA 1260
TGCAGCCGTA GGAGCACTTT GCTAACTGCC AACGTGAGTT CAGATTCTTC AGGGTATTTG 1320
GCACCCAGGT CTATGGTGCG GTGTGAGATC TGTGATGTAA GGTTTGATGC CTGCCCCAAC 1380
TCCAGTCTTG CTAACACACA TGAAACATTT GGCAAATCAT GACCCTACCT TGGGGAAAAG 1440
AGCAGTCTGG GAGAGCTTCT TCAAGGCAAC CTGACTTCAG TGCAGTCTGA GGCATGGCTG 1500
AGATAGGCTT ACGTGGCAAG GAATCAGGAG GGTATCTGGG CCAAGAGCTG CAGTGTGGGC 1560
AGAGGTGTAG TGTGGGCTGC AACGAGGACA GCCACTGGAC AAAGCAGAGA ACAGAGACAG 1620
AATGAGGAAG AGCTCTGTGG GCAGGGTGGG GCGCAAGGTG GAGAACCTTC AAAGTCTGAA 1680
AAGTTTGACT TGTTGGGGCT CAATGCTGTG GGCAGTAGGG AACCACAGAA GGCTCTTAGG 1740
TGGAGAAATG ACAGCTGGAC TTTAGCGAGC AAGCCCTATC TCCATGAGCA GCACGGGTGA 1800
TCCTCTAAGC ACACCAGGCA CGAGTGTGCA GGGAGCTGGT GCAAATGCCT CTGTGTGCGG 1860
GTGAGCTTCT GTGTTGTGAC TCTGCCCACA CGTGTGCTTC AGTGTGCTGA GTGGCTGCAT 1920
GCCCCAGATC CATGCTGCAC GCGCCGCCGG CCAGTGAGGG TGCTGGGCAC TGGGAGGTGG 1980
CGGGGAAGGA GGCGTATGCG TGTTGTTTGT GGGCATGTGT GTTAGCGTGT GCATGTGGGC 2040
CATGGGGCCT CACAGCATGT GTGTGCACGC CCGGGCGTGT GCGTGTGTGT GTCCCCCACC 2100
CCCAGGCCGG CCCCACCCGT GCGTGTGAAC TGCCATGTTG ATTTCGTGCT 2150
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