| Tag | Content |
|---|
EnhancerAtlas ID | HS108-06533 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr10:121203260-121205320 |
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 | chr10:121205027-121205046 | TGCTGCCCCCTGGTGGACA | - | 8.3 | | PLAG1 | MA0163.1 | chr10:121204058-121204072 | CCCCCTTGGGGCCC | - | 6.44 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I119444 | chr10 | 121204461 | 121205441 |
|
Enhancer Sequence | GATGGTGAGC TCCTGGTGGC CAGATGCCAC CCTCAAGCTG GTGGCTCCCC TCCCTGGGCC 60
TGGCCCCAGT CTGTCCCCAG AACAGCAAAC AGGCTGAAGG GACAGGGGTC TGAGCATGGG 120
GGTGGGGGTT GCAGCCCACC AAGCTAGAGT TGAGGGCACT CCTTGCTGTG GACTGGGGTG 180
GTCAGCGGAG ACTTCCAGGA GAAAGCCTGG GTGGGGCAGG GACACCCAGG AACCAAGGGA 240
AGAGGGGTGA GGGGAACAGT GTGGAACACC CTCACATCCA GCCTGTGGGG GGGTCCACAC 300
AGGGCGGAGA AGAGATGGTC TGAGCTGGTG CCCCAGACAC AAAGCAACCT TGGGCCAAGC 360
CCCGGCCCCT GCCCGTGGGC CTCCTGCTCC CTCCACCTCT GGATCCTAAG GTGTTGGTTT 420
AAGACGAAGG GCTACAGGGG GTGGGGGCGA CGATTTCAGT CTTTGAACAT CTTATAACAA 480
AGTTTTCCAC CACTAGATGG ACTGCTGGTC ACGCCAGCCT GGCTCCTGCA TGACAGGGTC 540
TAGGGATAGT GAGGTCAGAC CCACCCAAAA GCTGGGTGGG TGGGGCCAGA TGGGGGGACT 600
GGAAGCCAGA TAAGGAGTGA CAGGAGCCAT TGGAAGTGGG GGATATGGGA GTGGAGTCCG 660
CCCGTGCACC CCTGCCACTG GGCCGCCCCA TGCCGGCCCT CAGGCCCTTC CCTGGGAACC 720
AGGACTAGTG GCTGGCTTTG TGGGGAGATG GCCACTTCCT GCTGCTGCCT GGCTCTCAGC 780
CCCCAAGTCC AGCCCATGCC CCCTTGGGGC CCTCCTCCTT ATGGTCCCCA GCACAGCTGT 840
GCTGGCACCC CCACTGCAAG CAGCTGCCCT CTAATGCCAG CCTCATAGGG ACAGGAGGGG 900
CCGGAGCACC CAGCTCCACA ATTGCCAGCC CACAGACTTC CTCTCCTCTC CCTGGAGCCA 960
CAGATGTACC CCGTATCCCA TGTACCCGGA GCCACAGATG GGCAAACCGA GCCTGGGAGG 1020
GGGGAGCCAC ACTTCCCACC CCTCTACATC TGCAGGCACT TTTGGGGCAG ATTCAGCGTG 1080
TGCATTGACA ACCCAGGCAA CTCCCGGAGT TTAGGAAGCA GCAGTCCTGG GAGTTGATTA 1140
AAAGTCGCAA TGCTTCTGCT CAGGAAGACC TGAGATCTGC GCCGCAAGCG GCCCCAGGAG 1200
GGTCTGGCTC GGCTCCTCAC CCCAGAGGCC CCTCTCCTGC AGCCAGACAC CTCTGCTTGG 1260
CCCCTTCCTG TCACCAACCT CATCCTCACA TCACAGAGCT GTGGGAAGAA GTCCTGTGTG 1320
TACAGCAGAC CCACACTCTA ACCCCACAGC TGTTGGCCCG CCATGCAGCT GGGGCCTCAG 1380
AGAAAGCCAC ATGGTCATCG CAGCCAGGGC TAGGGTGGGG GGACCGGAGG AGCAGTGCAG 1440
CACTGGTCGG GTAAATGGAA ATGTGGGTGT GAGCCATACT TGGCTGTCTC ATTGGGAGAT 1500
ATCTGTCAGG TGCGACAAAA CGAGACAAGG GAAAGAAGAA GGGGTCAGAC AGCCGTGGGC 1560
AGAGCATCAC CAAATGTCCC AGGTCAGGGC CAGGCAATCA GAGAAGCAGG TCTTGAGAGA 1620
TCTCAGCAGG GATATGGGAC GTACTAAGAG GATGACGAGG CGGAGAGGGC CCCAGTCCCA 1680
CCCCCAGACC CCAGACACCC ACCTTGGCCC CTGGCTTTGG AGCTGGGATC TCCTGCTGCA 1740
GCCTGGACCA GGGTGCTGCT GTCCCTCTGC TGCCCCCTGG TGGACACTGA GAGAAAGCCT 1800
GCTGCTCCCG GAGGACCTGT CCCGTGGGTA CAAAACCACT GTCCTCTGGA AGCCTCTGGC 1860
CTTGCTGCGG CTTCCCTTAC AAATGATCTT TGGTCTTGGG AGTCTAGTCT TAGGCCTCCT 1920
TCACGCCCTT GACTGCAGCA TCTCCGGCAT CTAGGCCTAC CTTGTCCCCT CCAGCTGGTG 1980
GCAGCTCAGG ACACTGCAGA GCCTGACTTG CCAGGAGACC TCGCAGGTCC TGGGTTCACA 2040
GGGCTATTTC TAGGCTCTGG 2060
|
