| Tag | Content |
|---|
EnhancerAtlas ID | HS101-08271 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:69149700-69151540 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr11:69150975-69150990 | AATGCTGAGTCATGC | - | 7.77 | | Nfe2l2 | MA0150.2 | chr11:69150977-69150992 | TGCTGAGTCATGCTG | - | 9.03 | | Nr2f6(var.2) | MA0728.1 | chr11:69150082-69150097 | TGACATTTTGACCCC | - | 6.54 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I069336 | chr11 | 69151441 | 69152968 |
|
Enhancer Sequence | ATAGCTTCAC CACACACCAC AATCATTTCA CCCATCGGCT TCTGTTGTAA CAGCACTTTG 60
CTTCTGTCTG TCCTCCCTGC CTCCTCTCTA AGGACCCTGA GATTCAATTT AGAGCCCACT 120
TGGATAATCC AGCTCGGGAT CATTTCCTTA CTCACATCCG CACAGCCCTG TGTGCATATG 180
CACAGCTCTG TTTGCGTATG CATGACCCTG TTTGCATATG CATGAATCTG TTTGCATATG 240
CACGACCCTG ATTGCATGTG CACAGTTCCG GGCATCAGTG TGTGGACACC TTTGGGAGGC 300
TGGCAGTCAG TGCCCCACAG CGTGGCCTGT GCCCAGGGAT GCCTTGATGT GGGGCAAAGA 360
GCCTCGGTGG ACACACCTGG GTTGACATTT TGACCCCCCA TTCAATGCCA GTGGGGCACC 420
CCTGGATGAG TCATTTGATC TCTCTGGAGC TCTTCATCCA GGAGATGGAC ATGATAGTTC 480
CTGCTCCTCA GGGCTGCGGA AACTGAATGA GACCATACAG CTGTTTGTAA ATGTGTCTTT 540
CAGTGGCAGA GACTTCCTTT TCATCAGAAT CTGGTGAGGA ATCTCCTAAC ACACAGAGGT 600
GATGGAAACA CGGCTGCTGG GACCGGTGGA CTCCCCACCT TCCCCACACA GGGCCACCCC 660
CTTCCTGCCT GCAAGGACCC AGGGCTAGGA ATGCAGTCGG AGAACCTGTG CGATAGAATG 720
CAGCCTTGGG GTTCACAAGC AGGGGACGGG GACAGCTCCT CACTCTTCTA CCTTGCTCTG 780
TCCCACCCCA TGGAGGGAGT GACACGGGAG CTACGCAGAG AAAAGAGCAA AGTGTGTCAG 840
TGTCATGACT TGCCAAAGCT GATTGGAAGA TGTGGCAGAT TGTGTTTCTT TTCCCAACAA 900
TGACTGTCTC CTCCCTTAAG AGAATGGGAT GTCCCCACCA ACGCCATGTG GCTTGGCAGT 960
GCCGCCTGCA GAAAGCGCCT CCATTCCTGT CCCTGTGCTG CTGGGGAGTA CCACCTGCTT 1020
GCTTTGGTCA ATGGAAGATG AGAGGACAAC ATTGACCCTT GGTCTGAGTG CAAGCGCTAA 1080
GTGCCATTGA GGTTGACGTG AGAAGAGCAT GTGCCACCAG GAGCTGTGCC TTCAGCATGA 1140
GCCCTGGCAC GCAAGCTGTG GGCAGACTCG TGGCTCCCAT GCAAAGTGCA GGGGACATAA 1200
ACCTTCACTG CTATACACCT CTGAGAGGTG CGGTGGTTTA TACCACAGCA AAACTGCCAG 1260
GCAATGTAGC TTCCGAATGC TGAGTCATGC TGGGCTAATG ATGGCCCTGT CTACTCGTAC 1320
CTGGAATCCA GCCCTGGCCA AGCCCACTGA GGGATGTCTA GATTTGGGCA CACGAACTTA 1380
GCTATATGTT ACGTTATCTA GCCTGGGGCA GAGAGGGAAG GCAAGATATC AAGCCCCATG 1440
CCTAGGACTT TAAAAAAAAT ATCAGTTTTT ACAGAGGAAC AATTTACGTT CAATACATTG 1500
TACATCTTTT AAGAGTGAAG CTCAATGATC TTTCTTTGTG AGACAGGGTC TCACTCTGTC 1560
ACCCAGGCTG GAGTCCAGGC GTGCGATCTC AGCTCACTGC AGCCTTGACC TCCCAGGCTC 1620
AAGCGATCCT CCCACCTCAG CCTTCCAAGT AGCTGGGACC ACAGGCATGT GCCACCACAC 1680
CCAGCTAATT TTTGTATTTT TTGTAGAGAT GGAGTTTGAC AATGCTGCCC AGGCTGGTCT 1740
CAACCTCTGG GCTCAAACAA TCCTCCTGCC TTGGCCTCCC AAAGTGCTGC GATTACATGT 1800
GTGAGCCACT GTGCCCGGCC ACAATGACTT ATTTTTATTT 1840
|
