| Tag | Content |
|---|
EnhancerAtlas ID | HS091-08577 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:100698000-100700850 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Znf423 | MA0116.1 | chr11:100700314-100700329 | GCCCCCTAGGGTGGC | - | 6.23 | | Znf423 | MA0116.1 | chr11:100700314-100700329 | GCCCCCTAGGGTGGC | + | 7.12 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I100827 | chr11 | 100698177 | 100699810 |
|
Enhancer Sequence | TGGGATTACA GGCATGAGCC ACAACGTCCG GCCAAGCCTT ACATCTTTAC ATAGAGTGAT 60
GGGACCTTCA ATGGAATCAC TTGGAAAACA CCATGTGATT TTCCCCTAGT TGTGGGGTCA 120
TGGTAGTCTG GTATGCAACT CATACTTTGT GAAGCTGATG TGGCCTGTGG CATGTGGAAA 180
AGACAGCACA ACTTGCAGCA GGTGGCTGCA TTCCTAACCC AAAGGTGCAT GGATCCCAAG 240
GGCCTGTTGG TGAACCCACA GTGGAAATGT TTACCTGGGG TCATTTTCTA CAAGGGTAAT 300
GCCAGTAGGA TGGGAAACCT CATCAGTATG AGGCTGTGGG GAATACCATG GGGTATAGAA 360
GCTGAGGGGT AAGGTGTGGC TGGCCACAGG AGAGGCACTG CCCACATTGG CAAAGTCATA 420
GTTGTGGAGG CCTACTAAGG AAGTAAGTCT CAAATAACCT GTGAAAATAA TATTCACAAG 480
AGAGAGCTGG CTCTAGCCCA TCTCCTTGGC CAGAGAAAAG GAATCTTTAA GTATCAAGCA 540
AGAACTTTCC TTCACTATGC CCCACAGTGA TCTTGGAAGT GGTTAGTAAT AGAAAAGGAG 600
ATGTGTGGAA GAGAAAAAGT CAACTAGAAT CTACCCTTTA CAAAACATAG GTTCTCTCCT 660
TCACCACATG GGAGTGGGGG TAAGAGATTT AGAGGCTTTT TATTTCCTAA GTGTTCAGAA 720
AAGCCACAGG GTCTGCCCAC AGTCTCATCC CTGAGAGCAG GTGAAGGACT GCTGCCTATC 780
ACTGAGCAGG TGAAAAATGG GAAGTAAAAG TCATGGCTCT TAACATTCCA GGGGTCCTGC 840
TGTTGAGAAT GCCTTGCTTT GTTTGACACT ATCAGTCCTC CAAGTGGTCT CACTTGCCGC 900
TAAGTGCTGA TTTGTAGTCA GTGGCAAAGC ATGAGGGTAA TACTTTTCTT CCTTTTGTGT 960
TACACCCTTT AGAAGGATTT TCCCCAGTTT AAAAAAAAAA ATCCTTAGTG TTTTGCAAAG 1020
TTCAGGGGAA GAACTCTTGT GGTTTTGCTT AGAGCTTTCT TTATTTCAAG CCCTCAGAGC 1080
TGATCCAGGG ACAGATTTGA CAAATTGCTG CTATACATGC TGTGCTCACC CCTGTTCTCT 1140
GATGACTGAG CTTGTTTGTT CAAGGAAACT ACCTCATTGT CTCTGACTAG GCTTCTGTGA 1200
AATAGTAATG CAGTTCACCA GATATGCTCA AATATGTGTG GACCCCTGGT GGTGGTTTCA 1260
ACCTGAGCAA GGTATGAGGA ACCATTATAA ATAGGCATGC ATCAGGGTAT CAGAGCTGCC 1320
TAGACAGACC TGCAGAACTC TCAGATTCAA CATACATGAC TTTAAGGGGG AAAGGGCCTA 1380
CCTACTATTA ATTGTTGAAA GATACTGCTT TTCTGTTTGT CTTTTTTTTT TTTTTGGAGA 1440
CAGGGTCTTG CTCTCTCACC CAGGCTGGAG TGCAGTGGCA TGATCCTAGC TCGCTGCAGC 1500
CTCAAACACC TGTGCTCAAG TGATCCTCCC GCCTTGGCCT CCCAAAGTGC TGTGATTACA 1560
GGCGGAAGCC ACCATGCTCG GCCTACCTTA CCATTTTGTA GATGTGTAAA GTGAGGCCCA 1620
ACAGTTGCCA CATGCCCAGG ATGCACAACT AGTGAATATT ACAGCAAGCA AAGTAATTTT 1680
GCACGTTTGG CTGCAAGTAA TACAAAACAC AATAGTGGCT TAAATCATTA ATGAGTTTAT 1740
GGGCCTTATG CAAAGAGGAA TCTGGAAATA GGCAGCCAAG GTGATGCCTC CAGGAGTGCA 1800
GGCTCCTTTG CTCTCCTTTC CTGCCATCCT TAGTCTGTGG CCCTTATCCT CATGCTTGTC 1860
ACACCACAAG CATAGCTTTG TGGCAGTTGG CACTTTCTGG CATCAGGTTC ATGTTTCAGG 1920
CAGGAAGAAT GGTGGCTTGG GGAAAAAAAG CATGGTGGCT TCCGCCTGTA ATCACAGCAC 1980
TTTGGGAGGC CAAGGCGGGA GGATCACTTG AGCACAGGTG TTTGAGGCTG CAGCGAGCTA 2040
GGATCATGCC ACTGCACTCC AGCCTGGGTG AGAGAGCAAG ACCCTGTCTT CAAAAAAAAA 2100
AAAAAGACTT TCAAGACTTT CAAGAACCTC ACCAGGTTAA TTCTGCTATC ACAGGACCAG 2160
TCATAGTTAC AAACTGGGTT GGAGATGTAT TTTAACTGGA CACACTGGCA GCTCTAGTAG 2220
TGCTGACCAG GGCATGCAAA GAATCTTCTT AGCTTCAAAG GCATTACCCA CTTTACTATG 2280
ATACAGACAG CTCCTCCTCA GTGACTCCTC CTCTGCCCCC TAGGGTGGCC AGTGACTGCC 2340
ATATTGTTCA GTGATAGAAA TTACCCTTTT TCATATTGTG CATGCATATA ATAAACTTCA 2400
ATTTTGGCAT TTTCCAATGG TTAATGATTC CTTTATCTGT TTACGGTTGT ATGTTATTTT 2460
CCCCCTTGTT GTCTGATTGG TGATTATTAT AAATTGTTTC TAAAATCTTC TAATTACCCA 2520
GGTATTCCTT GATTATAAAT CACATGAGCA AAATCGGCTA GTTCTTTACT CTGAAGTTTA 2580
TTTTTAACAA AATTCATCCA TTCATTTAAG ATGTTTACAA TTACTTTGTG ATGATAAGAC 2640
TAAGTCCTAG AGTTCATACT TTTGCAGCAT TAGCAAGGAC AAAATTCTGA TCAAAGCTAC 2700
ATACTTTGGA TTCTCCAAAG GTGTGTTTGT ATCTTTCAAA TATGTGTTCT GTAGGACAGT 2760
AGAATAACAA TAAAAGCAAT ATTAATAGGA TGTTAGTAAG GGCTCAGAAG TTAAAATCTT 2820
CTTCCATGGT CAGATTACTT TGAAAACTCC 2850
|
