| Tag | Content |
|---|
EnhancerAtlas ID | HS091-11109 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:121459310-121461790 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr12:121460954-121460966 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr12:121460958-121460970 | GTTTGTTTGTTT | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr12:121461311-121461326 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr12:121460108-121460123 | CGATCTCTTGACCTC | - | 6 |
|
Enhancer Sequence | TCCAGAAGAA ATATAAGCCT TGGCTGGGTG CAGTGGCTCA CGCCTGTATT CCCAGCACTT 60
TGGGAGGCCA AGGCGGGCAG ATCACTTGAG GTCAGGAGTT TGAGACCAGC CTGGCCAACA 120
TGGCAAAACC TATCTCTACC AAAAAATGCA AAAATTAGCC GGGTGTGGTG GCGTATGCCT 180
GTAGTCCCAG CTACTCGGAA GGCTGAAGTG GGAGAATCTC TTGAACACAG GAGGTGGAGG 240
TTGCAGTGAG CTGAGATCGC ACCACTGCAC TCCAGCCTGG GCAACAAAGG GAGACTCTGT 300
CTCAAAAGGA AAACAAAAAA AGAAAAAGAA AAAGAAATAT AAGCCTGGCA TTGCCAAGTT 360
TTCTGACTAG CCAAGATAAA AAATATTTGC ACAATGTTGT GTGTGTTTGT TTTGTTTTTT 420
GAGACAGGGC CTTGCCCTGT CACCTCAGGC TGCAGTGCAG TGGTGCAATC TTAACTCACT 480
GCGCCTTGAC CTCCCAAGCT GAAGCGATCC TCCCGCCTCA GTTTCCTGAG TAGCTGGGAC 540
CACAGGTGCG TGCCACCACA TCTGGCTAAG TTTTGTTCTT TTTTTTTTTT TTTTTTTTCA 600
GATGGAATCT CACTCTGTTG CCAGGCTAGA GTGCAGTGGC ACGATCTTGG CTCACTGCAA 660
CCTCCGCCTC CCAGGTTCAA GCGATTCTCC TGCCTCAGCC TCCCTAGTAG CTGGGACTAC 720
AGGCACATGC CACCACACCC AGCTAATTTT TGTATTTTTA GTAGAGATGA GGTTTTACCA 780
TGTTGGCCAG GATGGTTTCG ATCTCTTGAC CTCGTGATCT GCCCACCTCG GCCTCCCAAA 840
GTGCTGGGAT TACAGATGTG AGCCACCGCA CCTGGCCAAG TTTTGTATTT TTAGTAGAGA 900
CGGGGTTTCA CCATGTTGCC TAGGCTGGTC TTGAACTGTT GGGCTCAAGG GATCCACCCG 960
CCTCAGCCCC TCAAAGTGCT GTGATTACAG GCGTGCGCCA CTGCCCCCAG CCTACAATGG 1020
CTTTTATATT CAGGAAAAAT CCAGAGGCGT ATATTTTCCA GCCCATGGGT GGGCCTCCTC 1080
ATTTGGCCAG CGGGTCCCCC CGTTTATACT CTATGTACCT TACTGGAGCC TCTGATTCTG 1140
CTTCTGCCTT CTGCTCCAAG CAGTTCAGTC TCCTGTCCTG TACACATCTT GCTCATCCCA 1200
GCCTCCCATC CTTTACCCCT CATCATCCTT TGTCCTCTGT TCTGAGTGTC TATATCTCCC 1260
CCCGGCCTTT AGGGCTCATT TCAACTCCTA ACTTTTTAAA GGAATCTTCT CTGGTGACTT 1320
CAGTTAACAT TTATTCTGCT TCCAGACCCC CAGAGCCCCT GGTTCTGCTG CCTCTTAGCA 1380
GAGTGCCCTT AGTTAATTAA CCTCTCTGAG CCTCAGTTTT CTCTTCTGTA AAATGGCAAT 1440
AATAGTAATG ATGATAATAA TAATAAAGAT AGTGATAACA CTCGACCTTC TTACTTTACA 1500
GAATTGCTTA TGAGGATCAA CTGAGACAGA CCTTGGACAA GAGCTTTGCA CACTAGAAAG 1560
TGTGATGTTA ATAAAATAGA TTTTTGTGAT CTCTGCCTAT ACTATAGGTT TGGCATCATA 1620
TAATAATATG ACTTAGTATT TTTTGTTTGT TTGTTTGTTT TCAGAGTATC TTGTCTTCTC 1680
TGGTAATTCT AGCAGTTTTG TGTAAGTTTG TTTCATGGAT TTGCTTCCTG ACAACATAGG 1740
GTGAGTTCTC TGAGAGTGAG GGTGGTGTCT TTTTTTTTTC TTTTTTTCTT TTTTTTTTGA 1800
GGCAGAGTTT CCCTCTTGCT GTCCAGGCTG GAGTGCAATG GCACGATCTC AGCTCACTGC 1860
AGCCCCCAGC TCCCGGGTTC AAGCGATTCA CCTGCCTCTG CCTCCGGAGT AGCAGGGATT 1920
ATAGGCACCT GCCACCACGC CCGCCTAATT TTGTATTTTT TTAGTAGAGA TGGGTTTTTT 1980
CCATGTTGGC CGGGCTGGTC TTGAACTCCT GACCTCAAGT GATCCACCTG TCTTGGCCTC 2040
CCAAAGTGCT GGGATTACAG GCGTGAACCA CCGCACCTGG CCGAGCGTCG TGGTCATGTC 2100
TTATTTCTGT GCCTGTGTTG TCCCCCAGCC CACATCCCCT ACCCCATCCC TGAGAACAGC 2160
ACTGGCACAG AATGGCTGAT TGAGCTGACT TGGCTGGACC CAACTCACGC AAAGAATGAT 2220
CAGGAACACA GAACTGATTC TCCAGTAAAT TATGGGAAAA AGAAAGGAAA GGAGAACAAG 2280
AATTTGAAGG TAAGAAACCC AAGGCTCTGA GAGCCAAAGA ATTTGTCCAA GTTCACGGAG 2340
CCCATGGGTG GTGCAGCTGG CCCTTAAACG GTGACTCTAA AGTTCTGTTC TCCATCAACA 2400
CAGAACTGAA TGAGTAAATA CTGAGTAGTT TATCTGTCGT TCTGACCTTC AAGCCCTTGA 2460
CAGCCCAGAG AGGAGCCATT 2480
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