Tag | Content |
---|
EnhancerAtlas ID | HS037-09498 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr12:115888950-115890950 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr12:115890854-115890866 | TGCCTGGGGGCA | + | 6.04 | Sox6 | MA0515.1 | chr12:115889467-115889477 | AAAACAATGG | - | 6.02 | ZNF263 | MA0528.1 | chr12:115890054-115890075 | CCCTTCCTCTCCCTCTCCCTC | - | 6.3 | ZNF263 | MA0528.1 | chr12:115890022-115890043 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 | ZNF263 | MA0528.1 | chr12:115890027-115890048 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 | ZNF263 | MA0528.1 | chr12:115890032-115890053 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I115451 | chr12 | 115889005 | 115891497 |
|
Enhancer Sequence | CCTCGGCAAC CCTCGGGGAA AGACAGGTTA TTAGAGTCTT GGGTTGATGG CCCAAGGCCC 60 ATTTTTCTGA GAAGGAATAT GGGACCCTGA GCCAGGAGTT GACTTGGCCA TTCCCGAGGG 120 AGGCCAGCAG GCACACCCAG GACTCCTGGC CTCCTGCAGC CGAGAGGAAG GAGACTCCGA 180 GGCACCGATC CTTGGGGTTA GCAGGAGGTG GATGTCCACC AGCTCCTTTG TCAACCCTTC 240 CCCAGCCCCA CTAATGATGA TAACACCAGC CTGGTCCTAC AGAACAGCTT CTATGTGTTG 300 GGGACTGTTG AACCACTTAT ATCTTTGCCT GTCTTTAACC TCCCGGCATC CCTGTGACGC 360 AGACACCTTT ATTCTTCCCG TTTCCCAGGG GAGAAGATAG AGATGCAGAG AGGCAAGACA 420 CTAGCCCAAG GCCACAGTTA GAAAAAGGCA AAGTTCAGAT GCAAAGCCAG GTAGGCCCTG 480 CTATTCAAGG CTCTGCTAAC TTCAGCCAAG CAAGTAAAAA ACAATGGATG TCCTGTGAAC 540 AGTGGCATCT TTGGAAAACG TCGCTGTTTT TATTAATCTC TCTCAAGATA GATGTTGCTC 600 AAACACAGCA GCGTCGTGAC AGTGCCAATA GCCAGCAGTC TCCTGTCCGC GTGGGTTGCG 660 AGCCCCGGGC GTGGACGGAG TTGGGAGCGG AGGGCGGCAG GTGCCAGCGG GGCCCGCCTC 720 TCCCTGCAGG CGGCCCCGGC AAGTTCACGG CCGGCCCGGG GCGAGGGGCG AGCGGCGCGC 780 GGCCGTGCGG CTCATTCTAC CGCCCTGCGT GCGAAGGGGA GGCCGCGCCC CCGCGCCCCT 840 CGCTCGCGCC GTGCCTGCCG CCGCCACCCG CCCGGCCGCC GGGCCGGCCA CTGAGCGGCC 900 GCTGCAGACT CGGCGGCGCC GGCGCACCTG CAATCAGGCC CCGCGCCGCG CCGCCTCCTC 960 GAGCCCAAGG CCGCCGCGCG CCGCGCTCGC CGCTGATAAG AGGCGGCGGG GGAGGGGCGC 1020 AGGATGCTGG CGTTGCGGAA GGGCGGGGGA TGGGTGGGCA GCTGGAGCGG GCTCCCCTCC 1080 CCTCCCCTCC CCTCCCCTCC CCTGCCCTTC CTCTCCCTCT CCCTCTGCGA TGTCTCTCCC 1140 GAAAGTGTGT GACTTGCCCA TGTCTGTCTC TTGTCTGCGC CTCTCCCCTA AATTCCCTCC 1200 CTCCCCAGCC CTCGCCGCGA GCGTGTGTGC GCGCGTGTTC GTGTGTGTGT GCGTGTGCAT 1260 GTGTGTCTGT GTCTCCAGTT GCTCCCTGTC TCCTGTACCT GTCTCTGTGC ACTTCCTGAC 1320 CTTTCTGTCT CCTACTCCCC ACCTCTCTGA TTCTCTCCAC CTCCTGCTGA TTCTGTCGCT 1380 CTCTTCTCTC TTAGCATCCC CTCTTAGTTT CTCCCTCTCT CCCTGTTCTA TTTCTCTCTT 1440 CCTCACCTAA CTTGGAGCCA GTCCCTCCCC TCTCCCTGTG TCTGTCTTCT CTCCCTCTCT 1500 CCATCTTTCT GACTCTGACC TGCCTCTCCC CTTCTCTCTC CCTTCCCTGT CTCTCCGAGT 1560 CCTTGCCTGT CCTCCTCTCT CTGCATCTTT TCTTTCTGCG TCCCCAACTC CCTCTCACTT 1620 CTCCGTTCTT TCACTCATTT GTCTGTATCT TCCCTTTTCT TTTCTCGCCC TGGGCTCCTC 1680 CCCATAACTC TGCGTGTCCC CTGCCCATCT CAGCATCCTG TGGCACTTTC TGCATGGCCG 1740 GCCCGCCTGC AGGGACAAGG CCTTCAGAGC CAGCGGTTGC AGGAATAGCT GGACCCCACA 1800 AGGGGCTAGG CTCAGCAGGT GTCCTGACTT CAGGGGGCAG GACTGTGCTC ACCTGTGCCT 1860 TTCATGTAAG GCTCTGGCGC ACTTCACAAA CAGTCATTAA GGCCTGCCTG GGGGCAGGTC 1920 AGGGAATATC ACAGCCTGGG CTGTTTGGTT ATCTTCATTA TTAATACACA CTCCCCTGCC 1980 TTAAATGAGT TTAGTGCAGG 2000
|