| Tag | Content |
|---|
EnhancerAtlas ID | HS073-03495 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr12:120972770-120974600 |
Target genes | | Number: 22 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr12:120973085-120973096 | TGTGACTCATC | + | 6.14 | | JUND | MA0491.1 | chr12:120973085-120973096 | TGTGACTCATC | + | 6.14 | | NFIC | MA0161.2 | chr12:120973608-120973619 | TGTGCCAAGTA | - | 6.32 |
|
Enhancer Sequence | GGTAAGGACG GGCCTGCGGC AGTGGGCGGG GGCGACTGCC CCTGCTGCTG GGGAGAGTCG 60
TTGCTCTCAT CGGCTGGGTT ACTCGGGGAC AGGCTCCACT TTCTTTTATA GCTCCTACCT 120
GCCCTTTTCC ATGGCTCTCA TTTGCAGTTA CATTAATGAG CGCTGTGCTG CGTGGTTTAC 180
GTGGATCATT TACATTAATA CTCAAAACTG CTCGATTAAG CAGGTGCTGT TCTTATCGCC 240
ATTTTGCATA TGATGAGAAA GGGTAAGGTC ACCCAGCTAG TATTTGGCTC ACAGCAGGCC 300
TTAAGACTTG GTTTGTGTGA CTCATCAGTC CACGCTCCTA AAACCACTAA GTTGTTCTAC 360
CCTTTAATGT TGAATTAACA TTGGATAGTG TTCAAGTTTA GATGGGTGGG TGAGGGCCCA 420
AGGACCTTTC AAACTCAGAT CTCTTATTTA ATAACCTGGT CCCAGATCCA TTCCTCTGTC 480
GAAGAGGAAG TCATCCTTCA GTGGCTATTC ATTGTGGGGT TAAGAGCGCA GACTATGAAT 540
TCAGTCTTTT TGGGTCCCAG TTTGCCAGAC CTTGAGTGAG TGCCCCGAGT TTACTTACTT 600
GTAAAGGTAG GTGGAGGTAA TATAATTAAA TAAACTTAAA AAACTAATTA AAAACAAAAC 660
AAATGAACTA AGGTCTTAGG ATATCTGGCG TCTATTTTGC GCCAAATACA CATAATGTCT 720
ATTGTTGTGT GTTGGACTAT AGGATTGTCC TTTAACAGGG AAGGTTTTAT TTCTGTAATC 780
AAGTCTGTCA ATATTATGAC CATGTTGATA ATAGCTACCT TTAATTGAGG GCTTACCATG 840
TGCCAAGTAC TAGGTGAAGT TTTTACCTCT GTTTTCACTG TGCCAGTCAC TGACTTGTCT 900
ACCAGGGTGA AATTGTTCAT ATTTAAAGAA GGAATAAACT GAGCAGGTAG GATGTTAGGA 960
GTTGGCAGAG GCTAGAGTCC CGGTGTTCTT CATTTTATTT CGAAGTTTGT ACTAATCTCT 1020
GCTCTCTTTT GTATTTCAGT CACATTAGCA GTAATAGGAA GGTGTTTTCA GCGACAGTGG 1080
GGATGTTGTG GCAGAGAGGG AAATATTTGA AGTCCCTAAA TGTGGAGGTC CAGTTTAAAA 1140
CTTGTCAAGA TTAAAAAAAC TGTTTAGAGT GAGACCGGGC GCGGTGGCTC ATGCCTGTAA 1200
TCCGAACACT TTGGGAGGCT GAGGTGGGAG GATAGCTTGA GCCCAGGAGT TTCACACCAG 1260
CTTGGGCAAG ATAGTAAGAC CCTCGTCTCC ATAAGAAAAA AAAAAAATTA GCCGAGTGTG 1320
GTGGCACACA CCTGTAACCC TACCTACTTG GAAGGGTAAG GTGGGAGGAT CGCTTAAGCT 1380
CAAGGAAGTT GAGGCTGCGG TGAGCTATAT CACGATACTG CATACCATCC AGCCTGGGTA 1440
ACAGAGACCC CCATCTCTAA ACAGTAAAAA GAAAACTAAG GCTGACTTAA AACAAACAAA 1500
AAAAACAGAA AATTGTAAGG TCTGCTAACT CGCTCAGAGT TCACCTGCTG GATATGGCAA 1560
ACTTGTTTAC CTGGTGTGAG ACCATTGGAG TATGGGTTCT CGGGCCGTGT CAGGAAATGG 1620
CATGTATGCA GACTGATTTT GCAGTTCTGC ACATGCGTAG CTTTGCCATA GATCCCTCAA 1680
AAGATAGAAG GTAACCAGTC CTTTTGGTCA GTGTTGGAAC TGGTTTAGAG TGGTCTGTTC 1740
AAAGCAATTG ATAAGTAAGT TTATTTTTGT ACTCTATTCC CAGATGTATG TTAAGGATTT 1800
GGTTCTCCAA CTGTGAATTC TCAACTAATT 1830
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