| Tag | Content |
|---|
EnhancerAtlas ID | HS067-00008 |
Organism | Homo sapiens |
Tissue/cell | GM18522 |
Coordinate | chr1:1574180-1575550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR2 | MA0472.2 | chr1:1575294-1575305 | CCGCCCACGCA | + | 6.32 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_23152 | chr1:1574692-1576308 | Colon_Crypt_1 | | SE_23805 | chr1:1574726-1575197 | Colon_Crypt_2 | | SE_24735 | chr1:1574763-1576431 | Colon_Crypt_3 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001639 | chr1 | 1574693 | 1576431 |
|
Enhancer Sequence | AGCCAGGTGC AAGGGCTCAG GCCTGTAATT CCAGCACTTT GGGAGGGCAA GGCAGGAGGA 60
CTGCTTGAGC CCAGGAGTTC AAGACCAGCC CGGCCAACAT AGCAACACTC TGTTTTCTAT 120
TTTTTTTTTT TTTTTTTTTG AGACGGAGTC TCGCTCTGTC ACCCAGGCTG GAGTGCAATG 180
GTGAGATCTC GGCTCACTGC AACCTCCACC TCCTGGGTTC AGGCGATTCT CCTGCCTCAG 240
CCTCCCTAGT AGCTGGGAGT ATAGGTACGC ACCACCACGC CAGGCTAATT TTTGTATTTT 300
TAGTAGAGAC AGGATTTCAC CATATTGGCC AGGCTGGTCT CGAACTCCTG ACCTCTGATC 360
CGCCCACCGC CTCGGCCTCC AAAAGTGCTG GGATTACAGG TGTGAGCCAC TGTGCCCGGT 420
CAAAACTCCT TTCTACAAAA TAAAAAAATT AGCCAGGCAT GGTGGCTTGC GCCTGTAGTT 480
CCAGCTACTC AGGAGGCTGA AATGGGAGGA TTGTTTGAGC CTGGGAGGTG GAGGCTCCAG 540
TGAGCTATGA TTAAGCCACT CCACTCCGGC CTGGGTGACA GAGACAGACC CAGTCTCCAA 600
AAAAAAAGCC ATCCCAAGAG TCTCTTTGTC AAACTGGATG TGTCCCCTGC TTGTACCAGG 660
ATGACACTGA GGACGGGCCC TACCTGCCAG GCGCAGCATG ATGCCCCATG CCAGGGCACC 720
TACCCCTCCG TGTACCTTGG GGCCGGTGCC CAGGCCGGAT GTCATGTACT CGGGGTGGCC 780
TGTGGCCCGA CGCCTACGCT CAGCAGCACT AAGGGGCAGA GGCGCTCACA AGGCATAGGG 840
CAGTCGACAG AGGCCTGCTG CATGCGCCAG AGAGAACCTC TCCGCCCACA GGCACCAAGG 900
AGGGGGCCGA GTCCCTGCCG GTCTCCCAGG CCCCAGAGGC CACTGGCACC TTCTCAGGCT 960
TGTCCCTTCC AAATCGCTCC CAACAATATC CTGCCTTATT GATAGCTGCC TAAGCAAAAG 1020
GCTTCTGGTC ACACATCTAC ACTGACTCCC GTAGCCGCTC CCCCATCCAA GCCCTGCACA 1080
GATGCCGGTA ACAAGGCCTT GGTGCCTACA TAACCCGCCC ACGCAGGGGT CAAGTGGAAG 1140
GCACTGCTCT CCAGTGCGGA GGAGGACGCA ACTCGGGCAG CAGTGACAGC AGCGCGGCCG 1200
CACGCCCAGG CTGCCTTTCA AGCCGCAGAG CAGTCCTGCG GGCAGCTCCC TGTCCACCCA 1260
GTTCCGTCCA GCATGAGAAA GAGGCGGGAC CTAGAAGCAT GAGGGGCCAG TGGCTGTGCC 1320
CGCCCGTCAC TGCCCCAGTG GGCCCAGCAG CCCTGTGAGG CGACAGACGC 1370
|
