| Tag | Content |
|---|
EnhancerAtlas ID | HS098-00037 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:1573950-1575630 |
Target genes | | Number: 28 | 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) |
| EGR2 | MA0472.2 | chr1:1575294-1575305 | CCGCCCACGCA | + | 6.32 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23152 | chr1:1573189-1574218 | Colon_Crypt_1 | | SE_23152 | chr1:1574692-1576308 | Colon_Crypt_1 | | SE_23805 | chr1:1574726-1575197 | Colon_Crypt_2 | | SE_24735 | chr1:1573260-1574278 | Colon_Crypt_3 | | SE_24735 | chr1:1574763-1576431 | Colon_Crypt_3 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001639 | chr1 | 1574693 | 1576431 |
|
Enhancer Sequence | CCCTGGGAAG GAAGCGCCTG TGTGAGGTCT CAGTGGCCAT GCCAGCTGGA GGGAGGGCGG 60
CTGCGTCCAC AGGCACGGCA CACCCGGCAC GGGGCAGGTG CAGGGCAGAG CCTTGGGACT 120
GGGCCGGGGG TGGAGCCGGG AGCAGCTCAG TTCTTTCAAA GTCTCTTTCC TTGCAAAACC 180
ATCTGACACT TTATTATGAA ACAAAACCAG TGTGAACAAA AGGCCATCCC AGCCAGGTGC 240
AAGGGCTCAG GCCTGTAATT CCAGCACTTT GGGAGGGCAA GGCAGGAGGA CTGCTTGAGC 300
CCAGGAGTTC AAGACCAGCC CGGCCAACAT AGCAACACTC TGTTTTCTAT TTTTTTTTTT 360
TTTTTTTTTG AGACGGAGTC TCGCTCTGTC ACCCAGGCTG GAGTGCAATG GTGAGATCTC 420
GGCTCACTGC AACCTCCACC TCCTGGGTTC AGGCGATTCT CCTGCCTCAG CCTCCCTAGT 480
AGCTGGGAGT ATAGGTACGC ACCACCACGC CAGGCTAATT TTTGTATTTT TAGTAGAGAC 540
AGGATTTCAC CATATTGGCC AGGCTGGTCT CGAACTCCTG ACCTCTGATC CGCCCACCGC 600
CTCGGCCTCC AAAAGTGCTG GGATTACAGG TGTGAGCCAC TGTGCCCGGT CAAAACTCCT 660
TTCTACAAAA TAAAAAAATT AGCCAGGCAT GGTGGCTTGC GCCTGTAGTT CCAGCTACTC 720
AGGAGGCTGA AATGGGAGGA TTGTTTGAGC CTGGGAGGTG GAGGCTCCAG TGAGCTATGA 780
TTAAGCCACT CCACTCCGGC CTGGGTGACA GAGACAGACC CAGTCTCCAA AAAAAAAGCC 840
ATCCCAAGAG TCTCTTTGTC AAACTGGATG TGTCCCCTGC TTGTACCAGG ATGACACTGA 900
GGACGGGCCC TACCTGCCAG GCGCAGCATG ATGCCCCATG CCAGGGCACC TACCCCTCCG 960
TGTACCTTGG GGCCGGTGCC CAGGCCGGAT GTCATGTACT CGGGGTGGCC TGTGGCCCGA 1020
CGCCTACGCT CAGCAGCACT AAGGGGCAGA GGCGCTCACA AGGCATAGGG CAGTCGACAG 1080
AGGCCTGCTG CATGCGCCAG AGAGAACCTC TCCGCCCACA GGCACCAAGG AGGGGGCCGA 1140
GTCCCTGCCG GTCTCCCAGG CCCCAGAGGC CACTGGCACC TTCTCAGGCT TGTCCCTTCC 1200
AAATCGCTCC CAACAATATC CTGCCTTATT GATAGCTGCC TAAGCAAAAG GCTTCTGGTC 1260
ACACATCTAC ACTGACTCCC GTAGCCGCTC CCCCATCCAA GCCCTGCACA GATGCCGGTA 1320
ACAAGGCCTT GGTGCCTACA TAACCCGCCC ACGCAGGGGT CAAGTGGAAG GCACTGCTCT 1380
CCAGTGCGGA GGAGGACGCA ACTCGGGCAG CAGTGACAGC AGCGCGGCCG CACGCCCAGG 1440
CTGCCTTTCA AGCCGCAGAG CAGTCCTGCG GGCAGCTCCC TGTCCACCCA GTTCCGTCCA 1500
GCATGAGAAA GAGGCGGGAC CTAGAAGCAT GAGGGGCCAG TGGCTGTGCC CGCCCGTCAC 1560
TGCCCCAGTG GGCCCAGCAG CCCTGTGAGG CGACAGACGC CAACACGGGG GCCAGGCTTC 1620
GCTCAGCCCC TGTGGTAACT CCGACTGCCA ATGCGGACAG TGGCCTGGGG CGAGGGGAGG 1680
|
