| Tag | Content |
|---|
EnhancerAtlas ID | HS101-01477 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:46656460-46657760 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2B | MA0660.1 | chr1:46657182-46657194 | GCTAAAAATAGT | + | 6.11 | | MEF2C | MA0497.1 | chr1:46657180-46657195 | GTGCTAAAAATAGTA | + | 6.59 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_23257 | chr1:46656032-46657214 | Colon_Crypt_1 | | SE_31897 | chr1:46655935-46657326 | Gastric | | SE_34180 | chr1:46655907-46657050 | HCC1954 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 46656860 | 46656987 | | chr1 | 46657071 | 46657228 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I046190 | chr1 | 46655908 | 46657326 |
|
Enhancer Sequence | AGTGGGTATG AGAGTGAAAA TCAGCACCTC ACATTGTCTG GCCCACACCC ACTTGCTGAC 60
CAGCCAGACA TCTATAAGAC ACACAAATGA AGTCCTAGAC CTGTAAAGAG CCCTCTAATT 120
TCCCACCGTC TTCTCCATCC TCTTTGCAGC ATCCTCAGCA AGCTCTTACT AGCTTTAATT 180
TGGCCTCCAC CATTGCTGGA GAGCTCATGC TGTCACGGCA GCTCACACTA CTGCACCACA 240
GACCCATGAA CTAGCAGTCC CTGCCTCTTG TAGTTCTCCC TGGGCCTGCT GTTCTAGAGC 300
CACAGATGTC AGAAACAGGC CCTGCAGGAG GTGGTGGGCA AAGGGACGGG CTGGGCTGGG 360
AAGGAAAAAA CTACTTTGAC TCTGGTACTG AGAGTGACCT GAGGGAAGCG CCTGCCCCTC 420
TCTGGGAGAG GAATGGGGCT CGCGTATTAG TCAGCCTCTG AGGGACCTCT GGCTTCTAGG 480
AGGTTCCAAG CTGGACGCTA TTCATTCCTT TGGGCTGGGC TGGCTCAAGG CCTCCCTTGC 540
TGTAACTGGG GAATGGTCCT CTGAATGCAG CCAGGTGGGT TGGCGGTACC TAAGGACTTC 600
CCTGTTCTCC TCAGGCTGAA GCATAGGCTC CAGCACTTGC CAAAACAGGA AAGGGCAGAG 660
ATTGCAGGGC TGGACCAGTA CTTAGAGGCA GAAATACTCT CCCCAGACAC CCACAGTCTA 720
GTGCTAAAAA TAGTAAAAAT AAAAACAATA CCAGCTGACC CTTATATATG TTTATAATTC 780
AAAGCACTTT ACATATATTG ACTCATTTAA ACCTCAAAAT ATCGTAACCC AGTGAGGTAG 840
TAGTATTTTA TCCTCTTTTT TTTTGAGATG GAGTCTCGCT CTGTCACCTA GGCTGGAGTG 900
CAGTGGCGTG ATCTTGGCTC ACAGCAAGCT TCGCCTCCTG GGTTCACGCC ATTCTCCTGC 960
CTCAGCCTCC CAAGTAGCTG GGACTACAGG CGCCCATCAC CAGGCCCGGC TAATTTTTTG 1020
TATTTTTAGT AGAGATGGGG TTTCACCATG TTAGCCAGGA TGGTCTCGAT CTCCTGACCT 1080
TGTGATCCAC CCGCATCGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCGCGCC 1140
CAGCCCTTTA TCCTCATTTT TCAGATAAAG AAACTGAGGC AAAAATAGGA TAGCTCTTTC 1200
CCCAAGGTTA CATGGCTAGC AAGTAGCAGA GCTAAGATTG CTTCAGAGTC CATGTTCTTG 1260
TTCTTGACTG TCATGCCACA CTGTGCCCTG CTCCCTGCCT 1300
|
