| Tag | Content |
|---|
EnhancerAtlas ID | HS101-22298 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr19:49042690-49044160 |
Target genes | | Number: 37 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:49043186-49043201 | GAGGTCAGGAGTTCA | + | 6.22 | | ZNF263 | MA0528.1 | chr19:49043674-49043695 | TTTCCTTTCCTCACCTCCTTC | - | 6.02 | | Zfx | MA0146.2 | chr19:49043916-49043930 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27310 | chr19:49043349-49043973 | Esophagus |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH19I048539 | chr19 | 49043057 | 49043258 | | GH19I048540 | chr19 | 49043350 | 49043973 |
|
Enhancer Sequence | GCTGAGATTG TGCCATTGCA TTCCAGCCTG GGTGACAGGG CAAGACTTTG TCTCAAAAAA 60
AAAAAAAAAA AAAAAAACAA AACTGCCCAG GAAATTCTTA CGCGCAGTCC TACGTGGGGA 120
CTAGCGGCCC AGAGCTACTG CTTATTAAGC ATTTATTATG AGCCAGGAAA GGTGCAAAAT 180
GTTTTATCCT TGAGTCTAGT TCATGCCTCC AGCAGAAGCC CAGGCCCCTG GGTTCTAGCA 240
TGGTCTTCTG CCAGCTTCGA CTTGGACAAG TGACGTCAGT GCCCTGTATG TTGGTTTTCT 300
CATTGGAAAG ATGGAGATAA TAATAGTGCC TACTCATAGG ATCATCATGA GGCTGAAACG 360
CGTAGCTGTG CAGATCTCTT GGCACTGTGC CAGGCACTGA GTATGTTCTA CACAAGTGTT 420
TGACAAATAT AATAAAACTG ATGGCTGGGC ACCTGTAATC CCAGCACTTT AGGAGGCCGA 480
GGCAGGTGGA TCACTTGAGG TCAGGAGTTC AGGACCAGCC TGGGCAACAT GGTGAAACCC 540
CCTCCCTACT AAAAATACAA AAATTAGCGG GGCATGATGG CGGGCACCTG TAATCCCAGC 600
TACTCGAGAG GCTGAGACAC GAGAATCGCT TGAACCCGGG AGGCAGAGGT TGCCGCGAGC 660
CAAGATCGCA CCACTGCACT CCAGCCTGGA TGAAAGAGCG AGACTCCATC CCAAACAATT 720
AACAAAAATA ACTGACTGTG TATCTTGGAG TGACAGAGCT GTCCCTGCTT GTGTAATGTG 780
CCTATCCATG CATTGGCGAG GCGTGTCGAT CCTGCAGCTG GGAGAGAGTT TGCATGGGAG 840
GAGGCAGCGT GAGAGATCAG TCCCCAGGCA CAGAGGAAAA CCGAGCTGGG ACTCAGCTCT 900
CACGGTCCTG CCATTCAGCC AGCTGAGAGG CACAGTCCCA CATCCAGACC CTTACTTGTG 960
CTGTCTCCTC TGTCCAGAAC ACTCTTTCCT TTCCTCACCT CCTTCAAAGG CTTGTTCCAA 1020
TGTCATCATC TTGGTTTAAA GTGGAGATTC AGCTTAACCC CTTCCCCACC TGTGCCTACT 1080
GTCTCTCGAT TGGCCTTATT CTTCTCCATG GCCCTCAATG TACACGTTTA CCTGGAAAGT 1140
GCTCCCTGCA AGGCAGCTGC ATACCATTAT TAAGACTCTG TGACAGGCCG GGCGTGGTGG 1200
CTCATGCTTG TAATCCAGCA CTTTGGGAGG CCGAGGCGGG CGGATCACTT GAGGCCAGGA 1260
GTTCCAGACC AGTCTGACCA ACATGGTGAA ACCCCGTCTC CACTAAAAAT ACAAAACTTA 1320
GCCTGGTGTG GTGGTGAGTG CCTGTTATCC CAGGTACTCG GGATGCTGAG GCAGGAGAAT 1380
CGCTTGAACC CGGGAGGCGG AGGTTGCAGT GAGCCGAGAT GGAAACACTC CACTCCAGCC 1440
TAGGTGACAG AGCGAGACTC CGTCTCAAAA 1470
|
