Tag | Content |
---|
EnhancerAtlas ID | HS101-24807 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr2:128155120-128156350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr2:128156301-128156322 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | JUN(var.2) | MA0489.1 | chr2:128155988-128156002 | ATGAGTCACCACCT | - | 6.13 |
|
| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_09644 | chr2:128155087-128156513 | CD14 | SE_23461 | chr2:128155077-128156312 | Colon_Crypt_1 | SE_24894 | chr2:128155366-128156060 | Colon_Crypt_3 | SE_28345 | chr2:128155229-128156626 | Fetal_Intestine | SE_29146 | chr2:128155181-128161071 | Fetal_Intestine_Large | SE_52838 | chr2:128154976-128156395 | Small_Intestine |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I127397 | chr2 | 128155228 | 128156376 |
|
Enhancer Sequence | AGAGAGGACC TCAGAACCAC CTGACAGGCT CTCCCTCACT CTGTTCCATG GTACCTCCCA 60 AATGCCCATC CCAGAGCCCC TCCCCACTGC CTAATGCACC AGGGCACCAC TCCCTGTCTT 120 GCCAATTTCA GCTGCCCCTC TGCCTCCAAG ATCAGCCTTG CCATCCTTGA CACCACAGGC 180 TTCCTTCATC CAAGCCCTCT GAGCCCCTCT CTGGGCGGTT TGGAGGATGC TAAGCCCTCT 240 CAGTGCACCA TCCAGGGGGT CCATGTTGCA GAAATGAGTG AGGAGGTAGT TATCTTCATC 300 CTCACAGCTC AGCATATGCC TCGACCCAGT GCGATGTAGA TCCTTCCCCA ACTGCTTCCT 360 GCAAGTCAAG TCACAAAGGT TGGCATTGGT TCTTCACCAT AGGCTAGCCT GGCTGAAGCT 420 CAGCTGCACA GAGTCTGTCC TGAGAAGCAG AATGCCACTG TCCCCTGGGC CCTCCAGACT 480 GCCAAGGCTG CTCAGTTTCA GAGAGCAGGC TCCCTGTGGC CTCACACGCC GGCTGCCAGC 540 TGGGCCAGGT AACTCTGGCC AGGCTGCACT GTGAAGAACA CGAGAGTCGG CGGAGACCTG 600 TGCCTGCTCT TCTCAGCCTC AATGTCTGGA AGACAAAAAA AGGCATCCTG CTCCCAAGAT 660 TGTGGTGGAG GCCAGCAGGG TGACGCACAT GAAAGCCACT GGAGATAGAT GGCACTTGTT 720 CCCACCCACT GCCCACAACA GGCCCAGGAC TGCCTCAGCC CCGGTGGACC CCAGAGCCAG 780 CAGGCCCTTC AGAATGGAAG GTGCCAAACA CCATCGGAAG GCGTGGTTCT TTTCAGAGAA 840 CCAGACTCTG AGACTGTGGC CTCCCACTAT GAGTCACCAC CTCTGATTCC TGAGGTCCCC 900 TCCAGTCATT GGCTCTCTCC CAAGCCAGCC AGCTGATCAG CCTTGAGGAC AGCAGAGTGT 960 CTGCCAAGAG AGATCTGTGA AGTTTCCCAT CACCGTGGCA GTCCACAATG TGAAGCCCCT 1020 GAGGCCACCC TTCTCCATGT GTCCCCCACA CTGTCCCTGA CCCTCCCACC ATCCTAGAAA 1080 ACCAGCCTCC CAGGTCCTCT GTCATGGAAG TAATTTACAG CAAGGCAGAA AGAGCTGAAA 1140 GATTTATAAA TGTGTAAAAT TTACAAAGGT GTTTCTTTCT TTCTTTCTTT CTTTTTTTTT 1200 TTTTTTTTTT TTGAGGCAGA GTCTCACTCT 1230
|