| Tag | Content |
|---|
EnhancerAtlas ID | HS101-35680 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr5:133961270-133962690 |
Target genes | | Number: 23 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr5:133962204-133962219 | GAAGAGCAAAGGTCA | + | 6 | | Nkx3-2 | MA0122.3 | chr5:133962588-133962601 | AAAAACACTTAAT | + | 6.42 | | Nr2f6(var.2) | MA0728.1 | chr5:133961772-133961787 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27855 | chr5:133959146-133963362 | Fetal_Intestine | | SE_28731 | chr5:133959104-133963559 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I134623 | chr5 | 133959195 | 133963477 |
|
Enhancer Sequence | GAAAGGAGTG CCAGAATTGT GCCAGCAAAG TGGAAGAGAA TATAGGGGGT TCAAGAATTC 60
AAGAGAAGTT CAGGGTTGGG TGGTGGCAAA CTCCAAGGCC TGGCTCTGGC ATGGACGATA 120
AAGAAAAATG GAGGTGACAG ATACTGGAAG CCAGGCTAGA GGGTACACTG TCCACATTGA 180
CAGGCAGTGT AATCACCTGG AAGACTGGAG GGCACTGATA CAGACTGTGA ATCAAGTGGC 240
AAAGTCCTCA CTGAAGATGA TTGTTGGTAG GTGAGAGCTA AAGAATGGTG AAAAGCCTTG 300
ACAGAAAAAG GATTTTTTGC ATAAGGATGG TACCAATTTG CTGTTGTAAA ATTTGTCCCA 360
AGAGAGATAA TCTAAGAAGA CACAAACTCT GCTTTGGAAG ATAATAATAT ATATATTTCT 420
TTAAAATTGT GGTTTCAGCC AGGCACAATG GCTCACACCT GTAATCCCAG GACTTTGGGA 480
GGCTGAGGCG GGTGGATCAC CTGAGGTCAG GAGTTCAAGA TCAGCCTGGC CAACGTGGCA 540
AAACCCCATC TCTACTAAAA ATACAAAAAT TAGCTGGGTG TGGTGGTGCA CACCTGTAAT 600
CCCAGCTACC CAGGAGGCTG AGGCAGGGGA ATCACTTGAA CCCAGGAGGC AGAGGTTGCA 660
CTGAGCCGAG ATCGAGCCAC TGCACCACAG CCTGGGCCAC AGAGCAAGAC TCTGCCTCAA 720
AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA TGTGGTTTCT AGGAACCTTA AAACAAACTA 780
GGAGTAATTA GAAACAGAAT TAACTGTTTT TTTATTGTTA TTTTAAGTAG AAGTAAAAAT 840
GCCCAACTAA GAATAAAAGT TACTTAGCTG CAAACAGATA CCTGAGCCCA GAAAACAGGT 900
TACACAACAC CATGAACACA CTATTAAGAC ATGTGAAGAG CAAAGGTCAA GAACAAGGAA 960
ACATACACAC GTCAGCAGAT TTATTTATTG CACCAATACC AAACAGGAAA AGTCTCTCTG 1020
CAGATTAGAA AAGTGATCTA CTCAAGTAAC ATGAAAACCA GTGCAAAGGA TGTAATGGAA 1080
CAGAATCTCA GATTACAAGT AACTTCTTAA AGCCTTGTTC CATTAAACTA CATGGATGGC 1140
TCATTTAAAT GAAATATCCT GGATAGATAA ATCCATAGAG TAAGTATATT AGTGGTTGTC 1200
AGACTGAAGG AAGGAAAAAT GGGGAATGAT TGCTAATGGG TACTGGGTTT CTTCTTGGGA 1260
TGATCACATG TTCTGGAATT AGATAGTGGT GATGTTTACA CAACAATGTG ACTATACTAA 1320
AAACACTTAA TGTACAATTT TAAAAGGTCG ATTTTATGGT ATATCAACTA TATCTCAAAA 1380
AAGCTATTAT AGAAAAATTT TAAAAGCAAA TTTTAAAAAG 1420
|
