| Tag | Content |
|---|
EnhancerAtlas ID | HS012-02640 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr11:17553090-17554000 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr11:17553613-17553628 | AGAGGACAAAGTCCA | + | 7.11 | | Hnf4a | MA0114.3 | chr11:17553614-17553630 | GAGGACAAAGTCCACT | + | 6.8 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28323 | chr11:17551402-17556297 | Fetal_Intestine | | SE_29229 | chr11:17551426-17556292 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I017529 | chr11 | 17551501 | 17556212 |
|
Enhancer Sequence | TGTGGAGATG CCGGGAATGC CTGGAGCCTC ACCCCTGGCC ATGACCTCAG GCACCCAGGG 60
ATTCCAAGAG GAAGCCATTT CAGCCACTGG GCCCAGGCTT AGGAATGGAG TAGACCACTC 120
CTGAAAAGCC CAGAGCTCTT CACACCGGGC CAGTGCCTGA GAAGACTTTG TTCTCTTATA 180
TAAATATCCC CAGGAAACCA GTCTACTAGG GATTGTTGAC TCATTTTGCA GATGAGATGA 240
AGCCAGGATT TCAAACTCAG CGCTGCCTAT CTCGGCTGTT GGGATCTTTC CAGAGGGGAA 300
AGCTCTGTGT GAGATGCTGA CAATTCCTCA CACACTCATC ATCTCCACTC GTATCTGCTG 360
CTAAGCTCTG TCAATTTCAC CTCACCACAG TTCACATGCC TCCTCCCTCA TGCTGTTCAG 420
ACCTTCGACT GCAGCTGCCT GCCCATGTAC TCACTGTCAC GTCATCTTTT CTCAGTGTAA 480
GGCACTCCCT GGCTTAAAAC CCTTTGATGG CCCCTTACTG CCCAGAGGAC AAAGTCCACT 540
CTTCTCAGCA GGCTCAAGGC CCTCCATGAC CTGTCCCCAT GGAGCTTCTC CAGCCTTGTG 600
GCTATTTATG ATCTCCGTGC CCTCCCAAGT CCTACTCCCC CAGATTACTT ATCTCCATTC 660
ACACCCTTGC TTTCATGCCT CCACACTTTG GCTGATGCTG ATCCCTCATT CTGGAATGCC 720
CTTCCCAGAT ATTCCACCTA CCAAAATCTT TTTCTTTTAT TATTATTTTT TTGAGACAGG 780
GTCTTGCTGT CTTGCCCAGG CTGGAGTGCA TTGATGCAAT CATGGCTCAC TGCAGCCTTG 840
ACCTCCTGGG TTCAGGTGAT ATTCCCACCT CAGTCTCCTA AGTAGCTGGG ACTACAGGCA 900
CGCGCCACCA 910
|
