| Tag | Content |
|---|
EnhancerAtlas ID | HS091-21126 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:73606340-73607680 |
Target genes | | Number: 46 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:73606738-73606756 | CATTTCTTCCCTTCTTCC | - | 6.31 | | HNF4G | MA0484.1 | chr17:73606718-73606733 | TGGACTTTGTCCCCT | - | 6.81 | | Hnf4a | MA0114.3 | chr17:73606716-73606732 | GCTGGACTTTGTCCCC | - | 6.83 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23082 | chr17:73605173-73608547 | Colon_Crypt_1 | | SE_24179 | chr17:73606008-73608531 | Colon_Crypt_2 | | SE_27754 | chr17:73604916-73614604 | Fetal_Intestine | | SE_52698 | chr17:73604933-73614611 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I075608 | chr17 | 73604632 | 73614479 |
|
Enhancer Sequence | GTGCAGGGGC TTGGGTGGGG CGGTTCAGGG TAGAAGCCAG GCTGCCTGAG CTGGCCGAGC 60
TGGCCAAATC CCAGCAGCGT TGACCCTCTC AGCCCGGCCT CGCACGGGCT GTGGCTTCAG 120
ACACAGTGCT CCTTGAACTC ATCCCTTTTC CCTCCGGCCG GGGTAGGCCG GGGCCCTTGG 180
GAGGTGCTGT CTTCCTCCAT CCCTGCCTAC TCTCCCCAGG GCCTGGCTCT TCCCTCTTGC 240
CTGGGGTTCC CATCCCCTCC AGGCCTCCCC TGGGCCCCGT CCGCTCCCCT CTTTTGCATG 300
ATGACTCAAA TCTAAGGTCT ATAAAGCGAC TCAAAGGTCA ATGCCCACGT GCTACCCCCT 360
CTCTGGCCCC TCCCTGGCTG GACTTTGTCC CCTGGGACCA TTTCTTCCCT TCTTCCTGCC 420
CTCTTCCCGG TGCCCTGGCA GATGGGCACA GACGCCCACA GTGCTAAGGC TGGTGAGGGC 480
CCTGGAGGGC CAGGGGTGGC TGGCCCCTCC TGATCTGTTC TCACTCCTTT GCTGAGAACC 540
TCCCAGGGGC AGGAGGGGAC AGCTGAACTT CAGAGCTGGG GAGGTGCCCC CAGGTGACTC 600
ACATGGGAGG CATCAGCTCT TCCCACATCT CTTCCAACAG CTTGGGCGTT GGCAGGGCTG 660
GCATAGCAGC GAAAGGGCCT TGGAGAGAGT GCCAAGCATG GTAGGTGGCC TGGAAAGTGG 720
GGGGTTTTAC ATGGGGCTAT GAACCTGCTG AGACTGGGAC AGCTTAGAGG GCTGCCAGGG 780
TGCTACCGTG GGTCTTGTCC CTCAGGGCCA TGCATTGCAC CTCCTGAGAA GAGGACCGGG 840
GTGCTCTTGG CTCTTGGTTT CCCTCAGAGG GTCTTTGGGG CTCTGTTTGT TCGAGTGTCC 900
AGGGTCAGAA TCCTTGGTCT TTGGCTGGGT GTGGTGGCAC ACACCTGTAA TCCCAGCACT 960
TTGAGGTCGA GGTGTGAGGA TTGCTTGAGC CCAGGAATTT GAGACCAGCC TGGGCAACAT 1020
GACAAGACCC CATCTCTACA AAAACAATAA AAATTAGCTG GACACAGTAG CACATGCCTA 1080
TAGTCTCAGC TACTCAGGAG GTTTGAGGTG GGAGGATCGC TTGAGCTAGA GCCTCAGAAG 1140
TCAAGGCTGC AGTGAGCCAT GATGGTACCA CTGCACTCTA GCCTGGGTGA CAGAGTGAGA 1200
CCCTGCCTCA AAAAAAAAAA AAAAAAAAAA TCCGTGGTCT TTGGAAGGGA TGTTTATAAT 1260
CTTGGGGTTG AGGGTGTGGG GAGGGACACT GGTCCCTAGG CCCCTCCTGT GGATCCTGGG 1320
TAAATGAGTC CCCTCTGCCA 1340
|
