| Tag | Content |
|---|
EnhancerAtlas ID | HS091-00678 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:19979820-19981500 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:19980354-19980373 | CAGCGCCACCTTTTGGCAG | - | 6.12 | | FOXH1 | MA0479.1 | chr1:19980510-19980521 | TGTGGATTCGA | - | 6.14 | | GFI1 | MA0038.2 | chr1:19980913-19980925 | GAAATCACAGCA | + | 6.22 | | Gfi1b | MA0483.1 | chr1:19980914-19980925 | AAATCACAGCA | + | 6.62 | | TEAD1 | MA0090.2 | chr1:19981247-19981257 | ATGGAATGTG | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_24802 | chr1:19981234-19982168 | Colon_Crypt_3 | | SE_26994 | chr1:19979780-19980770 | Esophagus | | SE_26994 | chr1:19981202-19982584 | Esophagus | | SE_52799 | chr1:19981212-19982414 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I019654 | chr1 | 19981203 | 19982711 |
|
Enhancer Sequence | ATGGCCCATG GTAGGATTGT CCTAAATGGG ATGCCCAGTC CCAAGCCACC TGACTCCTGG 60
TGCTGGGCTT CTGTGGGGCC ACTGGGACCA GGACTTGTCC CCTCTTCCTC CTGATTTAGC 120
CTCATCCAGG CCCCTCTAGG GACTGTCCCA AGGTAAAGAA TCCCTGACTG AGCGCATAGC 180
TGCCTAGGAA GCCTGATCAA AACGCAGACT CCTACCCACC CTAGAACTTT TACTCCACAA 240
GTTCCTAGGG AATTCTGATC AAATTTCAGG TTTGGGAACC ACTGGCCTGG CTCACTGCAC 300
TCATTTTACA GGTGGTGGGG AAACAGGTCT GAGTGTCCCG GTCACCCAGC ACACGTGGAC 360
CCATGCCCTT TCTCGGCTGT GCCGTCCTCC GAGGGTTTGG GGGCCTCCTT GAAGAAGGCA 420
CTGCCCTCAT CTCTGAAGCC TCCCTCTCCC GTGCTTTTTG CACTGGGGGG CATGGGTGAA 480
ACTTACCTGG GGCGAGTCTC CTGAAAGCGG AATCCTTTGA CACAGACTGC CCTGCAGCGC 540
CACCTTTTGG CAGATCCTGG TATTGTTTTA GTATCTCACT CCATCCTATA GCAGGGGAAT 600
TTGCAAATGG CCAAGTGCTT AGCTTTGATT GGCTCCCGCT TGACTCACGT GTTAGAATGG 660
GGCTGGGGAC AGTGATCTGT GTAGAGCCCT TGTGGATTCG AGTTTCTGGT GAGGCATCTT 720
AGAGAACAAT ACTGTCTGGT TCAGGGTCAG TTTTTTTGCC TGAGGTCTGG CCAGCCAAGG 780
TGGCCCAGGA ATTCACTGCA GGCCAGGTGC GGTGGCTCAC GCCTGTAATC CCAGCACTTT 840
GGAATGCTGA AGCAGGAAGA TCGCTTGAGC CCCAGGAGTT TGAGACCAGC CTGGGCAACA 900
CGGCGAAACC TGGTCTTTAC AGAAATTAGC CAGGTGTGGT GGCGGACGCC TGTAGTCCCA 960
GCAACTCGGG AGGCTGAGGT GGGAGGATCA CCTGAGCCCA GGGAAGTCGA GGCTTCAGTG 1020
AGCCGTGATC ATGCCACTGC ACTCCAGCGT GGGTGACCGA GTGAGATCTT TTCTCAAAAA 1080
ACAAAACCAA AAAGAAATCA CAGCAACGTG AAGGTTAAGG CTAACTTTTC AAACATCAGA 1140
ATCCTGACAA TGGTTGCAGT AGCTTTCAAG GAGACATGGT GTGTGGCCAG CCCCTCCAGG 1200
GCTGTGTGGA CAGCTTTTTG TGTATTTTCC TGGGTGACTC ACAGCATCAA AGGGAGAAAG 1260
GAGGTAGTAA TTGTTCAGCA CTTGACATGT GCTTGAACAC TTCGTAATCG CAATCCTGTG 1320
CCAGGCAGTG GCACCATCTC CCCTTTTTAG ATGAAGAAAC CGAGGCACCG AGATAAAAAG 1380
TAACTTGCTC AAGGCAATTT AGGAAGTTGT AAAACCAACC AACACATATG GAATGTGTAT 1440
TATCTGCTAG GCTCATTTAA TATCTCATCT GACCTTCCAG ATACCCATCT GATGTAGGTA 1500
CCACTCCCAG CTCCAATTGT GAGATTCAGA GGGGAGAAAT AACTTGTCCA AAGTTGCACT 1560
TGGTTAGTAA GTGGGAGAGC TGGGGTTGCG CCAAGGAGTC GGATGCCAGA GTCCATGCTG 1620
TAACACCACT ACCCGGCCCC CTGCACCTTG CTGTGCCTCA CCTGGCACCT GTGCTCCGTT 1680
|
