| Tag | Content |
|---|
EnhancerAtlas ID | HS052-00453 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:19979750-19981500 |
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 | CCTGGGCAAC AGAGCGAGAC TCCGTCTCAA AAAAAAAAAA AAAAAAAAAG TACCTGGCTT 60
TGCCATCTCC ATGGCCCATG GTAGGATTGT CCTAAATGGG ATGCCCAGTC CCAAGCCACC 120
TGACTCCTGG TGCTGGGCTT CTGTGGGGCC ACTGGGACCA GGACTTGTCC CCTCTTCCTC 180
CTGATTTAGC CTCATCCAGG CCCCTCTAGG GACTGTCCCA AGGTAAAGAA TCCCTGACTG 240
AGCGCATAGC TGCCTAGGAA GCCTGATCAA AACGCAGACT CCTACCCACC CTAGAACTTT 300
TACTCCACAA GTTCCTAGGG AATTCTGATC AAATTTCAGG TTTGGGAACC ACTGGCCTGG 360
CTCACTGCAC TCATTTTACA GGTGGTGGGG AAACAGGTCT GAGTGTCCCG GTCACCCAGC 420
ACACGTGGAC CCATGCCCTT TCTCGGCTGT GCCGTCCTCC GAGGGTTTGG GGGCCTCCTT 480
GAAGAAGGCA CTGCCCTCAT CTCTGAAGCC TCCCTCTCCC GTGCTTTTTG CACTGGGGGG 540
CATGGGTGAA ACTTACCTGG GGCGAGTCTC CTGAAAGCGG AATCCTTTGA CACAGACTGC 600
CCTGCAGCGC CACCTTTTGG CAGATCCTGG TATTGTTTTA GTATCTCACT CCATCCTATA 660
GCAGGGGAAT TTGCAAATGG CCAAGTGCTT AGCTTTGATT GGCTCCCGCT TGACTCACGT 720
GTTAGAATGG GGCTGGGGAC AGTGATCTGT GTAGAGCCCT TGTGGATTCG AGTTTCTGGT 780
GAGGCATCTT AGAGAACAAT ACTGTCTGGT TCAGGGTCAG TTTTTTTGCC TGAGGTCTGG 840
CCAGCCAAGG TGGCCCAGGA ATTCACTGCA GGCCAGGTGC GGTGGCTCAC GCCTGTAATC 900
CCAGCACTTT GGAATGCTGA AGCAGGAAGA TCGCTTGAGC CCCAGGAGTT TGAGACCAGC 960
CTGGGCAACA CGGCGAAACC TGGTCTTTAC AGAAATTAGC CAGGTGTGGT GGCGGACGCC 1020
TGTAGTCCCA GCAACTCGGG AGGCTGAGGT GGGAGGATCA CCTGAGCCCA GGGAAGTCGA 1080
GGCTTCAGTG AGCCGTGATC ATGCCACTGC ACTCCAGCGT GGGTGACCGA GTGAGATCTT 1140
TTCTCAAAAA ACAAAACCAA AAAGAAATCA CAGCAACGTG AAGGTTAAGG CTAACTTTTC 1200
AAACATCAGA ATCCTGACAA TGGTTGCAGT AGCTTTCAAG GAGACATGGT GTGTGGCCAG 1260
CCCCTCCAGG GCTGTGTGGA CAGCTTTTTG TGTATTTTCC TGGGTGACTC ACAGCATCAA 1320
AGGGAGAAAG GAGGTAGTAA TTGTTCAGCA CTTGACATGT GCTTGAACAC TTCGTAATCG 1380
CAATCCTGTG CCAGGCAGTG GCACCATCTC CCCTTTTTAG ATGAAGAAAC CGAGGCACCG 1440
AGATAAAAAG TAACTTGCTC AAGGCAATTT AGGAAGTTGT AAAACCAACC AACACATATG 1500
GAATGTGTAT TATCTGCTAG GCTCATTTAA TATCTCATCT GACCTTCCAG ATACCCATCT 1560
GATGTAGGTA CCACTCCCAG CTCCAATTGT GAGATTCAGA GGGGAGAAAT AACTTGTCCA 1620
AAGTTGCACT TGGTTAGTAA GTGGGAGAGC TGGGGTTGCG CCAAGGAGTC GGATGCCAGA 1680
GTCCATGCTG TAACACCACT ACCCGGCCCC CTGCACCTTG CTGTGCCTCA CCTGGCACCT 1740
GTGCTCCGTT 1750
|
