| Tag | Content |
|---|
EnhancerAtlas ID | HS053-21715 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr2:109537550-109539820 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr2:109539484-109539495 | TCCTTTGTTTT | - | 6.32 | | Sox3 | MA0514.1 | chr2:109539485-109539495 | CCTTTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26844 | chr2:109537399-109541786 | Esophagus |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I108922 | chr2 | 109538681 | 109538830 | | GH02I108923 | chr2 | 109539621 | 109539750 |
|
Enhancer Sequence | AATCACCCCC CTGAAACCCT CTGCTTCACA GAGGTGCAGA GAAGCTGCCG TCTCTTTAAG 60
GATAGGAGGT AATTGCATTG CACAGGTGCC TAGGCATAGG GTTAGAGCCT GGGAGGTGTG 120
GGGCAGAGCT GTGGGCACTC CTAGGCTGGG GAGACCCTGA CACTGACCTG GGCTCACTCC 180
TGGCTGGTGT CTCCCCTGCA GCTGCGACCC ATTGTCTGCT GTAGCTCTCC TAGGTGGGTG 240
TCATCCTCAG CCAGGGGCCC TTGGCAAGTC TGACGGTGGT TTGCGTAATC CACCATTTGT 300
TGCTGCAGAG TACCAAGGAT GTGCACTTTG TTTGGCGAGG GCCCAGGTAA ATCAAGAAAA 360
CAGAGGGGAG GAAGAGGTGC TCTTGACCAC AACTGTGGGT TTGACAAAGA CAGGGCCTGC 420
TGGACCTGGG CAGCCAGTTG GCAACTTCGG GCTCCTGATG AAATGTTTGC TGCCCAGAGT 480
GGGGCTGCTG ATGGCAGTCC TGTGTGTGTG GGTCTTAGTG ACTCCATGGG GCTTTCTAGC 540
TCCGACGTTT TTGCTGACTG CTGGGCAGGT GCTCTGAGTA AAGAGATCTC TGGATTGAGA 600
CCAGGGCAGG CCCAGGGGTG GAGGGCATCA CTCTGTTTGG CATTCACACC GAGGCCCTAA 660
CCCAGAGGGC TCCATCCACC CCAAGGCCTA TCTGGCCGCA TCTCCCCATT TCCCAGATGG 720
GCAAGCCGAG GTCTGGGGCC TTGCCCAAGG GGCCTCTAAT GGGAACACAG CAGGACTGTC 780
TATTTCTCTG CTGACCTCCT TCAGGGCCGG ATTCTAAGGC CCTACCCCGA GGCTTTCCTC 840
GGAGCCGGCT TTCAGTAAAG CAGGCAAGGG CTGGGGGTGG GAGTGGGGTG CGCTCATCTT 900
TAAAATCTTG AGGACTCAGG GGACTTTGCT TGCTTTCCAC ATGTGATAGA CCTCATTGCT 960
GGACTTAGAG AGGCGCCCCT GCCGTGACTC AAGTCTGCTC TGGCTGCCAG ACATTGAACA 1020
TTGAAGGCTG TGCCATGTGA GAACTCTTGA ACAGAAAAGC CCCTGAGGAG GACTGCTCCT 1080
CTCCCAGGTT CCACAGGCAA AGATGCTTTT GTGAATAGGT GGGGAGTGTC TGACATCTTT 1140
CCAGACTGGT TCTTCAACCC AGAATGATCT GGCCTTGAAT CAGCCTAGAT CCCCACAGAG 1200
GACATGCGGG CCATGGCAGC TGGCTTCACC ATGAGTCAGG CTGGCAGCCG AGCTGCGGCC 1260
TCCTCTAATT TGTGAATTAA TTAGCATATG GCTGGCCAGG AAAATGGCTT TGAAGACGAG 1320
CAAACACATT GGTGCAGGGC TCATGCATTG CTCCTCCTGC AGCACAGCCC ACAGCACAGA 1380
ACCCTCCTCC TGGCTTGACC AAAAGGAGAG AGGAGATGCT GCGCCCCATT CCTGCTCCTC 1440
CCCTTCTTTC CAGCGTGATA AGACGCAGGC TCTCCTTCTT CTCCTGGACA ACATTATTAT 1500
GAGACATGGG GGTAGTGGCG CCTTATGGAG AGCAAAGAGA GGCAGGGTCC CAGGGTCAGC 1560
TCCTCCTCCA CCCTTGAAGG AGCCAGAGGG TGGCAAGTGC TCCTGCAGCC CGGCACCAGA 1620
CACCCAGCTT CCTCCCAGCT GCTTGTCCTA CCTGCCTCCG TCTCTCCCCA GACCACACAT 1680
CTAAGAGTCT ACACAGCACA TTCCTCTGAG GCAGAGGTAC CTGGCCCTTC GTCATAAACA 1740
GATGCCCATG AAAGCCAGAA AGGATAACAG GAAAGAAACA CCCCAAGGCA GGATTATAAA 1800
CTCCTGAGAC TGTTTACATG TGCTTTGTGG AATCTGTTTC ATTAATTGTG ATCACATTTA 1860
TATTTTCCTT GGCCTCACTG TCACCTAGCA CTTTGTAGTA CTTTGCAAAA TAGTAGTACT 1920
TTGCCTCTGT GATCTCCTTT GTTTTCACAA TGACCGTGAG AGATGGGAAG GTCAGATGTT 1980
AGTACCCCCA TATTACCGAT GAGAAAACCG AGGCTCATGG AGGTTAAGTG ACTTGTCAGG 2040
TAGCTGGTGG CCAACCTGCA CTAGAACCTC AGCCTCTGAC TCAAGGCTCA GATGTGGCAA 2100
ACATCCCTCC CTTCATAGAC CTGCCTGGAC AGGCCACAGG AGCACTTTCA CTAGTGCTGT 2160
TACTGTGATT CACCTTGTCC AGGTGCCAGG ACCGGCTCTT TCCTACACCC TCTGTAGTGA 2220
AAGGGATCCG TGCTGAACAA ATACCGTGCT GGTGGAAGGA CAAAGACACT 2270
|
