| Tag | Content |
|---|
EnhancerAtlas ID | HS177-11273 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr2:2850050-2851640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr2:2851060-2851073 | TACATTTGCATAT | + | 7.12 | | ZNF263 | MA0528.1 | chr2:2851195-2851216 | GAAGGAAGTAGAGAAGGGAGA | + | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_33649 | chr2:2847186-2856385 | H2171 | | SE_66981 | chr2:2847186-2856385 | H2171 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I002846 | chr2 | 2849874 | 2851350 |
|
Enhancer Sequence | CTTGGAGAAA GCCCCGTCTG TTCCCCCTTC CTCACTGCGT AATCCTTCCC ATACGCCCCT 60
GCTCGCTGCC ATTTCTGAAG GACACAGGGG GCTTCTGTTA CCTGAGCCCT TTTTCCCTCA 120
CAGATGCCTG CAGGCTGAGG CTTGCTGGGG AGGCCTCTTC AAGGGACGCC TAGCCCCTGG 180
ACATCATCCA AGTTGGCAGC TTCACCACAG AGCTGCTGAG AGAAAGGCGC GGGGGGCAGC 240
CTGGGCTGGC CTGCTGAGCC AAGATAAAGC TGCAGGAACC TGCTGCTGCC AGAAGGGATG 300
TTTGCTGGGT TCCCACAGGT GACCAATGCA GGCAGAGACC AGCCAGGACT CCAGCTCAGG 360
GACAGTGATG GGCACAGGGT CACGCAGGGC TCTAGGCTTG GCCCAGGTTT TGAGCCAACA 420
ACACCAGCTG CCTGGTGGTG GGAACAGACA CAAGCACCAG GCTCAGTTTT CAAAGCTCTC 480
CTCCTCCTTC TCCTGTTATT TAAGGTCATA CCACATTGGA AGTGAGTCAG GCAGGTGGAG 540
CCCTTTATGT CCATGAGGCA GGTGCAGCAG CCCAGGGAGG CAGGGTGGCC TTTCCCAGGA 600
ATAGCCAGCG TCACCTGGAG GCAGAGCCAG GCGAGGGCTG TGTGGGTGGC TCCCAGCCAT 660
GTGGACAGCA GGCCTGACTG TCCCTGTCCC CATGAGCCTC ATGAAGGTGC CGCGGATCCG 720
TCCAGGCGTG GGTGTTGTTC TCTTCCGGCC CAGCCTTCTC CCTCTTTCCA CACACACGAT 780
TGGGCCAGCA TCTCCCGTCT GCTGCCATCT CCTCTGCTGG TGGGGGTGCG TCAGCTGACC 840
CTGTGCCCTC TGGCCTCATT TTTCATGGGT GTTGCCACTG TCTGGCTGTC TGCCCCTTCC 900
CACATTAACT CTCACCCTCT GGCGGCAGAG ACCTTGTCTT GCCCATCTCT GTATCTCCAG 960
CCCCCAGTGG CCCTCAGTGC GCATTTGCCA AGGGAAATAT ATGCAAAAAG TACATTTGCA 1020
TATCACAGCC CTGTGAGGCA GACACACCCA GAATCATTGC TCCTGCTTTG CAGAGAGGGT 1080
CTGTCCCTGG ACCCCGTCTT TGACTGCTGG GGCCTGAGGG TGTGGGCGGA CAATGAGGCA 1140
CATCAGAAGG AAGTAGAGAA GGGAGAGTGA GAGCCTGTCT TTCGTCCAGC TCCCTCCCTG 1200
CAGGGCCACC CCTGGCCAGC CTTAGACCAA AGGACACAGA TGCCAGCAAA TGTCTCTGCC 1260
AGCCCCCGGG GCTGGCAGGT GGCCTCCCTC CCAGCCACAC TCAGATGCCA TGGCTGTGAT 1320
TACAAAGAAC ACAGGGACCA GGGCACTTGG GCTCTGTGTG ACAACCCTGT GCAGCTGGGG 1380
ACACACACAC ACCACAGCAT GCCACATATA CATACACACA CACACATCAT ACACACCACA 1440
GCACAGCACA CACACAAACC ATACACACCA CAGCACAGCA CACACACACA CAAACCATAC 1500
CCACCAGAGC ACAGCACACA CACAAACCAT ACACACCACA GCACAGCACA CACACACACA 1560
CAAACCATAC ACACCATGGC ACAGAACACA 1590
|
