| Tag | Content |
|---|
EnhancerAtlas ID | HS098-47043 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:170864020-170865000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr5:170864502-170864523 | TCTCTTTCCCCTTCTTCCTTT | - | 6.11 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41295 | chr5:170859499-170865221 | Left_Ventricle |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I171436 | chr5 | 170863666 | 170865035 |
|
Enhancer Sequence | GCCAGGCCGG AAAAGCGGAG ACTGCTGCGA GGCCTCCTGG TCCTTGCCAC TCACTGGGAA 60
AGCACCTGCC CCCACCCATT CCTGCCTTCT CAGGCCCAGG TTCTAGGAGA TGGCCCAGGC 120
CCCAGCCTTG GGCCTGGGGA TCTGGGGCCG TGGTCCTGTG TGTGGGGCCA AACCTGCCAG 180
CCTGAGCGTT TTTGGGACGA TGCCCCGCCT GCCTGCCAAC CCTGCCCGTT GCAGTCAGGA 240
CGTGACAACA AGACAAATAA TTTCTTGGAC CTTTTATCTT GGACACCATT TATTTTCCCT 300
CAGCCCCGGG GCAGGACTGA CCTCATGGTA GGGCCCAAGC GTGGCAGCTG CACCGTCACT 360
GGGGGCTGGG CCAGGCCAGG CCAGGCTGGG CAGGGCTGAG CCATGCTGGG CTTGTGCACC 420
TCCGGGCCAG CTGCCTCCCT TCTCCCAGGC ATCACTCTTT ACCGCCTCCG TTCCCCTCCC 480
ACTCTCTTTC CCCTTCTTCC TTTCGCAGCT TTTCCCCGTT CCCCGTTTTG TTTTTGTCCA 540
CCTCTCTGTC CCCCTCCCCA CCAGCTCTGT CTCCCTCCTT CGGACCACAG CTTCCCTCCT 600
CCCCACCTCT CCCAGGCCCT CTGCTGGCTG CCTCTATGGG GCCTCCCATC CCTCGTGGCC 660
CCCTCCACAG ACGCCTGGCT GTGCTAGGCT GACCCAGGTG GTGGTTTTCC CTCGGATCTG 720
CTGTCCAGTG GCTGCCAGAA GGGGCAGCTG GCTGGCCGTG GCAGGAGGAG GTGCCCTTCT 780
GGGGAGTCCC AGAGCTCTCA TTGGCCCCTC CAGGCTGGGA GAGTACAGGG GGGTCAGACT 840
CTGGTCTGAA CCATCTGTCC ACGCCCTGAG ACAGGAGGCG GGAGCTCGAG AGGGAGGGGA 900
GCCTGGAAAT GGCCGGCCCC TCACCCCAGA AGTCACTTGC CCTCTCATTC CCTCTGCCTG 960
AACTGGGAAC TCAGGGAATC 980
|
