Tag | Content |
---|
EnhancerAtlas ID | HS184-18398 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr20:48839150-48840340 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF410 | MA0752.1 | chr20:48839756-48839773 | CACATCCCATAATGATA | + | 6.78 |
|
| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_00214 | chr20:48831408-48844173 | Adipose_Nuclei | SE_26761 | chr20:48839876-48842025 | Esophagus |
|
| Number: 1 | ID | Chromosome | Start | End |
GH20I050218 | chr20 | 48835339 | 48844536 |
|
Enhancer Sequence | AGTATGTCAC CTTCCACACT GCAGGGACTG CTGTCTGTGG TGATCACGAT GCTTTCTGAG 60 CACTCAGCAC AGGGCCCCGC ACACAGTAGG GGCTCCACAG AGATTTGTTC AATCAGTGAA 120 TGGGCGCGCA GGAGGGGTGG CTGTTGGCCC AGATGATGCT TCAGCAAACA TCACAAGTGT 180 CCTTTCTCTG GCTGATGGCT CGAGGCTGGT GCCCAGAACA GGCTGCTGTG GAGACGGCTT 240 CCCTGACCAC CCTGTCAAGT AGCTCCGACT GCCCAACCCA CACCCATGCT CTCCAGTCCC 300 CTCGCCCCAC ACTTCCCACA GTCTCAACTT GTTTTGCTTC TGTATTTTTC ATGGGCCCCT 360 CCTCCCCCGA GAATGGAGCT CTCTGAGAAC AGGGTGTCCT CTGTTGGCCC CACTGTCATC 420 CCCCTGAGTG TCCAGTGCAG GACCCGGCAC CCCATGGGAA GTGTTTCATG GCAGGTTGAT 480 CAGGGTTTGC ATCGGATGCC CCATCTGCCG GGCTAGTTCT GGCTGGGAGG GTGTTAGGAG 540 GAGATGCTGT GCTCGGACCT GCGAAGTCAC GGGGGAGATG GGGACCCACT TGGGCCTTAA 600 TTATAACACA TCCCATAATG ATATGGTGTT ATAATACGCA CACAAAGTGT CCTAATCTGA 660 TATTATATCT GGGTTTTGTA CAATAGATAC AATCGGCTGG CTGCAGTTTG CTAATTCATT 720 CTCGACCTAT CTCCACGCTC CACCTAGATG ACTATCGGCT TCCTTAATTA AGTGGAAGGC 780 AAGCTCTGCA GGCGATGCTT GCAGTCCCAG CACCGACGAG TCCGGCCTGG CCCTCCCATA 840 AGCTGGGATA ATAGCTACTC CCACATGGGG CGAGGCTGGT TCTGCCTTCT TCATCCCAAC 900 CTCCTGTCCC AGTCTTGGGC GTGACAGGCC TGCTCCAAGG CCTGGTAAGC CACAAACGCC 960 AACCACCAAG GGCTCAAACC GGCGGCCTGT GGGCCGGGCC GGCCTCGAGA TGTGTTGGGT 1020 TTGGCCTGCA TGGTGCTTTT GCTGCAAGTT AAAATGAGTT GCCAACTATG AAAAATCAGA 1080 ATGTCGTACA CAAACATCCA GATTCCCGGC TTCTCTTGGG AAATGGGAAG ATGCAGGGAC 1140 TCGGGTTCAT AGTCCTGGGT GCTGGGGCTG GGGAGTGGCT GTCCCCTCTA 1190
|