| Tag | Content |
|---|
EnhancerAtlas ID | HS184-12933 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr16:89568370-89569260 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr16:89568877-89568888 | GGCCACACCCT | + | 6.32 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_35155 | chr16:89567874-89569896 | HeLa | | SE_36659 | chr16:89568308-89569273 | HMEC | | SE_50805 | chr16:89568216-89569455 | Sigmoid_Colon | | SE_52882 | chr16:89568136-89569769 | Small_Intestine | | SE_62639 | chr16:89542302-89575973 | Tonsil | | SE_65143 | chr16:89568583-89569301 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I089501 | chr16 | 89568311 | 89569832 |
|
Enhancer Sequence | ATGACCACCT GTTCCTTGTC AAACCAGCCC TTTAAGTTAC AACAAAAAGA AAGCCCTCCT 60
CCTGCTCCAT GTCCACACTG AGCCTGGTGT CTGCGGCCCT GTCCTGGCGT TTCAGAGGCC 120
GGTCTGGAGA CTCACCCTCA TCGCCCTCAG CAGCTGGGCC ACCAGCAGCC ACATGCTGGC 180
CTCTGCTGGC TTCTCTCTTC CTGGCGCTGC AGATCAGAGA ACGCAGCCCA GAGTGGGCAC 240
CAAGACACCC CAGGCTTTAC TGGATCCTCT GGGAGAACCA GCCCCATGCC TCGGTCCTGC 300
CAGGATCCTT ACCTTCTGGC ACTGCTGCAA AAGCCTCCCT CCTCCCTGGC CTCACATTCC 360
CACCTCTGGC CTCTCTAGAG TCCATTCTCT CAGCAGCCAG TCATGCTTTT ACCACAGACT 420
TTATTAGTCC TCAGCAGCAC TCCCCCTCGG ACTCTCCAGC ATTCCCTGGC CGCTCCCCAC 480
TCCCCTGCTA CCTGCCCCCT CCCAACTGGC CACACCCTGG CCATCAGTTA GTCGGACTGC 540
AAGCTTGTCC AGTCCAAGAG ACTAAACGGT CCAGTCGAGC CACTCCCAGA TTCCTGACCC 600
TCAGAAACAG AGTGAGATAA GCATTTGTTG TTTTAAGTTG CCACGTTGGC GAACTCGGAA 660
TGCACTGCCC AGGGCCGTGG GGATTCCCGT CACGTGGAGA GGACATAGGC TGTCCCTTCC 720
AGGTCCTTAA ACACCTGCCC AAAGTCCCAC ACCCAACAAT CTAAAGAAAC GCTGAGGAAT 780
ACATGATTAT TTAGTCATGC TCAAATTCCT GTACAGGTTT CTTGCTAGTA GAAACGGACT 840
TTCCGCCAGG CGTGTTGGCT CACGCCTGTA ATCCCAGCAC CCTGAGAGGC 890
|
