| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08488 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:111385510-111386650 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr12:111385832-111385843 | TAATCTAATCA | + | 6.32 | | TCF3 | MA0522.2 | chr12:111385992-111386002 | AGCAGGTGTT | - | 6.02 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I110947 | chr12 | 111385202 | 111385960 | | GH12I110948 | chr12 | 111385981 | 111386130 |
|
Enhancer Sequence | TTATTATTTT ATAGTTCTGG GGGTCAGAAT TTTAAAATGA GTTTCACTGG GATAAGATCA 60
AAGTGTCAGC ACAGCTGCAT TCCTTCTGGA GGCTCTAGGA GGAATCTATT CCCTTGCCTT 120
TTCCAGCTTC TAGAGGCCAC CTGAATTTAT GGCTTGTGGC TCCTTCCTCC ATCTTCAAAG 180
GCAGCAATGA CAAGTCAAGT CTTGTCACAT GATGTCACTC TCACACTCAC TCTTCTGCCT 240
CCCTCTTTCA CTTATAGGGA CCCTTGTGAT GACATCAGGC CCACCTGGAT AATCCAGAAC 300
AATCTCTCCA TCTCAAGATC CTTAATCTAA TCACATCTAA AAAGTCTCCT TTGTCATGTA 360
ATTTAACATG TTTATGGGTT CCAGGGATTA GGGCATGGAC ATCTTCAGGG GCCATTATTT 420
TGCCTACCAC AGCTTTCTTT TCTCTTGGGT AAATACCTAG GAGCAGAATG GCTGGATCCT 480
GCAGCAGGTG TTTAACTTTT TTAAAAAAAT TGCCAAACTG GTTTCCAAAG CGCTTGTACT 540
ATCTTACATT CCCATCAGCA ATGTACAAGA GTTCCAGTTC CTCCACATTC TTCCCCAGCA 600
TTTGGAATGG TCAATATATT AGATTCCAAG GGTTGCTGTA ATTAATTGCC ACAAACTGGG 660
GGTCTTAAAA CAAGAGAAAC GTGTTTTCTC ACAGCTCTGG AGGCCAGAAG TTTAAAGTCA 720
AGAGTCAGCA GGGTTGATTC CCTCTGGAGG CTCTCAGGGA GAGAGCTTCT TGCCTCTTCC 780
AGCTCTGGTG GCCACAGATA TTCCTGGGCT TATATATACA TCACTCCAAT CTCTGTCCCT 840
GGCTTCACAT GGCATTCTCT TCTCTGTGTG TCTCTGTGTC TTCATGTGGC CTTCTTAAGG 900
ACAACAGTCA GTCAGTAGAT TTAGGGCCTA CCCTAATCCA CTATTACCTT GCTTTAACTA 960
ATTATCTGAA AATATCTTAT TTCCAAATAA AGTCACATTC TGAGGTTCCA GTGGACATGA 1020
ATTTGGAGGC GACCCTATTC AACTCAGTAT AGCCAGTCTT TTAAATTTAC CATTCTAATA 1080
GGTATGTAGT AGTGTCTCAT TGTGGTTTAA ATTTGCATTT TTGTAATGAC TAATAATGCT 1140
|
