Tag | Content |
---|
EnhancerAtlas ID | HS197-06313 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr13:111683140-111685090 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr13:111683755-111683765 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr13:111683755-111683765 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr13:111683755-111683765 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr13:111683755-111683765 | AACAGCTGTT | - | 6.02 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH13I111030 | chr13 | 111683002 | 111684871 |
|
Enhancer Sequence | ACTATGGCCA CAAGAGAAAG CCCAGCTCAT TTAAGTAAAG TAATTGATTT TGACATCTGA 60 AAACTAACAG CAGTTAGAAA TTTTAGAATG AATCACTGAG TAGACCAAAT GAATTTAAAT 120 CAATTATCTG AGGTTTAATG TTTAAAGGGG GTTTAATTTT ATGTATCTAG TTGCACCTTG 180 ATTATTCAGT TTTGAAGTTC CATGCATCAA AGTTTTAATC TCAGAATGAA CACTAGACTC 240 CCTGGGCTTC CCCTGCAGAC TGGTATGTGC TTAGGGAACG CAGGTGAGCC ATGAGGCAGC 300 CAGTCATGAA GTCAACCGAG GCTTCTCAGC TGCCATGCCA GCCGCTGTAG TAGTTCCCGA 360 GCAGAGTTCA CCCTCAGCGT CGTCACAGAC AACTTTTGTG GAGAGCTCAT GTGTGCTTGC 420 CAGTTCTCTG TGCCTCTGTG GCTTTCTCAC AACGGGCAAC ATTGGGTCTA AATCTTAACT 480 TTCTTGCAAA GAAGTCACAC TTCTCAAATA CAGGCTGTGT TAAGCGAATG ATCATTTGGG 540 CAGCCATGTT TAATAGAAAT GCTGTTGCTA TCCCAGGCTC ATTCTTGCTA TCTTAAGATA 600 GATTTGTTCA TCATTAACAG CTGTTTCACC AATGGGTGTC TGTTTGCTGA ATGACAAGTC 660 CTGCAGTCTC ATGACTTCAT GCTGGATAAC GCCAGGCGCA GGTGCATTTA GAAGGGTGAA 720 GTGGCTCTTT CTGTAGGCCC AGGCCAGCTC TGGCCTTTCT CTTGTAGCCA ATGAGCTGTG 780 GTAGAGACAC CTGTCCCCAG GAAGCAGCTC ACTCCTGTCC TACAACCCTG AGGCGGGCAG 840 GGCAGGCACT ACCGCCCAGC TGTCCTAGTC CTGATGTGAG TCAGTGACCT AGAATCCGGA 900 GCCTTCCCAA CAGCCAGTGG AAACATCCTG TCACATGTGG TTTTTATTTC AGAACTCGGG 960 CTTGTGGTGC TGCCCTGCAC CCTGAGACAC CCTTGCTGTG GTCGGATTCG TGGAAGCACA 1020 CTGGCTTACC CAAGTACCTC AGTCGATTGC TCAGCAGCTC TTACTTGTGA TCAGAGCTGA 1080 TGGGGTGAGC AACTTATTCT TGGGGAGAAT TAGCTCCTGG AAGGTCTGGC TTGGGGCTGG 1140 TGCCGCATCC CATGGCCTCA GCTTGAGGAT GGAGGAAGGG GTCAGCTGGG GAGTGTGGAG 1200 GGATGGGGAG CTGTTCCCAA GCTTCACACC ACTGCTCACC ACTGGGCAAT CCAGTGAGCT 1260 TCCATGGATC TGACCACACT TATGGGGTCT CAGGGCACAG GACTCTGCAC CGAAAGCCCA 1320 AGGTTTGAAA TGAAAATAAC ATGTCCTCCA CTCCTCCAGG GGAATGTGTG TAGAACAACC 1380 TGGGACCAGC CAGAGAAACA TGGTGGGCGG GTTCCTGGCT TGGTGCCCCT TTCCCACTCC 1440 TCTCCCAATA ATCTGGTCCT GTGAGGATGC CCCACACTCC TGACCACCTC AGGCCTGCAC 1500 CCTCGTCTGA GCTAACCCTC ATCTGAGCTG TTGGGCCTTG CTGGAGAGAT GGGGGCTGAG 1560 CAAGCACAGG CCTGCTGGGG CCTCTGGATC CTCTCACTGT GGTGATGGCC AGGCCACCTC 1620 CTGCAGGAAC TGCTGGTGTC TCCTCCATGA CCAGAGGCCA CCACTGGGGA TGCCCAGGCC 1680 TCCCTGTCAC ATCCTCCCCA CTTCTGGTGC AAACTCTCTG AGAGACACAT GCAGGACAGT 1740 GCTTGGACCC AGGCCCACAC TAGCTTCCTA CCAGTCACTG CACCCCAAAT CAACTCATCC 1800 ACTCAGCCAC AGGTGGGGCA ACTGCACCCC AGCCCAGGGG GGTTCCTGAC GGGGAGAGTG 1860 AGTGCATGTG TGTGAAGAGT GGCAGGTCCT GCAGACCGAG AGAGTCTAGA ACATCCTCTT 1920 GCGGGAGGAA TGGCCTAGAG TCAGGGGAGG 1950
|