| Tag | Content |
|---|
EnhancerAtlas ID | HS161-08465 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr19:56177950-56179870 |
Target genes | | Number: 25 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr19:56179366-56179377 | TCTTATCTCTT | + | 6.02 | | MYC | MA0147.3 | chr19:56179734-56179746 | GGGCACGTGGCG | - | 6.74 | | RREB1 | MA0073.1 | chr19:56178558-56178578 | TGGGAGAGGGTGTGTGGGGG | - | 6.84 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23398 | chr19:56178044-56179214 | Colon_Crypt_1 | | SE_23398 | chr19:56179431-56180404 | Colon_Crypt_1 | | SE_23969 | chr19:56179550-56179870 | Colon_Crypt_2 | | SE_27904 | chr19:56178304-56180119 | Fetal_Intestine | | SE_29198 | chr19:56178255-56180189 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I055666 | chr19 | 56178334 | 56181342 |
|
Enhancer Sequence | TGAATCAGCA CTTGGCCTGA GCTGTTCTCA CACACGTGGC TCACACGATG GGCACCAGGG 60
TTCTTCCCAT TCTACAGATG AAGACACTGA GGCCCTTGGA GGCTCATATG GTACAAACAA 120
GACTTGAACC CAAGGAGCCA TGAACCCAGG GAGCCCAACT CTTGTATCCT TGGCTCTGTG 180
TTGCTCAAGT GAGACGGGCA GAGCCAGGGC TCGCGGCTGA GCTTCCAGTG TGACCCATTC 240
TTCCTTGGAC CCAGGCAGAG CCTGCAGCCT GCCATGCTGC CTGTGGGGAG TCACAGCTGA 300
GTGTGGGCTC TGGAGGCTGC CTTTTTCCTG CCTGTGTGTC TTTGCTCTGT GCCTCAGTTT 360
TTGCCTTCTG TGCTGTATGT ATAGCATTGC AGTAGGAGGT TGAAAGTCTT ACAGGATGCC 420
TGGCCCATGG GGTGAGTGCC CGGTGTGTGT TCCTGCTCCC GGGCTGCTGC TACTTGTCCC 480
TGTAGCATAG GAGCTGGGTC TCCTGGGGTC TGTGTGGCCC CAGTCTGGTG GTTGGAGCTG 540
GCTGGGTTGG TGCTTCCAGT TCTGTGGGGG CAGCGTCATC ATGGGCTGGA AGGGCTTGAG 600
TGAGTAGGTG GGAGAGGGTG TGTGGGGGCA TCTCCCCTCC TTCCATGGGC ACAGCGGCTC 660
ATGCTTCTGA GGCTCTTTCC CATTTCCTGT CTTACCTATT CCTTCCCAGC ATCAGGATGG 720
AGGTGGGATG GGGCCACTCA CACTTGGTGT GGAGGCTGCA GAGGAAGGGG AGGCCATATG 780
GCCTAGGTTT TGAACTTGGG AGTCAGGCTG GTTGGTTACC GGGGCCTGGC ATAGCTGATA 840
TCTGACAGGA CGGCGTCAAG TTACATTGGC AGAGCCTGTG GGGTCTCAGG TTGAATCATC 900
CCACCAGCAG GCACTTGTCT GTGAGTCCAG AGTTCAGTGG ATAGGGCAGG ATCGAGGGCC 960
AGTAAATTCA GCTGATAAGC CCCCACTCTG GTATGTCAGC CCTCGAAGAC ACTGGATCCT 1020
GCATCCCACA GTCAGCCCAC AGTTCCCAGT GAGATCAGAG CAGCTAATGC TGCGGATGCT 1080
GTTCTGAGAC TTCCCGGGCA GCCGCGGCTG CTCATCGTGT CGTGCCACCC CTGTGAGGGC 1140
AGTTGCACCC CTGCAGTGGC ACCTGCAGTT CTGACAGGGC GTGAAGGGAA GGGACTGAGC 1200
TTTTTTTTTT TTTTCCTTTG AGATGGAGTC TCACTCTGTT GCTCAGGCTG GAGTGCAGTG 1260
GAGTGATCTC GGCTCACTGC AACCTCCGCC TCCTGGGTTC ACGCCATTCT TCTGCCTCAG 1320
CCTCCTGAGT AGCTGGGACT ACAGGTGCAC GCTACCACAG CCCGCTAATT TTTGTGTTTT 1380
TAGAGAGACG GGGTTTCACC ATGTTGGACA GGATGGTCTT ATCTCTTGAC CTTGTGATCT 1440
GCCCGCCTTG GCCTCCCAAA GTGCTGAGAT TACAGGCGTG AGCCCCCGCG CCCGGCCGGG 1500
ACTGAGCTTT AATGGGAGCC TTGCCTGGGT GGCTGTCAGA GAAGGGGTGG GGTGTGTTGT 1560
GACTCACCAG TAGGTCCCGA GCCCAGGTGA CCTGCCAGCA TTCCACAGCA GCAGGTAGCA 1620
GATGTGGGTG TGAACTTTGT GCCTTTGGAG CGTTCTGGAG GATGTTCTAG TTTGAGGTTC 1680
CCCTGAGGCT GGGCAGATTT GGGAGACATG GTGCGTTCTC CCCGAGGAGC CTCTGTGTGC 1740
CACTGCCCAG GACCCTCACT GGTCAGATAA GGCTGGGGTG GGGTGGGCAC GTGGCGACCC 1800
CTCCCTCGTC AGATCAGGCA GGAAGTGTTC TCTTTGGCAA TTGAGGAGCT CGCCGTAGAC 1860
TGTCCAGGTT TTGGGAGATA ACCTGGTACT GGAATTGAAG TCCTCCTCTT CTCTACCCAT 1920
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