| Tag | Content |
|---|
EnhancerAtlas ID | HS047-15211 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr17:73552580-73554230 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr17:73553238-73553249 | CATGAGTCACT | - | 6.14 | | Nr2f6(var.2) | MA0728.1 | chr17:73552890-73552905 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr5a2 | MA0505.1 | chr17:73552898-73552913 | GAGTTCAAGGCCAGC | + | 8.25 | | RARA | MA0729.1 | chr17:73552890-73552908 | GAGGTCAGGAGTTCAAGG | + | 6.73 | | Znf423 | MA0116.1 | chr17:73553867-73553882 | GGCCCCCTGGGGTGC | + | 6.42 | | Znf423 | MA0116.1 | chr17:73553867-73553882 | GGCCCCCTGGGGTGC | - | 6.57 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23798 | chr17:73551444-73552902 | Colon_Crypt_2 | | SE_23798 | chr17:73553213-73554927 | Colon_Crypt_2 | | SE_28701 | chr17:73551300-73554667 | Fetal_Intestine_Large | | SE_41669 | chr17:73551532-73552852 | LNCaP | | SE_41669 | chr17:73553153-73554910 | LNCaP | | SE_47745 | chr17:73552503-73552972 | Pancreas | | SE_47745 | chr17:73553056-73554946 | Pancreas |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I075555 | chr17 | 73551481 | 73554876 |
|
Enhancer Sequence | TTCAGGAATC CCCCAGTCCC GGGCAGGGGG TGAGGCTGCT GGGGGGCTCA GAGACCTGTT 60
TTGCAGGGGT TGTATTGGTG GATCCAGAGG GAAGGACCTG ACGCCCATGT CTCAGCCAGT 120
GATCATTCAG TGAGTGGCTG GCTGGTGCGC CAGTAGCAAG GCCTAGGCCC TTCTGTGCCC 180
CTGCCTCCCT CAGCTCCCCA CCTCACCACC AGAAAAGCAA GTTACAGGGA CCCCTCTTGT 240
CGCTAGGGAT GTTTTTAATT TAAAAAAATT TTTTTCGGCA CTTTGGGAGG CTGAGGCGGG 300
CAGATCACTT GAGGTCAGGA GTTCAAGGCC AGCCTGGTCA ATGTGGTAAA ACCCTGTCTC 360
TACTAAAAAT ATTTTAAAAG TTATCAGGGC GTGGTGGCAC ATGCCTGTAA TCCCAGCTAC 420
TTGGGAGGCT GAGATGGGAG AATCGTTTGA ACCTGGGAGG CAGAGGTTGC AGTGAGCCAA 480
GATTGTGCCA CTGCACTCCA GCCTGGGCAA CAGAGTGAGA CTCTGTCTCA AAAACTTTTT 540
TTTTTTTTTT TTTTTTTTTT GTGGAGACAG GGTCTTGTGA TCTTGCCCAG CCTGGTCTTG 600
AACTCCTGGG CTCAAGCAAC TCTCTCGCCT TGGCCTCTCA AAATGCTAGG GTTACAGGCA 660
TGAGTCACTG CACTCCCAGC CTGCAGTTTT GTTTTTTAAC CTATCTCGAT AAGAATCAGA 720
GGTGGACTGG CCCCAGGGCC CTATCCACAA GCAGAGATGG GGTGGCCTTG GGCCAGGAGA 780
GCAGGGCTCG GCAGCTGTCT TCCAAATTCC ACCCCCACTC CCACAGGCGG CAGAGAGTGG 840
AGAGGGCTCT GCCTGGCAGG GACAGTCCTT CCCCGGCCTG AGGCTGGATG TTGTCCAGTT 900
GGGTCATCTT TTATCCAGAG CACTGGTTCT GGCCGACTGG GGGCTCCCAG TGTTTTCAGA 960
GATGAAAAAC CGGATCAGGT TGGGCACCCC GCCAGTCTGA TCTGTGCTCC CCTCAGGGCA 1020
GGGCCCAAGG GAGTTGAGAG ATGAGGGACC ACCTCCAATA GCTTGGCTGC CACCTCCAGC 1080
GGAGCCTGAC CTCCCTCTTC CCCTCTGCCC GGTGTGGGGG AGGGGTATGG AGCACTCGAG 1140
TTCCAGGCTG GGCTGGTGTA CACAGGGGGC CAGGGCCTTG CTGCGGGCTC AGCCTTCCCT 1200
CGGCTGGTTA ATCATTGCCA GGCCACAGCC AGACTCTAGT TACCAATCCC TGGTGCCAAG 1260
ACTAATGGGC CAAGGCTGTT GGTGATAGGC CCCCTGGGGT GCCGTGTGTT TTTTCACAGG 1320
TGCTACCAAG CGACAGCCAA CATGTCTTTT GCAGCTCAGG ATCAGGGTGG CAGCCTGACA 1380
GTTGCCAGGG TAGGGCTTCG CCTTTCTATG GAGTTGCTCC CACCGGCCTG ACTGGGAAAA 1440
ATCTCCCAGG GATCAGGTCA CTGGCCTGGT GCCCCAGGGC CAGGGCTGCT GTGTCTCCTC 1500
CCCACCCTAG GCTCCATGCA TGGGTCCTGC TGCCTCGGGG GAGGGCAGCC CCTCTCTGTG 1560
TTTGCATCAT TGCACATGGG CCCCGAGGGC CTGGCACTCA AGGCAGGCAG GGGATGGTGT 1620
CCGACCTTCC AGAGCTTTCC TGAGCCTACT 1650
|
