| Tag | Content |
|---|
EnhancerAtlas ID | HS044-13464 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr9:91392220-91393580 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr9:91393147-91393167 | TGGGTGGTGGTGGTGGGGTG | - | 6.82 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_36802 | chr9:91389349-91392745 | HMEC | | SE_38646 | chr9:91388475-91394098 | HUVEC | | SE_56572 | chr9:91385647-91393268 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I088773 | chr9 | 91388661 | 91393535 |
|
Enhancer Sequence | TCTCAGACGC AGCATCAATC GTCAGCAGTA GTTGTGGTTC CTCCTTCTGC GTGGTCACCT 60
GTGGAGGGCC TGCAGTGAGT GTGCATGTGT GTGTGTGCAT GTGTACGGGG CATAACACTG 120
GTGGCAAAAC ATCAGGGAAA ATCTGGGGCT TCTGTGTTCA AGAAATTAGT TTTATTGTAA 180
TTGTACAGAG ATAAAATCCC TACTTTCACA GAGTATTCTT ACGCACTACT TTCTTTTCTT 240
GGAAATTTTG GGGGGAAAGA CTAACAATAC ATGTTTCTTA GCCGTGGCCT TTCCTAATTT 300
CCAAGAGCTG AATCTCATCC TGCTAAGGTC TCCCTGAAAC CAGACTGCTC TGCACCCTCC 360
TCCGCACTCC TCCCCACGGC ATGACAGTTA CTGCCCATCT TCTGAGATAA CTTCAAGGCA 420
ACTATGGCAG CTTGTTTTAT TTTCTCTTCC TGCAACTCTC TCTGATTCTC TCTTTCAGCA 480
TTTAAGGATT GTCTTACTCT AATCAGCAAC TCCACCAGGA ACCTTTTGTG TTTTTTCGCT 540
CTGTTTCTCC CCCACTATTT GGGGCCAGAG CCCTCTGAGC CTCACATAAT GAAATTCAGG 600
TCGCTGTGCA GAAAATATTG AGCACAGAGA AACAAACCCC AGGAGGCAAA CTCTGAGGCC 660
GGAAGGTAGA ATTAGGAGCA GCCAAAAAGG ACAGCAGGCG AGTTCAACCG GATGCATGAT 720
CATTTCCTGT TCTTAAAATT CCCTTTAATA TCCCCAGCCC AGCCCGCTGA GTCGGTGAGA 780
AGCTGGGGAG GAAGAGCCCT GGCTGGGGTC AGGGGCCCAG GCTGCAGGCC CAGCTGGTGG 840
CTCGCTAGTG AGGCCCTGGG GAGACCTCTC AGGCCTGTCT TCAAGTCAGT AAGGAGGGGC 900
CAGTCCTGCA GCTCTACCCT CAGAGCATGG GTGGTGGTGG TGGGGTGTGT GTGTGTGTGT 960
AAGGCAGGTC TGGCTCCAAG CATCAGGAAG TGAGAACTGG GGAGAGATGT CTTTTGTGGG 1020
GTTCACACCC TCCCCAGCCG GGTTCTCCCA CTCTCCTGGA AGGAACGGGC AGCTAACACC 1080
TCAGAGCTCC TGGAACAGGC AGGGGATGCC CACCTCCTTA TCTCAGGGAG TAACCTGTGC 1140
ACAGTCCTGG GAACAGGCAC GGTCATCTTA GTGATAGTGA CAGTGTGGCC TGGCCTGCAG 1200
CAGTGAGTTC TGCACACTTC ATTGCGGGGA AGCTGGATGG TAGAAAGTGG AGACATTCAA 1260
CCAAGATGAC GCAGTTGTTT GCAGCCACAT GTAGAATTGA CGCCTGTCTG AAAACCTCCC 1320
CACCATTTGG CCACGATCAG TGCTGACCCT CACTCTGTCC 1360
|
