| Tag | Content |
|---|
EnhancerAtlas ID | HS165-15797 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr9:91391570-91393700 |
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 | GACAGGGTCT GTGGCTCAGG GTGTATCATA GCAGAGCCTC ACCTGACTGC TCAAGGCGAC 60
TGAAATGATG AGATTTTGGA CTTGAAGTGG GTGTTCTAAT GGAGTGAGAT CTTTGTTGTC 120
ATGAGACAGG ATAGATGCAT TTTGCAGATG AGAGAGAGGA ATGTGGTCAG AGGGTAAACT 180
ATAGCAGACA AAATTTTTGC CTCCCCCATT TTAGACCTGC CTTTTAATGG ACTTGCTTAG 240
TCATTGGGGT TAACTATGAG CAAACACAGT CCCCAGTACA GCAGAACAGA GAAACAACAA 300
TGTACCAGGT TAGATCAGAG CAAAGGAATG TTTGAAAACT GGAAACATCT CATATTTAGA 360
AAACAAGAAG TGGGCAAGAA ACCAGAGTGT CTGGGGAGCC TATAAGTGCA TATGAAAAAG 420
TATGGGCCCA CGTTGGGCAT GGTGGCGCAT GCCTATAATC CCAGGAGGCT GAGGTGGGAG 480
ATCGGGTGAA TCCAGGATTT CAAGGCTTAA GTGAGCTCTG ATTGTGCCAC TGCACTCCAG 540
CCTGGATGAC AGAGTGAGAC CCTGCCTCAA AAAAAAAAAA AAATAAAGGC ACAAATGGAA 600
GGTGTTTGTA TCAACAGGGC CAGGGCCATG GGCTCTTGGA GTGCCAAGTG TCTCAGACGC 660
AGCATCAATC GTCAGCAGTA GTTGTGGTTC CTCCTTCTGC GTGGTCACCT GTGGAGGGCC 720
TGCAGTGAGT GTGCATGTGT GTGTGTGCAT GTGTACGGGG CATAACACTG GTGGCAAAAC 780
ATCAGGGAAA ATCTGGGGCT TCTGTGTTCA AGAAATTAGT TTTATTGTAA TTGTACAGAG 840
ATAAAATCCC TACTTTCACA GAGTATTCTT ACGCACTACT TTCTTTTCTT GGAAATTTTG 900
GGGGGAAAGA CTAACAATAC ATGTTTCTTA GCCGTGGCCT TTCCTAATTT CCAAGAGCTG 960
AATCTCATCC TGCTAAGGTC TCCCTGAAAC CAGACTGCTC TGCACCCTCC TCCGCACTCC 1020
TCCCCACGGC ATGACAGTTA CTGCCCATCT TCTGAGATAA CTTCAAGGCA ACTATGGCAG 1080
CTTGTTTTAT TTTCTCTTCC TGCAACTCTC TCTGATTCTC TCTTTCAGCA TTTAAGGATT 1140
GTCTTACTCT AATCAGCAAC TCCACCAGGA ACCTTTTGTG TTTTTTCGCT CTGTTTCTCC 1200
CCCACTATTT GGGGCCAGAG CCCTCTGAGC CTCACATAAT GAAATTCAGG TCGCTGTGCA 1260
GAAAATATTG AGCACAGAGA AACAAACCCC AGGAGGCAAA CTCTGAGGCC GGAAGGTAGA 1320
ATTAGGAGCA GCCAAAAAGG ACAGCAGGCG AGTTCAACCG GATGCATGAT CATTTCCTGT 1380
TCTTAAAATT CCCTTTAATA TCCCCAGCCC AGCCCGCTGA GTCGGTGAGA AGCTGGGGAG 1440
GAAGAGCCCT GGCTGGGGTC AGGGGCCCAG GCTGCAGGCC CAGCTGGTGG CTCGCTAGTG 1500
AGGCCCTGGG GAGACCTCTC AGGCCTGTCT TCAAGTCAGT AAGGAGGGGC CAGTCCTGCA 1560
GCTCTACCCT CAGAGCATGG GTGGTGGTGG TGGGGTGTGT GTGTGTGTGT AAGGCAGGTC 1620
TGGCTCCAAG CATCAGGAAG TGAGAACTGG GGAGAGATGT CTTTTGTGGG GTTCACACCC 1680
TCCCCAGCCG GGTTCTCCCA CTCTCCTGGA AGGAACGGGC AGCTAACACC TCAGAGCTCC 1740
TGGAACAGGC AGGGGATGCC CACCTCCTTA TCTCAGGGAG TAACCTGTGC ACAGTCCTGG 1800
GAACAGGCAC GGTCATCTTA GTGATAGTGA CAGTGTGGCC TGGCCTGCAG CAGTGAGTTC 1860
TGCACACTTC ATTGCGGGGA AGCTGGATGG TAGAAAGTGG AGACATTCAA CCAAGATGAC 1920
GCAGTTGTTT GCAGCCACAT GTAGAATTGA CGCCTGTCTG AAAACCTCCC CACCATTTGG 1980
CCACGATCAG TGCTGACCCT CACTCTGTCC CTGGGCTGTG GCTGACACAC ACAGGGTCAC 2040
TGCCAATTGC TCAGGGCTCC TGTCTCTCAA TACATGTATT TTCACAAAAA GGACACTCAC 2100
TAAAGTGATG TCGAGAGCCA TCTTGAAGAG 2130
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