| Tag | Content |
|---|
EnhancerAtlas ID | HS080-29067 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr5:122433510-122435340 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr5:122435171-122435192 | GTTCTCTTCTCCTCCTCCTCT | - | 6.26 | | ZNF263 | MA0528.1 | chr5:122435314-122435335 | GCTCCCTTCCCTTCCTCCTTC | - | 7.65 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_01647 | chr5:122432976-122436252 | Aorta |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I123097 | chr5 | 122433360 | 122436028 |
|
Enhancer Sequence | GCCCAGCGGC ATGGACACTT CTCTGCTTTC CGAAACAAGT TGTTGCTTTT CACTTCAGAG 60
GTCTGGGGAC ATTTCTGAGA AGCTTGCAGC CCTCATTCTT CCAGCTCTCT TGGGAGGAGT 120
AGAGGAGTAG CTGCTGACTG AGGCAAAGGT TTGGCTGGCT AGAGCCCCCT CCAGTGAGAC 180
AGGAGGCTTA CATAGTCAGC CCTCCTTTGC TGTGAAGCAA ATGGCAAATC GAGGGCTCCC 240
TTACCATGCT GGGTTGCGAT TAGCTGTTCC TGACACAAAC GTTTCATACA GACTCACAAG 300
TTTCTTGGGC ATTTCGGTCA TTTCAGCGCA GATAGGGCAC ATCCAGGGTG ATCCAACAGG 360
CCTGGCTGCG GCCAAGGCTG GCGGCGGCAG GTACCCGGGT GCCCCGAGGG CCACCCGCCG 420
CCCCGCTCTG GCGCATCCAT CAGTGGCCAG CTTTCACCGT GTCTGCCAGG CGGGACTCGC 480
CAGGTGTCAG GCTCAGTGCC ATAAGCCTGA CACTTGCGCG GGGTCGCCGT GGCTCCTCAG 540
GGAAGCTGGG CCAAGGAGGC TGGGTCGCGC CGGCGGGCGC CGAGGCCACC TTCTCGGGGC 600
AGGCCATCCG CGCTGAGGCG CAGACACGGC GGCTCCTCCA GGCCCATTAA TAACCCGGAG 660
GGCGCTGCGA TCCGACAGCG CAGTCGCCAC AGGCTCTATT TCCCGTGGCC GCCTGCCTCC 720
TTCCAGCCCA GTTCGAGTGG AGGGATACTG GGCGCCCACT ACCGCCCGGC CCGGAGGGTG 780
GGGGTCCCTC TCGCGCAGGC TGCTTTGGAG AGTGTCGGAG AGAGACAGCT TTATCTACAG 840
CTTCACCCAT TGTATAGCAC AACAGAATCG CATTTAGCCT GGAGAACAGC CGTCGGGGCA 900
GGAGTTGGTG CCTTCTCTAA CAATTAGGCT GATCGTTAAA TTTGCTATTC CTTTCTTCCG 960
GCGTCTAGGG AGAGCGTGCA CACCAAACCC TCCAGAACAG CACCCCGGTC CCCCACCCCG 1020
CCCCACCTGT CCCCGCCCTG CTTCAGTGCC TGGAGGGAGA ACTGACTGGT CGCTTGAGGG 1080
ACCCCATTTC GGGCGCGCCC TTGGAGTCCT GGGGCTGCGG CTCCTGCTCT ACCGGGCTGC 1140
AGGCTTGCTC TGCCCCGTCC CGTGGCGTTT GGGAGGCAGT CGAGGAAGCC TCCGAGTCTC 1200
TGGGTCGAAG GAAGTGCGAA TGGCACCCGC GATAGACTGG CCGTCTCCCC CACCCCGCCC 1260
CGTCTGGTGA TTTTAAATCG TCTCCTGTGT AATTGTAAAA AGAGGAAAGC TGAATACCCA 1320
GACGACCAGT ATAGAATCTC TTCGAGACAG CAGATTGGGC AAGAGACGGG CTTTTTTTCG 1380
CAATACAAGG ATAAACACAT CCTGAAACTC CAGATAGAAA CCTCAGGAAT GGGCGAGAGG 1440
GTCAGAAGGA ACGAGAGACA GTAGGGAAGA GAGAGAGAGA GACAGAGACA GAGGGAGAGA 1500
TGCAGAGAGA CTGAAACGGG AGGAAGAAGC CTGGAACTGT CGGTTCCGTG GAGAGCGGAC 1560
ATGCTATCTG CGCCCAGATC CGAAGGCTTT TTGGGGAGCC TAGAGTCCTG GCCCGGTACC 1620
AGGCAGATCT GGGTGCGGCG AATTCCAAGG GAGCGGCGCG GGTTCTCTTC TCCTCCTCCT 1680
CTGAGTTGCT TCGGTGCCCC CAAGGCATCA CCTTCCTCGA AGGTGGCTTA CCCAGGCGGG 1740
CGGTGATGCT GTTGTCTCGG GAGTTTACTC AAAGATGGGC CGCTCGGGGC GGCCGGATTA 1800
ACCCGCTCCC TTCCCTTCCT CCTTCTTGTC 1830
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