| Tag | Content |
|---|
EnhancerAtlas ID | HS040-24941 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr3:4909230-4911040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr3:4910267-4910278 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr3:4910267-4910277 | GCCCCGCCCC | + | 6.02 | | NRF1 | MA0506.1 | chr3:4910169-4910180 | GCGCCTGCGCG | + | 6.14 | | SP4 | MA0685.1 | chr3:4910264-4910281 | ATCGCCCCGCCCCCTCC | + | 6 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_18602 | chr3:4908063-4912293 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19590 | chr3:4908204-4911214 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20241 | chr3:4907902-4911210 | CD56 | | SE_49889 | chr3:4905767-4910143 | RPMI-8402 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 4909917 | 4910799 | | chr3 | 4910393 | 4911000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I004866 | chr3 | 4907845 | 4911822 |
|
Enhancer Sequence | GAAAAAATAA TCAATGAAAT GCTTCCTTTA TCTTTTCTAA AACACTAAAC TAGAAAGATG 60
TGCAAAGTAA GACTGAGCAG CTTTTTCTAC GGCAGGGATC AATGGGAGTG TACGTAATAA 120
ATGAATAATT GCATTCCTTC TCCCTGGCCA GCCGACAGAG TGGAAATCGA CCTCTGTTCG 180
GCGGGCATGC ACAACCGGCT GGCATGGTGT CTGCGTTCCC CTCCTATGAA AGGATCAGCT 240
CTAGTTACAT GCCCTGTGCG CGGCCTGAAG CCTGTAACCG GGATTACGAG CCCACTATGA 300
GCCAGGGACT AAAGGTGACA CAGATTTCAC CTCTTTTCAT TACCTTTGAA GGAAGTTCTG 360
TGCCCTGACG AGGAAACTGG GGCCAAGCTC GCATAGGCAG TGCGGCCGAG TCAGCCCTGT 420
GGCCCCCAAG CTGGGGCACG AACCCACCGC AGTGCTTGCA CCAGGCACTG GCTCCGAGAG 480
CAAAGGCATG ACTGGGCACC TAAATACCCA CTAGGCAGGC AGTGACTGCG ACAGTAACTC 540
TCTTCTTTTT GGCCACTCTC AGGCCGCAAG TCCTCCAGAA AACGGAAAAC TGAGGCGCGA 600
GCCAAGTCAC TTTCCAAAGG TCACAGCTGG TAGCAGGCCG AGGAGGGCCT CCAGGCCTGG 660
TGCTTGCGAC CCTCAACGAC CATCTGTAAT AATGCCCAGA GCCTCTGCCA GGATTCCCCA 720
GCCCTATGTT CCCGCGGCCT TTGAGGGGAA AGGGCCAGGG CCTAGACGTT CCCCTCCCGC 780
GTGGTTTTCC CGTCAGCAGC TTTCGTCTGC AAGGGAAAGC GGCGGCCCCA CCCGCAGACA 840
GCTGCGAGGC ACCGCGCCAA GCGTATGCGC CTGTTCCCAG GCACTCCCTC CTCCGCCTTC 900
ACCCTTTTGC CACCTCCGCC CTCCACCCAG CCCCGCCGTG CGCCTGCGCG CCCCGGCCCG 960
TGGGCCAGCG GGCAGTCTAC TCACGTGGGC CTCCGCATGG CCCAGCGCCG CCAAGGGCAA 1020
GGCGGAGCCT CGCGATCGCC CCGCCCCCTC CGTGCCCCGC CTCCTGTAGG GAGCGCGGGA 1080
CCCTCGGCTG GCGCGGGCAC TTCCCAGCCC AGCCCGGGGC GCCGGCTTCG CCGCGTGCGC 1140
GTGCGCATGG TGGGGTTTGG CTGGCTGCGG GATGCGGTCG AGGCCGCCGA GGCCGCAAAC 1200
TCCAGTGGGA AGGCGGCGTG CCGCGGCCGG CTTCGGTGGA GGAGGGGGCG TTTCCCCGGA 1260
AAAGGAAGGA AGTGGGTGTC ACGGGCCTCA ATACGGCCCC TTTGACGTCT TGAGTGGGAA 1320
ATCACAAGAT ACTGCTCCAG ATTTTCCCAT TTTATGGCTA AATCCAAATG ACTCGGACCC 1380
CCTGCCCCAT CACATCAGGA ACTTCAGCAG TTCCTTCCAC CAAAGCTCAA CTATTGCTGC 1440
AAGCGCTTTG GTAATCACGA GCATTATCTA TGAAGCTACT GCTGTGGTCA GGGCCCCAGT 1500
CGTCCTGCTG AGTAGCAGAC TTTGAAAGAC GGTGTCCAAG GCCACCCTGC TGGTCAGTGA 1560
CCTGCTCTAG AGGCTAAGCC AGGGCATGCT TAGAACTTTG ATATTTAGAC TTCTTACATT 1620
AACTTAACCC AGTTAACAGG TTTGTGGGGG CATTTTTTGT TTGTTTTTTT GAGACCGAGT 1680
CTCGCTGTGT CACCCAGGCT GGAGTGCAGT GGCACAATCT CTGCTCACTG CAGCTTCTGC 1740
CTCCCGGATT CAAGCAATTC TCTCACCTCA GCCTCCAGAG TAGCTGGGAT TAGACGTGTG 1800
CCACCACACC 1810
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