| Tag | Content |
|---|
EnhancerAtlas ID | HS148-08613 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr19:19701420-19702760 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr19:19702034-19702048 | GAGAGGTGACTCAT | + | 6.35 | | LMX1B | MA0703.2 | chr19:19701796-19701807 | GTTTTAATTAA | + | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_12109 | chr19:19700241-19703035 | CD3 | | SE_18839 | chr19:19700276-19704898 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19648 | chr19:19700122-19703992 | CD4p_CD25-_Il17p_PMAstim_Th17 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I019589 | chr19 | 19700502 | 19703700 |
|
Enhancer Sequence | GCATATGCCA CCACGCCCAG CTAATTTTTA TATTTTTAGT AGAGACGGGG TTTCACCATG 60
TTGGCCAGGC TGGTCTCGAA CCCCTGACCT CAAATGATCC CCCCACCTTG GCCTCCCAAA 120
GTGCTGGAAT TACAGGTGTG AGCCATGGCG CCTGGACACA CATTTTGTTT TTCTAGTTAT 180
CATGGACATC AGGTTGTTTT CAGATTCCTT AATCTGTATA TTTATATACA ATGATCCACT 240
TCTCTGTCCA ACAGACACTT TGGCAATGAT AGGATGTTCT AGACCTTTCT ATTATAGGAG 300
GCACCAGCCC TGTGTGGCTG CTGAGACTTG AAATGTGGCT GGTGTGGCTG AGGAATGCAC 360
TGGTTAATTG CATTTGGTTT TAATTAATTC AAATGTAAAC AGCCCTGCGT TGAGTATCTG 420
GAGCCACCCA GCTGATGAGA CTCAGGGGCT CAATTTGTGA GTTACCCTGA GACTGAGGGG 480
AGGAAAGGAT ACTCCAATCA ACCTGGAGAA TAAGTCCCCC AGCTGCCGGG GTCTACTCCC 540
ACAAGAACCC TAAAGAAATG TACATGGGAC TCAGCCCCAG GGTACAGCTA ATTAGAAAAA 600
GGATCTCAGT TCCAGAGAGG TGACTCATAG GCCTCAGGGT GACTGCTAGG ACCCAGGAAA 660
GCCCCATGAG CACCATGACA CCCCAGCTTC CTGGCTGAAT TTACAGAACC CGATTCTGTA 720
ATTGCAACAG ATCCGACCAG CTGACGAGGA AGGGAAAGAA TGAGAATGGC TTATGCCTGC 780
CAACTACTAG CAAGGCCAAT CATTAGTCAG GAAGACAAAA AGGCATTCCC TGATGTTATG 840
CATTATTTAC ATTTACTCCT CTGAATGGGG CTCTGTGCGT TCCTACAGCA CAGCAAGGGT 900
TCCTGCAGCA CAACAGCCCT GGCTGAGAAA CTTCTTGTTC CCCAGAGACA CAGTCACAGG 960
GTGGAGAAGG CAAAGCAGGC CCCTTCTCAA GAACGGCCCA GGATGGGATG GCCGAGTGGG 1020
TCTGCAAGGG GCCTCTGGGG CTCAGCACAC CGCCTCGGAG CTGCCTACCC ACTCGAGATC 1080
TGAGATCCGA AGCTTTTCAC ACAAGCTGTC ACTCATGCTC ATGTGGAGGT AAAGCCTGAC 1140
ACATTCCAAC GTGCCAGGCT GTCCCTGCTC TGGTGCCAAA CACCACTGTG TGAATTCAGG 1200
CCACGCCTCA GTCCTCACTG GGAACATCAA TGTGACAAAC CTTATTTTTT ATTTTTATAT 1260
TTTTTTAGAG GCAGAGTCTC ACTTTGTCGC CCAAGCTGGG GTGCAGTGGT GTGATCTCAG 1320
CTCACTGCAA ACCTCACATC 1340
|
