| Tag | Content |
|---|
EnhancerAtlas ID | HS176-24873 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr22:19971080-19972670 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR3 | MA0732.1 | chr22:19971879-19971894 | CCACGCCCCCGCAGC | + | 6.03 | | KLF16 | MA0741.1 | chr22:19971878-19971889 | GCCACGCCCCC | + | 6.62 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_02031 | chr22:19969294-19974834 | Aorta | | SE_29732 | chr22:19969800-19974744 | Fetal_Muscle | | SE_41259 | chr22:19969834-19977368 | Left_Ventricle |
|
| | 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 |
| GH22I019982 | chr22 | 19970033 | 19973042 |
|
Enhancer Sequence | GGAAAGAAGT GGCCACAGAA GGCACCTCCC CCTCTCCCAC AGGCAGGGTC TTGGAGGATG 60
ACAGATAACT TTATAGATGG GGAAACTGAG GCCTGGCAGG GGGAAGAGGA TTTACCTAGA 120
ACTTCACAGT CCAAGTGGGA TTTCAAGCAC CCCCAGAGAA GGCAATCTGG CAAGGAAGGC 180
TTTGGGCCTC ATCTCGCCCT CAGTCTTGAG ATGTAGGTGG AATGCCTGCT GTGGACCTGG 240
CTAGGAAAAG GGGACCTGTT CCCTGGGAAA AAGAAATAGA CTGAGGCCTA GAGTGGGGAC 300
AACTGGCACG CTGCCAGGCA GGGCAGGCTG GGCTCTTCTC CAAAGGCACT GGGGAGCTGG 360
GACTGCTCTG AAGCAGGAGA AGGCTTGTGT GGCCCATCAC TGCTGGGGCT GGGCTGCCCC 420
ATCTGTATCT GGCAAATGTG TGTCAGGCCC TGAGCTCTCT CTGCTGGGCC CTGGGCGGGG 480
CTCATCTGAG TTCAAGCAGG GGCCCAGGCA CTGAGGGGCT GCAGTTCTGG CGACAGAGTG 540
AGGAGGGTAT AAAGCAAGAC TGAGGAAACG TTACCCAGGA CTCTGCCAGT GGGATGTAGC 600
CCCTCATATA TGTATATATT TACATCTATT AAAAACTCAG AGAAAAACCC CCTCTTCCCT 660
AGCTAGGCAG TGGGGGTAAG CGGGAGAGGA AAAGGGGAGG ACATCTCAGG ACCCCGATGC 720
CACTCTGTGG CCCAGCTTAT CCCTCCCACC AAGGCTGTGG TGAGGGTCTG ACAGGCAGAG 780
CTGGGGTGGT CCAGGAGAGC CACGCCCCCG CAGCAAGACC TGGCAACCCT GCGGCACCAC 840
CCATCAGCCC CGGCCTAGCA GCCCCGCAGT AGGATCCAGA GGCCCCAAGA GTCCCTGCTG 900
GCAAATGACC TCAGGGAGCT AAAAACGAGG GATGACTTCA CCCGGGTGGC AGGTGCATGA 960
GTCAGCCAGT GATCACAGGA AAGCCCGGCC CCTGCTACAC ATGCCCAGGC ACACACACAT 1020
GCATATACAT GACCCCTCAG ACAGGGACAC ATGCATGTAC ATACACGTGT GCAAGTACCC 1080
AGCCCGGCAC AGGCCGAGCA CATCAACCCG TGTGCTCTAA CAGCACCCCA AGGGCACGGC 1140
GCCCACTGTT CCCAGAGGCA CACTCGTGAG CACACATCCT CCCGTCCTCC ACCGTGTATC 1200
GGAGACCCTT ATCCATGCAG GGCCTCACAG AGTCTCAACA CACAGGGACA GGGGCCACCA 1260
ACTCTGCCAA TCATCTGCCC AGCATCCACT CTGGGAGTCT CAGAGCTGGC TGGCAGATGG 1320
AGAAACTGAG GTGTAGAGTA GTGAGAGGCC CATAGCCAGC TGGTGGCTCA GCTCTCTGCA 1380
ACATCTTTAG GGTGGGGCTG TGGAATGGTG GGCTGACTCT CAACAGGAGT TGGCTGCAGT 1440
CCCTGGATCC CTGTCTGGCC CCAGTGTCCA TGTCTGACGT GCACCTGCCC AGGCTGGCCC 1500
ACTCTCAGGG ACCCTGGCCC TGCAGCCCCA CACAGCCTCT GCCTCAGACC CAACTCTGGG 1560
CTGCTCCCCT CTGTACCCTA GACATGGGCT 1590
|
