| Tag | Content |
|---|
EnhancerAtlas ID | HS098-34348 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr20:22672180-22673120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr20:22672438-22672457 | TTGACAGTAGAGGGCAGCA | + | 6.25 |
|
| | 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 |
| GH20I022691 | chr20 | 22672253 | 22672838 |
|
Enhancer Sequence | GCCAGGCCTG CTGCTGCTAG ACCCTCTGCC AGACACTGAG AAGGAAGACG TTTGTGCCCT 60
AGGTCAAAGG CAAACCCTGG GTCCTAGGGA ATGTCATTGA GGTTTGCTTA AGTAAAATGT 120
TTTCATTTAG GTTATCTATG CCAATAAAAT GATGCAAAAT TCATAAAAGC AGGTGGAAGC 180
AAAATCGTGT CTGAATGTAG GACCCTCTTC TAGTTCCCTT TTGAAGCAGC CGCTTAGGCC 240
GTCTGCAATT AAGCCGATTT GACAGTAGAG GGCAGCAGAG GGTGCCGTTT CAGGGTTCAT 300
TCGGCCGCAC AGGCACAAGC TCCCTACCGG CTCGGCCTCA GCCGGAGGCC CTGGCAGAGC 360
TAACAATGGC CGGCTCCGCC AAGGCGCGAG CAATGAGCTG GATAAAGTCT CAAGCGACCC 420
CCAGCTCAGG CCTGATGGAG AAGCTGGTTA TGTGCACAGC CTCTAACTCT GACCAACAGC 480
AGGTTAGGTC AGAGGCAGGA CTAAGGGGAG ACACATTCCC GGTGTTTCTT TTCCTTGTCG 540
GCATGTCCAG GGTGTGGGGC AGCTGCCGGA TAACCCCAAT TGGGGTTATC GTGGTGTTCA 600
GGCTTCCCTG TCCCTCCTGC AAGCAGCGAG CAGTACCTTG AGCCTGCAGG GAACATATGA 660
AGATGAAGAA CCTCATCTTC TAACTCCTCC AGCTCCCAGA AAGCTTGCCT GGAAGCTTCC 720
TCCTTGGGCA TCCTCTCCCG GTGGGGATGG CTGGGCATGG CCAGACAGCC CTTCTTCCTT 780
CCTCTCTCCA TCAGTGCTGA GATGAGCACG GTGAAAATAT CCAACAATGG GGAAGAGAAA 840
AGATGGAGGC AAAATGCAAG CACTTGGAGA GGAAAGAGGG CCTGGGAAAA AAAAGTGAAT 900
CACATTTTGA GCCATTTTCC TTGTTTTTTG TTTCTAAAGA 940
|
