| Tag | Content |
|---|
EnhancerAtlas ID | HS051-18131 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr21:46498130-46499550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr21:46498666-46498684 | CCTTTCTTCCTTCCTTGC | - | 7.78 |
|
| | 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 |
| GH21I045078 | chr21 | 46498144 | 46500155 |
|
Enhancer Sequence | TGTATTTTTA TTGGAAGTAC AGTGAAATGG AAGCTCTACT TGCTTCTAGT TTGGTGATTT 60
TGGAACCTGG TTCCATTTCA TTTGCTTGTT CATCCAACAG GCATTCACCC ATGCATCCTG 120
GCCCAGGTAC TGTTCTAGGT ATTGGAGATT CAGGATGAGC CTGATGAGGA GAGTTCCTGC 180
CCTCAAGCGG TTCATTTTCT TGGGAAGGAG GAGAGCAGTA AACAAGCATT TGGTGTCCTA 240
ACTGCTTCAA AGGGCAAATG AGGCAGGGTA GGTGAGAGAA GGTCAAATAG GTGGTGAGGA 300
TGGAGTGAGC TGGGCTGAGG TCACGGCAGC AGCAGCCTCT CAGGCACAGG GAACTCTCGG 360
GTGAAAGTCC CTGAGCCTCC TTGTAGTATG GTGGTCACCT CAGGGAGGCC ATTGCTGCCA 420
GAGAGGCTGG GCGAGTGGTA GGAAGTGAGA TGGGAGTGGA GGAGAGCTGC ATCTTGGAGC 480
ACACAGGCTG TGGTAAGGAA TTTAGATTTT AAGTTTGATG GGAAGCCTTA AGGGAGCCTT 540
TCTTCCTTCC TTGCGAATGA CATGATCTGA TTTATCTTTA AAAAGTACCA CTCTGGCTGT 600
TGGGCTTACA ATATGCCAGG CTGTTTTAAG AGCTTTACAT ATATTAATTC ATTTATTCTT 660
ATGACAGTCC AAAAAGTAGG CATTATTATC ATTATTCCCA TGTTACAGGG GGGAATACCT 720
AGGCACAGAG TGGTTAAGTG ATTTACCCAA GGTCACACAG GAAGTGGCAA TGGCAGGATG 780
TACCCTTACC TCCTTACTGC AGCTTGCTTT TTGCACCTCC ACTACTGCAG ACTGGAGGAG 840
GAATATCAGC AAGGAGATCA GTTAGACTTT TGTGAAAGCT GGGTGACTGT ACCGGCACCT 900
CAGACCAGGG CGGAAGTGGT GAGATCAGAT TCAGCCTACT GAATTTCAGC ATTTGTAAGA 960
TGCCATCATT TTTAAGTTGC ATCATCATTT CTTATGCTGC TAACAAAGGG AAAATGTAGC 1020
CAACTAGATT GTGACACAAT GCTTTCTTGT TACCCAGCAT TCATTTATAC TCATTGAAAG 1080
AGCTTAGACT AAGCATTGAC TTTTAAAATC ATATAATTCA TGCACTTTCA TAAAAAAGGA 1140
AAATACAAGT AAAATAAAGT AATTCTGAAA TTTCTTCACA TCTAGAATCT GATTCTTCCA 1200
ACTCAGCTTT TGACTTGGCG TTGGTGCCAG GTATGAGATA GGGAAGTCTG GGAAGAGCCA 1260
GTGTTGGGAT TTGAACATGT GGAGCTTGTG ACTGGAAGGC AGCCCAGCTC AGCAGCTCCA 1320
CTCAAGGGCC AGATCTGGAG GACGAGGGTT GGGTCATTGT GCAGCTACTT CCTAGATGAT 1380
CTTGAGCAAG CAGTCTAATC TCTGTGCTTC AGTTTTCTCA 1420
|
