| Tag | Content |
|---|
EnhancerAtlas ID | HS080-22325 | Organism | Homo sapiens | Tissue/cell | H9 | Coordinate | chr21:44225740-44227950 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr21:44226030-44226051 | AAAGGAGAAAGAGGGTGAAGG | + | 6.18 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr21 | 44226540 | 44227640 | | chr21 | 44226661 | 44227178 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH21I042806 | chr21 | 44226181 | 44227500 |
| Enhancer Sequence | ACGGAGAGAA GGGGTCGGGG GGTTCTTGCC CCCCAGAAAA GCAGTACTTG CCGCTAAGGG 60
TGAAGGACCA AGGCAGGTGT CCCCGCATGG TCAGACACCT CTGAAATGTG GGTGAATAAT 120
CAGGCAGGCG TCCCTGTGTG ATTAAACACC AAGGGAAGAT TGTCTTCCCG AGTCTGTGAC 180
TGGCGCCAGA GTTTTGCGTC CATGGATAAA ACACGTCTCC TGTCTCTATG AGAAAAGAAA 240
AGGAACTGAA ATTAAGAGAA GGGAGAGATT GAAGTGTGGC ACCAAGATTG AAAGGAGAAA 300
GAGGGTGAAG GATAGTGAGA GAGGTTGGAG AAGAGAGTAA GAAGAGGCCA CTTACCTGAT 360
TTAAAATTGG TGTGATGTTC CTTGGTCTGG TTGGTCTGAG GACCTGAGGT CGTAGGTGGA 420
TCTTTCTCAT GGTGCAAAGA GCAGGAGGAT GAGATTGATC TCCCAAGGGA GGTCCCTCAG 480
TCCGAGTCAT GGCACCAAAT TTCACTCGCA TCTGTGTGAA GAGTCCACCA AACAGGCTTT 540
GTATGAGGAA CAAGGCTGTT TATTTCACCT GGGTGCAGGC AGGCTGAGTC CGAAAAGAGA 600
GTCAGCCAAG GGAGATAGGG GTGGGGCCAT TTTATAAGAT TTGGGTAGGT AAAGGAAGAA 660
GGGGGGTTAT TCTCTGGCGG GCAGGAGTGG GGGTCACAAG GTGCTCAATG GGGGAGCTTT 720
TTGAGCCAGG ATGAGCCAGG AGAAGGAATT TCACAAGGTA ATGTCATCAG TTAAGGCAAG 780
GACTGGCCAT TTTCACTTCT TTTGTGGTGG AATGTCATCA GTTAAGGCAG GAACAGGCAA 840
TTTAAATATC ACTTCTTTTG TGATTCTTCA GTTACTTCAG GCCATCTGGA TGTATACGTG 900
CAGGTCACAG GGTATATGAT GGCTTAGCTT GGGCTCAGAA GCCTGACAGT ATCTAATCCA 960
CTTTGCTATA CAAAGGCGTG AGATTCCTAC TGTCTTTCCA ATCCTTTGAG TGGATTCCTG 1020
GGATGCACAT TACATTCTCG TTAAATGCTT CTTTGATAAT GCAATGGCTT CCTTCCTCTT 1080
CTGCTTTGTG GAGAGGTTTT CTTGGGTTGG GAGGAGGCTT TGTTTCTAAT TCTGCTTCCC 1140
CAGTACAGTC TTGGCTGGTG GAGCAGCTTT CCCATTTGTC AGCGTTTCAA GTCCTTTTAT 1200
GTTTCTGCGT CAGTTTCCTT AATATGTGGC ATTGTGGAAA CAAGCAAAGA CCACCTGCCT 1260
AAGACCAAGC ACGCGCCGTG TATTCCGAGC TGGCTCTAGT GAGGGGGCCA CCTCCACCAC 1320
CTGCCTTTGG CAGAGACTCA GGGAAGGCAT GGGGGAAGCT TGGTGATGGA CGACAGACCC 1380
CGGGGTGCCC GGATGAGGCC TTTTTCAAAA GGAAGCTGGG CAGGCTCGTG GGAGCGGACA 1440
TCCTAGGGGT GCATATTTGA CTTTCTCTAG TTAGTCCAAA ATTGGAAGCA GGGACAAAAA 1500
TGAGGGAAGC TGACAGTTAT TAATCAAATC CTGGGCAGTT TGGACCAATT GTTAGAGGGG 1560
TCATTGTTTG GCTTCCCTGA CCAGTTACCT GTGGTAACAG GCTTACTACA GAGCTGACTT 1620
AGAGAGAGAA GGCTGGCTCC CGGGGCTGGT TACAGGGGAT CACAGGTTGG TTTCCTGAGC 1680
TGGTTGCACA GATTATAATT CGGGGTTCTG TTTTTATATG AGGTCTGACC ATTGTTCATT 1740
TGTATATTCA GTTTCTCAAT ATTTGCCATC AAGGTGACCT CATGGTCCTA ATGTAGCAGG 1800
ACGAGCCGCG GACAAAATCC CTCAGACACT GAGATAGTGA AGGGAGTGGC TTTAATCAGC 1860
TGGGAGCATG GGCAGGCTAG CGTCTTAAAA TCCGAGCTCC TTGGGTGCTC AACTTCTGTC 1920
CCTTTTAAGG GCTCACAACT CTAAGGGGGT CCGCGTGAGA GGGTCGTGAT CGATTGAGCA 1980
AGCCAGGGGG TACGTGACAG GGGCTGCGAG CACCGGTGGT CAGAGTGAAA CAGAACAGAA 2040
CGGGAGGTTT CACAATGTCC TTCCATACAA TGTCTGGAAT CTATAGATAA CATCAGTTGC 2100
TAGGTCAGGG GTTGAATTTT AACTACCAGG CTTAGGTCAG GCAGGCCCAG GCCTGGTTTC 2160
AGGTCTGGTT CCTAGGCACC GGGCTACCTG CCTTTAGTTT TGCTTCTCTT 2210
|
| |
|
|
|
