| Tag | Content |
|---|
EnhancerAtlas ID | HS089-01877 | Organism | Homo sapiens | Tissue/cell | Hela | Coordinate | chr10:71766570-71767990 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr10:71766655-71766666 | AAATCTCAGCA | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAGGACAGGG CCCCACCTTG CAGGACAATG GAGGTGAAGA AAAGAGAAGA TCCACATGAA 60
AATAGAGGAG ATGAACAGAG CCACAAAATC TCAGCAAGGA CATCACTATA TTTTTTAACA 120
CTTCACAAAA CACTCCTTGA AGAGGGAGCT CTAGCAAGTT AGCAAAGCCA CTCTGCATCA 180
TAGCTTCTTC CAAAAGTTTA GGAAATTAAT TTTGCATGAA ATCGAATAAC AGAAAAGCAT 240
GCACATCAAA GTCCATATAA AGTTATTATA AGAAAAAAGA TCACGAACAA AATAACATTC 300
CTACAGATCA TGAAAATATG CCACTAAAAT AGGTCCCAGA ACTGATCAAA ATGTAATCTT 360
CCATTTCAAA ATGAGCTAAG TGGCATTTTT AAATGATATA ACACATGCAA TAACATAAGT 420
AAGAACTAGA GCAACTCAGA AATGCAGCGA CAGCTCATCA TTAAAAACCA CATACTGGTG 480
ACAGGTGTTT CGACAACTGT TCGGCTGAGT CTGCTGCAAA GCCGTGTGGT CCGTAAGGCC 540
GCTGGGAGTT TTTCTTTGTT CTCCTGTTCT TTGTTCCCAA CAGCAGACCC AGGTTGTTGG 600
ACAGAGGGAC CTGAGCTGAG CAGCAGGTAT TATCTCACTC ACCTTTACAG ACAGCAGCAG 660
CAGGGTCCAA GGTGAGGGTG GGTTGCAGGG CTGACTGTAG TTCCAAAGCA AGCTGGGTTC 720
TTCTGAAAAA TGACAGCGTC TTAAGTCTAC AGAGCTGCCT CTAGCAAAAG GTTTGTGTGA 780
GTCCGTGTAT GCTGAGCTTT TTGTTGTTTT TTTAGATAAG AAACAGAAGA AAATCATCCC 840
AGATTCTGTC ATTCCCTGGA AAGAGAAGGG GAATTCCAAG TTTCTCAGAG GCTCTTTGGG 900
GTCACTAGCC AACCACCCAC ATGTAGGAGT TAACACCTAC CATCACTGGA GGTTTCAAAG 960
ACCTGGCTTG GAGAACATGC AGGGAGGAGG GCCGGGATGT GCCCATGCAG AGTCCCCTTG 1020
GTGTCACCAT GGGCGCGTCA CAGCCAGTCA GGCTCTGGAT TCTACACCGT GTGTAGCATA 1080
GAGAAGTAAC TTCTTGTTGT CATTCATTAC TACCTTAAAG AACTGGAGGA ATCATCTCCT 1140
AGGAAACAGT GCCATGTTTG TGCCCAGCAA ACAGTGCCCA GGTGCCATCT GGGAAGGGGC 1200
AGTTTTATTG AAAGATGTCT TACTGCTTAT TCTAGAGTTT TTAGCAACTC CCCTTCTTGC 1260
CTCCACCCCC CAGACCTTAC TTTTTACCAG CTTGTCTTTT TTTCTTCTTC TTTATCCCAA 1320
AGGTTTTAAC CTCCAGTCCC TTCTTGATGC CCACTTGATG GAATTCTCCA GCACCATCTG 1380
CCCTTGTTCA CTCATCTGCT TTTCCTTCTC TTCTCCCTGC 1420
|
| |
|
|
|
