Tag | Content |
---|
EnhancerAtlas ID | HS167-03244 | Organism | Homo sapiens | Tissue/cell | Retina | Coordinate | chr2:173098670-173101050 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAX | MA0058.3 | chr2:173100742-173100752 | AGCACGTGGT | - | 6.02 |
| | 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 |
GH02I172234 | chr2 | 173098785 | 173100945 |
| Enhancer Sequence | TGTTGTTGGA CATCCAGGGC TGAATGCTGT CATGAAATTC TGCTCCTTGG TAGCTCACCA 60 TCCACCGTAA GCTCACCATC CACTGTATGT GAATTGTCCC TAAGTGAGAA AACAGACTGC 120 AGCAGGCCAG TGAACTTTTT GAGAAACTGG CAGACCAGCA GACATTCTGG CGCCAGCAGG 180 ACACCAGTGG GAACTGAAGG TCTTTGTACC AGGAATAAAA CAGTGCTTCT TCCTTGAAGG 240 AGAGGGAGCC TTGGCACTTG GAAAACCCTT GGTAGGAATT GGGTAGTGAA GCTTGAGGGA 300 AGGGCCTGGA GACTGGTGAG TAGCTCTATG TGTAACCGGG GAGAGGAATT TCTTCTCCTG 360 GGTGAAACAA GGGATGTAGG GGTGAGAAGG GAGTGGGGAC AGTAGCTGAA AGTGTCAGTC 420 AAGAGGTGTC CTCTCTGGGT GGAAACCCTC TCGTTTTCAG TGAAATCTCT CAGGAACTGC 480 TTCATGGCAG CAGATTTTGA GAACCAGTGA AAGGGCTGCA TTTTGCATTA GGGTCGGTGG 540 GGGAACTAAA AGAATCACAG GCAGATGCAG GGCCTGGGAA TTGGCACGAT TCAGGGGTAG 600 GGGAGTGAGG AGGAGTTTCG GACATTCCTA GACTGCAGAA TTGGTGGATT CAAGACAATT 660 TCACCCAGAT CTTACAGGGC AGAGATCCAC ACCTGTGGGT CATGTGTTTG AAACAAGGTC 720 CACAAGCAAC CCCGTGGGTC CATTCTGTTT TCCCCGAAGA ATACTGAATG GGATGGGAGG 780 TTCCTGGGGA GCGTGCTTTG ACCCTGGGAC AGCGCACGGG AGGAAGGCCC CGCACAGTCT 840 GGCTGCCTGG GGGTCTTGTC GCCTGGGGGC GGCGGAGAGC GCCAAGGCAG CCAAAAGAAG 900 CTTGTGTCGT GGAGCAGCGG CGGGCACGGG GGACACTGGG GGGAGCAGCG GCGGGCATCT 960 GGAGGCATCG GGGGACAGCG GGGGACATTG AGGGGCAGTG AGGGCGGCCG AGTTGTCGGC 1020 GGTGGGCGGC GCCGGGGGAG CCGCGCTCGG GGACAGCTGG CGGCTCAACG GCAGCATCGG 1080 CAGCATCGAG AAAGGTGACG AGTTCTGCAA ATAACAGCTG CGGAGCAATC GTTATGTTTG 1140 GACAACGTGG GAAGGGCCAT TGTTCACAAA TTGTTCTCTT CAACAACACC TGCATGCACA 1200 GATAATAATC CATTGTCGGT CTCCGGCTTC AAAGACAAAA GGCAGCCGCG GAGGGAGGAG 1260 TCAGCAGAGC CTGGAGATAA CAGGACCACT TTGCAACCGG GGAGAGTGCA AACGAGGACT 1320 CCAAGTCGCG TCCCGGGTCT GCCGCGACGG TCGCTCACCG CAGGGGTCTC CTTCCTCTTC 1380 TGGCAGCGAG TGCGACCTCT TTTATCCTAG CAGGCCACCA CCTTCGCGGC AACAAACATC 1440 ATTTCCTATG CAGTTGCAAA GCATGCTCCC TTGCAATCAG CGATCAATAC TGGCAAAGTG 1500 GCTCCAGGAT AGGAAAGGTC GCACGTGTGT TGGTAAATGG AAAGGTTTAT GAGGCGCAGG 1560 TGGTCGTGCT CCGCGGAGAT TGTGGTATTA GCATGTCAAA GACAAAACGG AACCAAGGTA 1620 TACAGGCACA GAGTCTCTTC CTGGGGCTCC GGGAAAGCTT GGCACGACCC TCTTGAGCCT 1680 TCAGTTTAAA ATGAAACGCT GGCGCCAGAT GTGGCCACCA CATTGCTGAT AAGTCCAGTA 1740 CCTTCCGTTT GTGCAAAGCT TTGTGATTTA AGGTTAAGTA GTTTTGCTTA CTTCTCTCAT 1800 TTGAGCCTTA TAAAGACAGT GTGAAGTCTG TAGTGAGTAA AAGCCCTATT TTAACAGAAA 1860 AGGAACCAAG GGACCAAGTT GGAACTTGAA TCTGGGGTCT ACTGATGTTC CATTCACTAC 1920 ACTGCTTGGT ATAACTGCAT ATCAGGTTAT TTGGATTTTA TTTTATTTTT TTCTTTTTCA 1980 GCCTTTATTC AGTAACTACT ACCAGATTAG GTAATAGGCA CATAGAGACA TGAGACATAC 2040 ATTCCCTACC TTGCTATGCT GTTCAACATA GTAGCACGTG GTAATTTAAA TTTAATGAAA 2100 AGTCAATAAA ATTTAAAATT AACTTTCTCA GTACAACTAG CCATATTTAA AGTGCTCAGA 2160 AGCCATATGT GCCTAGTGGC TGCTGTATTG GGCAGGGCAG AAAGTTCTAC CGGGCAGCAC 2220 TGTGTCTACA GGCTAACAAT CTAATGAAGA TTAAAGACAG TCTCACTTCT TTTCTGTCCT 2280 ATTTGCTACT TCCTTGCAGT TCATTCGTTC CTTGGTACAT GTGTGCCTCT TGCTTTCTAA 2340 AAGACACCCT GAGCAGTTTC CAGCTTTATT GAGGTCAAAT 2380
|
| |
|
|
|