Tag | Content |
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EnhancerAtlas ID | HS098-29100 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr2:20564990-20566170 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr2:20565956-20565967 | TCTGATTGGCT | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 20565226 | 20565440 | chr2 | 20565144 | 20565451 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I020365 | chr2 | 20564898 | 20567277 |
| Enhancer Sequence | AAAAACAAGG TAACAAGACT TCACCTGAGT GTACCGTGCA GTACATGCAT GTTCTAACAC 60 ACACGTGAAG TGGCACCCTA CCTGTACAAT GCACTCATCT GCATTTGCAC CCACATGCCT 120 GCCATCAGCG TCATGGTCCT CACTGTGCCC CTTTCGTATC TACGTGCCCA TCAGCATGCA 180 CATTTGCAGG GTCAGCAACT TCAGTCAACC ATGATCCCTG TACCCTGGTC CTTAGCATGT 240 CCTTTTCTTG GTTCCTGATT TTCGTTTTCT TTTCAGAGAA ATGCAAGATG CTGAGTTGAA 300 AGCATTTCCC CATAGTAGCT GCATTCTTCC TATTTGCTCA GCTCTGAGTC ATTTCAGGAG 360 TCATCTTTGA CTTTCATCTG TCTCTAAAGC CTTACATATA AGTCATCAGA AAATCTGCCT 420 TTGAGATATA TCTCCAGATT CTGTGAATTT CCAGGTACTT CCACCACAAC TGTGGTCCAC 480 GCTACCATCA TCTCTCAGCT GGGTTACTGC AAAGCCTCCT GTCTCCCTGC TCCCACACTT 540 GGCCAAATCT AGTTTAGTTT GTAGCCAGCC AGTGTGTTCC TTTTATAACT CAAATTGGAT 600 CATGTCACTT CTCTGCTAAG AACCCTTTAA TTGATCCTCG TGCTACTTGG GAAAAATCCA 660 AAATCTCTAC CATATCTTCA TGACCTGGCT CCATGCTGCC TCTCAAATCG CCTACCCCTC 720 TCACCCTCAC TTGAGCCACA CTGGATGCTT TGCTGTTCCT CAAACACACC AGACACACTT 780 ACTTCAGGGT CTTTGTGTTT TTAATTCCTC TGCCTGGACC ATTTTCTCCC AGATACACAC 840 AGACATCACT TCCTCACTTC CTTCAGGTTT CTGCTCAAAT TCATTGTATC AGGAACCCCT 900 CCTCTAAAAA CTCTTTCTTG GATAACACAC ATTCATATTC TTCCTAGCCA TTCTGTGCCT 960 CCTTACTCTG ATTGGCTTTT CTTCAGAGCA CTTATCACTG CCTGAAATAT TATTTGTTTA 1020 TTGTCTGTCT TCCTGCACTA GAGTGTAAGC TCCCTGAGAC CAGGGAGTTT GTTCTGTTCA 1080 TGGCTTACCT CAGCTTCTAG AACAGTGCCT GATATGGGGT AAGCCCTTAA GAAACAGGTG 1140 TGGGGCTGGG CAGGGTGGCT CATGCCTGTA ATCCCAGCAC 1180
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