Tag | Content |
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EnhancerAtlas ID | HS181-01371 | Organism | Homo sapiens | Tissue/cell | Sperm | Coordinate | chr1:244318020-244319440 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:244318717-244318735 | GGAGGGAGGGAGGGAGGG | + | 6.03 |
| | 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 |
GH01I244154 | chr1 | 244317838 | 244319404 |
| Enhancer Sequence | GAGTCCACGG ACATTGTTTT ATCTACCTTG TAAGCTCAGC CCATTTGCTG GATTGGGAAA 60 TAAAAAGGAC TGAGTTTATC TTCCAGCCTT CTTCATTTAA GTGTCCTATA TAGTCAATGA 120 TTTACACACT GTGCTCCTGT AGAAACGCTG GGGTCCTACC AACCCATTGT TCACAGACAG 180 CAAATTCTGA CTTGTTTTTC AGTAGAAGTG ACACCCTGCC GTCAGTTCAA CCGTCCCTTT 240 CTTGTCCTGT CTCCCCCTGT GATCATCAGA GGCTCACATT TATGAGCCTT CTGGAGTCAC 300 AGAACAAGTG TGTGCAACTA ACCAGCCCAC CTGGACGTCA GACTTGCCTC GTGACCTTGG 360 CTCAGGTTAT GCTTAACAAC TGGCAGAAAG GTAACTGCCA GAGCCGAGCT GGACATAACA 420 CACGATCCAC AGCCCACAGC CAGGCGTGGC TTCAGCAGCC CCTGGACCCT GAGGGCATGG 480 GGCCCATGCC GGGCTTTGTG GGCAGGATGT GTGCAGGGGG CCGGCAGCTG CTTTGTGCCA 540 GCACAAGTGG GACAGCTGCA ATGAATGGGC CAAAGAGCCA CCTCAAAGGC ACACTGTGCC 600 CAACTTCAAA CACACGGCCT TGCTGCGGAC AGCTGAGGAA CAGCAGCAGC GGCGGCAGCG 660 GCAGTAGCAA CAAACAGGCC GCCTGGGCCC AGCTTTAGGA GGGAGGGAGG GAGGGACTCC 720 CCACTGTGCA GGGCAGCCCG CTGGCAGCGT TGGACAATGC CCAGTCCACA GCAGCTGCAA 780 CCGCCGGCCA AAAGCGATCT GCACATGCGA TCCGACTGAC CTCAGCTCAG TCAGAGTAAG 840 GGACATCGAT CTCTAAGGTC CCACCAGATT GTATCTGTAA CGGGCGTACA GGCGATGTTG 900 CTATGTTCTG GTTCTACCTA CCTCCATTAG AATGTTTTCC GAATCTGCTA AGGACCACCG 960 ATAGGACCCC AGCTATGGAG CTGTCAGCGT AAATATAGAG GCTGGTTACA TGGGCTCCTC 1020 AAACTCTCCC ACCGTATAAC CCTGCTTGAT TCATTCCTGT TTCTTTCCCC GACGCCAGTG 1080 TCTCCAGGAG GAGTGGGCAT CACAGGCGGC TGCGTGCTTA TTACCCCCTC TTCCTGCCGT 1140 GTAGGGGTGG TGGAAGTTGT TGGGATAAGG CACACAGATG CTCCACCACT GAGGACGTCC 1200 TTTGATTGAA TTGTATTAGT TCTCTCTAAA TGGGTACTCC CCTTGCATCC TGTGCGTTAC 1260 CATGCTGTTT ATATTAACAC CCAGCACTCA GCTCATCCAT GATGAACGCT CAGAGAAAAG 1320 TGGGTGGGCT CAAACATAAT TCGATCACTA AGAGCGAATG TTTAAGAGAG GCTGATACAC 1380 TAATCGCTTA GTGATACACA CACACCCCCC ACCAGATGTT 1420
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