Tag | Content |
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EnhancerAtlas ID | HS064-00991 | Organism | Homo sapiens | Tissue/cell | GM18507 | Coordinate | chr1:161186320-161187770 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr1:161187349-161187360 | TTCTGTGGTTT | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGTTTCTAT GGGTCATTGT TAATGCTCCA TTCTGTCAGC AGTTGATAAT GAGGGTGGGC 60 AGCATGAGAT CCCCAGTTCC AGAGACCTGA GCGTCAGCTG AGAAATAGAG GCAGAAATGG 120 GAAGGTCTCT GAAGCTCTAC AGCTCCAGCC ACTATCTAAG AATTCTCACT CCTCGTTCAC 180 TCTGTGTTGT CTGTGCTGGA TTGGTGTGTG TGTGTTGGTG GCAGCTGGGT GTTGGGGAGG 240 AGGAGGTCAG TAAACTTCAG GGAAACTGTG GAAATTGAAA GAGAATGACT GGGGAGGAAT 300 TCCAGCAGCC TAGCTGAGAA GGTGGGAGCA AGTATTAAGT TAGCCACTGG TCTGCTGCCG 360 TGGGATGAGG AGGGAGGAGG CCCGCTGAGG CACAAAGGAA AGCATGGGCT TTAGAGGCAG 420 AAAACCTGCA TTTGAGTTCC AGCTCTGTCA CTTAACTCTG TGGCTCTGAG TGAGTTACTT 480 AGCTTTTCCG AGCCTTGGTT TCGTCACCCA TAAAATGGCG ATGATGATGT TTCCCTCACA 540 GGGTAGTTTT AAGATTTGTG CAATATCGTG TGTGTGAAAG AGTGTTGCAG AATAAAAAGT 600 ACTTGACCGA TGTCAGCAAT TGACTGACGT TAGTCACATG TTCCCTACTG GTCCTCTGAT 660 ACGGGGTGAG AGCAGTCTCT GGAGCCCAGA CTTGATTTGA TTTTTTAAAT TGCACAAAAC 720 TTCCCCTCTC AGAGACCCAG AGAGTGAGTA ATAGGGCAGA GTAACAGGAG CTGGAATCCA 780 TATAGCTGTG GTCATTCCCC CAGCCTTGTG TTCAGGGCCA AAGGTATCTG TAAGGTCTGG 840 GAAAAACAGA CACACTTTTT TTTTTTTTTT TTTTTTTTAC ATATTTAAGT GTCTTGTGGT 900 GGGACAGAAA GCAACAAGGC TGAGGCTAGG AGATGACCAA TGATAGAGTA ATTGCCTTCT 960 CTCCCTTCCC CAGCTCACAT CCTTCCTGTC CAGCCCTCAG CCACAGGTCA CAGGACTTAG 1020 TAGAGACACT TCTGTGGTTT CTTCACTGAA ATTTGCCACT ACCTCTCCCT CCCACTACCC 1080 ATCTTGGCTG AGGTTTTGGT TTCAGTCCAG TGGACTCAGA TGGGTCCCTT GAGGTGGATA 1140 AAGTGCTCAA TGGTGCCTGA AGAACCCACA GTGCTAAAAA GAAAAGGTTG GGGGCTGAGG 1200 GGGAAGGCCT CAATTATTAG TCCGTGTGAG TCCCATTTCA ATAGAACCCT CAAGCTTCCT 1260 ATCCTAGCCT GACCCTATGG TGTGGGAGGA GGGAAAGGTA AGGGCAGTGG AAGGCCAGAG 1320 AGAAACAGAA TTTCTTCCCT TAGACGGCTC CCCTCCAGGC CCTGTCCTAC CTCCCAGAGC 1380 CCCTTCCCTT CTCTCCTCTG AGTACCAGAT CCTCCCTGAT ACCCCCGACC CCATGGGCAT 1440 CCTCTATCCC 1450
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