Tag | Content |
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EnhancerAtlas ID | HS056-01037 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chr1:161186380-161187770 | 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 | AGCATGAGAT CCCCAGTTCC AGAGACCTGA GCGTCAGCTG AGAAATAGAG GCAGAAATGG 60 GAAGGTCTCT GAAGCTCTAC AGCTCCAGCC ACTATCTAAG AATTCTCACT CCTCGTTCAC 120 TCTGTGTTGT CTGTGCTGGA TTGGTGTGTG TGTGTTGGTG GCAGCTGGGT GTTGGGGAGG 180 AGGAGGTCAG TAAACTTCAG GGAAACTGTG GAAATTGAAA GAGAATGACT GGGGAGGAAT 240 TCCAGCAGCC TAGCTGAGAA GGTGGGAGCA AGTATTAAGT TAGCCACTGG TCTGCTGCCG 300 TGGGATGAGG AGGGAGGAGG CCCGCTGAGG CACAAAGGAA AGCATGGGCT TTAGAGGCAG 360 AAAACCTGCA TTTGAGTTCC AGCTCTGTCA CTTAACTCTG TGGCTCTGAG TGAGTTACTT 420 AGCTTTTCCG AGCCTTGGTT TCGTCACCCA TAAAATGGCG ATGATGATGT TTCCCTCACA 480 GGGTAGTTTT AAGATTTGTG CAATATCGTG TGTGTGAAAG AGTGTTGCAG AATAAAAAGT 540 ACTTGACCGA TGTCAGCAAT TGACTGACGT TAGTCACATG TTCCCTACTG GTCCTCTGAT 600 ACGGGGTGAG AGCAGTCTCT GGAGCCCAGA CTTGATTTGA TTTTTTAAAT TGCACAAAAC 660 TTCCCCTCTC AGAGACCCAG AGAGTGAGTA ATAGGGCAGA GTAACAGGAG CTGGAATCCA 720 TATAGCTGTG GTCATTCCCC CAGCCTTGTG TTCAGGGCCA AAGGTATCTG TAAGGTCTGG 780 GAAAAACAGA CACACTTTTT TTTTTTTTTT TTTTTTTTAC ATATTTAAGT GTCTTGTGGT 840 GGGACAGAAA GCAACAAGGC TGAGGCTAGG AGATGACCAA TGATAGAGTA ATTGCCTTCT 900 CTCCCTTCCC CAGCTCACAT CCTTCCTGTC CAGCCCTCAG CCACAGGTCA CAGGACTTAG 960 TAGAGACACT TCTGTGGTTT CTTCACTGAA ATTTGCCACT ACCTCTCCCT CCCACTACCC 1020 ATCTTGGCTG AGGTTTTGGT TTCAGTCCAG TGGACTCAGA TGGGTCCCTT GAGGTGGATA 1080 AAGTGCTCAA TGGTGCCTGA AGAACCCACA GTGCTAAAAA GAAAAGGTTG GGGGCTGAGG 1140 GGGAAGGCCT CAATTATTAG TCCGTGTGAG TCCCATTTCA ATAGAACCCT CAAGCTTCCT 1200 ATCCTAGCCT GACCCTATGG TGTGGGAGGA GGGAAAGGTA AGGGCAGTGG AAGGCCAGAG 1260 AGAAACAGAA TTTCTTCCCT TAGACGGCTC CCCTCCAGGC CCTGTCCTAC CTCCCAGAGC 1320 CCCTTCCCTT CTCTCCTCTG AGTACCAGAT CCTCCCTGAT ACCCCCGACC CCATGGGCAT 1380 CCTCTATCCC 1390
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