Tag | Content |
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EnhancerAtlas ID | HS030-01780 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:161186220-161187770 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr1:161187349-161187360 | TTCTGTGGTTT | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GAGAGAGAGA GAGAGAGAGA TAACCCTTTA GGAAGGTAGG ACTCTGTTCT TGTGCTTGGG 60 AGTAAGGCAA GGATATAGCC AAGACAAACA GACGGGATTG CTGTTTCTAT GGGTCATTGT 120 TAATGCTCCA TTCTGTCAGC AGTTGATAAT GAGGGTGGGC AGCATGAGAT CCCCAGTTCC 180 AGAGACCTGA GCGTCAGCTG AGAAATAGAG GCAGAAATGG GAAGGTCTCT GAAGCTCTAC 240 AGCTCCAGCC ACTATCTAAG AATTCTCACT CCTCGTTCAC TCTGTGTTGT CTGTGCTGGA 300 TTGGTGTGTG TGTGTTGGTG GCAGCTGGGT GTTGGGGAGG AGGAGGTCAG TAAACTTCAG 360 GGAAACTGTG GAAATTGAAA GAGAATGACT GGGGAGGAAT TCCAGCAGCC TAGCTGAGAA 420 GGTGGGAGCA AGTATTAAGT TAGCCACTGG TCTGCTGCCG TGGGATGAGG AGGGAGGAGG 480 CCCGCTGAGG CACAAAGGAA AGCATGGGCT TTAGAGGCAG AAAACCTGCA TTTGAGTTCC 540 AGCTCTGTCA CTTAACTCTG TGGCTCTGAG TGAGTTACTT AGCTTTTCCG AGCCTTGGTT 600 TCGTCACCCA TAAAATGGCG ATGATGATGT TTCCCTCACA GGGTAGTTTT AAGATTTGTG 660 CAATATCGTG TGTGTGAAAG AGTGTTGCAG AATAAAAAGT ACTTGACCGA TGTCAGCAAT 720 TGACTGACGT TAGTCACATG TTCCCTACTG GTCCTCTGAT ACGGGGTGAG AGCAGTCTCT 780 GGAGCCCAGA CTTGATTTGA TTTTTTAAAT TGCACAAAAC TTCCCCTCTC AGAGACCCAG 840 AGAGTGAGTA ATAGGGCAGA GTAACAGGAG CTGGAATCCA TATAGCTGTG GTCATTCCCC 900 CAGCCTTGTG TTCAGGGCCA AAGGTATCTG TAAGGTCTGG GAAAAACAGA CACACTTTTT 960 TTTTTTTTTT TTTTTTTTAC ATATTTAAGT GTCTTGTGGT GGGACAGAAA GCAACAAGGC 1020 TGAGGCTAGG AGATGACCAA TGATAGAGTA ATTGCCTTCT CTCCCTTCCC CAGCTCACAT 1080 CCTTCCTGTC CAGCCCTCAG CCACAGGTCA CAGGACTTAG TAGAGACACT TCTGTGGTTT 1140 CTTCACTGAA ATTTGCCACT ACCTCTCCCT CCCACTACCC ATCTTGGCTG AGGTTTTGGT 1200 TTCAGTCCAG TGGACTCAGA TGGGTCCCTT GAGGTGGATA AAGTGCTCAA TGGTGCCTGA 1260 AGAACCCACA GTGCTAAAAA GAAAAGGTTG GGGGCTGAGG GGGAAGGCCT CAATTATTAG 1320 TCCGTGTGAG TCCCATTTCA ATAGAACCCT CAAGCTTCCT ATCCTAGCCT GACCCTATGG 1380 TGTGGGAGGA GGGAAAGGTA AGGGCAGTGG AAGGCCAGAG AGAAACAGAA TTTCTTCCCT 1440 TAGACGGCTC CCCTCCAGGC CCTGTCCTAC CTCCCAGAGC CCCTTCCCTT CTCTCCTCTG 1500 AGTACCAGAT CCTCCCTGAT ACCCCCGACC CCATGGGCAT CCTCTATCCC 1550
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