Tag | Content |
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EnhancerAtlas ID | HS191-02480 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr1:161186260-161187770 |
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 | ACTCTGTTCT TGTGCTTGGG AGTAAGGCAA GGATATAGCC AAGACAAACA GACGGGATTG 60 CTGTTTCTAT GGGTCATTGT TAATGCTCCA TTCTGTCAGC AGTTGATAAT GAGGGTGGGC 120 AGCATGAGAT CCCCAGTTCC AGAGACCTGA GCGTCAGCTG AGAAATAGAG GCAGAAATGG 180 GAAGGTCTCT GAAGCTCTAC AGCTCCAGCC ACTATCTAAG AATTCTCACT CCTCGTTCAC 240 TCTGTGTTGT CTGTGCTGGA TTGGTGTGTG TGTGTTGGTG GCAGCTGGGT GTTGGGGAGG 300 AGGAGGTCAG TAAACTTCAG GGAAACTGTG GAAATTGAAA GAGAATGACT GGGGAGGAAT 360 TCCAGCAGCC TAGCTGAGAA GGTGGGAGCA AGTATTAAGT TAGCCACTGG TCTGCTGCCG 420 TGGGATGAGG AGGGAGGAGG CCCGCTGAGG CACAAAGGAA AGCATGGGCT TTAGAGGCAG 480 AAAACCTGCA TTTGAGTTCC AGCTCTGTCA CTTAACTCTG TGGCTCTGAG TGAGTTACTT 540 AGCTTTTCCG AGCCTTGGTT TCGTCACCCA TAAAATGGCG ATGATGATGT TTCCCTCACA 600 GGGTAGTTTT AAGATTTGTG CAATATCGTG TGTGTGAAAG AGTGTTGCAG AATAAAAAGT 660 ACTTGACCGA TGTCAGCAAT TGACTGACGT TAGTCACATG TTCCCTACTG GTCCTCTGAT 720 ACGGGGTGAG AGCAGTCTCT GGAGCCCAGA CTTGATTTGA TTTTTTAAAT TGCACAAAAC 780 TTCCCCTCTC AGAGACCCAG AGAGTGAGTA ATAGGGCAGA GTAACAGGAG CTGGAATCCA 840 TATAGCTGTG GTCATTCCCC CAGCCTTGTG TTCAGGGCCA AAGGTATCTG TAAGGTCTGG 900 GAAAAACAGA CACACTTTTT TTTTTTTTTT TTTTTTTTAC ATATTTAAGT GTCTTGTGGT 960 GGGACAGAAA GCAACAAGGC TGAGGCTAGG AGATGACCAA TGATAGAGTA ATTGCCTTCT 1020 CTCCCTTCCC CAGCTCACAT CCTTCCTGTC CAGCCCTCAG CCACAGGTCA CAGGACTTAG 1080 TAGAGACACT TCTGTGGTTT CTTCACTGAA ATTTGCCACT ACCTCTCCCT CCCACTACCC 1140 ATCTTGGCTG AGGTTTTGGT TTCAGTCCAG TGGACTCAGA TGGGTCCCTT GAGGTGGATA 1200 AAGTGCTCAA TGGTGCCTGA AGAACCCACA GTGCTAAAAA GAAAAGGTTG GGGGCTGAGG 1260 GGGAAGGCCT CAATTATTAG TCCGTGTGAG TCCCATTTCA ATAGAACCCT CAAGCTTCCT 1320 ATCCTAGCCT GACCCTATGG TGTGGGAGGA GGGAAAGGTA AGGGCAGTGG AAGGCCAGAG 1380 AGAAACAGAA TTTCTTCCCT TAGACGGCTC CCCTCCAGGC CCTGTCCTAC CTCCCAGAGC 1440 CCCTTCCCTT CTCTCCTCTG AGTACCAGAT CCTCCCTGAT ACCCCCGACC CCATGGGCAT 1500 CCTCTATCCC 1510
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