Tag | Content |
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EnhancerAtlas ID | HS141-01301 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:161186290-161187770 |
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 | GGATATAGCC AAGACAAACA GACGGGATTG CTGTTTCTAT GGGTCATTGT TAATGCTCCA 60 TTCTGTCAGC AGTTGATAAT GAGGGTGGGC AGCATGAGAT CCCCAGTTCC AGAGACCTGA 120 GCGTCAGCTG AGAAATAGAG GCAGAAATGG GAAGGTCTCT GAAGCTCTAC AGCTCCAGCC 180 ACTATCTAAG AATTCTCACT CCTCGTTCAC TCTGTGTTGT CTGTGCTGGA TTGGTGTGTG 240 TGTGTTGGTG GCAGCTGGGT GTTGGGGAGG AGGAGGTCAG TAAACTTCAG GGAAACTGTG 300 GAAATTGAAA GAGAATGACT GGGGAGGAAT TCCAGCAGCC TAGCTGAGAA GGTGGGAGCA 360 AGTATTAAGT TAGCCACTGG TCTGCTGCCG TGGGATGAGG AGGGAGGAGG CCCGCTGAGG 420 CACAAAGGAA AGCATGGGCT TTAGAGGCAG AAAACCTGCA TTTGAGTTCC AGCTCTGTCA 480 CTTAACTCTG TGGCTCTGAG TGAGTTACTT AGCTTTTCCG AGCCTTGGTT TCGTCACCCA 540 TAAAATGGCG ATGATGATGT TTCCCTCACA GGGTAGTTTT AAGATTTGTG CAATATCGTG 600 TGTGTGAAAG AGTGTTGCAG AATAAAAAGT ACTTGACCGA TGTCAGCAAT TGACTGACGT 660 TAGTCACATG TTCCCTACTG GTCCTCTGAT ACGGGGTGAG AGCAGTCTCT GGAGCCCAGA 720 CTTGATTTGA TTTTTTAAAT TGCACAAAAC TTCCCCTCTC AGAGACCCAG AGAGTGAGTA 780 ATAGGGCAGA GTAACAGGAG CTGGAATCCA TATAGCTGTG GTCATTCCCC CAGCCTTGTG 840 TTCAGGGCCA AAGGTATCTG TAAGGTCTGG GAAAAACAGA CACACTTTTT TTTTTTTTTT 900 TTTTTTTTAC ATATTTAAGT GTCTTGTGGT GGGACAGAAA GCAACAAGGC TGAGGCTAGG 960 AGATGACCAA TGATAGAGTA ATTGCCTTCT CTCCCTTCCC CAGCTCACAT CCTTCCTGTC 1020 CAGCCCTCAG CCACAGGTCA CAGGACTTAG TAGAGACACT TCTGTGGTTT CTTCACTGAA 1080 ATTTGCCACT ACCTCTCCCT CCCACTACCC ATCTTGGCTG AGGTTTTGGT TTCAGTCCAG 1140 TGGACTCAGA TGGGTCCCTT GAGGTGGATA AAGTGCTCAA TGGTGCCTGA AGAACCCACA 1200 GTGCTAAAAA GAAAAGGTTG GGGGCTGAGG GGGAAGGCCT CAATTATTAG TCCGTGTGAG 1260 TCCCATTTCA ATAGAACCCT CAAGCTTCCT ATCCTAGCCT GACCCTATGG TGTGGGAGGA 1320 GGGAAAGGTA AGGGCAGTGG AAGGCCAGAG AGAAACAGAA TTTCTTCCCT TAGACGGCTC 1380 CCCTCCAGGC CCTGTCCTAC CTCCCAGAGC CCCTTCCCTT CTCTCCTCTG AGTACCAGAT 1440 CCTCCCTGAT ACCCCCGACC CCATGGGCAT CCTCTATCCC 1480
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