Tag | Content |
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EnhancerAtlas ID | HS073-01077 | Organism | Homo sapiens | Tissue/cell | GM19238 | Coordinate | chr1:161186840-161187760 | 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 | ATGATGATGT TTCCCTCACA GGGTAGTTTT AAGATTTGTG CAATATCGTG TGTGTGAAAG 60 AGTGTTGCAG AATAAAAAGT ACTTGACCGA TGTCAGCAAT TGACTGACGT TAGTCACATG 120 TTCCCTACTG GTCCTCTGAT ACGGGGTGAG AGCAGTCTCT GGAGCCCAGA CTTGATTTGA 180 TTTTTTAAAT TGCACAAAAC TTCCCCTCTC AGAGACCCAG AGAGTGAGTA ATAGGGCAGA 240 GTAACAGGAG CTGGAATCCA TATAGCTGTG GTCATTCCCC CAGCCTTGTG TTCAGGGCCA 300 AAGGTATCTG TAAGGTCTGG GAAAAACAGA CACACTTTTT TTTTTTTTTT TTTTTTTTAC 360 ATATTTAAGT GTCTTGTGGT GGGACAGAAA GCAACAAGGC TGAGGCTAGG AGATGACCAA 420 TGATAGAGTA ATTGCCTTCT CTCCCTTCCC CAGCTCACAT CCTTCCTGTC CAGCCCTCAG 480 CCACAGGTCA CAGGACTTAG TAGAGACACT TCTGTGGTTT CTTCACTGAA ATTTGCCACT 540 ACCTCTCCCT CCCACTACCC ATCTTGGCTG AGGTTTTGGT TTCAGTCCAG TGGACTCAGA 600 TGGGTCCCTT GAGGTGGATA AAGTGCTCAA TGGTGCCTGA AGAACCCACA GTGCTAAAAA 660 GAAAAGGTTG GGGGCTGAGG GGGAAGGCCT CAATTATTAG TCCGTGTGAG TCCCATTTCA 720 ATAGAACCCT CAAGCTTCCT ATCCTAGCCT GACCCTATGG TGTGGGAGGA GGGAAAGGTA 780 AGGGCAGTGG AAGGCCAGAG AGAAACAGAA TTTCTTCCCT TAGACGGCTC CCCTCCAGGC 840 CCTGTCCTAC CTCCCAGAGC CCCTTCCCTT CTCTCCTCTG AGTACCAGAT CCTCCCTGAT 900 ACCCCCGACC CCATGGGCAT 920
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