| Tag | Content |
|---|
EnhancerAtlas ID | HS086-05415 | Organism | Homo sapiens | Tissue/cell | HEK293 | Coordinate | chr17:42679370-42680520 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chr17:42680154-42680168 | TTTTATCTTATATT | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 42679653 | 42679703 | | chr17 | 42680200 | 42680262 |
| Enhancer Sequence | TTTTATTTCT ACATGTGGGG GTGCATGTGT GCGTACATGC TTGTGGCCGC ACAACTCCCA 60
GACTCACCCT GGGGTCTCCG GGTGCATGTG TGTGCCATGT GCCAGGATGT CTGCATGTGT 120
CCACGTGTGT GACTGCTTGT CAAACAAACT CCCTGGAGCT AGGGCTCTGC AGGAAGGGTC 180
AGACGGCAGT CTGAGACACT TTTCATGTGT CAGGAAAACC AGGCTCCCCT TTCAGGAAGC 240
CTGCCCAAGG AAAATAAACT AGCCCAGCTC CTGGGGCAGA GGGGGAGGGC GCAGGGGGTG 300
GGGAAAGAGA GAAGGTGGCT GAGACGGGTG GCGGGGGTCA CAGAGCAAGG CCGTCAAATG 360
ATGCCCCTTT GACCCCACTC CATCGACCCT CCTGGAGACC CTCTTCCCTC AGCTTTGTCC 420
TAAGGGGGCT TTGTCCTCTT TCTCTTCTTC AGGCTCTGTT TTCTCCTCTC CATCTCTCTT 480
CTGTCTCCAC GATTTCTTCT CTGCCTTCTT TTTCATTTGC CCTTCTCCCT CCATGTTTCT 540
CTCTCCCAAC TCCCATTACT TTGCAGCTGG CGGCCTGCCA GTCACCTGTC TCCTTTCTTA 600
TCTCCACTGC AGAAGCCAAA GCCGTGGTCT ACCTATGAGA ACAGGTGGTC AGAAAATCCC 660
GAAGGCCACG GTGCAGGTTT TTATTAACTT TTATCCTTCG ATGCCAGGTT GGCTGCAAGT 720
CTCTGGCCAT TACCTCCAAC ATGGAGGTGA TCTTTCATTC ACCAACTGGC TAATTGATGT 780
CATCTTTTAT CTTATATTGA TTAAGCACCT GGTTTGTGCC AGGCACTGTG GTTGGCTCTA 840
GAGCTGCCGT GGTGGGCAAT AAGCGGGAGA AATGAATGGG TTCTGCCTCG CAGAACTTTC 900
AGACTGATGG GGAGTCAGAA ATTAGTCAAA GTCACACACA AATGTAAAAG TAACTTAAGG 960
GCTGCAGACA GAGGGGTAAA TACCTGTATA TAAGAGCCGC TAATGAGGGA ATTAACATAG 1020
GAGGATGGGA AAGGTTTTGT AAGGAAGTGA TAGCCTAGGT TGGAGGGAAA AGCAAGAGTT 1080
AATCAGGCCA AGGAGTGGAG GGGGTGAGTG TGCATGAGGC AGCTGGTGGT AGGCAGAGGG 1140
AACAGCAAGT 1150
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