| Tag | Content |
|---|
EnhancerAtlas ID | HS073-13392 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr7:99921600-99923310 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr7:99922288-99922309 | ATTTCCTTTCTCTTTCTTTCT | + | 6.7 | | Nr2f6(var.2) | MA0728.1 | chr7:99921668-99921683 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr7:99922513-99922528 | TGAACTCCTGACCTC | - | 6.22 | | RELA | MA0107.1 | chr7:99922284-99922294 | GGGAATTTCC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CACCATGCTT GGCTAATTTT AGTATTTGTA TTAGAGACAG GGTTTCGCCA TGTTGGCCAG 60
GCTGGTCTTG AACTCCTGAC CTCAGGTGAT CCGCCCACCT TGGCCTCCCA AAGTGCTGGG 120
ATTACAGGCA TAGCCACCGT GCCTGGCTGA CTTCTAGAGT TTCAATAACA GAGATGTGGT 180
TCAAGAAGAA AAGGGAGACA TGTTTTGTAG ACAGCAGGAG CTTCATGAAA AGAAGCCAAT 240
GAAGGGCAGG ATGTGTAGCT GTCTACCTAC AGGAAACCAG CCAGGAGCCT CCCCGCAGGG 300
AGTTCAGCAC AGACGGCCGG GAAAATCTGC ATTAACCTGA GCTCTGGACC TAAGAGAGGA 360
CAAGGCCTTG ACTGTTTCTA CAGACTCACA AGACGCAATC TCTGCGGTCC ATGCCCGTGG 420
TGTGATCTGG GAAACAGGGG GCCTTCTAAA TGCCAACAAC AAGGAAATCA AATGCGCAAC 480
AGACAGAAAT ACCGGCATTG ACGCGGGCCA TGGAGAGGCC TAAACAGATG ACTGCAGTCC 540
ACTGCCAAGG TCATCAAAGG GGTGACTCTG AAATAAGAAA TTTCAGACGC CACGGCCCAA 600
ATAGCTGCAC GAGGTGGGGA AGTCCTCCAC ATGCCTCTGC TTCCTTCAGT ACCTCTTCAT 660
GAAATAAGCG GAGGTACTTC CCTGGGGAAT TTCCTTTCTC TTTCTTTCTT TCGAGACAGA 720
GTCTTGCTCT GTCGCCCAGG CTAGAGTGCA GTGGCGCGAT CTCGGCTCAC TGCAACCTCT 780
CCCTCCCGGG TTTTGGCAAT TCTTCTGTCT CAGACTTCTG AGTAGCTGAG ATTACAGGTG 840
TGTGCCACCA TGCCCAGCTA ATATTTGTAT TTTTACTCGA GACAGGGTTT CACCATCTAG 900
GCCAGGCTGG TCTTGAACTC CTGACCTCAT GATCCACCCG TCTTGGCCTC CCAAAGTCCT 960
GGGATTACAG GCACGAGCCA CCGCACCCAG ACTTCTTTAT TTTTTGAGAT GAAGTTTCGC 1020
TCTTGTTGCC CAGGCTGGAG TGCAATGGCG AGATCTCAGC TCACTGCCAC CTCCACCTCC 1080
CAGGTTCAAG TGATTATCCT GCCTCAGCCT CCCGAGTAGC TGGGATTACA GGCACCCAAC 1140
ACCAAACCCA GCTAACTTTT TGTATTTTTA GTAGAGATGG AATGTCACCA TGTTGGCCAG 1200
GATGGTCTTG AACCCCTGAC CTCTAATGAT CTACCCGAAT TGGTCTCCCA AAATGCTGGG 1260
ATTACAGGCG TGAGCCACTG TGCCCAGCCC CTCCCATACC TCTTTTGGCC AAGGCAGTAC 1320
AATTCAGAGA ATCTTGCCAG GGAAGACTGG TAAATGGACG TCAACATGAT GCCTATGGCT 1380
CCTGGTGGAT TTAGATACCT CCTGGTGCTT ACTGATACCT TTACCAGTTA CATGGGGGCT 1440
TTTCCATGCC AGACTGAAAA TGCAGGAGAT CACTGATCAA CCTTCAACTA TTTACTAGCA 1500
GAACACTGAG GGGACTCTGC AGTCACCAAT ATCTCCTATT GCACTTGGAT AAACACCTCC 1560
CGGGAAATAG AGATGAATAG AAAGGAAATA GTCAAACAAG CAGAATGGCT ACATTCCTTC 1620
AACCAGAAGG GTCCATTAGT CTGTTTTCAC ACTGCTATAA AGAACTACTG GAAACTGGGG 1680
AATTTATGAA GAAAACAGGT TTAATTGACT 1710
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