| Tag | Content |
|---|
EnhancerAtlas ID | HS060-23461 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr22:41853020-41855120 | 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 | chr22:41853139-41853160 | AAAAAAAAAGTGAAAGGATGA | - | 6.83 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAAGAGGCTG AGGCAGGGGA ATTGCTTGAA CCTGGGAGGT GGAGGTTGCA GTGAGCTGAG 60
ATCATGCCAC TGCACTCCAG CATGGGTGAC AGAGACGCCG GCTCAAAAAA AAAAAAAAAA 120
AAAAAAAAGT GAAAGGATGA ATCCCCTCAT GCGGGCAGAG CCTTCATGAC CCAATCATTT 180
CTTGAAGGTC CCACTTCTGA ATACTGCCAC ATTGGGAATC AAGTTTCAAC ATGAGTTTTA 240
GAGGGGACAA ACATTCAAAC CATAGCAATC ACCTCACTGA TGCATTAGAA TTGCTCAGAG 300
CTCCCTACAC ACATCGCCCT AGGCTGGGGG TGGTGGCTCA TGCCTATTAT CCTAACTTTG 360
GAAGCCAAGG CAGGCAGATC GCTTGACCTC AGGAGTTCAA GACCAGTCTG GCCAATATGG 420
TGAAACCCTG TCTCTACAAA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAGCTG 480
GGCATGCTGG TTCACACCTC CCAGCTACTC AGGAGGCTGA GTTGGGAGGA TTGTTTGAGC 540
CCAGGGGGTC GAGGCTGCAA TGAGCCGTGT TCATGACACT GCACTCCAGG TTGGGGGACA 600
AAGTGAGACC ATATCCGAAT CAATACATAT CACCCTGTTC ACGACTGTCT TTGCTCAAGT 660
TGATGCCCCC CCCAACAAAT GCCCTTATTT GCCTACTGCA CCCTTTGCCT GTAGGTTCTG 720
ACATATCAAA GTCCAGTTTA TTATCCAGTT TCCTTGACTT CAAGCATTCA TTCAATACTG 780
AACACCTACC TGCTACCTAC TGGGCAAAAC AAACTTGCTT CCTGCTCTTG TAGACACGGT 840
CGTAGGTTAC TTTCACTAAT CACCAAATGC TTTAAGAAAA CACATAGGGT TGGGTGTGGT 900
GGCTCACACC TGTATTCACA GCACTTTGGG AGGCTGAGGC AGGAGGGTAA CTTGAATCCA 960
GGAGCTTGAG ACCAGTCTGG GCAACACAGC GAGACCTTGT CTCTATAAAA AATACAAAAA 1020
ACAGGCCAGG CTTGGTGGCT CACGCCTGTA ATCCCAGTAC TTTGGGAGGC CAAGGTGGGC 1080
GGATCACGAG GTCAGTTCAA GACCAGCCTG GCCAACACAG TGAAACCCCA TCTCTACTAA 1140
AAATACAAAA AATTAGCTGG GTGTGGTGGC GTGCATCTGT AATCCCAGCT ACTAGGGAGG 1200
CTGAGGCAGG AGAATCACTT GAATCTGGGA GGTGGAGGTT GCAGTGAGCG GAGATTGCGC 1260
CACTGCACTC CAGCCAGGGC AACAGTGCAA AATTCCATCT CGAAAACAAA AACAAAAAAC 1320
TAGCTGGGCA GGGTGGTGCA TGCCTGTAGT CCCAGCTATT CCAGAGCCTG AGGTGGGAGG 1380
ATTGCTGAGT CTGGGAAGTA GAGGTTGCAG TGAGCTGAGA TCGTGCCACT GCACTCCAGC 1440
CTGGGTGACA GAGATGCCGT CTCAAAACCA ACCAACCAAA CCAAAAAACC ACATAGGATG 1500
CTAAGTGGGA GTACAAGGGG AACTTAGATT AAGGGTCCGG AGAGGCATCT TTGAGGAAAT 1560
ATTTGGCTAA GGTCAGAAGG GAGTAGGGGT TAGCTGAGTA AAAGGGAGGG GGGCACAAGC 1620
ATTCTAGAGG GATCAACATG TTAAAAATAA ACCCAAAGCA GAAGCCAAAA GGAAAGCAGC 1680
AGTTGTGGAA CTGAAAAGGA GCCTATGGCT GCAGTGCAGA GAAAGGGGTG GCCAAAAGCG 1740
CCCGGAAAGT GCTGTAGTCC TATGGCCATG GCCTTCCCCT GCCTTCCTGT GGTACCTCCA 1800
AGCTAGGCCT AGAACCCTTC CTTTGTGCAT CCTCTGGGTT ATACTGGAAC CTTTTTTTGT 1860
GTGTGTGTGA GATGGAGTTT CACTCTTGCT GCCCAGGCTG GAGTGCAATG GCACGATCTC 1920
GGCTCACTGC AACCTCTGCC TCCTAGGTTC AAGCAATTCT CCTGTCTCAG CGTCCCGAGT 1980
AGCTGGGACT ACAGGCGCAC AGTGCCACCA TGCCTGGTTA ATTTTTGTAT TTTTAGCAGT 2040
GACGGAGTTT TGCCATGTTG GCCAGCCTGA TCTCGAACTC CTGGGCTCAA GTGATCCGCC 2100
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