| Tag | Content |
|---|
EnhancerAtlas ID | HS182-10372 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr18:21618940-21620410 | 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 | chr18:21619788-21619809 | GTTTGGTTTCAGTTTGATTTT | + | 6.67 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTCAAATTA GGGGTTAGGG CTTCAACATA GGACTTTTTG GTGGACGCAG TTCAGACCAT 60
AGAAACAGAG ATACATAGCA CTTACTTGGG ACCCCCAGTT TGCCAGGAAC TGTGCTGGCA 120
TCCTCATTCA GTCCCCCCAT GCACCTGTAA GGTGGGTACT GTCATTTCCC CCTACTTTAC 180
AGATGATGAA ACTGCAACTC GAAATAATTA TTTTCCAAGG ACACTTCACT TAGCAGAGCC 240
AGGACTTGAA ACCAGGGCCA TGGGAATTGA GGGAGTGTCA GAGGAGGTGC CTTGAGAATG 300
AGCAGGGAAG TCTCCCAGGG TACTGGGGCA GAGCCAGCAT CCTCAGACTA GGCATGTGTT 360
ATAGTCAGGG TCAGACTGTT CTGTGGCCGC ACAAAGAGAA GTGTATTCAA GGGAATGATG 420
GAAGTGGACA CACATGATAG GTGGGTCTGT GTTCTATGTA GAACCATGGA TTTTACCCTT 480
TTCCACTTGG GTGGTAAGGA GCCATTGGCA GGTTTTTGTT TTGTCTTGTT TTGTTTGTAG 540
AGACGGAGTC TCAGTGTGTT GCCCACGTTG GTCTCAAACT CCTGGCCTCA AGCGATCCTC 600
TTGCCTCGGC CTCCCAAAGT GCTAGGATTA CAGGTGTGAG CTGCCATGCC TGGCACCATT 660
GGTGGTTTTT AAGCAGAGGA GTGACATGGG TTTGTGTTTT AGAAAACTAA TTCTGGGGAC 720
ACTGTACACA GTAAGCCTGG AGGAAAGAAA ACAAGTTAGA GAGCGACTGT CATAGCCCAC 780
ATGGGGTCTG GGGAGAGCAG GGGAAATATG TGTGAAATGT TATAGGAGGT AGATTCAGCA 840
GGACTCCTGT TTGGTTTCAG TTTGATTTTT GGTTGTGGTT GGGAGGAAGG AGGAGGAATT 900
GAGGATGTTC GGGGTCACTA GTTAGATGGT GCGGCCATTC AGAGCAAGAG AGGGAATACA 960
GGAAGAGGAA CAAATTTGAA GGATTAAGCA ATGTTATAAT TTCTTCACCA ATTTGTCATC 1020
AACTGGGAAA TGTTACACCA ATTATTTTAA CTCTCTTGGG AAAGAAATGT ATGTAGTACT 1080
GAATATTGAA AAAAGACTTG AAGTAGCTGG AGGAGTAATC GGAGGCCTCT TGATTGGGAC 1140
CGTGATTGGG ACCACTAGTG ATGATTTATT ATAATTTAAG AAGTCAGTTA AAGCAGGGGA 1200
TTCTAAAAAT GATTAACGTC AAATAAACAT TTTATTACTT TTGATGTGGG GCTGAGGCTT 1260
TCGCTTTGTG AGTTTGGTGA TGGATTTTTA ATTTGACTTT CTTGCGTAAG CCGCATCTAT 1320
AATATATTTC TGTGTCTTTC AGTATTGGGG TCACTGAAGT GGAGTAAGAG GTTAAAATCA 1380
TTTGTGAAGC AATATTGGGT AAATGCCCCT CAGCTTTACA AGCCTTTTCC ACTTATCTCG 1440
CTTTCACCTA ACCCTAACGT AACTTTTAAA 1470
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