| Tag | Content |
|---|
EnhancerAtlas ID | HS182-21956 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr9:124424810-124426220 | 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 | chr9:124425281-124425302 | AAAAGGAAAAAGAAACTCAGG | - | 6.31 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCTACAATGG CAGAGTTGAA TAGCTGAGAC AGAGACCATA TGGACTTGTA AGCCTGAAAT 60
ATTTGCTATC TGGCCTTTTA TGGAAAGTTT GCTGACGCCC AAGATACAGC TAAAGCCACC 120
TACTCTCTCT CCAGGCATAA CTGGCCACCT AAAGGTGGTG GGTATCCTGC CTACATGTGC 180
TTTCTGCTTT TACATAGAAG CCTATGCTTC CAAGTGTGTC GAATTGCATT GTGTGTTTAA 240
AAATGGATAT GGTGAAATTG CACATGGCAG AGAGGAGCAA ACACATATGG ACACCCTGAG 300
ACCTCCTTAG TTTCCTGAAC TCCAGCAGCA CAGAGTAAAT GCCAGCTCTC TGCCAGCCCT 360
GGAATGGGCC CTGCAGATGC AGAGAAAAGA ATCGTGGGAA GAAAACTCCA GAAGAAAAAA 420
TGGGGAAAGT GACACTGCCG ACTCAAATTA CTAGAAATCC TCAGAAAGTA AAAAAGGAAA 480
AAGAAACTCA GGGTTGAGAG AAGACTTTGG GCCGGTGAAT TCATCCTTGG AGTGTTCAGG 540
AAATCCAGAG ATTTTTGGAA GGCTGGGAAT TCTTTGGAAG TGAGGCGTGT CTGGAGATAA 600
GGAATAGGAA GCATGGGCTG TCAAAAGCAA TTGTTAGGGA GCTCAAGTAG AGAAGCAAAA 660
GGAAAACCTG GGGACAAGGT CGACAGATGC TGAAAACCTT GTAGGATTTA TACTAGGCTA 720
CACCAGACTA TTAACGCGGC CAACCAGAGA CCAACAAGGG AGCAAACCCT TGCACTGTCC 780
TTGCGGAAGG GCCCTACCCA GCATCCTGGG ATGTAACTGG GAAGGATGTG TCTCATTAGC 840
ACCTCTGCCC CACCTCTGGA ATACCAGCTC CAAGCCAAAC ACGTCCCCTC TGAGCAGCTG 900
CTGTGCCCTG CCCCCGAGTG CTCTATGTTG AGGATCCTCC GGGCAGGAAT GGTGGGCTGG 960
ATGCTGAGCC CTCTACAGTT GTCCCCATGT CCCTCTCCCA CCAGACTCCA CTCCCCAGCA 1020
GCAGTGGGCA ACCTCCTCTG ATTCTGAACC ACCTCCTGAG CTTACAGACC ATTGGAACTC 1080
GATCCCAGTT CCCTTTAGGA GACAGCAGGC TATCATAGTT CCATGGCCTC AGGACACTGT 1140
ACCTGTACCA CCTCCAAACT CAACATCATA AAACCAAAAC GTGAAATCAA CATCCCTCAT 1200
CTCTTTCTGC CAGGTAGCTG GGACTGAGCT GGGCCCTGGG GACATAGAGA GAGGCCAAGG 1260
GCCAGGCGCG AACTCAGCTT CCTGAGTCAC TTGGGAGCAC TGTCTTCTCA CTCATCTCTG 1320
CACAGTGCCA TTCCTTTCCC ACATTGGGGC AACCCTTAGA TTCAGAGATA TCCGGGCTTG 1380
AATCCTGTTT TCAACGTTTC CTAGCTGTGT 1410
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