Tag | Content |
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EnhancerAtlas ID | HS182-00868 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr1:46670990-46671940 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr1:46671635-46671650 | GAGGCCAAGGTCAGT | + | 6.15 | RFX1 | MA0509.2 | chr1:46671783-46671799 | TGTTGCTATGACAACC | + | 6.71 | RFX1 | MA0509.2 | chr1:46671783-46671799 | TGTTGCTATGACAACC | - | 6.73 | RFX2 | MA0600.2 | chr1:46671783-46671799 | TGTTGCTATGACAACC | - | 6.65 | RFX2 | MA0600.2 | chr1:46671783-46671799 | TGTTGCTATGACAACC | + | 6.75 | RFX5 | MA0510.2 | chr1:46671783-46671799 | TGTTGCTATGACAACC | - | 6.36 | RFX5 | MA0510.2 | chr1:46671783-46671799 | TGTTGCTATGACAACC | + | 6.67 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAGAAAAGAA AACAGAGGCA CAGGGAGTTT AATAACTGCC CAACATCACG CAAAAAGCAG 60 GGCCATGATT TGAACCCAGA TCATCTGACT GCACTTTGCA TCTTTACTTT GAGACCTGCT 120 TTGTGCCAGA TAGTCTGAAC ATTTTATGTC ATTGAAATGA GAAAACTGGT CATCATTTCT 180 CCCATCTTAC AGATAAAACG TGCTTGCAGA TTCTGAACTC ACATAGGGAG TCAGTGGAAG 240 AGCCACGCCC AGTCTCTGGC TCTCTTCTCT GCCTTGGTGG AAACTATCTG TAAACTTTAA 300 GGGGCTGCAT TTAACTTTTG ATTTTGTCTC TCTGTATTCT TGACCCAGCT TGCCTGGGGC 360 CTGAGGCTGC CCGAGAAAGG GCACAAGGGA GGGAGCCTTC TGGGGCCAGA ATGAGGAGAG 420 ATCCCCATCC TATTTTTTCT CCTTCCTCAG GCCAGGATGT TATTAATATT AATCTCTTCT 480 TGTGCTCTGC CCTGCCTACT GGGTTGCACC CAGGAAGGAC AAGGGGTGGG GCAAGGGATT 540 TGCCTTCGGG CTACTGAAGG CAGGACTGGT TCAAGCCCTC TAAGGACTGT CCTTCAATTG 600 TTCCTCTCCC AGCTCTCCTT GCACAAAGGG GGAAGGCCTA CCCTTGAGGC CAAGGTCAGT 660 CCTGCCTCTA GGCCTCGTCC CTCCTGCTTT CTTCCTCTAC CCTCCATTCA AAGGTTGAGT 720 GAACAAGCCA GACTGGGATA TGTGGGAATG GGAAACAGTG GCAACTTCTT CTTAGTTCTC 780 CCACCCAAAG AACTGTTGCT ATGACAACCC ACCTCCACAG AGGCAGTTTG AGAAAAAGCT 840 TTAGGCAAGG AAGAATGCAC GGGTTCAAGT CTTGGCTCTG CTTCTGAAAC GTTTTGTGGT 900 CTTGAGCAGC ACTCTGTCTC TCTCCTGGCC TCAGTTTTTC CTCCTTTTGG 950
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