Tag | Content |
---|
EnhancerAtlas ID | HS182-00193 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr1:11518330-11520030 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr1:11519247-11519262 | CAGCTCAAGGCCAGC | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCCATTGGAT GAATCCAATG ACTGTTGTCT TCATAAGAGA GAAATCTGGA CACAGACGTA 60 GACAGACGGA GAACAGCACA TGATGATGTG ACAGAGCTTG GGGCGACGCA TCTACAAGCC 120 GGGGACCCCA CGATTGCCAC CACCAGAAGC TGGAGACACT CCTGGAACGG AATTTCCCTC 180 AGGGCCTCCA GAAGGAGGCA ACCCTGTCCA TACCTTGACT TTGGACTTGT AGCTTACAGA 240 ACAGTAATAG AATAAATTTC TGTTGTCTAC TGTTTGTGTT AACTTGTTCC AGCAGCCCTA 300 AGAAACGAAT ACACTGTTAT TTCAACGCAG CAAAGCGAGC GCGGTTCTGG GTATACAGTG 360 GTGCCCAATA AGCTCCACTC CCTCATTGCT GACCCTCTGC CTTCACTATC CTCCACCCCC 420 ACTCCCCTCC CCACTGGCTT CTCAGGCCAG GTCAGTCTGG GCTGGGGGGC ACCTGCTGGG 480 CCAGGCAGGC AGAGCAATTC CTGTGCCCTG GCTGAGGCCT GCGGCACCTC ATTACCAGGC 540 AGAATGTACC TCGATTTCAC CCATGACTGG CACTGAAAAG CAGCCCTGGC TGGTGTCATG 600 GATGGGCCAG AAGCTGCTCC GGGCGCCTCC TGCCCCCTCC TGGGCCTGGC AAATCTCTGA 660 AGCACCCAGA AGCTGGCAGG CAGCACGCTC CACAGCTGAG CCACACAGAT AAACCTCAAC 720 AGGCGCTGGG CTGTTCGGTC CTGGAGCAAA CATCAGGAAA TTAATAGGCC TTTCTGTGGG 780 CAGCGCCTGG CCTGGCCCCC ACTTCCCCCT CACTCCCGCC TGCCCCCCTC CCCTCATCCC 840 AGGCTTTGTT TCCTTTTTCC CTTTGTTTCC TGTTTGCGAT AAACACGATT CATGCCAGTC 900 CAGCCGGGCC CCGTCACCAG CTCAAGGCCA GCCGTATTTC TCAGCAATGA GCCCCGAGCT 960 GGCTGCAGTG AGGATCTGGG CCATGGACAC AGGCGTGAGG AAGGGGCACT GTGGGCAGAG 1020 ACAGGGCTGA TGTGGGGGCG CCAGCAGGGA GCAGGGTGCC GGGTCTCTGT GAAGTGCCGC 1080 TGAGCACTGG GCACTGAGGG GAACTCAGAG AAGCCACCAT GGCCAGACCC TCCCTATCTG 1140 GGCACAGCTG TGCCCACCCT TCCTACATGG ACATAGCTTC CTGAGGCTGC TGTAACAAAG 1200 TGTCACACAC CAGGCGGCTT AGAGCAACAG ATATGTATTC TCTCGCAGGT CCGGAAGCCA 1260 AAAGTCCAAG CTCAAGGTGT CAGCAGGGCC ATTCTGTCTC TGAAGGCCCA AGGGAAAGCT 1320 CCCTCTGGCC TCTTCCAGCT CCTGGTGGCA GCGGCCACCC TTGGCATTCC ATGCCTGTGT 1380 GGCTCCAGCC TCCGCCTCTG TCTTCACACA GCCTTCTCTT CCCTGCGTCC CTCCCCTTCT 1440 TGTAAGGACT CCAGTCGTAT TAGGACCTAA TCTTAACCAA TGTTAAGTAA GACCTAATCT 1500 TAACTAATGA CATCTGCAAC GATCCCATTT CCAAATAAAG GTCACATTCA CAGGTACTGG 1560 GGGTCAGGAG TTCAATACAT TTCTTTTTGG GGACAGAATG CAATGCATCC CAGCTGCTGA 1620 GGCTCCTGGT GGCATCTCTC ATCACCGCCT GTCACACCTC AGCCATCCAG CCATCCTGGG 1680 CACCTGCAGC TTCCTAGTTG 1700
|
| |
|
|
|