| Tag | Content |
|---|
EnhancerAtlas ID | HS182-00613 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:31319590-31321300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6 | MA0677.1 | chr1:31320725-31320739 | CAGGTCATAGGTCA | + | 6.56 | | Rxra | MA0512.2 | chr1:31320725-31320739 | CAGGTCATAGGTCA | + | 6.06 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I030846 | chr1 | 31319734 | 31321163 |
|
Enhancer Sequence | GGAGGAAGGG GACTGGCAAG GAGCCAAAAG CCTATAATAC CCCTGGGTGG CCTCCAGACT 60
TTCCTGAAGA CACACTCAGT GAACCTGCTC AGATTTCATG GGCTAGAATG TGTCATGTGG 120
CATCCCAATA AACCAGGGAG AAGGGGAAAA AAAACAGTTT TGGTCTTTTA GTCTGGGCGC 180
CTTTTGCCAC CATGAAGAAA GTCTGGGCTC TGTGAGTAAA AATGAAGAGG GTGGCAAGCA 240
ACTGGGTCCA CCCCAGGGGG CCTGAGGCCA GCCCCAGCCT GCCATTAACC TGTTGTGTGG 300
TTTGAGGCAT GTCCCTTCCC CTCTCTAGCC TCAATTTCCC CATTTCAAAA TGGGAGAACT 360
GGGCCAGATG CTATGGGACT TTATTCAGCT TTGACTGGCT GGTGCAAATC CTGACGCTGC 420
TACCTATGAG CTGTGTGACC TGGGGCGGCT ATTGGACAAA CCTTTGGCTC AGTTTCCTCA 480
TCTGTAAAAT AGGGGTAATC GTGGAGCTGC CTCATAGGGT TCTGAGGACT GGATGGGCTG 540
TTACTTGTAG GGCGTTCAGC AGAGTCTGAC AGGAAGGCAC AGACAAAAGC CATCAGTGAC 600
GCTGTTATGC TAAGCTCTGA GAGTCCACGA GTCCTGAGTC CTGCTTCTGC GCGCCTCTGT 660
GTGCTGGGTG ACCTGAGGCA GGTGCCTTCC CCTCTTGGGG CCCAGCAGGT CTGAGAGTTG 720
CCTTCAGAAG CTGGGCCTGG CTGTGACAAG AGAGTGAGTC CCTTCCTGGG CTGGGAGGGG 780
GAACAGGAGC GGACGGAGTC AGCCGGTTTC CTGCAGCCGG GGCAGTGACC TGGGCAGCAG 840
GGACTTCCTG TTTCCCAGAG GGAATCCGGG CCACTGCATC CAGCCCCTCC CTCCCCTCCC 900
TGCAGCTCCC CTCTGTAATG GAGGAAACTT GTCGCTGGGG CAACCTTCCC TGCGTCATCT 960
CCCGGGGCGG GCGGCCCTGT GTGGGTGAGA GAAGCACCAG CAACAATCGC CCTTTGTCTC 1020
CAGCTCAGCT GCTCCCAAAG CGCTTTCTGA CCTTGCCCTC GTCTCAGCCC TGAGAGTCTC 1080
ATGCCCATTT TCCAGATGAG GAAACTGTGG CCCAAGGAGG TGAGGTGACT TGCCCCAGGT 1140
CATAGGTCAC AAGGCTGGTG AGAAGTAAGG CTGGGATTAA AACCTGAGTC TTCTGAAAAC 1200
ATGGGCCAGC TTCATCTGGG GCCCTCGGCA CCCAGTGGAC CCTCAGTCAG GGCCCCCGAG 1260
ACACTGTCAG AGCCTGGAGC TTGACTTTTC AGTGCCCTGA TGACCTAGGA TGTGATCCTC 1320
GGCCACTGTC GCCTCCCCAG CTGGAGCCCT GAGGAAGGAG GCTTGGGGTC TCCTGCAGGA 1380
CCCCTTTGTC TTTAACATGC ACACACCATC CGGCTTCGTG ACACTTGTCC CTGGGGACAC 1440
AGAGACCAGC CAGACCCACT CTGCAAAACC TGGGCACAAA CAACTTTAAC TCAAGGTGGC 1500
CAGTCTGACA TGCCACTGGC TAGGAGCAGA GGCTTTGCAT CCCCGGGTGC AAATCCTGAC 1560
CTTGGTACTT GCCGGCTGTG TGCCTTAGGC TAGTGACTTA ACCTCTCTGA GCTTCTGTTT 1620
CCTCGTCTAT GAAATAGAGG TCATGTTAGT TCCCTAGTGC TGCCATAAAC AAACTGCCAC 1680
AAACTTGTTG GCTTAAGACA ACAGATATTC 1710
|
