| Tag | Content |
|---|
EnhancerAtlas ID | HS080-00717 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:31319880-31321040 |
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 | TGTTGTGTGG TTTGAGGCAT GTCCCTTCCC CTCTCTAGCC TCAATTTCCC CATTTCAAAA 60
TGGGAGAACT GGGCCAGATG CTATGGGACT TTATTCAGCT TTGACTGGCT GGTGCAAATC 120
CTGACGCTGC TACCTATGAG CTGTGTGACC TGGGGCGGCT ATTGGACAAA CCTTTGGCTC 180
AGTTTCCTCA TCTGTAAAAT AGGGGTAATC GTGGAGCTGC CTCATAGGGT TCTGAGGACT 240
GGATGGGCTG TTACTTGTAG GGCGTTCAGC AGAGTCTGAC AGGAAGGCAC AGACAAAAGC 300
CATCAGTGAC GCTGTTATGC TAAGCTCTGA GAGTCCACGA GTCCTGAGTC CTGCTTCTGC 360
GCGCCTCTGT GTGCTGGGTG ACCTGAGGCA GGTGCCTTCC CCTCTTGGGG CCCAGCAGGT 420
CTGAGAGTTG CCTTCAGAAG CTGGGCCTGG CTGTGACAAG AGAGTGAGTC CCTTCCTGGG 480
CTGGGAGGGG GAACAGGAGC GGACGGAGTC AGCCGGTTTC CTGCAGCCGG GGCAGTGACC 540
TGGGCAGCAG GGACTTCCTG TTTCCCAGAG GGAATCCGGG CCACTGCATC CAGCCCCTCC 600
CTCCCCTCCC TGCAGCTCCC CTCTGTAATG GAGGAAACTT GTCGCTGGGG CAACCTTCCC 660
TGCGTCATCT CCCGGGGCGG GCGGCCCTGT GTGGGTGAGA GAAGCACCAG CAACAATCGC 720
CCTTTGTCTC CAGCTCAGCT GCTCCCAAAG CGCTTTCTGA CCTTGCCCTC GTCTCAGCCC 780
TGAGAGTCTC ATGCCCATTT TCCAGATGAG GAAACTGTGG CCCAAGGAGG TGAGGTGACT 840
TGCCCCAGGT CATAGGTCAC AAGGCTGGTG AGAAGTAAGG CTGGGATTAA AACCTGAGTC 900
TTCTGAAAAC ATGGGCCAGC TTCATCTGGG GCCCTCGGCA CCCAGTGGAC CCTCAGTCAG 960
GGCCCCCGAG ACACTGTCAG AGCCTGGAGC TTGACTTTTC AGTGCCCTGA TGACCTAGGA 1020
TGTGATCCTC GGCCACTGTC GCCTCCCCAG CTGGAGCCCT GAGGAAGGAG GCTTGGGGTC 1080
TCCTGCAGGA CCCCTTTGTC TTTAACATGC ACACACCATC CGGCTTCGTG ACACTTGTCC 1140
CTGGGGACAC AGAGACCAGC 1160
|
