| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00858 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:31319780-31320840 |
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 | CATGAAGAAA GTCTGGGCTC TGTGAGTAAA AATGAAGAGG GTGGCAAGCA ACTGGGTCCA 60
CCCCAGGGGG CCTGAGGCCA GCCCCAGCCT GCCATTAACC TGTTGTGTGG TTTGAGGCAT 120
GTCCCTTCCC CTCTCTAGCC TCAATTTCCC CATTTCAAAA TGGGAGAACT GGGCCAGATG 180
CTATGGGACT TTATTCAGCT TTGACTGGCT GGTGCAAATC CTGACGCTGC TACCTATGAG 240
CTGTGTGACC TGGGGCGGCT ATTGGACAAA CCTTTGGCTC AGTTTCCTCA TCTGTAAAAT 300
AGGGGTAATC GTGGAGCTGC CTCATAGGGT TCTGAGGACT GGATGGGCTG TTACTTGTAG 360
GGCGTTCAGC AGAGTCTGAC AGGAAGGCAC AGACAAAAGC CATCAGTGAC GCTGTTATGC 420
TAAGCTCTGA GAGTCCACGA GTCCTGAGTC CTGCTTCTGC GCGCCTCTGT GTGCTGGGTG 480
ACCTGAGGCA GGTGCCTTCC CCTCTTGGGG CCCAGCAGGT CTGAGAGTTG CCTTCAGAAG 540
CTGGGCCTGG CTGTGACAAG AGAGTGAGTC CCTTCCTGGG CTGGGAGGGG GAACAGGAGC 600
GGACGGAGTC AGCCGGTTTC CTGCAGCCGG GGCAGTGACC TGGGCAGCAG GGACTTCCTG 660
TTTCCCAGAG GGAATCCGGG CCACTGCATC CAGCCCCTCC CTCCCCTCCC TGCAGCTCCC 720
CTCTGTAATG GAGGAAACTT GTCGCTGGGG CAACCTTCCC TGCGTCATCT CCCGGGGCGG 780
GCGGCCCTGT GTGGGTGAGA GAAGCACCAG CAACAATCGC CCTTTGTCTC CAGCTCAGCT 840
GCTCCCAAAG CGCTTTCTGA CCTTGCCCTC GTCTCAGCCC TGAGAGTCTC ATGCCCATTT 900
TCCAGATGAG GAAACTGTGG CCCAAGGAGG TGAGGTGACT TGCCCCAGGT CATAGGTCAC 960
AAGGCTGGTG AGAAGTAAGG CTGGGATTAA AACCTGAGTC TTCTGAAAAC ATGGGCCAGC 1020
TTCATCTGGG GCCCTCGGCA CCCAGTGGAC CCTCAGTCAG 1060
|
