| Tag | Content |
|---|
EnhancerAtlas ID | HS180-01121 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:31319690-31321270 |
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 | GGCTAGAATG TGTCATGTGG CATCCCAATA AACCAGGGAG AAGGGGAAAA AAAACAGTTT 60
TGGTCTTTTA GTCTGGGCGC CTTTTGCCAC CATGAAGAAA GTCTGGGCTC TGTGAGTAAA 120
AATGAAGAGG GTGGCAAGCA ACTGGGTCCA CCCCAGGGGG CCTGAGGCCA GCCCCAGCCT 180
GCCATTAACC TGTTGTGTGG TTTGAGGCAT GTCCCTTCCC CTCTCTAGCC TCAATTTCCC 240
CATTTCAAAA TGGGAGAACT GGGCCAGATG CTATGGGACT TTATTCAGCT TTGACTGGCT 300
GGTGCAAATC CTGACGCTGC TACCTATGAG CTGTGTGACC TGGGGCGGCT ATTGGACAAA 360
CCTTTGGCTC AGTTTCCTCA TCTGTAAAAT AGGGGTAATC GTGGAGCTGC CTCATAGGGT 420
TCTGAGGACT GGATGGGCTG TTACTTGTAG GGCGTTCAGC AGAGTCTGAC AGGAAGGCAC 480
AGACAAAAGC CATCAGTGAC GCTGTTATGC TAAGCTCTGA GAGTCCACGA GTCCTGAGTC 540
CTGCTTCTGC GCGCCTCTGT GTGCTGGGTG ACCTGAGGCA GGTGCCTTCC CCTCTTGGGG 600
CCCAGCAGGT CTGAGAGTTG CCTTCAGAAG CTGGGCCTGG CTGTGACAAG AGAGTGAGTC 660
CCTTCCTGGG CTGGGAGGGG GAACAGGAGC GGACGGAGTC AGCCGGTTTC CTGCAGCCGG 720
GGCAGTGACC TGGGCAGCAG GGACTTCCTG TTTCCCAGAG GGAATCCGGG CCACTGCATC 780
CAGCCCCTCC CTCCCCTCCC TGCAGCTCCC CTCTGTAATG GAGGAAACTT GTCGCTGGGG 840
CAACCTTCCC TGCGTCATCT CCCGGGGCGG GCGGCCCTGT GTGGGTGAGA GAAGCACCAG 900
CAACAATCGC CCTTTGTCTC CAGCTCAGCT GCTCCCAAAG CGCTTTCTGA CCTTGCCCTC 960
GTCTCAGCCC TGAGAGTCTC ATGCCCATTT TCCAGATGAG GAAACTGTGG CCCAAGGAGG 1020
TGAGGTGACT TGCCCCAGGT CATAGGTCAC AAGGCTGGTG AGAAGTAAGG CTGGGATTAA 1080
AACCTGAGTC TTCTGAAAAC ATGGGCCAGC TTCATCTGGG GCCCTCGGCA CCCAGTGGAC 1140
CCTCAGTCAG GGCCCCCGAG ACACTGTCAG AGCCTGGAGC TTGACTTTTC AGTGCCCTGA 1200
TGACCTAGGA TGTGATCCTC GGCCACTGTC GCCTCCCCAG CTGGAGCCCT GAGGAAGGAG 1260
GCTTGGGGTC TCCTGCAGGA CCCCTTTGTC TTTAACATGC ACACACCATC CGGCTTCGTG 1320
ACACTTGTCC CTGGGGACAC AGAGACCAGC CAGACCCACT CTGCAAAACC TGGGCACAAA 1380
CAACTTTAAC TCAAGGTGGC CAGTCTGACA TGCCACTGGC TAGGAGCAGA GGCTTTGCAT 1440
CCCCGGGTGC AAATCCTGAC CTTGGTACTT GCCGGCTGTG TGCCTTAGGC TAGTGACTTA 1500
ACCTCTCTGA GCTTCTGTTT CCTCGTCTAT GAAATAGAGG TCATGTTAGT TCCCTAGTGC 1560
TGCCATAAAC AAACTGCCAC 1580
|
