| Tag | Content |
|---|
EnhancerAtlas ID | HS180-15317 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr14:78113600-78114940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr14:78113791-78113806 | GAGGTCAAATGTTCA | + | 6.25 | | RARA | MA0729.1 | chr14:78113791-78113809 | GAGGTCAAATGTTCAAGA | + | 6.34 |
|
| | 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 |
| GH14I077647 | chr14 | 78114341 | 78114490 |
|
Enhancer Sequence | GAGCTCTGGC TCTAACATTA ACACACATCG CTCTGCTCAC ATTTTTTGGC CCAAACAAAT 60
CACATGGTCA AAGCCTGATG TCAACAAGCA AGGAAATATG ATCCTATTCA AGAAAGGAGA 120
CAAGAGGGCT GGGCTGGTAG CTCATGCCTG TAATTCCAGC ACTTTGGGAG GCCAAGGCAG 180
GAGGATCACT TGAGGTCAAA TGTTCAAGAC GAGCCTGGCC AACACAGCAA AACCCCATCC 240
CTACTAAAAA TACAAAAATT AGCTGGGCGT GATGGCGCAC GCCTGTAGTC CTAACTACTC 300
AGGAGGCTGA GGCAGGAGAA TTGCTTGAAC TCAGGTGGTG GAGGTGGCAG TGAGCCGAGA 360
TTGTGCCACT GCACTACAGC CTGGGCAACA CAGCAAAACT TCATATCAAA AAAAAAAAAG 420
AAAGAACGAA AGAAAGGAGT AAAGAATACT CATAAACAAC AATAGAGTCC ACCACAGCAA 480
AATACCGTAG AAATCTGCAG TAACAGAAAA GTTGTTAGAA ATGGTAAAAG CTAACCTTGC 540
AATCTTAAGA AGTCTCTATT TAAATGAATT CCCAAGCTCA AAAGGAAAAG GAGAAAGTTT 600
GTTTCAAAGT TGAATCCCTA AGCCCTGAGA TTCTTACTTA TCATAAGTTA GACTACAAGC 660
ATCTAATCTT AAAATGAGTA TTAAAACAAC CTGTATTATT TATCACCATG TGATATGATA 720
AGCATTCACT TTTTATTGCA CAATTGACTC TTAGTCTGTG ATAAGAGTGG GTCCCTAGGA 780
GATACGCCTG AACTTTGATC AGCATTCAAA TGAGGGCAGG ATGCATGCAC TTCATTGTGC 840
ACCCACTTGG ATAATTTCTT ATAAGCCGAT GTGCCTAGGC CTGGAATCTT TTTAAAGGAA 900
CCAGAGCTAC AGTCTTCCTA ATCAGTGACA CATTTCCAAG GTGTCCAAAT ACACTCACAG 960
ACATGACAGA CAAATCCACC CCAAGGTGGT CTCCAAAGTC TAGCTGCACT GGTTATCATG 1020
TTGTGGTTCC AAATAAAAAA GTAGAGGCCG GGTGCGGTGG CTCATGCCTG TAATCTCAGC 1080
AGTTTGGGAG GCTGAGACAG GCAGATTGCT TGAGCTCAGG AGTTCAAGAC CAGCCTGGGC 1140
AACATGGTGA GACACCATCT CTACTACAAA TACAAAAATT AGCTGGGCGT GGTGGCACGC 1200
ACCTGTAGTC CCAGCTACTC GGGAGACTGA GGTGGGAGAA TTGTTTGAAC CTGGGAGGCA 1260
GCGGTTGCAG TGAGCTGAGA TCATACCACT GCACTCCAGC CTGGGTGACA GAGTGAGGCC 1320
ATGTCTTGAA AGAGAGAGAG 1340
|
