| Tag | Content |
|---|
EnhancerAtlas ID | HS180-38464 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr5:40791460-40792380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr5:40791892-40791903 | AAGCAATAAAA | + | 6.32 | | Foxd3 | MA0041.1 | chr5:40791833-40791845 | AAACAAACATTT | - | 6.27 | | TBP | MA0108.2 | chr5:40792282-40792297 | CCCTGCCTTTTATAC | - | 7 |
|
| | 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 |
| GH05I040790 | chr5 | 40791054 | 40792491 |
|
Enhancer Sequence | CACATTACTC AGAGCAAATA TTACCAGCAT TCACAATGTC CCCCTCACAA GAATAGCAGA 60
TTAGTCAACT AAATATTAGC TAACAACCAT GCTATTGCTA TCTAAAGGGA ACTTTGTCTA 120
ACTGCATAAC ATTGTAACAA ATGCTCTTCT AATTAGATAT ATAATCCTGA AGGGAAACAA 180
GATCATACTT TGAAACAGAG GATTTTAATA GGACAGAGAA GCAGCAAAGA TAGAAATATC 240
TACTAAAGAT ATTCTAGACA CCTAACCATT TCATTCCCAC TTTAAAATTG AAAGAATAAA 300
AACGTGTTAA GGAAATAGCT TAATCCTGGG GAAGGGTGGG CTTTAAAAGC TATAGATCGT 360
AATTTAAGAA AGCAAACAAA CATTTCAAGC ACACCAAGGG CATTCCAAAT ACCCATGAGC 420
CACCATCAGC TTAAGCAATA AAACATTACA AATACAACTC AAGCCCTGCA TGACTCCTCC 480
CAGATTCCCT TATCCTTCAT CTGTCCTCAG AAGTAACCAC TATCCTGAAT TTGGTGTTTG 540
TGTTTCCCAC GTTTAAATAT TTTTACATGG GTAGGAATCC ATAAAAAATA TAGTAACATT 600
ATTTTTCATA TTTATTTTTA CAAATGTCAT TGCATATATT TTGATAACAC AATACCTGCA 660
CTATACACAC AGTTCAAAAG TACAAAAGCA TCTATGGTGC AACACAATGT CCTCCTTTAC 720
CTAGTCCCCT ATACTGAGCA ACTAACGTAA CCAGTCTTGT GTGTATCTTT AAAGAGACAT 780
ACTCTATATA TAAAAGCAGT CACATTTAAG ATACAGATTT GCCCCTGCCT TTTATACATA 840
AGTGGTAGGC ATATTGAACA CACTGTTCTA CTTTTTCCTC TTAAAAATAC ACCTTGGAAA 900
TTGTTCTCTA AAATATACAA 920
|
