| Tag | Content |
|---|
EnhancerAtlas ID | HS180-04408 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:209914430-209915510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:209915196-209915208 | GAATGTTGGTTT | + | 6.04 | | Nr2f6 | MA0677.1 | chr1:209914716-209914730 | TGGCTCAAAGGTCA | + | 6.04 |
|
| | 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 |
| GH01I209741 | chr1 | 209915319 | 209916725 |
|
Enhancer Sequence | CAAAGAGCCG GGATTACAAG GATGAGCCAC CATGCCAGGC CTGCCCTGAA ATTTTATGTC 60
TGCCTTCCCT GCTTGTTTTT TCTCCTTAGT ACTTATTATT ATCTATATTG TTGGTCATTT 120
ATCTTGTTTA TTATCTGTCC TTGTCCCAGT TACTATGGTG ACATAACAAA TCATCCCAAA 180
ACTCAGTGGC TTAAAACATA AAATGACATT CGCTTCGCTT GCAAATCTGT AGTCTGAGCA 240
GGCTCAGCAG GGATAGTTAA TTTCTGCTCC ACTCAGCAAG ATTGGGTGGC TCAAAGGTCA 300
GGAACTAGAA TCACCTAAAA GCGTGATTGT GCCTGCCCTG GGAAGACATG AACAGCTGGA 360
CTCTGAAACA GGTAGGGCAC TTTAGGTGCC TGGCTCCTTG GGCACCTGGA GCTAAGCAGG 420
GAGGGCACAG CAGGAGTCTC TCTCATCTTT GTGTGATCTC TCCACATGGT CACTTGGAAT 480
GGCAGCTTTA GGGTTGCCAG ACTGCTTGGA GGACTTGAGA TCTCCAAAGG CAAGTGTCCC 540
AAGAGAAAGA GCCAGGCAGA AGCTATATTG CCTTTCAGGA CTGACCATAC ACTTTTGGTC 600
GAAGCACTTC TGAAGATGCA CCTCATTTCA AGGAAAAGGA ATACAGACCC CACCTGTTGA 660
TGGAGGACTG TCATTGTCAC ATTGTAAGAA GAGCATGTGG GATGGATGGG CTAAAAATTG 720
CTGCAGCCAT CTTTAGAAAG TACCATCTGC CACATTCCCC CTGCTAGAAT GTTGGTTTCA 780
TGAGGACAGG AGTTTTTTCT GTTTAGTTCA GTGTGCCCCC AGCACCTAGA GGAGCACCTG 840
GCACATACGT GTGGGCCAGA GAAGATCATG AGGTATCTAG ATGCAAGTGA TAAACTGTTG 900
TACCAGACCC AGAATCAGGA GCTTCTGAGG GTCACATAAA CACAGGAAGA AGGCAGGTTT 960
GCAGGAGCCA AGGCCCTGCA GATTGTCAAG AGGACAGGAG TGGGAGGGCT GATTAGGAGG 1020
TGAGGAAATG AGTACAGAGA CAGAAACATG GTCAGGTGAC AAATTGATAG CCAAAGTCAA 1080
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