| Tag | Content |
|---|
EnhancerAtlas ID | HS012-13194 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr14:75365200-75366170 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr14:75365586-75365601 | TGACCTTTGATCTTA | - | 6.12 | | Nr2f6 | MA0677.1 | chr14:75365586-75365600 | TGACCTTTGATCTT | - | 6.69 | | Rxra | MA0512.2 | chr14:75365586-75365600 | TGACCTTTGATCTT | - | 6.14 |
|
| | 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 |
| GH14I074898 | chr14 | 75364941 | 75366129 |
|
Enhancer Sequence | AGGTGAGTTG CTTGTGGCTG GAATTGGAGA GGTCCTGGGA GGTAGGTGTA TGAGCACAGA 60
CCTGCTCCCA CATGCAGAGG ATCAACAGAC CAAGGCTTTT TATTTGCTAC CTATAGAAAT 120
ATCAGTATCT TCCCCAGGGA TTTCTTGGTT CACCTTCCTG AAGCAGCATC ATGATTACTT 180
TCTACCCGCC AGCTGGGCAG AACAGTTTCT CTTCCCAGTG TACAGCTCGG CAGCTGCTCA 240
GGCAGCAGGC AGTTCTGGGA TAGCCCAGCT CTCCAGGCTG TCTCCTGTCA AGGTGGAAGC 300
ACGTGTTCTG GCTTCCTCCC CTCCCCCAGC TCCACAGGCC CTGTTACCTT GGGGCCTGAC 360
TTCCACAGTT GGTGTAGGCT CCTGGCTGAC CTTTGATCTT AGGTCGATGG GCCTCACTGG 420
GAGCTTCGGC TTGGCCTCTC ATGGACCTGG TGCTTATTTT CTTTCCTTTT TACTTACCTA 480
CGTCATTGTA GTGTTGACCT AACAAGCACT TTGTTTTCCT GTTGACACAC TTCTCTGTTC 540
CTTGGGAGAT TGGAGAGGGG TCAGTGCTAC TTTTGCCATC CTCAGCAGTG TCAGGGGCCC 600
TAAAGGTCTA GAAGTAGAAG CCCTAGTCCC TCCTGTTGAG TGGTGCTCTA GGGAGGTAGA 660
AGGCCATCTT TGTTTTGCCC AAATGTATAC CTCTTCTTTT TCCCATTCTT CTCATGCCTC 720
CCTGACTGGC TCTCATCTTT TTCAGTGGCC CCCTTCTGCT TGCCCACACA TGTAGGCGGC 780
TCTCAAAAGT TCTCGTGGCC TCTTTTTCAC ATTACATGCT TCCTCTGGAT GTCTTATCTA 840
ACAATACAAC ATGGACTTTC TGCGGAAATG ATTCCCAAGC CTTTATTTTC CCATTAGTTG 900
CTAGGTGTAC ATTTTCAGAT GCTGGTTTGC CATCTCTTGA GGTAGCATAT TTCAAAGCCA 960
GATCACCCCG 970
|
