| Tag | Content |
|---|
EnhancerAtlas ID | HS012-16837 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr2:201923440-201924580 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA | MA0729.1 | chr2:201924552-201924570 | GAGGTCAAAAGTTGAAGA | + | 6.25 | | Stat6 | MA0520.1 | chr2:201923995-201924010 | GTTTCTCTGGAAAAC | - | 6.42 | | Zfx | MA0146.2 | chr2:201924528-201924542 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | 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 |
| GH02I201056 | chr2 | 201921426 | 201924123 |
|
Enhancer Sequence | AATCACAGAA ATTTTCATAT CGAATTACAT TTGTTTCTTA TCACTATGTC ATGACACTTT 60
TCTCTGGTCA GAGAGCTTCC ATTCTACCCT GGATAAAAAT GTTTCCAATC TCATCTCCAT 120
ATATTTAGCT AAACATTTTT CTGGGTGTTT CCATATGAGA TTAACATTTA AATCTATAGA 180
CTGAGTAAAG CAGACTGCCT TTCCTAATGT GGTGGATGTC ATTTAATCAG TGGAAAGCCT 240
GAACAGACAA AAAGGCTAAG CCTCCCCCAA GTAGAGAGTC AGTTCCTCCT GCCTAAGGAC 300
ATTGGCTTTC TCCAGCCTTC AAACTCAAAC TGAAACATTA GCTCTTCAGA GTCTCAAGCC 360
TGAGTGACTG CTACTATGTT ATCTCTGGTT CTCAGGACTT TGGACTGTGT CTGACTGGAA 420
CTATACAGTC AGGTCTCCTG AGTCTCCAGC TTGCCAACTA CCCTGCAGAT CTCGGGACTT 480
GTCAGCCTCC TAAATTGTGT AAGCCAATTC CTATAATAAA CCTTATAATA AATCACACAC 540
AACCTTATTG GTTCTGTTTC TCTGGAAAAC CCTGATGAAT ATAGTTCCTG ACTTGTTCAG 600
AATGACCTAA GGATATATGC AGAATCCATC TCTTATACCT CTCAGAACAG GAATCCAAGT 660
TATAGATGGG AATGCCTGGC CCTGGTATCA GGCATTCCAT TACCATGTCT TCTTCAGTAG 720
AACAGGGGCA TATAAGTGAG ATTGGTGGCT AGGCAGATAC CCAACCAAAG AGCAAATGTA 780
AATCTCTCTT CTTAATGACA GAGAGTGACT CTTTCAGGAC CTCCTTATCT TGACTTTTGG 840
GAAGGAAAAA ACCCTTTCCT TTCCCCTCAC AGAGCAGGGA ATAGTTTCTT TCCATTAATA 900
CTCCCCTTCC AAAGAAGGCC TCTCCCCTTC TCCCTCTTAA GCCTCATAAA TTGATGGGGT 960
GGGCAGAATC ATAGTCACAA CAGCCCATAG TACTCAACAT CTTATGTTGT CAAAGACCTG 1020
TGTGCAGGTT GAAGAGCCCT CTTATTGACT GGGTGCAGTG GCTCATGCCT GTAATCCTCG 1080
CACTTTGGGA GGCCGAGGCG GGTGGATCAC CTGAGGTCAA AAGTTGAAGA CCAGCCTGGC 1140
|
