| Tag | Content |
|---|
EnhancerAtlas ID | HS012-12052 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:121178880-121180350 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr12:121179374-121179394 | GGGGAGGGGGTGTTTGGAGG | - | 7.24 | | STAT3 | MA0144.2 | chr12:121179020-121179031 | CTTCTGGGAAG | + | 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 |
| GH12I120741 | chr12 | 121179620 | 121180698 |
|
Enhancer Sequence | CCTGACCTGG GCCTGGTCCA GGGCCCCGGG GAATAGGAGT GCGCTTCTTT GAGCGAATTT 60
AGGTCCTGAT TTACCCCACA GGCAGGGTGT GCGCAGAGCC CACGGGTAGT GTGTTCCCTG 120
CTAACGAGGC ACACCTGTGG CTTCTGGGAA GCGCGTCCTC CTGGGCTCCC GAGGTCAGTG 180
GCGTCCTGCG CAGTCTGCAG AAGTTTGGGT CCCTGGGCTT TCCTCCTGGC TCCAGGTAAG 240
TGCCGCCTGC AGAAGTTTGG GTCCCTGGGC TTTCCTCCTG GCTCCAGGTA AGTGCCGCAG 300
GGTCTTGGCT CCTGGCTCAC ACTCTCTCGG GGTCTCCTGA TCTGCTCCTG TCCCTGCCCT 360
GGGCTCAGGT GCAAGCCAAA GGTAGCAGAG CAGAGGGGGA CCCAGGATGC TTCCAGAAGC 420
AGCGCATTTG AGCCCTTCCA CCTGGGGGCA GATGAAGGCC TGTCATTCCC TGTCCCCATG 480
AGCCCGGGGA CAGTGGGGAG GGGGTGTTTG GAGGCGCTGT GCCCCCGCCC GGCGAGGCAG 540
CGCTGCTCCT GACGCAGATG CGGCGTGGGG TTGAGGTTGT CTTTGGGCCC TTCCTCCAGG 600
TGATGGGGGA GAGGAACCCA AACAGCATTC ATCCCAGGCT GGGGACCTGG CTGTCTTGGC 660
TGGAGTTCAG GCCCCTCAGC TCCCCTGCCC TACCCGCTGA GAAGGGTCTG GGCCCTGGAG 720
GGTCAAAGGT AGCCGACTTG AGCCACACCG CTCCCAGCAG GGCAGAGGGC TGGAGTCAGC 780
ACAGGCCGAG TGGCAGCCCT GGAGGGGTTT CTGCTTCTCA GACCTGCCCA GGGCTCGTTC 840
AGGTGGCCAC GAAGAGCCTT TCCAGGAAGT GCAGCCTCGG AGGCCTGGGG TCCTCCATTT 900
CAGATGAAGC AACCCAGGCT CCGACCCAAG AGCCAGTCTG TGCACTCGGG GGCTTTGAGG 960
TGCCGTCGTG GGTCCGGGGT CTGTCCTTCG GTGAGGGAGA GTCGGCACAA ACCCTTGGCT 1020
TTGACGGGGT GCTGCCCGTT AGTGGAAGCT CCTCCTAACT TAGAACTGAA TGTGGACTCT 1080
GCCCCCGGGC CACTGGAGCC CGAACTGTCC TAGAGCCCAT GCCCCTCTGG ATACAGTTTC 1140
CTCAGTGTAG ATTTCCTAAG GACAAGGACG TTCACTTACA GAACAACAGG ACCGTTTCCC 1200
ACCCTGGTCA ACTTTCACAT CTGCACACTC CACTCGGATT GTGCCAGCTG GCACGGTGTC 1260
TGCGAAGTCA GCTCTTCTCA AGGTCCAGGG GCCTGCATTG CATGTAGCTG AGAGGCCACC 1320
TGTTTCCTTC CCTCTAGCCC TCTGGGACAA GTTCTCCATG CTTTGGTTCT TTTTTTTTTT 1380
TTTTTTGGAG ATGGAGTCTC GCTCTGTTGC CAGGCTGGAG TACAGTGGCG CAATCTCGGC 1440
TCACCGCAGC CTCCACATCC CGGTTTCAAG 1470
|
