| Tag | Content |
|---|
EnhancerAtlas ID | HS050-03606 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:110044560-110045550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:110045108-110045128 | AGGATGTGGGTGGTGGGTGG | - | 6.38 | | RREB1 | MA0073.1 | chr1:110045119-110045139 | GGTGGGTGGGTGGGGGGTGT | - | 6.55 | | RREB1 | MA0073.1 | chr1:110045115-110045135 | GGGTGGTGGGTGGGTGGGGG | - | 8.93 |
|
| | 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 |
| GH01I109497 | chr1 | 110040120 | 110046097 |
|
Enhancer Sequence | GTTCTCTCAG GCCATGGTTC CAACCAGGGA GAGTAAACAA GCTGACTAGA TTGGAGGCGT 60
CAGGGCAGGT CTAAGTGTCT TCACCATTTT GCATTTTCCA CCTAAGAGTG TAGAAGCCTG 120
ATGAAGGGGC TTGACTGGCA GCTGCTTTAG CCTTCCTCTC TCAAGCCCCA GGAGAGGAAG 180
CATTCAGCAC AGGCTGACTG TGACTAGACC AGAAAAGCCA ACCGTCCCAC TGCAGGGGCC 240
TGAGCCTTTT CTGCTATGTG GGTGGAGAAA GTGAAGCTTC CCCACTGGTT TCCTGGGAGA 300
TACAAGATAA GTGGTGCAAG AAGTGCATGC AGAAAGGGAA GGAGTTGAGA GACTGGGGGG 360
AAGAGAGGCC AGGTTAACCA ATGCACTGAA CTCTTACCTA TTCTCAAAGA AAACTGTCAT 420
ATTAGCCTCC TCCCTCCCCG CAAGTGCTAC CTAAGAGGAG CCAGGGTAAG TGCTGCAAGG 480
CATGGCAGAC AAAATTGCAC ATCTTGGCCA GAATCTAAGG AACTTCTTGT GGTTTGGGGG 540
AGGTGGTGAG GATGTGGGTG GTGGGTGGGT GGGGGGTGTT GAAGAGATGC AGCCATGGAC 600
TTCCTTGGGC TTGGCACAGG CCAAAACAGA AGAGAGAACT CCAAACTCCA AGTAGTCCTC 660
ATCAGACTTG CTCTCCTTAT CAGCTTCATC CTGTCAGCCA AATTGTCAGC CATAGAAAAA 720
CTGCTTTGCA GATGAAAAAC TATATAAATG CAGAGTATGG GAGTGCTCTG ACATCAACAG 780
CTGTCATTTC ACTGACTGCC AAGGTTGACT TGTCTGATGT GGCTGGTTGT GCAGTAGCTC 840
CACCCCTCGT CACCTTGGTT GTTCCTCCTG AAGTGAAAAA CAACTTTCCA AATAGAGGAG 900
GGCTGCCCTT CGGTCAAGAC TTTAGGTAAG TATTCAAATT CGCATTCTTT TAATTTTTTT 960
CCTGGTATCA TTTCCTCTCC CTCTTTGGAA 990
|
