| Tag | Content |
|---|
EnhancerAtlas ID | HS180-02594 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:110044260-110045520 |
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: 2 | Chromosome | Start | End |
| chr1 | 110044800 | 110045479 | | chr1 | 110044516 | 110044800 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I109497 | chr1 | 110040120 | 110046097 |
|
Enhancer Sequence | GCCCCCTAGC ACCCCTATCT TTAAAGCAGA TACCCAGTTA TCTCATGGTG CTTTCTAAGG 60
ATGCTCAGTT CTGCTCAGGC CCCCCAAAAG CAAACTATGA CCAAGTGAGG GAGCAGTGGG 120
AGGTAAGGGA AATGCAGCAC AAAGTACAAT CCAACTCCAG TACTTGCCAA CCTGTATGTG 180
TGCGCACATG CACGCATACA CCAGCCTTGG AGGCAATGAC TCCTGCCTAA TGTATGCCAG 240
TGCCAAAGGG CATCCAGAAG TCCCACTGCA GGGCTCCACG TCCTGGCTCA CTGCAGGTTG 300
GTTCTCTCAG GCCATGGTTC CAACCAGGGA GAGTAAACAA GCTGACTAGA TTGGAGGCGT 360
CAGGGCAGGT CTAAGTGTCT TCACCATTTT GCATTTTCCA CCTAAGAGTG TAGAAGCCTG 420
ATGAAGGGGC TTGACTGGCA GCTGCTTTAG CCTTCCTCTC TCAAGCCCCA GGAGAGGAAG 480
CATTCAGCAC AGGCTGACTG TGACTAGACC AGAAAAGCCA ACCGTCCCAC TGCAGGGGCC 540
TGAGCCTTTT CTGCTATGTG GGTGGAGAAA GTGAAGCTTC CCCACTGGTT TCCTGGGAGA 600
TACAAGATAA GTGGTGCAAG AAGTGCATGC AGAAAGGGAA GGAGTTGAGA GACTGGGGGG 660
AAGAGAGGCC AGGTTAACCA ATGCACTGAA CTCTTACCTA TTCTCAAAGA AAACTGTCAT 720
ATTAGCCTCC TCCCTCCCCG CAAGTGCTAC CTAAGAGGAG CCAGGGTAAG TGCTGCAAGG 780
CATGGCAGAC AAAATTGCAC ATCTTGGCCA GAATCTAAGG AACTTCTTGT GGTTTGGGGG 840
AGGTGGTGAG GATGTGGGTG GTGGGTGGGT GGGGGGTGTT GAAGAGATGC AGCCATGGAC 900
TTCCTTGGGC TTGGCACAGG CCAAAACAGA AGAGAGAACT CCAAACTCCA AGTAGTCCTC 960
ATCAGACTTG CTCTCCTTAT CAGCTTCATC CTGTCAGCCA AATTGTCAGC CATAGAAAAA 1020
CTGCTTTGCA GATGAAAAAC TATATAAATG CAGAGTATGG GAGTGCTCTG ACATCAACAG 1080
CTGTCATTTC ACTGACTGCC AAGGTTGACT TGTCTGATGT GGCTGGTTGT GCAGTAGCTC 1140
CACCCCTCGT CACCTTGGTT GTTCCTCCTG AAGTGAAAAA CAACTTTCCA AATAGAGGAG 1200
GGCTGCCCTT CGGTCAAGAC TTTAGGTAAG TATTCAAATT CGCATTCTTT TAATTTTTTT 1260
|
