| Tag | Content |
|---|
EnhancerAtlas ID | HS060-19556 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:75658100-75659440 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr2:75658677-75658697 | TGGTTGGGGTGGGGGTGGGG | - | 6.16 | | RREB1 | MA0073.1 | chr2:75658682-75658702 | GGGGTGGGGGTGGGGGGGTT | - | 6.29 |
|
| | 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 |
| GH02I075427 | chr2 | 75655008 | 75659421 |
|
Enhancer Sequence | ACCCCTATCT CCCTTCTCTG ACTCTCTTTT TGGACTCAGC CCGCCTGCAC CCAGCTGGAA 60
TAAACAGCCT TGTTGCTCAC ACAAAGCCTG TGGTGGTCTC TTCACATGGA CGCTGTGTAA 120
GTTGGGGTGC AGCTTGGTTT TATACATGTT AGGGAGACAT GAGACTTCAA TCAAATACAT 180
TTAAGAAATA CATGAGTCCA GTTCAGAAAG GCAGGACAAT TTGAAGTGGG GGGCTGGGGG 240
GAGCTTCCAG ATTATAGGTG ATTTTTAAAT TTTCTGGTTG CCAAATGGTT GAGTTTATAT 300
AAAGACCTGG GATCAATAGA AAGAAAATAG ATAATGTCTG GGTTAAGATA AAGGATTGTG 360
GAGACTAAAG TTCTTAGTGT GCAGAGAAAG TCTTCAGGTA GCAGGCTTCA GAGAGAATAG 420
ATTGTAAATA CTTCTTATCA GACTTAAGGT CTGTGTTGAT GTTAATGCCA GAGAGGCGTA 480
ATGAGGCATG TCTGAGCCCC ACTTCCTGCA ATGGCCTGAA CCAATCTTTC AGGTTAAATT 540
TTAAGAGTGT CCTGGCTGAG GAGGAAGTCC ATTCAGATGG TTGGGGTGGG GGTGGGGGGG 600
TTAGAATTTT ATTTTTGTTT TACAAGGACT TAGGTGTTTT TGGGGAACAT AATTCAGCCT 660
ACCATATCAT GCAAGAGAAT TTAAACTGTA CTGTGTCAGC CAGGGGTTAA AATCTTAATG 720
CCTACCAGGG CTAGGCAGGT AAAGAAGCAT CTTAGTCCAT TTTGTCCTGC TATAAAAGAA 780
TACTTGAGGC TGGGCAATTT ATAAAGAAAA AAGATTTATT TGGCTCACAA TTCTGGAGTG 840
CTGAAAAGTT CAGGATTGGG CATTTGCATC TGGCAAAAGC CTCGGGCTGC TTTCACTCAT 900
GGCAGAAGGC AAAGGGGAGC CAATGTGTAC AGAGATCACC TGGTAAGAGA GGAAGTGAGA 960
GAAGGAAACT CTAGGTTCTT TTTTAATAAC CAGCTCTCAT GGGAACTAAT AGTATGAGAA 1020
CTCATTCATC TCAACCCCTC CCCAGAGAAA GGATTAATCT ATTCATGAGG GATCCACCCC 1080
CAGTGACACA AATACCTCCC AGTAGTTTCC ACCTCCAACA CTGGGATCAA ACTTCAATGT 1140
AAGATTTGGT GGGACAAACC AACCATATAC AAACTCTAAC AGAAGTAAAT AAAGCAGTCT 1200
GGTTATTAGC CAACAGGAAA AAGTGAAGAA AGTGAAAACT CAGAGAGTAC TATCTAAAGT 1260
GAGTTCTGAG TGTTATCAAA ATAAATGCAA ACCAGTGTTG CCTGATTACC TGATTCTTTT 1320
GGAGAAGCTA AGATCCAGAT 1340
|
