| Tag | Content |
|---|
EnhancerAtlas ID | HS165-01331 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr1:212855440-212857660 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:212856887-212856905 | CCTTCCTTCCTTCAGCCC | - | 6.57 | | EWSR1-FLI1 | MA0149.1 | chr1:212856883-212856901 | GCTGCCTTCCTTCCTTCA | - | 7.33 | | ZNF263 | MA0528.1 | chr1:212856401-212856422 | CCTCTTTCCTTCTCTTCCTCC | - | 6.82 | | ZNF263 | MA0528.1 | chr1:212856404-212856425 | CTTTCCTTCTCTTCCTCCTCT | - | 8.06 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 212856204 | 212856981 | | chr1 | 212856011 | 212856573 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I212682 | chr1 | 212855380 | 212855525 | | GH01I212683 | chr1 | 212855710 | 212857342 |
|
Enhancer Sequence | ATTGAGCCTT CTCTGGGTTT GTGACATTCT GGAAGGTACT TTTTGGTCTT GCCATTAGCC 60
TGAAGGAAAG CCTAAGGAAG CTCTGTGAAA GCTGAGGATG CTTGGAAAAT GGTCCTTTCT 120
CTCAGGCTTC TGGGCAACAG TAATGATTAC ACATTGTCCA AGAACCTGCC ACCCCCAAGT 180
TCAAACAACA CAGGGGCCAA TTCAGAGCAC AGCAGAAGCT TATATCCTAC ACAAGGCAAC 240
CGAAAACTTA ACCCAGTTCC AGATGAGTCT TGACTAAGAA ATGAATAGAT AAGTAGCAGG 300
TTATTAAGGG AAATCAGGGA AGTTCCAGAG CCCATCTCTG GCCTTTCAGG ATGGTGTGGT 360
AGAATGCAAA CAATGGACTC TCCCTTGCAC TTTCCCTCAG GGCTGTGGTT AGAATTCTGT 420
GCTAGTAGCC TTCGTTCTGA TCTGTGATGA TATTTCTGGT CTTCTCAAGA ATATCATACC 480
AGAAAAAGGT GATGCTAGAA CAGCCAAGAG AACAGGTGAG CTGTTTCAAG GGGCAGTTTG 540
TCTTGAACAC AGCCTTGGAC TTAGGGTTCA AGCCCTTCAA GCATACCACG CCAAGAGCAC 600
TACCACTGCT AAATACAAAC TTTTGGTGTG GGTCACGCTA ATGGTGATGA TGTCCGTGGT 660
GGTGGTGTTG ACCACACCTA TCTCCTTTGT CTCACAAAAA TAGGGTGGGA CGCTTTCATC 720
AAGGTGGTCC ATTTCCAAAT GGGCACTCCA GAAAAGTTCC CTTGACTCCA AGCATACAAC 780
AGTTTCGAGA TTTGGGCCTT GGTTGGCCAC ACCCCCAAAC CTCAAATTAT GCAGCATTAT 840
GGGGGTGTGA GGGAACTTCC CCCAGCACAC CCTCCTGTGG ATTCAGCAAA ACCGTCCCAG 900
GAGAAGGGAT GATTTAGATT CAGAGAACAA GGATCCCCAT TCCCTCCTTC CCTTTTCCAA 960
CCCTCTTTCC TTCTCTTCCT CCTCTCCATT CTTGCTTTCT TTTTGCTCCC TGGCTCTCTT 1020
CTACAGGCCT CCTTCATGCA GCACGGATGA CCCTGCCAGG ACTTCCTGGA CCTCAAGGGA 1080
GGGAAGGTGT GTCACTGAGA GCTGGGGCCT CCCTTTTTTT TTTTTTTTTC TAGTTCTTGC 1140
TGGGGCAAAG CCCACAGCCC TGTGTCAGTA AATACCTCCC GGGTGGCGGA GACCCCAGCA 1200
TTGGTGGGAA AGAAGAGAGG GGCTTTTGGG ACTGTCGCTT TCCTGTCTGT TAAGAGTCAT 1260
CATTCTTTAC CAAGATTTGG GGTCAAAATT GGGTCCTGAT TACTGAATGG AAACCCCAAG 1320
GTTCAAGGCT GGCTGGTGCA ATACAGGGCG AGATTGCGGA CAGGAAGTGG TGTGGCTGTG 1380
TGGGTGTGAA GGAAGGACTT CCTCCCTCTC TGACACTTTC TATGCCGAGG GGGCCTTTCT 1440
CAGGCTGCCT TCCTTCCTTC AGCCCAGCAG GCAGCCGCTC TGAGACTTGA GATGCAGATG 1500
CCCAGCACAA GTCCTGGTGC CCAGCGGCAG TACGAATAGA ACCACGCAAA TCCAGTCCTC 1560
AGCACCTTGT GTACTACCCT AGTCCCTCCT GGAAGAATAC AGCACCTTCT CAGGCTTATA 1620
CTCTGCAGAA CTTTTACTTT TTCAGGTAGG AGTAGCCCAG GGGACATTTG TTTTTCAGGA 1680
CTCTGGTCCC ATCTCCAGTT ATCTCAGAGG GGACATGACC CTCAGCACCA TGGGCTGCCT 1740
TAGTTTTGCT TCCCTGCTTC CAAATATATT GCTTTCACAT TGAAAGTGGA GGCAGTCTTG 1800
ATCCTCCCAA AATTCAAGCT CAACCTCAAG CTCAACACAG CAGCTAGGGA GGAGGACGCC 1860
TGATTCAGTG GCTAATTTGA ATAAAGTTCT CAATCACAGA TAAAGCAATT GACAAATTGC 1920
AGCAAAGTAG CTGGATCTGG GAGATATTTA GGAGACATAA TGGACAGGAC TGGGTAGATT 1980
AGCTTGGGAA CACAGAGAAA TCAATAGGTT TCTAGCCAGG TGGGTGATGG ACCCTTGATT 2040
AAATAGGTAA AAACAGATTG AGAAGCATGT TTGAGGGGAA GATGACGAGA TCATGAGTGT 2100
ATCTTGCGCC ACGTTGAGTC GTTGAGTGGA ATGTGCTGGA AACATCCTCC GAGAGACACC 2160
TAACAGGCAG CTGGATGGAT CCACAGGGCT GCCCGCTGGA GAGAGGACTG GGCTCTGGGT 2220
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