| Tag | Content |
|---|
EnhancerAtlas ID | HS182-01899 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:212855400-212857830 |
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 | CTTTCTTGCT TTCTCAATTT CAGAAAGTAC TGCCTGGTGA ATTGAGCCTT CTCTGGGTTT 60
GTGACATTCT GGAAGGTACT TTTTGGTCTT GCCATTAGCC TGAAGGAAAG CCTAAGGAAG 120
CTCTGTGAAA GCTGAGGATG CTTGGAAAAT GGTCCTTTCT CTCAGGCTTC TGGGCAACAG 180
TAATGATTAC ACATTGTCCA AGAACCTGCC ACCCCCAAGT TCAAACAACA CAGGGGCCAA 240
TTCAGAGCAC AGCAGAAGCT TATATCCTAC ACAAGGCAAC CGAAAACTTA ACCCAGTTCC 300
AGATGAGTCT TGACTAAGAA ATGAATAGAT AAGTAGCAGG TTATTAAGGG AAATCAGGGA 360
AGTTCCAGAG CCCATCTCTG GCCTTTCAGG ATGGTGTGGT AGAATGCAAA CAATGGACTC 420
TCCCTTGCAC TTTCCCTCAG GGCTGTGGTT AGAATTCTGT GCTAGTAGCC TTCGTTCTGA 480
TCTGTGATGA TATTTCTGGT CTTCTCAAGA ATATCATACC AGAAAAAGGT GATGCTAGAA 540
CAGCCAAGAG AACAGGTGAG CTGTTTCAAG GGGCAGTTTG TCTTGAACAC AGCCTTGGAC 600
TTAGGGTTCA AGCCCTTCAA GCATACCACG CCAAGAGCAC TACCACTGCT AAATACAAAC 660
TTTTGGTGTG GGTCACGCTA ATGGTGATGA TGTCCGTGGT GGTGGTGTTG ACCACACCTA 720
TCTCCTTTGT CTCACAAAAA TAGGGTGGGA CGCTTTCATC AAGGTGGTCC ATTTCCAAAT 780
GGGCACTCCA GAAAAGTTCC CTTGACTCCA AGCATACAAC AGTTTCGAGA TTTGGGCCTT 840
GGTTGGCCAC ACCCCCAAAC CTCAAATTAT GCAGCATTAT GGGGGTGTGA GGGAACTTCC 900
CCCAGCACAC CCTCCTGTGG ATTCAGCAAA ACCGTCCCAG GAGAAGGGAT GATTTAGATT 960
CAGAGAACAA GGATCCCCAT TCCCTCCTTC CCTTTTCCAA CCCTCTTTCC TTCTCTTCCT 1020
CCTCTCCATT CTTGCTTTCT TTTTGCTCCC TGGCTCTCTT CTACAGGCCT CCTTCATGCA 1080
GCACGGATGA CCCTGCCAGG ACTTCCTGGA CCTCAAGGGA GGGAAGGTGT GTCACTGAGA 1140
GCTGGGGCCT CCCTTTTTTT TTTTTTTTTC TAGTTCTTGC TGGGGCAAAG CCCACAGCCC 1200
TGTGTCAGTA AATACCTCCC GGGTGGCGGA GACCCCAGCA TTGGTGGGAA AGAAGAGAGG 1260
GGCTTTTGGG ACTGTCGCTT TCCTGTCTGT TAAGAGTCAT CATTCTTTAC CAAGATTTGG 1320
GGTCAAAATT GGGTCCTGAT TACTGAATGG AAACCCCAAG GTTCAAGGCT GGCTGGTGCA 1380
ATACAGGGCG AGATTGCGGA CAGGAAGTGG TGTGGCTGTG TGGGTGTGAA GGAAGGACTT 1440
CCTCCCTCTC TGACACTTTC TATGCCGAGG GGGCCTTTCT CAGGCTGCCT TCCTTCCTTC 1500
AGCCCAGCAG GCAGCCGCTC TGAGACTTGA GATGCAGATG CCCAGCACAA GTCCTGGTGC 1560
CCAGCGGCAG TACGAATAGA ACCACGCAAA TCCAGTCCTC AGCACCTTGT GTACTACCCT 1620
AGTCCCTCCT GGAAGAATAC AGCACCTTCT CAGGCTTATA CTCTGCAGAA CTTTTACTTT 1680
TTCAGGTAGG AGTAGCCCAG GGGACATTTG TTTTTCAGGA CTCTGGTCCC ATCTCCAGTT 1740
ATCTCAGAGG GGACATGACC CTCAGCACCA TGGGCTGCCT TAGTTTTGCT TCCCTGCTTC 1800
CAAATATATT GCTTTCACAT TGAAAGTGGA GGCAGTCTTG ATCCTCCCAA AATTCAAGCT 1860
CAACCTCAAG CTCAACACAG CAGCTAGGGA GGAGGACGCC TGATTCAGTG GCTAATTTGA 1920
ATAAAGTTCT CAATCACAGA TAAAGCAATT GACAAATTGC AGCAAAGTAG CTGGATCTGG 1980
GAGATATTTA GGAGACATAA TGGACAGGAC TGGGTAGATT AGCTTGGGAA CACAGAGAAA 2040
TCAATAGGTT TCTAGCCAGG TGGGTGATGG ACCCTTGATT AAATAGGTAA AAACAGATTG 2100
AGAAGCATGT TTGAGGGGAA GATGACGAGA TCATGAGTGT ATCTTGCGCC ACGTTGAGTC 2160
GTTGAGTGGA ATGTGCTGGA AACATCCTCC GAGAGACACC TAACAGGCAG CTGGATGGAT 2220
CCACAGGGCT GCCCGCTGGA GAGAGGACTG GGCTCTGGGT ACAGATGGGA AAGTTACCAG 2280
CATAGAGACA GATGGTGGCT GAGAAGAAGC AGGTAGAGCA AAGAACAAAG GTAAAGGCCA 2340
TTTTCATAGG CTGTTGGGAA GTAAAGGAAA ATAAGACTTG AGATGTGACC ATTAGATTTA 2400
GTGACCAGAG CTTACTGGTA AACTCCAAGG 2430
|
