| Tag | Content |
|---|
EnhancerAtlas ID | HS056-01297 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr1:212855320-212857800 |
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: 3 | Chromosome | Start | End |
| chr1 | 212855380 | 212855525 | | chr1 | 212856204 | 212856981 | | chr1 | 212856011 | 212856573 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I212682 | chr1 | 212855380 | 212855525 | | GH01I212683 | chr1 | 212855710 | 212857342 |
|
Enhancer Sequence | AAAGAACTTC TGGGAGGTAC TTTCATTTAT TCTTTCCACT CTCAGCCTCA GGTTGTTGTC 60
CGCCACTGGT GTTTCTCAAA CTTTCTTGCT TTCTCAATTT CAGAAAGTAC TGCCTGGTGA 120
ATTGAGCCTT CTCTGGGTTT GTGACATTCT GGAAGGTACT TTTTGGTCTT GCCATTAGCC 180
TGAAGGAAAG CCTAAGGAAG CTCTGTGAAA GCTGAGGATG CTTGGAAAAT GGTCCTTTCT 240
CTCAGGCTTC TGGGCAACAG TAATGATTAC ACATTGTCCA AGAACCTGCC ACCCCCAAGT 300
TCAAACAACA CAGGGGCCAA TTCAGAGCAC AGCAGAAGCT TATATCCTAC ACAAGGCAAC 360
CGAAAACTTA ACCCAGTTCC AGATGAGTCT TGACTAAGAA ATGAATAGAT AAGTAGCAGG 420
TTATTAAGGG AAATCAGGGA AGTTCCAGAG CCCATCTCTG GCCTTTCAGG ATGGTGTGGT 480
AGAATGCAAA CAATGGACTC TCCCTTGCAC TTTCCCTCAG GGCTGTGGTT AGAATTCTGT 540
GCTAGTAGCC TTCGTTCTGA TCTGTGATGA TATTTCTGGT CTTCTCAAGA ATATCATACC 600
AGAAAAAGGT GATGCTAGAA CAGCCAAGAG AACAGGTGAG CTGTTTCAAG GGGCAGTTTG 660
TCTTGAACAC AGCCTTGGAC TTAGGGTTCA AGCCCTTCAA GCATACCACG CCAAGAGCAC 720
TACCACTGCT AAATACAAAC TTTTGGTGTG GGTCACGCTA ATGGTGATGA TGTCCGTGGT 780
GGTGGTGTTG ACCACACCTA TCTCCTTTGT CTCACAAAAA TAGGGTGGGA CGCTTTCATC 840
AAGGTGGTCC ATTTCCAAAT GGGCACTCCA GAAAAGTTCC CTTGACTCCA AGCATACAAC 900
AGTTTCGAGA TTTGGGCCTT GGTTGGCCAC ACCCCCAAAC CTCAAATTAT GCAGCATTAT 960
GGGGGTGTGA GGGAACTTCC CCCAGCACAC CCTCCTGTGG ATTCAGCAAA ACCGTCCCAG 1020
GAGAAGGGAT GATTTAGATT CAGAGAACAA GGATCCCCAT TCCCTCCTTC CCTTTTCCAA 1080
CCCTCTTTCC TTCTCTTCCT CCTCTCCATT CTTGCTTTCT TTTTGCTCCC TGGCTCTCTT 1140
CTACAGGCCT CCTTCATGCA GCACGGATGA CCCTGCCAGG ACTTCCTGGA CCTCAAGGGA 1200
GGGAAGGTGT GTCACTGAGA GCTGGGGCCT CCCTTTTTTT TTTTTTTTTC TAGTTCTTGC 1260
TGGGGCAAAG CCCACAGCCC TGTGTCAGTA AATACCTCCC GGGTGGCGGA GACCCCAGCA 1320
TTGGTGGGAA AGAAGAGAGG GGCTTTTGGG ACTGTCGCTT TCCTGTCTGT TAAGAGTCAT 1380
CATTCTTTAC CAAGATTTGG GGTCAAAATT GGGTCCTGAT TACTGAATGG AAACCCCAAG 1440
GTTCAAGGCT GGCTGGTGCA ATACAGGGCG AGATTGCGGA CAGGAAGTGG TGTGGCTGTG 1500
TGGGTGTGAA GGAAGGACTT CCTCCCTCTC TGACACTTTC TATGCCGAGG GGGCCTTTCT 1560
CAGGCTGCCT TCCTTCCTTC AGCCCAGCAG GCAGCCGCTC TGAGACTTGA GATGCAGATG 1620
CCCAGCACAA GTCCTGGTGC CCAGCGGCAG TACGAATAGA ACCACGCAAA TCCAGTCCTC 1680
AGCACCTTGT GTACTACCCT AGTCCCTCCT GGAAGAATAC AGCACCTTCT CAGGCTTATA 1740
CTCTGCAGAA CTTTTACTTT TTCAGGTAGG AGTAGCCCAG GGGACATTTG TTTTTCAGGA 1800
CTCTGGTCCC ATCTCCAGTT ATCTCAGAGG GGACATGACC CTCAGCACCA TGGGCTGCCT 1860
TAGTTTTGCT TCCCTGCTTC CAAATATATT GCTTTCACAT TGAAAGTGGA GGCAGTCTTG 1920
ATCCTCCCAA AATTCAAGCT CAACCTCAAG CTCAACACAG CAGCTAGGGA GGAGGACGCC 1980
TGATTCAGTG GCTAATTTGA ATAAAGTTCT CAATCACAGA TAAAGCAATT GACAAATTGC 2040
AGCAAAGTAG CTGGATCTGG GAGATATTTA GGAGACATAA TGGACAGGAC TGGGTAGATT 2100
AGCTTGGGAA CACAGAGAAA TCAATAGGTT TCTAGCCAGG TGGGTGATGG ACCCTTGATT 2160
AAATAGGTAA AAACAGATTG AGAAGCATGT TTGAGGGGAA GATGACGAGA TCATGAGTGT 2220
ATCTTGCGCC ACGTTGAGTC GTTGAGTGGA ATGTGCTGGA AACATCCTCC GAGAGACACC 2280
TAACAGGCAG CTGGATGGAT CCACAGGGCT GCCCGCTGGA GAGAGGACTG GGCTCTGGGT 2340
ACAGATGGGA AAGTTACCAG CATAGAGACA GATGGTGGCT GAGAAGAAGC AGGTAGAGCA 2400
AAGAACAAAG GTAAAGGCCA TTTTCATAGG CTGTTGGGAA GTAAAGGAAA ATAAGACTTG 2460
AGATGTGACC ATTAGATTTA 2480
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