| Tag | Content |
|---|
EnhancerAtlas ID | HS108-06955 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr11:11010760-11012980 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| | | 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 |
| GH11I010990 | chr11 | 11011801 | 11011950 |
| Enhancer Sequence | TATCTTCAGG GATGGAGCGG GAAAGGGGTA CTAGGTGCCC TGTGGTCTTC AGGATGAGCT 60
AAGTCATGGT TCACAGGGGA GAGGTGAGGC TGTGATGCCA GTGAGTCCTT GCACAGGCAA 120
AGTCTCCAGG GTTGGAGAAT TGCAGGGGAC GGGGGTGGCA GATACTGAGT TCAGAAAGGG 180
AGCAAGTTCG TGATAAGAAA GGCTAGTTAT GGGCTAAAAC AGCCACTGTG GGCCGGCGGG 240
GAGCTGGTGT AGGGGTGAGT AGCCTGCATC ACTGAAAGAG AGTGAAGTGT CTACTCCACC 300
ATCCTGCAAC CAGTCCAAGG CACAGGCTTC ATACCCCTGC AGCTTCTGCC TCTGAGTTTT 360
CTGGTACCTG GGCCAATCAA GTAGCTCTGT TCTCCCATCT TCACTCCATC ATGTCCGCAC 420
TGGGTGCTGA TGTCCAGCAG TGGGAGGTTT GTGTGTGTGT ATGCATGCAT GTGTGTGAGG 480
TGCTTCAGAG TATGACGAAT TAAGAGAAAT GTAAGCCAAG ACAGGAGATG GGGCTGCTGG 540
TATTTGATGT CCCACTTTTA CCTGATAGCA AGTTGGTGTT TGTTTCTGAG CCCAGGCTCT 600
GAGCTTTGCT TCTTCACAGC CAAGCAGGGA GAGCAATGGA CGAGGAGACA AGACATGGGA 660
GACCTTGTCT TTGGTCTGCC TCTCACCAAG TGATAAGGGA GTTTAAAGTG TAAAGACAGG 720
CTCCCACACA TTAGCAAAAA GAGGTTCTCT CTCTTTCATC TTGGGGCAGG AGGAAAAGGG 780
GACCTGCTTC CTGAGTCTGT ACCTGCTGAG TATTATGGTG GCCACTGTAC ACACTGACTA 840
TGCCCTTGCA ATTTAGTTAG TCTTTCTTAA GTATCAAAAG TCACCTTTTA TTCAAGAATT 900
TGTATATACA CCAAAAAGAT TAGCAAAGAA GTAAGCTTAT CATATTTCAC TTACTCAACA 960
GTTAATCTAG TTGTAATTGT ATTTAACATC AGCCATAAAC AATATGAGGC ACCATTTCAG 1020
AACGGGCGGT GTGCTGACTG ACAACCCTGC CTTCCTGGGG TAGCACTGAC CTCAAGACAG 1080
AAGCAACTTA ATCACCATTC AGTTCCCTGC CATCTGCTTT GTCCTGATTC TGCATATTCT 1140
GCTGAATCAT TTCTGCTTCC CATGTTGGCC CACAACCTGT ACAGCCCCAC GCTGGTCATT 1200
TCCTTGTTCA GAGTGAACAC TTCACTCTCC CCAAACTCTC AGGCATTCCT GCTTTAGGGG 1260
ATCAAAATTT AGTCTTCAAG TTAATGGAGT TTTCATTCGT GTGTTTCTAG CTATTTCTAA 1320
TCCTATGTGC TACTGCACAG ATTGATGTAA TGGAGAAAGA TTGAAGGTAT GCTGTTCTCT 1380
TATATGAAAT GACAATGGCT ACTATAAAAC ACAATGTCAG CTCAGTTCTC ACTTGGGCTC 1440
CCAGAGCCAA GCCCAATAGG CCAGGCACCA GGATCGACAG TGGTCAGTTT CCAGACCTCA 1500
CTTCATCTTA CTGTTTTGCC AGGGTGCAAT TCTGGCAAAT TCCTATTCCT CCAGGGCCTG 1560
AGTGGATGGG AGGGCTAATA TTATGAGTCA ACTTGACTGG GCCGCATGGT GCTCAGATAT 1620
TTGGTTAAAC ATTATTTCTG GGTGTGTCTG TGAGATGTTT CTGGATGAGG TTAACATTTG 1680
ATTTGGAAGA CTGAGTAAAG CAGATTGCCC TCCCCAGTGT GGGTGAGCCT CATGCAATCT 1740
ATTGAAGGCC TAAAGAGGAA AAAAGGCTGA GTAAGAAAGA ATTCTTTCTC TCCCTCTGAC 1800
TGTCTTTGAG CTGGGACATC AGTCTTCTGC CTTTGGACTT GGACTCAGAC GGATTTATAC 1860
CATTGGCTCT TCTAGTTCTC AGGCCTTTGC ACTCAGACTG GAACTACACC ATTGGCTCTT 1920
CTAGGTCTTT ATCTTGCTGG CTACAGATCT TGGACCTCCC AGCCTCCACA CTTGTGTGAG 1980
CTAATTCCTG ATAGTAAATC TCTTTATTAT TTATCTATAT ATCTGTATCT ATCTACCTAT 2040
TCTATTGGTA CTGCTTCTCT GGAGAACCCA GACTAATACA GTAGGGCAAA GTCAATTGGG 2100
CAGGGCTGGG CAGGCAGACA CTCCAATTTG TGTCTCTCCT CCTTTAGACA TACAGACCAA 2160
AGGTGGGTAT TGATCAGAGG GTCCTCTGAT ATTGATCTAG CTTGATCATT TTATTTTTTA 2220
|
| |
|
|
|
