| Tag | Content |
|---|
EnhancerAtlas ID | HS103-04311 | Organism | Homo sapiens | Tissue/cell | HUES64 | Coordinate | chr11:69016730-69018590 | 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: 3 | ID | Chromosome | Start | End |
| GH11I069249 | chr11 | 69017341 | 69017450 | | GH11I069251 | chr11 | 69017600 | 69017750 | | GH11I069250 | chr11 | 69017861 | 69018010 |
| Enhancer Sequence | CCTGAATAAC GTGGGAGTCT TCTCTACAGA TCCTCCCAGG TGGTTCCACG GGGGAGCTGA 60
GTGGAGCTTC TGTGATCTAG TGACCTAGTC CCCAGCATGG AGTGCTCGGA AGTGCCCTCC 120
TTGAACATGT AAACATCCCA CCAAGTTGCC TCCCTTCTCT TGCTATTTTG ATGTAGCTTT 180
CTTTTCAATG GTCTTATTTC TGGGTCTAGC CCCCAGACAC ACTTTCCACC CCATGTCCTA 240
ACCTACACTC TGCAGCACAT CGCACCTGTG CAGGGTGATC GGTGATTGCA GGCCTGGGTC 300
CACGTCTCTG CTCTGCTTCT TGCTGGCCAC GAGGCTGCGT GCTCCTTACT GGCCCCTGCG 360
TGCTCATCTG TACAGTGTGC AGGAGCAGGA GCATCTGCCG GCAGACTTCT TGTGAGATTC 420
TAGTTCTGAG GCCTCCAGAC GGCGTGGGTG CACCGCCTGA GTCCTGCTGC ATTCTGTCTG 480
CTGCAGACCC AAGCCTGGTT CCTGCGTGGG GTCCCTCACG GGTGGTGTGT GTTTCACAGG 540
GCAGCAGGGA GCCAAGGGGC TGGGGCTGCC CGTGGGGAGT GTGTGAATCA AAGGAGCAGA 600
CCGCAGCTGG AGCCACCTCG CCTGGATTCC TGAACGCAGA CTCTTGACAG ACCGATTGTG 660
TAACGGCATT CCTCCCAAGG AAACACGCCT GCCCCCTCCA AGAAGGTGCG AGAGCTTCCC 720
AGACACAGAA AGGGCCCTGC TGGGTAAATC AGTTCTTCAT TATTCCGTTC CCGAGGCTCT 780
CCTATTGGCC AAGTGCCCGG CACCAGCAGA CGTCTGCCCG CACGGGGTCG GTCCGCATGG 840
GGTCGGTCCG CACGCAGCTG ACGCTGAGGC TCAGGTAGTC TCTTTGGTCC CACTAAGCGG 900
AGGATGCATT CAAAAGGATG CAAATTTCCA TCCATTTCCT GTCCCCCCTG CCTGGGATAA 960
GGGGCCTGTT GTGGCTGTGC AAGCTGGCTT TCTGGTATCT AAATACTTCT CTGGTGAGGA 1020
CACACCTGTT CACATCTGCC TGCACACCAC AGGCAAGCTG GCTTTCTGGT ATCTAAATAC 1080
TCCTCTGGTG AGGACACACC TGTTCATATC CTGCCTGCAC ACCACAGGCA AGCTGGCTTT 1140
CTGGTATCTA AATACTTCTC TGGTGAGGAC ACACCTGTTC ACGTCCTGCC TGCACACCAC 1200
AGGTGGGGTT TATTGTGTGG GGCTGGGATT TGGCCAGCCG ACTTCTGGAA CTCATTGTTT 1260
ATCTCTCCAT CACTGCAACA AATAACCCCC AGACCCGGAA ATGCCACCTT CGACTAAGGC 1320
CTCAGTGTGG GGTCATCAAA AATGGCAAGC TGGCCAGCCC CGAGGTGGGT GAGGACCAGT 1380
GCAGGCCTTG TCCTCTTGGA GTCAGGTAGG GCTGCTACTG GCAGGTGGCA TGAGGTCTCT 1440
ACCGCCTCCG AATGACCCCG CACCCCTTCT CCTTTCCTTT CTGCCCCTCC CTTTTTCATT 1500
CAGGATGGAG GCAGAAGAGG TGCTGAGTCT GGAACCCATG GCTGCTGCGG ACGAGGAGCT 1560
GGGTGATGCT TGCCTGGGCA CCGTATCGCT CTCATCCTGT TTTCTCGCCT GTGAAATGGG 1620
AATGGCGCTC ATGCTTCTCT GTGGGATGCT GGGAAAGGAA CATGAGGGCG TCCATGGAAG 1680
TGTTTGAGGC ATGCCTGCTC CAGGGGGAAG CTCCAGAAAT GACACCTATG ATCTCCCAGC 1740
TGTGTTCCCT TTAAGTTAAC AAACACTCGT CTGGTCTGGG GCTGGGGTAC AGCGATGAGG 1800
ATGACCTGGT CCGAGCCCCA GGAATGTGGG CCGTAGGAAG GGCATGGGCA TGAAAGACGT 1860
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