Tag | Content |
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EnhancerAtlas ID | HS182-22296 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr9:138818170-138819940 | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr9 | 138818727 | 138819161 | chr9 | 138819600 | 138819852 | chr9 | 138818447 | 138819258 | chr9 | 138819511 | 138819736 |
| | Number: 1 | ID | Chromosome | Start | End |
GH09I135926 | chr9 | 138818159 | 138819543 |
| Enhancer Sequence | CAGGAGAATG GCATGAACCC AGGAGGCGGA GGTTGCAATG AGCCGAGATC TTGCCACTGC 60 ACTCCAGCCC GGGCGACAGA GACTCCGCCT CAAAGAAAAA AAACAAGGAG AGCCCTGCAG 120 GCCCCTCCTT AGGCTGGCCT CAGAGGTCTT CAGTGGCCAG AGGGTGTGAG GATCTGCGGG 180 ACGTGCCGAC TGGGGCAGCC CCCACCACAC CCTGGGATGC ACCCTGGCTG GGACCAGTCT 240 CCAAATTCCC CTGCATCCGT CTCAGGCTGG AAAACTCTCC AACAAAGTTG CCTCCAGTCA 300 CTGGATGGGA AGCGGCCTCT CAGCTGAGCC GGACCCTCTC TCCTTCAGCT GGTGCTGCAG 360 TGACTCCAAG TGACCAGTGA CACCAGGTGT GGCAGCTGCG CACAGCCTTT ATCGTGCCGC 420 ACTCAAGGGC CCCGGGAAGG GAACCCAGGC AGGGCCCAGT GCCATGGTGG TCTCCACTTC 480 GCCGTGGAGA GAACGGCCAG GTGACCCAAC CACAGCGAGG CCTTCAGTGT GTTCCTCACT 540 TCCACCTGTG GCGGTCGCTT CTGGCTGTCA CCCTGAGCAC ATCCATGTGG CCTCTTGGAG 600 TGGCCTCTCC ACGTGGCCTA GGCTTCCTGG CAACGCAGCC GCCTCAGGGC AGTGTGACTT 660 CCTGATGGTG GTGACTCAGG ACAACAAAAG CGAGAGGCCC TGAGAGTCAG GCGGGCACCA 720 CAGGGCCTTG CTGAGGCAGC CGGGGACTCC CGCTCCCTCT GCTGACACCA TTGGTGGCCA 780 GTGAGTCAGA GGCAGAGGTG CCAGAGACCC CGCCCGAAGG GAGGAGATCT GAGAGCCTGC 840 AGCCACAGGC TCCTCCAGGA CTCGAGCACC GGGGCCGCAC AGAGAGCCCT TTCTCTCCTG 900 GGCAGGCCAG GCGGGGATCC CCCAGCGCCC TAACCTGCTC TGTGACCACG GCAATGTGGC 960 CTTGGGGATG TGCCCTGCCT CTCTGGGTTC CAGTGCAGGA CTCAGGGCTG GCCACCTGAG 1020 AAGCATCTCT AGGACATTCC AAAGCCTGGA ACAGGGACAG CATTGTGGCC CTGCTCTGGA 1080 AGGCTGCGTG GAAGCCAAGA AGTTGTCCTG GCCTGTCCTG GAGGTGCCTT TGCCCTTGCT 1140 TCCTGTCCTT GTCCCCAGGG GCTGCACCCA TCCTACTGAC TCTGCCAGCA GTGCCAGCCT 1200 GGTCCCAGGC ACCCTGGAGC TGCTCCATCC CCATTGGGGG CCAAGAGCTG CCGGCCCACA 1260 CCAGAGGCCC CGGCCACACA GGAGCCACGG GACAGCCGGA AGGGAAGCCA GGAGGCCTTG 1320 CTTGGGGAGC TGGGCACACG CCTGGCCTCC CCGTGATGCT CCCCTGGACG ACACACGCAC 1380 GCACACATGC ACGCCTGTGC ATGCACACAG AGCACACATG CACACACACG CACACCTGTG 1440 CATGCAGAGC ACACGCACAC ACACACAAAC CTGTGCATGC ACACAGCATA CACGCATGCA 1500 CGCCTATGCA TGCAGAGCAC ACATGCACAC ACATGCACGC CTGTGCATGC ACACAGCACA 1560 CATGCACACA CCTGTGCATG CACACACACA CATACATGCC TCTGCATGCA CACAGCACAC 1620 ACGCACACCT GTGCACGCAG AGCACACACG CACACACACG CACGCCTCTG CATGCAGAGA 1680 GCACACACAC ACACATGCAC GCCTGTGCAT GCACACAGAG CACACACGCA CACCACACCA 1740 CCACACACAC ACTTCAAAAA CCACACACGG 1770
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