| Tag | Content |
|---|
EnhancerAtlas ID | HS060-09119 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr13:24422260-24423470 | 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 |
| GH13I023848 | chr13 | 24422301 | 24423629 |
| Enhancer Sequence | CAGTTTCCTC ACCAGTAAAG TAGAAATACT TTCCAGGCTC CATTAACAAT TACAGAAACA 60
CATGCAATGA ACCTGGCATG GTTCCTGGAG AAAAGCAGGC ACACTGTAAA TTATAGCCAC 120
TATTATTGCT GTTAGACAGA GACACGGACA GGGACAAGAC TAAACCCAGC GGTTTCTACT 180
TCTATTCCAG TTCCCTTCTT CTACTCCTAT TCCAGTTCCC TTCTATTCCC CAAAGCTGAC 240
CTTACCTCTA AAAAGAAATG CAACACTGTG TCAAGAAGCT GTGTAGATGC AGTAAACTTT 300
CATTAATCAC CTGCCATGTG CCTGCATGAC AACTCCTCAG TGTGGAAAGA TGAACACATT 360
GTAACAATAA TGACGACCAA TCCAAATGAT CAGGGGCAGA GGAGCACTGC AAACAAGGCA 420
TTGGCTCAAA GATGAGGCTG TGGTCAGTTA CACCTGGCAG AGGGGAGAAG CTGGGAATGG 480
GAGGAACAGA GAGAACTACA AAGAAGAGGC AGCATCTGGA GCACACCTGG AAAGATGAGG 540
CTCCTAGAAG AGGGGGAGGG CACTCAAAGG GGAAGAAAGA GGGCAGCAAA GGCCCAAGGG 600
GATTCAAGCA AATGGGGCAG ACAAGCTCAA GCAAGCACTA GTGCCTTAGT CCTCACTCAG 660
CTGCCTCAGC CATCCAGAGC GAGACTACAT GCCTCTCCAC ACCCTCAGTG ACTCTCACCA 720
AATGCAGGCT ACTTCCTTCC TGAAGAAAAG CCAGAAGGAG AGAGGTCCAG AGAGGGTGGA 780
AGAGATTCAA AAAGCTACAG GGTGTTTCCC GCAGCTCCAA CCCACATCTG AGGGGCCCCA 840
AGGAGCAGTC CCACATGACC AGCCAGTCAG GAGGGCGTGA CTGCTGTGCT CTCAGCTCAC 900
GTCTTCAACA CGGAGTGAAA AAACATGCAC AGAGGGTGTT TGGGTGGTCA CAGGCCCCAG 960
TACAGCCCTC CACGCCAGGC TCATCATGTG GCTCCGCCTG CCTCCACAGA GCACTCCGAG 1020
GCTGAGGCCG ACCTGTGAAC AACCAACTGC ACCATCTCCA TCCACAGCTT CCTTATCTGC 1080
ATAGATGCTA CACATAAGAA CATTTTCCTC TCTCATCTAG AGACCCAAGA CAGTGGGAAA 1140
GCACCATGGG CAGCATATAG GACCTCACAG CACAGCAGAG CCACAACCAG CAGAGACAGA 1200
GCTTAGATGC 1210
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