| Tag | Content |
|---|
EnhancerAtlas ID | HS113-09588 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr12:121352150-121353560 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27043 | chr12:121352024-121353293 | Esophagus |
|
| | 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 |
| GH12I120914 | chr12 | 121352192 | 121353043 |
|
Enhancer Sequence | GAGCAAGACT CTGTCTCAAA AAAAAAAAAA AAAAAAAAAA AAGGGACGCA ACCACGGCGG 60
AAGAACAACT GCCAGTCTAA CTGTGCGTGA AGGCTGGCAG TGATGGGGCC GAGACTGGGA 120
ACCGCCCCTT CTCCCTGAGA CTGTTCATAG TGCTGTGGGT CACAGGAGTC ACCTTCAACG 180
TTACCACCAT TGACACCAAG AGACAGACTG AGAGAGTGCA GAAGCTGTGC CCAGGAGGGC 240
AGCTCCCATT CCTGCTGCAT GGCACTGAAG TGCACACAGA CACCAACAAG ATGGTGGAAT 300
TTCTGGAGGC AGTACTGTGC CCTCCGAGAT ACCCCAAGCT GGCAGCTCTG AACCCTGAGT 360
CCAACACAGC TGGGCTGGAC ATATTTGCCA AATTTTCTGC CTACATCAAG AATTCAAACC 420
CAGCACTCAA TGATAATCTG CAGAAGGGAC TCCTGGAAGC CCTGAAGGTT TTAGACAATT 480
ACTTAACATC CCCCCTCCCA AAAGAAGTAG ATGAAACCAG TGCTGAAGAT GAGGGCATCT 540
CGCAGAGGAA GTTTCTGAAT GGCAATGAGC TCACCCTGGC TGACTGCAAC CTGTTGCCAA 600
AGCTACACAT AGTACAGGTG GTGTGTAAGA AGTACCGGGG ATTTAACATC CCTGAGGCCT 660
TCCCGGGAAC GCGTCAGCAC TTGAGCAATG CTTATGCATG GGAAGAACCC GTCTCCACCT 720
GCCCAGATGA TGAAGAGATC CAGCTCGCCT ATGAGCAAGG GGCCAATGCC CTCAAATAAG 780
CCCCTCCTGG GACTCCCTCA ACCCCCTCCA TTTTCTCCAC AAAAGCCCTG GTGGTTTCCA 840
TATTGCAACC CAATGGACAC ACTCCAAAAT GGCCAGTGGA CAGGGAATCC TGGAAGACTT 900
GTTCTGGGAT GGTGTGGGGA AGAGGGGATG AGGGAAATAA ATGGGGGGCT GGGTGAGATT 960
TTTATTGTGG GGTGGGATGG GCAGGACAAC ATATTTCAGT AATAAAATAG AGAAAAAAAT 1020
GAAAAAATAA ATAAACAGCC GCATCTGTTA AAGAAATAAA GAAAAAATGT AAATACAATT 1080
TAAAAATATT TACTCACCTG TTTACCATCT CAAGAATTTT TTATTCCTTT CTATAGATCT 1140
GAGTTTTTTT TTTTTTTTTT TTTTTAGATG GAGTCTTGCT CTGTCACCCA GGCTGGAGTG 1200
CAGGGGCACC ATCTCGGCTC ACTGCAAGCT CCAACTCTTG GGTTCACACC ATTCTCTCGC 1260
CTCAGCCTCC TGAGTAGCTG GGATTACAGG CATGCGCCAC CAGGCCCGGC TAATTTTTTA 1320
TATTTTTAGT AGAGACGGGG TTTCACTGTG TTAGCCAGGA TGGTCTCGAT CTCCTGACCT 1380
CGTGATCCGC CTGCCTCAGC CTCCCAAAGT 1410
|
