| Tag | Content |
|---|
EnhancerAtlas ID | HS047-31025 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr7:73022000-73024370 | 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 |
| GH07I073606 | chr7 | 73021044 | 73022121 |
| Enhancer Sequence | ATCTGAGAGA AGGGGGCCAG GTCAGGGGCA CCCAGCTTCC TCATCCCCCA CCTCACCCCA 60
GGGGACTGGG ACTCAAGTGA CACCCTGCGA AATCCTGCTT GGCCTTTGAC GTTCAGATTA 120
AGTGCCCATG CTGCCTCCTC CAGGAAGTCT TCTCGGATGA TGCTCTAGCC TCCTAGATCT 180
TCCTTTTTTT TTTTTTTTTT TTGGAGATAG GGTTTCACTC TTGTTGCCCA GGCTGGAGTG 240
CAATGGCGTG ATCTTGGCTC ACTGCAACCT CCACCTCCTG GGTTCAAGCG ATTCTCCTGC 300
CTCAGCCTCC TGAGTAGCTG GGATTACAGG CGCCCACGAC CAGGCCCAGC TAATTTTTGT 360
GTTTTTAGTA GAGACGGGGT TTCACCATGT TGGCCAGGCT GGTCTCGAAC TGCTGACCTC 420
AGGTGATCCA CCTGCCTCGG GCTTCCAAAG TGCTGGGATT ACAGGCTTGA GCCACCTCAC 480
CCAGCCTGAT CTTCCTCTAC AGGGCACTGT GAATCCAACC TCCCACACCT TCTCTGGGTT 540
CCTCTGGAGC CCCATAGGTA CACTTGCAAA GACTGCTGAA TGGATTGTGG GGCCATAGGC 600
CACAGAGAGT GAGCTGCCTC CAGAAAGTCC TGGTTAGGGC TGGGTGCGGT GGCTCACACC 660
TGTAATCCCA GCACTTTGGG AGGCCTAGGT GGGTGAATAA CGAGGCCAGG AGATCAAGAC 720
CAGCCTGCCA ACATGGTGAA ACCCCGTCTC CACTAAAAAT ACAAAAATTA GCCGAGCATG 780
GCGGCACATG CCTATAGTCC CAGCTCCTTG GGAGGCTGAG GCAGGAGAAT CGCTTGAACC 840
TGGGAGGTGG AGGTTGCAGT GAGATCACGC CACTGCATTC CAGCCTGGTG ACAGAGCAAG 900
AATCCATCTC AAAGAAAAAA AAAAAAGAAA AAAAGAAAGT CCTGGTTAGA CTGGCAGGCC 960
AGGGGCCTAG AGCCTTGGGT CCTCTGCCTC AGAAGGCTAG GCACTACCCA CTTTCATTGC 1020
AGAGAACCAC CCTTGGTTCA CTTCTGACCA CCAACATGTG TCCTCTTCCA GGCCTCCACC 1080
TCCCCTCCCA GTCTCTAATT CTGACCTCTC CCCAGGCTCT TGCCCTTGGC CCCAACACAC 1140
ACTCCAGGCT CTTTTTTGTT TTTGTTGTTG TTTTGAAACA GGTTCTTGCT CTGTTGCCCA 1200
GGCCAGAGTG CAGTGGCGCA ATCATAGCTC ACTGAAGCCT TGACCTCCTG GGCTCAAGCG 1260
ATCCTCCCGC CTCAGCCTCT GGTGTACGCC ACCATGTCTG GCTAATTTTT AAATTTTTTG 1320
TAGAGACAGG GTCTCCCTGT GTTGCCCAGG CTGGTCTCGA ACTCCTGAGG TCAAGGAATC 1380
CTCTTGTCTT GGCCTCCCAA GGTGTTGGGA TTACAGGCGT GAGCCACTGT GCCTGGCCTC 1440
TTCCTTTTTA TTACTGTTAT TTTTAATTTT TTGGTAGAGA CAGGGCCCCA CTATGTTGCT 1500
TTGAGGACTG GCCTCAAATT CCTGGGCTCA CGAGGCTTTT CTTTATCTCC TAGCTTCCCT 1560
GGCCACTTTT TTTTTTTTTT TTTTTTTTTT TGAGATGGCG TTTCACTCTT GTTGCCCAGC 1620
CTAGAGTGCA GTGCCACGAT CCCAGCTCAC TGCAACCTCC ACCTCCCGGG TTCAAGCGAT 1680
TCTCCTGCCT CAGCCTCCCA AGTAGCTGGA ATTACAGGCA CGCGTTACCA CGCCCAGCTA 1740
ATTTTTTGTA TTTTCAATAG AGACGTGGTT TCACCATATT GGTCAGGCTG GTCTCAAACT 1800
CCTGACCTCA AATGATCCCC CAACTCAGGC TCCCAAAGCA CTGGGATTAC AGGTGTCAGC 1860
CACCTCACCG GGCCCTGGCC GCTTTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTATG 1920
CTTGAAACAA GGACTGAATC TGTTGCCCAG GCTGGTGTGT GTGTGTTTGA GACAAGGACT 1980
CAATCTGTTG CCCAGGATGG AGTGTGTGTG TGTGTGTTTG AGACAAGGTC TCAATCTGTT 2040
GCCCAGGCTG GAGTGCAGTG GCAGGGATCT TGGGTACTTC GATCTCCGCC TCCTGGGTGC 2100
AAGTGATCCT CCTACCTTAG CCTCCAGAGT AGCTGGGACT ACAGGTGTAT ACCACTGCAC 2160
CCAGCTAATC TGTGAATTTT TAAAAAAAAT TCAACATGGT TTCACCATGT TGCCCAGGCT 2220
GTTGTCAAAC TCCTGGGCTC AAGCGATCTG ACTGCCTCAG CCTCCCAAAG TGCTGGGATT 2280
GCAGGCGTGA GCCACCGCTC CCAGCCCCTG ACCACTTTTC ACTGACTCCT TTGCAATGCC 2340
CACCCTGCAG CCTCTCTCAC TCTGGCCCTT 2370
|
| |
|
|
|
