| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04493 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:161980530-161981720 | 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 |
| GH01I162010 | chr1 | 161980455 | 161982114 |
| Enhancer Sequence | GTGTGGTCGG GGGAGGGTGC TGGCTCTGGA GATCAGGTGT AAACCCACAC CACAGTCATG 60
GCCTACTTAT ATAACCACAT AGGGCAAGGG ATGAAACCTC TCTAGGCCCC AGGCAGGAAA 120
AGAAGGAATG ATGACACCTA CCTCACCCAA GCTTGGCACA GAGATGGATA AGGGGCTGCA 180
TGTGGTACAG TGCTGGGCAA GGAAATCAGG CTTGAGGCAT GTGGGTGAAG CTGGAGTGGG 240
AGGGACCCTT GGGGTCTCCA TAGCAGACAT GCAGGTGGAA AAGGAAAGGG AAGCCAGGGT 300
TTGGTATGGC TGGCATGGGG AGGAAGGTAA GAACCCAAGG CTGGTGTGCT GTAGAGAGAC 360
ACACTAGACA CCTGTGGGAG TAGACAAAGC CAGACTGCAG GTGAGGCAAA CCCTGGCCCC 420
AAGTCACACA GCAGGTGCAC ACAGCCATAT CTAAGGAGGC TGCCTGGGAG GCTGCCTGGT 480
AGGTCCTGTG GGCATCAGGA TTCCCTGGCA GATAGCTGGA TGCGCACAGG GCTAAGATAC 540
AGATGGCAAG CCCAAGGGCA GATGGGACAT AGTTTCTCAT GGGAGTGACC TGAGCAAGTG 600
TGAGGGTAAC TGGACCCAAG GGGGGAGGGC TCGTAGTTCC CATCAGCTCA CCGTGCTCAA 660
CCTTTGCACC CTCCAGGAGA CAGCTACGAC CAGATGGCCT GGGACAGCAA CCCCAGCTGA 720
CAGCTGTCTC CTAGCCCCTG GTAAGAGAGC TGGGGAAGAG AACAGCTGGA AACAGCCGGT 780
GCTCCTGATG GCAGGACAGG CAGGCCATGG CCTAATCCCT CCGACCACAG CTGATGGGAG 840
AGACAGGCAG GCCTGGGTTC AGGGAGCCAC CAGCTGCCCC ATTGAACATT CATCCAACCA 900
AACAGCTGTG GAGCATCTGT CCCACATCAG GTGCTGGACC AGGGCCTGGG AAACAAAGAT 960
GACTTGACCC AGCTTGCCCT TAAGAAGTCC AGGGCCTGGC AGGAAAGTCA AACAAGGCAA 1020
CAGCAAGAAG ACCCAGGCCT CTGGTGATGA ATTTCTATAT TAGGGTAATC TTACCCCTTA 1080
AAATAGAGCC ACTCGAGCCA TGCACACTTG CACATCCTGG CAGCTCTAAA CTGTTCCTAG 1140
GCCGACGGAT GGAGGGCTGA CACTCGCACT GTAAGTCTCT TCAGCCAAGA 1190
|
| |
|
|
|
