| Tag | Content |
|---|
EnhancerAtlas ID | HS042-00820 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr1:21475720-21477050 | 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 |
| GH01I021148 | chr1 | 21475116 | 21479692 |
| Enhancer Sequence | CTATGTGTAC ATAAATATGT ACAAAAATAT GTATACATAT ATAAACAAAA AATTCCTTCA 60
AGGAAATTTA TCGAAATACA TCAATGAGTT AGAGTTATGA GTAAACTGTT ATTCTTTTTT 120
TTTCCCTGTA TTTTCCATAA TGATCACATA TGGCTTTTCT AGAGAAGGGG GGCTTTTCTG 180
TTTCTCAAGC AAAAAAGCCT TTTCTCTTCA TCACACTGAA AGAGAAATGA ATGAAGTACT 240
GTGTTACTGC CTATCCAGAT ATACGGTATT TTACTGGTTG CTAAGCAGCA GATCCTGGTG 300
TTTTTACATC ATGCCTATCT CTAGTCACAG GCAGAAAGGA CAGGAACTCA GGCACAAACT 360
CACCCCATCC AAATGGCAGT GTATTTCCTC TTGGGAGTGG TCCAAAGAGC ACACACAGCA 420
ACTTTAATTC TCTACTCAAA CCACTCCCCA TCTCTCACCT TAACATACCA AGCAGATTTT 480
TTATATGGAA CAGTATTCCT CACACAAGCT GCACGAAAGG GAAGACCTTT TTAATCCTCT 540
ACTATATGCC ACCCACTCCA TCTCTGAGAG ATAATTCGCA TTTAAGTATG TTCACCCACC 600
AAGCTAGAAA TCACCATCAT TCTGGACATG TATCTGTCAT CAACTGACAC AGACAGGTAA 660
GCCTTGCTGC TTTCTGAAAA TAGCCAATCC TGCTCAGTGA ATGACAGCAT CAGCTAAGAT 720
TTCTTCTACT GCAGAGAATG GGTGGGTCCC CCCACTAATG CTGTAAATTC CAATACTCAG 780
TGTCATTCCC TCCAAACAGC AGAATCTACA GTATGGAAAT TCTTCCACAA GAAAAGCCCA 840
ATTCTTGTGG CCACAACCAT TAAGAGAATC CTGAGCCAGG ACATTCTCCC CAAGCTTCCC 900
CTCCTGCTTC TTCACAGGAA CCACAGCAGC CAAGTCCTAT ACTATGCCCG CCCCTGCTGC 960
AGCAGCAGCC ATTTTTGGCT CAGCCCTGCT GCAGTCCCAG ATGAAAGCCA GGACGGCAAG 1020
GACAAGATGG CAAAGGACTT TTAAAATGGA AACTCTTAAC AAAAATAACA ATGAAGCAAG 1080
CATCATAAAA AATGTTGCAA TAATATGCCA TGTCATTTAA AATAAGGCTT TAAAAAAAGA 1140
TGCCTATATT CAAGTACTTT AAACCATTTT TCATGGCGTC ATGAAAAATT TGAGGGAACC 1200
TAATTCATCA CAATGTGAGA TCAGCACTAT ACTGACACTA TGGGGAAAAC AATGCTTAAT 1260
GAGTTTAGTT TTCTACTCAA CTAACAGTTA ACAACAACTC CCTTGATTCC TGTGGAAAAT 1320
CTAAACGCAT 1330
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