| Tag | Content |
|---|
EnhancerAtlas ID | HS044-07689 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr2:202879060-202880290 | 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: 2 | ID | Chromosome | Start | End |
| GH02I202014 | chr2 | 202878969 | 202879110 | | GH02I202015 | chr2 | 202879174 | 202880398 |
| Enhancer Sequence | ACCTCTGGGA GAGAGGAAAA TATGCAATAA AAGAAGAGGT CGAAGAAGTC CCAGGTGTAC 60
GGAGTCAGCA TCCAGATTAC TGTATCTCTG AGCAATTTGC TGGACTGACA CAGCTTCATT 120
TTAAATGACA TAACATAACC AGCATGATTC ATCCTGCCGT CCAAGGGCTA TATAATAAGT 180
GTGGTAATGG GGGAGCATCT CCCGAGAGGG TACAGGAACA GCTGTGTGTG TCACCTGGGA 240
ATGGCACCCA CCTATAAATC CCATCTCTTT GACAACGATT CTAAAGTCCC TCTGTCACTG 300
TCACTCACCC ACAAAATTAG TGACTAAAGG GGAGAAGGAG AGGAAATGCC TCGCCCCTGA 360
AATAGAGAAA GACTGAGAGA GGGACAGAGC AAGTTAATAA ATAAAACAAG AGCCTGAAGG 420
GAAGAGCTGC TTTGTCAGAA TATAAATATT TCCCTTCCCC TTTTATCTTT AATGTAGTGT 480
GAGAAGCTTA TTAAAGGGAA ATGCTTCTCT GTCCCTGGAG CCCTCGCACA AGCCTTGCGG 540
GGAGCTGCCT GCAGAACGGG GTCGCCTAGC CCCACGCTTC TAAACTCTTC CCTGCTGGAA 600
GTGAGCGTAA TGTGCAGAGC AATAAAGAAG GGCTGGGGGA GGAAAGGGAA GACATTGTGG 660
CCATTAGGAT CCTTATCTTG ATGGGCCTGG TGTCAGGTTA TGTTAATCGC TGGGAGATGC 720
TGAGAGACTG AGGATGAGAA ATGCCTGTCT GCTCAAAGGC TTGGCCTGAG ATTCCAAGGG 780
AGGCTGACAT TGCTAGACTT ACCCTCTGCT CCGTTAGAGA GAACAACATC CAAATTTAGA 840
CAAAGGGGAA TTTGCCTGAT GGAGGCGTGG ATGGAGAGTC CTGTGGGTGT TCCTCTGAGG 900
AGCCCTTGGT GGCTGCACAT CTCACATCTC CAAGAAGACA GCCAGCACGA GCAGTCCCAG 960
CATACCCCCA ACAGAAGCCT ATTCCAAAAG CATGGAAGAC ATTTGCCGTC CACATCTCCT 1020
TCCTAAAACC CCTAAAAGGA TGGGACATTA AGGGCCTACA TACCAAGTCA GGCCAGCACA 1080
GAGCCTGGCA CGTGGTATGT GTGCAGTAAG TCTGTACGGC ACGACACGGA GACTGTACTG 1140
GGCTTGTTTA CCACTGTATC TGTGGGTCCA CACACAGGGG CCAGCACACT TGGTTTTGGA 1200
TGGATGAATG AACACATGCA TTTAGACACA 1230
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