| Tag | Content |
|---|
EnhancerAtlas ID | HS042-30122 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr22:29580150-29581690 | 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 |
| Enhancer Sequence | TTTCTGGCCT CAAGTGATCT TCCCGCCTTA GCCTCCCAAA GTGCTGGGAT TACAAGTGTG 60
CGTCACTGTG CCCAGCCTGT TATGTCCTTT CAGACACCCT GCCTCATTCC TTTTTACGAC 120
GTGCAGTCAA GCAGTTATCT GACCGTGGGT TTGTGTGTCT GTCTTTGAGG CTGGTCTTGC 180
TGGCTCCTGC ATTTCCAACA CAGAACCTGA GCTTTGGCTC AGAGTAGGCG CTCTGTAAAC 240
ACATGTGGGA CGAGTGAGGA CGTTCCCTGG ACGATGCCTG GGGTGCCCAG GCCACAGAGC 300
TGCCATTGAA TCTCCTGGGG GTTAAGGTCC ACCACGTTCC ACTCAGCAGG AAAAATTCAG 360
AGCTGACATT AATTCAGACC CCACATACGT GATTCTTACT GAGTTAGACA CCAAGACAAT 420
CTCGCCTTTT GTTGGGGCTG TGGGAGCCTT ACGTACGCCT AGAGAGAAGC CAGTCTAAAA 480
TCAGTCGCTT TTTGAAACCA TCAGCTCGAG AAATTAAGGA TTCTGTCAGC GTGCCCTGAA 540
TTTCTGGGCC CAGCAATTAA TTCCTTCTAG ATTAAAGGAT TGTTGTGTTT CTGATACATT 600
ATTATGCGGA GTGGGCTTGC TGTGAATTTT AAAACTTTAA CCAGAATCCT CATTAACTGG 660
GACCTTTTAT CTGTGTGCAA CTTCTAGAAG AGGCCAGTGG CTAGAAAGTG AGCTGATGCA 720
TCCAAAAAAC ACATTCCGGG TGTCCTGTTG CATATTCAGT CCAGGCAGCT GTTCTCCTTT 780
CTGATGGAAA CAGGGCCATT TACTTACAAT GTGCCTGGTG CCGGCTGTAT GTTGTACATT 840
GCGCCATTGA ATCATCACCT GCTCGATCAG GCAGCCACCG TCATTATTAG CTCCAGCGTA 900
CAGGTGAAGA GACTGGGGTT GAGAGAGATG GGGTCCCTGC TCAAGCCAAT GGGTGGCACA 960
AGTCTGTCCG ACCTCCAGGC CCCATGCTTG GCTCTCAGCT TCTGTTGCTT TCCCTTCTCC 1020
GTGGATGGTG AAGACCACTG TGCGGAAGGA TGATCACAAG GCCCTTTGGG CCACCATCCA 1080
GCCAAGAGCT ATTTCATCTG TGCTGGGCTT GAGGCTCTGC TGAGCCCGAG GGAGTAGGGA 1140
GGCCCAAGGG AGCAGACCCA GTCGTGTGTG AGGCTGACTC AGGGGCTAAG AGCTCCATCC 1200
TCTGGGAACA CCCACGGGGT TCAGGGCCCA GGGAGGCCAG CCCCTGCTGT CTATCATGAG 1260
CAGGCTCTGT CCCCTCCCTA GCATCAGTCC TCCTCCTGCC ATATGTCTGG GAACCTCAGC 1320
TTCTCTCAGG CAGAGTCCAG CCTAGCTGGA GTCTCACTTT GTTGCCCAGG CTAGAGTGCA 1380
GTGGTGCCAT CTCGGCTCAC TGCAACCTTC GTCTCCCAGG TTCAAGCAAT TCTTCTGCCT 1440
CAGCCTCCCG AGTAGCTGGG ACTACAGGTA TGTGCCACCA CGCCTGGCTA ATTTTTGTAT 1500
TTTTAGTTTT GCCATGTTGG CCAGGCTGGT CTTGAACTCC 1540
|
| |
|
|
|
