| Tag | Content |
|---|
EnhancerAtlas ID | HS095-20611 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr3:53142580-53144100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr3:53142636-53142651 | TGACCTCCCACCTCG | - | 6 |
|
| | 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 |
| GH03I053108 | chr3 | 53142945 | 53144950 |
|
Enhancer Sequence | TTATTTTTTA GTGGAGACGG GGTTTCCCCA TGTTGGCCAG ACTGGTCTTG CACTCCTGAC 60
CTCCCACCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCAT AAGCCAACAC ACCCAGCTTG 120
CTTTCATATC TTTAAATGGT TTTTTTTTTT TTTGAGACAG AGTTTCGCTC TTGTCGCCCA 180
AGCTGGAGTG CAATGGTGCT ATCTGGGCTC ACTGCAACCT CTGCCTCCCG AGTAGCTGGG 240
ATAACAGGCG CCTGCCACCA CGCCCAGCTA ATTTTTGTAT TTTTAGTAGA GATGGGGTTT 300
CACTGTGCTA GCCAGGCTGG TCTCGAATTC CTTACCTCAG ATGATCCGCC CACCTTGGCC 360
TCCCACAGTG CTGGGATTAC AGGCGTGAGC CACCGTGCCG GGCCAAAATG ACTCTTTAAT 420
GTTTGCAAAA AGTCCAGGCT CCTTAATTCT GTATTTGTGG GCTTTTATAC ACTGACCCCA 480
AGCTATCATT TTGGATTCCC TTTGCCAACC TCACCCTCAT CACCCTGTCA TCTTCTGCTG 540
CACCCTACCT CCCAGGTTTT AGCCCTCCAG CTGCTTTGAG TCAGGCTGGG CCCACCTTGG 600
CTCCTGTCAT TCTCACCACC TAGTGTGTCT TTTCTGCAGG GCCCTCCCTG TCTTTTGGCA 660
AAATAGACCT CTCCTTCCTA CATTCTATAG ACTCCCTGAG GGCAGGAGCC CCTCTCAGTC 720
ACCTCTATGA CCCTGGTTTC CTAGCAAAGC TCTAGGAAAT GAGTTTCCAA GTACCACACA 780
CCTCACAGCC AAGTAACAGT TAACCACATA AATGTCTGTG TCTTTGGTGA GAGAATGAAA 840
TGCCTGAGGC CATGGCCTGT TACTCATTCA TCTCAGTATT CTCAGCACCT GGCATAGTGT 900
TCAGGAAATG TGGGGGCAGA AGTAACAGCA CATACATTTT TGCTACTACA AAAAGTGATT 960
TCAAGCTGAG CTCAGTGGCT CATGCCTGTA ATTCCAGCAC TTTGGGAGGC CGAGGCAGGA 1020
GGATCGCTTG AGTCCAGGAG TTCAAGACCA GTCTGGGCAA CATCACAAGA CCCTGTCTCT 1080
ACAAAAAAAT TAAAATATTG GCTAGGCGTA ATGGTAGGTG CCTTGCCTGT AGTCCCAGCT 1140
ACTTGGGAGG CTGAGGTGGG AGGATCACTT GAGCCCGAGA GGTCAAGGCT GCAGTGAGCT 1200
GTGTTTGCAC CACTGCATTC CAGCCTGGGT GACAGAGTGA GACCCTATCT ACAAAAACAA 1260
AAAACAAAAA ACAAAAAAAA CCACCAGGGA TTTCAACTTT TTTAGAGCTG TAGTTTTAAA 1320
AATATATCGA ATCTGAGGAT CTCAGTCAGG CAACTTCCTT ATTTCACAGC CAAGGAGATG 1380
GAGGCCCTGA GAAGTTCCTA ATGGCACTCT GCCAGTCAGG GAGTCAGGCT AGGGGGATCC 1440
AACCATGGAG CAGGCTCCTG GCACCACATT CAGGTCGAGC TCTGGAGGCT TTAGTTTGCA 1500
GTAAACTTAA ACCAGCTGCT 1520
|
