| Tag | Content |
|---|
EnhancerAtlas ID | HS073-08309 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr2:69762660-69764040 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr2:69763018-69763036 | CAAAAGTGAAACTAATAA | + | 6.62 | | ZNF263 | MA0528.1 | chr2:69763340-69763361 | GGAGGAAGGAGAAAGGGAGAG | + | 7.12 | | ZNF263 | MA0528.1 | chr2:69763337-69763358 | GAAGGAGGAAGGAGAAAGGGA | + | 7.92 |
|
| | 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 |
| GH02I069535 | chr2 | 69762828 | 69763732 |
|
Enhancer Sequence | TTATGACAAG AATACAGCAG GTGAATGTAT GTAAGGTGAA GACGAATGTT ATTTTAAATA 60
GTATAGTCGG GGAAGGTCTC TCCAAGGGGA ACAGAGACCT GGATGAAGAA GGAGCAGCCA 120
TGTGCCATAT GGGGAAAGAG CATTCCAAGC AGAAAACAGT AGCACAAAGG CCCTGAGATG 180
GGAGTGTGCC TGAAGGGTCT GAGGCACAGA GGCAGGCCAC TGTGGCTGGA ATAGTGCTAT 240
GCATAGTACC AGTACTGCAA AGAAAGCTGA AAACATGGGA AAGGACCTAC TATGAACCAC 300
TGCTGTCAGG AAAGGGGAGA CAAGACAATG TGGAGCCATG GAGGAAGTGA AGGACTTACA 360
AAAGTGAAAC TAATAACAGG AACAAAGCAT AGAAACCAGA GTGATAATAA CAGTAGCAAC 420
TAACAGCACT TATTAAGTGC CAGACACTGC TCCACGCGCT TTTACCTAGA GTATTTCATA 480
TAATCCTTAC AAAGCCTTAT TGTCTCCCTT AATAGATTAG AAAAAAGAGG CCAGAGAAGT 540
TACCTAACTT GTCTGAGGTC ACAGGATAGT AGGGCAGTAT TTAGGCTCAG GCCACCGGAC 600
TGCCAGGACC ACACCCTCAC CCACCGTGCT GATGTGCATT GTGCAATTAA GGGGGATGGA 660
CAGTTGAGAT TGGCGAGGAA GGAGGAAGGA GAAAGGGAGA GGACCAGAGA AGCACACAGA 720
CAGCAGACTG AGGAAGGGCA CTTGGGCACC ATTCAGCATT TTTCTCAGGT CAGCAGCACA 780
TGAAGACAGC CATTTTATGA AAATTAGCTT GGCAAAATTG AGGGAGAAGA AAAGAAGGAA 840
GCCAACAAGG GCAGGTACAA CAGTCTGGGT GTGAGATGAC TAGGGCAGGG TATAGAGAAA 900
AATCAACAGG GATGGAAGTA AGCAGGTGTG AATAGATTAT GTGAGATTAA GAAGGTAGAA 960
ACCCAACTAG ACAGTCGTAC ACCACCTTCT GAAAGCTTCA GAGAATTTGC ATAGGGACTT 1020
TGTTTTTGGC AAAGTCCCTT AGGGTGAAGC TCAAGATTGT TTACCACTGC TTACAATCCC 1080
GAACCTTTCC ATTCTTTGAG AGTGCGATGC TGCTGACCCC ATTTCCTAGC CTCTCAGCTT 1140
AAGAGTGCAA TTGAAGTTGT CACTGTCAAA CTCTGCTTAC AGCTTTAGCA AAAAGATCTA 1200
AGAGGCTACC TCCTACTGAC CTCTTCATCT CAATATTATT CCAAACAGGT ATGGCATTAG 1260
GCATTTCAGT CAGAGAATGT ATTGCCACTG CAAAATTTGA AGGATTAGAT GAATGCAGGT 1320
TTTCAAACCT GTGTTTCTAA AAATGGGACA AGAATCTTCA TCCTATTATA CTTCATGAGA 1380
|
