| Tag | Content |
|---|
EnhancerAtlas ID | HS065-02225 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr17:44141660-44142420 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr17:44142237-44142250 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr17:44142238-44142251 | AATTAATTAATTT | - | 6.92 | | POU6F1 | MA0628.1 | chr17:44142239-44142249 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr17:44142239-44142249 | ATTAATTAAT | - | 6.02 | | ZNF263 | MA0528.1 | chr17:44141990-44142011 | CCCTCCTCCTCCTCCCTCTCC | - | 6.02 | | ZNF263 | MA0528.1 | chr17:44141987-44142008 | AATCCCTCCTCCTCCTCCCTC | - | 6.11 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 44141900 | 44141963 | | chr17 | 44142028 | 44142133 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I046062 | chr17 | 44139914 | 44142081 |
|
Enhancer Sequence | CACCATGCAA ATACTAATTG TTCCAGCAAT TCTCTCATCT CCCTTATTTG TCATTAGCAA 60
ATATGTTGCT AGTGGCTCTC TTAAGAAAAA TTCCCATTCT CTGCTCTCTT TTACAGCAAC 120
ATTCTTTGAA AATGTTATCT ACAATGGTTC CCTCAATTCC TTCTGTGGCC TTGTCTCCTG 180
AAACCACTCC AACCATGCTT TAATTCACCT TTCTCCCTCT ACCAAAACTG CTCACCAATG 240
TCTGCAACAA CCCCACCCCA CTAAATTCAA TGGTCTCAAT TCTCAGCCTT CATCTTACTG 300
ATCCTGTCTG TAACAACTGA CACAGACAAT CCCTCCTCCT CCTCCCTCTC CAAAACACTT 360
TCTCCCCTTG CCTTTCACAT ACCACACTCT CTTGGTTTTT CTTCTACTTT ATTCGTCACT 420
CCCTTCCCAA TCCTTTCCTC ATCTTTCACA GGAATGAGGA GGAATACCTA AGCTCTGGAA 480
TACATCAAAG GGCTAATCCA TATACCTCTT CTTTATCTGA GCTCTCCAGC ACTCTCTATT 540
CCCTCCTCTA TTGCATTTCT CTCTCCAGGA TTTTTTTTAA TTAATTAATT TTTTATTATT 600
ATTATACTTT AAGTTTTAGG GTACATGTGC ACAACGTGCA GGTTAGTTAC ATATGTATAC 660
GTGTGTTTTT TTTGTTTGTT TTTTTGTTTT TTTAAAAGAC AGAGTCTCAA TCACTCTGTC 720
ATCCAGGCTG GAGTGCAGTG GCACAACCAT GGTTCACTGC 760
|
