| Tag | Content |
|---|
EnhancerAtlas ID | HS098-24198 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:44141580-44142740 |
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 | TTCTTTTCTT TAAAGAGAAC ATGGCAAACT TACACAGTAC AACTGCATAC TAGAATAAAA 60
CAAGGAAAGT ACTGAAAATT CACCATGCAA ATACTAATTG TTCCAGCAAT TCTCTCATCT 120
CCCTTATTTG TCATTAGCAA ATATGTTGCT AGTGGCTCTC TTAAGAAAAA TTCCCATTCT 180
CTGCTCTCTT TTACAGCAAC ATTCTTTGAA AATGTTATCT ACAATGGTTC CCTCAATTCC 240
TTCTGTGGCC TTGTCTCCTG AAACCACTCC AACCATGCTT TAATTCACCT TTCTCCCTCT 300
ACCAAAACTG CTCACCAATG TCTGCAACAA CCCCACCCCA CTAAATTCAA TGGTCTCAAT 360
TCTCAGCCTT CATCTTACTG ATCCTGTCTG TAACAACTGA CACAGACAAT CCCTCCTCCT 420
CCTCCCTCTC CAAAACACTT TCTCCCCTTG CCTTTCACAT ACCACACTCT CTTGGTTTTT 480
CTTCTACTTT ATTCGTCACT CCCTTCCCAA TCCTTTCCTC ATCTTTCACA GGAATGAGGA 540
GGAATACCTA AGCTCTGGAA TACATCAAAG GGCTAATCCA TATACCTCTT CTTTATCTGA 600
GCTCTCCAGC ACTCTCTATT CCCTCCTCTA TTGCATTTCT CTCTCCAGGA TTTTTTTTAA 660
TTAATTAATT TTTTATTATT ATTATACTTT AAGTTTTAGG GTACATGTGC ACAACGTGCA 720
GGTTAGTTAC ATATGTATAC GTGTGTTTTT TTTGTTTGTT TTTTTGTTTT TTTAAAAGAC 780
AGAGTCTCAA TCACTCTGTC ATCCAGGCTG GAGTGCAGTG GCACAACCAT GGTTCACTGC 840
AGTGTCAACC TGGTGGGCTC AAATGATCCT CCCGCCTCAG CCTCCTGAGC AAATGGACTA 900
CACACGCTCG CCCACAGCAG GCTTTTTTTT TTTTTAAAGA TATGGGGTCT CACTATGTTG 960
CCCAGACTGG TCTCAAACTC CTGAACGCAA GTGATCCTCC TTCCTCAGCC TCCCAAAGTG 1020
CCAGGATTAC AGGTATGAGC CACTGTGCCT AGCCTCTCTC CAAGATTTAA TGCTATAGGA 1080
CACACTGCAG AGTTCATTTA TTATTTTCTT TCTCTTAACA ACTAGAATAT TTCATAGGGT 1140
AAGCACTTTT GTCTGTTTTG 1160
|
