| Tag | Content |
|---|
EnhancerAtlas ID | HS059-04677 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:246660440-246661260 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr1:246660849-246660859 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr1:246660849-246660859 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr1:246660849-246660859 | AATGGAAAAT | - | 6.02 |
|
| | 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 |
| GH01I246497 | chr1 | 246660721 | 246660890 |
|
Enhancer Sequence | AAACTGTAAG GAGATCAACA AGCACAATTT TCCCTCCAGA TCATACCAAC TCCAAGTAAA 60
ACTACTAGTT TCAAACATAG GTTTCGACTC TTATTGTGAA AAACATGGTC ATCATCAATA 120
AGCCACTATA CCATGTAAAT TTCATTAGTG AGTTTTATAT AGATATTTAT GACAAAATTT 180
AACTTGTTTG CCCTTTTTTG GTCTAATTCA AAATAAGAGT TAATGGCAAA TGTCAGAGGC 240
TAAGAACAGT TTGGAAAGGG GGTTCATGAA GGAGACCACT CAGAGACAGT GTTTTAGTGG 300
CTAAAAAATA AGTTGCCTTT CTGAAAAATA TTTGTATGCT TTTTACTCCA TTGTCCACCA 360
GAGGGAGCAT CACATCTGAT TAAGAGATAA TGGGGAACTC CCAGATAGAA ATGGAAAATC 420
ATCTGAAACT TGATCTACGA GGTGCTACAG ATGGTAGCAT ATACAGTTAA ATGTAAAATC 480
AAATCAGAGA ACCCCCAAAA GAATCTCAAA GTGAGTGGGA GGACAGCCTC CTAGGGAGAT 540
CTCATCTCTA AAAAAAAATT TTCTTTTAAT TAGCTGGGTA TGATGTTGCA CGCCTGTGGT 600
CTCAGCTGCT CAGAAAATTC TGGAGGCTGA GGAGGGAGGA TCACTTGAGC CCAGGAATTC 660
AAGGCTGCAG TGACCTATGA TCAAACCACT GCATTACAGC CTGGGTAACA CAGGGAGACC 720
CCAGTCTCTA GAGGAAAAAA AAAAAGAAAA GGAAAAAACA AGAAAAATGA GCAAAAGATA 780
AATACAGACA AATCACAAAA AGATATAAAT ATGGCCTTTA 820
|
