| Tag | Content |
|---|
EnhancerAtlas ID | HS064-10034 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr22:40169750-40170730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr22:40170302-40170315 | AGGATGATGTCAT | + | 7.34 | | JUND(var.2) | MA0492.1 | chr22:40170301-40170316 | CAGGATGATGTCATC | + | 6.5 | | NR2C2 | MA0504.1 | chr22:40170381-40170396 | TGAACCCTGACCTCT | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 40169815 | 40170473 | | chr22 | 40169800 | 40170600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I039773 | chr22 | 40169882 | 40170440 |
|
Enhancer Sequence | TGAAATAATT CAGATTGTAA GGTTAATTTA ATACCAAAAC AAGTACTAAG CAACTACAAA 60
TTTAGGCATT GCTTTAGGTT TAGAGGTATA AAGATGTGTA AGAGATTCAA ACAAATGATG 120
TCTGAACCAA GCTAAAAGCA TGAGAAAAAA GTCAAGAGAA GAAGGACACA AAAATTTCCA 180
AGTAAAGGGA ACAATTTCAG CAAAGAAATG AAGGCTGTAC ACAATGTGCT GTGTGGTAGT 240
GGCAGGGCAG GTACAAAGCA TTCAGCGTTA CGAGTGCACA GTGCACACAG AGAGCAGAGG 300
AGCTCAATCT AGAGACATAG ACAGAACCAG GGCTGGCAGA CGTCTTGACA GACAGGATTG 360
ATGAGAAAGA ATGAAACTGA AATCTTAAGA CCATTTCTTT GAAACTCATT CCTCTTCAGA 420
TGCCTCCAAC GAACTTTGCT GGCTCTCCTC CTATCTGTCT AGGCAATCTT CTCAACATTC 480
TTCCTGGCCC TGTTTCCTGT GAAATGTAAA CAGTCTGTCC TTGACTTTCC TCTTCTGCCT 540
TTACAATCTC CCAGGATGAT GTCATCTATT ATTATACTTA CACTAGATCT AGATGGTCAC 600
CTGTGGGCAA GTAATTCACA CATATTAATC CTGAACCCTG ACCTCTGCTG ATTTTTAGCC 660
CTAAATATCT ACCTATTTCT GTGTTCAGGG AGGTCTTATC ATCCTCCAGC CTCCTCATCC 720
TTGGGTGTTT GCTTTACCTC TGTTAATATG ACCATCAGCT TCCCAGTCAC TCAGGTTATT 780
TTGGAACTAT GGTTGTTACC ACAACTTCTA AGAGGTCTCT CCAGCTTACC CCCTCAGTCC 840
ACTCTACACA GCCCAGCCAG AGTGACCTTT CTAAAATGAA AGTTAGATGT TATTTCTCCC 900
CAATACTTCT TCAAATTATT TAACATGGTT TACAAGGCTC TGCATAAATT AGTCCCCATT 960
TACCTCTCTT GCCTCATCTT 980
|
