| Tag | Content |
|---|
EnhancerAtlas ID | HS148-13766 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr4:148281190-148282010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr4:148281514-148281530 | GATTGTTTATTTAATG | - | 6.24 | | Foxd3 | MA0041.1 | chr4:148281514-148281526 | GATTGTTTATTT | + | 6.62 | | JUN | MA0488.1 | chr4:148281574-148281587 | TATATGATGTCAT | + | 6.04 | | NFE2L1 | MA0089.2 | chr4:148281714-148281729 | ACTGCTGAGTCACTG | - | 6.71 | | Nfe2l2 | MA0150.2 | chr4:148281716-148281731 | TGCTGAGTCACTGAG | - | 6.6 |
|
| | 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 |
| GH04I147359 | chr4 | 148280497 | 148285022 |
|
Enhancer Sequence | ACGGACCTCA GGCCACACTC TTCAAGCAAA GAAGACTTGG CTTGATCTTG TGACAGCCAC 60
TTGTATTTAA ATGAGATGCT GGGAAACATA TGGAGACCTA CACAAGGGAA TACCCAAAAG 120
CTTCTTGGGC ATTACACTGA CCTACATAGT ATACGGTTTT CCATTTGGGC TGAGTCACAC 180
TGCCCCTGAT CAGGATAGAT GTTATAGGGA GATGGAACAG AAGGCAGGGA GTTCATAGCA 240
GTACTATCTG GTACCCCAGC ATCAGGGATG TCCCCAGCTT CCCGTGATAT TCATGTAGGC 300
CCTGGAAGCA CCGCTTCATA TAGTGATTGT TTATTTAATG TCCAAGTTTG GAATGGCTTA 360
GAAAAAGAAA AAGACCTAAG AGCTTATATG ATGTCATGGA AAGATAGAAG TCAGACATGT 420
GGTTTTCTTG GGTTCTTCAG CTTTTCCCAA TTTTCTCCAC CCCACATTCA GAGCTCTATT 480
TGCCTTCATC TGCAGAATCT CTGTAGGAAG CAGTTTTGAA AGGCACTGCT GAGTCACTGA 540
GTTGTACTGT GGTCTGACTC TCTGATACTT TAAATTCTGA TTTGAAGAAA TTGCTTGAAA 600
GCACTGATAT CTTTTTCTCA CCGCTGGCAA ATGGCAAAGT TTTCACTGAG TGAAAAGCAA 660
TGTTTCGTAA GTGAAAAATA TAAGAATCAA TTTGTCCATC ATTCCATTAT CCTGCCCAAA 720
CACTTAACAA TTAAGGGACA GGCCAGAAGG CTTCAGTTAA TTACATAAAA GGTTTTTTTT 780
GTTGTTTGTT TTTAAGTTAG GTTTAAAGAG TCCATGAGCT 820
|
