| Tag | Content |
|---|
EnhancerAtlas ID | HS056-12967 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr5:179278960-179280370 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr5:179279338-179279350 | AAGTAAACAGTA | + | 6.18 | | Foxa2 | MA0047.2 | chr5:179279335-179279347 | CCTAAGTAAACA | - | 7.22 | | Nr2f6(var.2) | MA0728.1 | chr5:179279064-179279079 | GAGGTCAGGAGTTCA | + | 6.22 | | ZNF263 | MA0528.1 | chr5:179279696-179279717 | GAAGGAGAGGAAAGATGAGAG | + | 6.07 |
|
| | 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 |
| GH05I179852 | chr5 | 179279263 | 179280597 |
|
Enhancer Sequence | AGCGAGACTC CGTCTAAAAA AAAATAAAAA AATAAAAAAT ATCAGGTGAA GGCACTCACC 60
AACATTATGA AATGTTTTTG TCTACGGAGG CAGGTGGATC ATTTGAGGTC AGGAGTTCAA 120
GACCAGCCTG GCCAACATGG TGAAACCCCG TCTCTATTAA ACATACAAAA AACAAATTAG 180
CTGGGTGTGG TGGCATGCAT CTGTAGTCCC AGATACTCAG GAGGCTGAGG CAGGAAAACT 240
GCTTAAACCC GGGAGGCGAA GGTTGCAGTG AGCCGAGATT GCGCCACTGC ACTCCAGCCT 300
GCATGACAGA GAGAGACTCC ATGTCAAAAA AAAAAAAAAC CCCAAAAAAC AGCAATTTAA 360
CTTTTAGGAC TTTGTCCTAA GTAAACAGTA AACAGCTGGT CACGTGGATA AAGAGGTTTT 420
TGTGAAAAGC TTCACGGTAG AGTTGTGCAT AACAGTCAAA AGGGAAATCA ACCTAAATGC 480
CCAACAAGGT TGGGCCAGTT CCTTACTCAC TCCACAAACA CCGAGCACTG TGCTAGGTGC 540
TGCGGATACA CCAGCAAATA AAAAGCCTCT GTTCTCACGG AACTTACAGC CTTAGATGGA 600
CAATCCGTGC ATAAACACAT GACTATGTAA CTTCCATAGG ATACTGAGAA GAGGGAGGGG 660
AACTCCACAG TGAGCACAAA GGCCTGAAGA GGGAGCAAAT TTGGGTTTAA GGTCAGAAAG 720
AAAGCACATG GCTGTAGAAG GAGAGGAAAG ATGAGAGGTG AAGGGAGAGG TGGCACTGGG 780
GCTGGAGCAG GAAAAGAGCA AGTTCAGTAA GGCAAAGGAT GCAGGACAGT TTGGGGTCCT 840
AGAGTTCAGG AGGGGCAATA CGGATGGACT GAAAAGACGT ACTGAATGCC AGCTGCAAAC 900
AGCTGGATGA GAGCATTTAC AGCCTGCCCC TGCCTGCCTC CACTTCCTGA GCCCACTATC 960
CCACACCTCC ACCTCCACCA ACGGCCTCTG CCCTTCCCCG GCTGCCCTGA TTCCTCTGTC 1020
ATCTTCTCAC AGTCCCCAGT GCTTTCCTTT CCTTGTGCTC AGCCGAGTTT TAAATTATGC 1080
AGATGCATGT GTGCATTAGT TTCTCTTCCC CTTCCACACA AGTGCATCTG TGAGGGCAAG 1140
AATGACAATG GGCTTACTTT CCACTGTTCC CCTTGTGCTT GGCACACAGA AAGTACTCAA 1200
GAAATACTTG CTGAATGAAG AATCAAATGG CAGTACCTTT CCAGATTCTG CTCCATCCAT 1260
TTCACTTCCT GAAGGAACAG GAAGCTCGGA AGCAGGAGCT CCGTGTCTGG GGAACTCTGT 1320
TTGAGAGAGG ATGATCCCAG CTGTGGCATG CTGGGACTCC CTGGAAGGGC TCGCTGCAGG 1380
CCTGCGCCCC ACTTGCTTTC TGTTTTGTAG 1410
|
