| Tag | Content |
|---|
EnhancerAtlas ID | HS108-39119 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:41426870-41427980 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr8:41427220-41427231 | CATGAGTCACC | - | 6.62 | | FOSL2 | MA0478.1 | chr8:41427221-41427232 | ATGAGTCACCC | - | 6.14 | | IRF1 | MA0050.2 | chr8:41426937-41426958 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | JUNB | MA0490.1 | chr8:41427221-41427232 | ATGAGTCACCC | - | 6.32 | | JUND | MA0491.1 | chr8:41427220-41427231 | CATGAGTCACC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr8:41427869-41427884 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr8:41427159-41427174 | TGAACTCCTGACCTC | - | 6.22 | | SPI1 | MA0080.4 | chr8:41427659-41427673 | AGAAAGGGGAAGTG | + | 6.22 | | SPIB | MA0081.2 | chr8:41427661-41427673 | AAAGGGGAAGTG | + | 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 |
| GH08I041569 | chr8 | 41426661 | 41427993 |
|
Enhancer Sequence | ACATTTTTTA TGCCAATGGC AGGTATTGAG GTTGAACAAG CAACATTCAC TTTATTTTTT 60
CTTTCTTTCT TTCTTTCTTT TTTTTTTTTT GAGACAGAAT CTTGCTCTGT CACCCAGGCT 120
GGAGCGCAAT GGCACTATCC TGGCTCACTG CAACCTCTGC CTCACGGGTA AGCGATTCTC 180
CTCCCTCAGC CTCCCGAGTA GCAGGGATTA CAGGTGCCTG CCACCATGCC CAGCTAATTT 240
TTGTATTTTT AGTAGAGACG GGGTTTCACC ATGTTGGCCA GGCTGGTCAT GAACTCCTGA 300
CCTCAAGTGA TCCACCCAAC CTTGGCCTTC CAAAGTGCTG TGATTACAGG CATGAGTCAC 360
CCCAACCGGC CACTTCATTT TTTTCCCTAA AGGGCCTGCC CCACCTGACT CTCGAACAAA 420
ACAGCCAGGG TGCCCTGCCA GGTGGTTAAC AGGGTAAAGG CAGAAGCAGC CAAACACACA 480
GGCTTCCAGG AACAGTGTGG ACAGAGCTGC AGCTTCCTCA TCTGATAATG GGAGCTATTG 540
CAATCGCTAC TGTTTCCCCC TTGCCTTCTA GAAGGCCTGA CTCCATTAAG GGTTGATCAT 600
GAATAGGGCA GGTGGACTTA TAGAGCATGC TGTCAGAGTT GGGGGTTGCT TTCAAATTCA 660
AGCTAGTAAA AATCAACAGA AAAGATGAGT AGCCAGCTGT AGAAGTGACG TACTCCTAAG 720
ATGTGTGGTA ATGTATTTCT AATGACATTA GAGTTTCTGA AATCCATCTC ATCATCATGG 780
CCTAGCACTA GAAAGGGGAA GTGCTGGGAG ACCACGTGGA CCAGGCGTCA CATTTAGAGA 840
GGGTCTGGGA CCTAGACTTT TGATACTATC TCCAAATTAA GTTACACATA CAACTACAGA 900
GAGAACTAAC AGGATTGAAA AAAGATGCTG CTCAGCTGGG CTCAGTGGCT CCTGCCTGTA 960
ATCCCAGCAC CTTGGGAGGC AGAGGCAGGT GGATCACCTG AGGTCAGGAG TTCAAGATCA 1020
GCCTGGCCAA CATGGTGAAA CCCAGTCTCT ACTAAAAATA CAAAAATTAG CTGGACATGA 1080
TGGCAGGTGC CTGTAATCCA AGCTACTCGG 1110
|
