| Tag | Content |
|---|
EnhancerAtlas ID | HS060-33022 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr8:21622000-21623250 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr8:21622592-21622613 | TCTTTCTTTCTTTTTCTTTCT | + | 6.14 | | IRF1 | MA0050.2 | chr8:21622596-21622617 | TCTTTCTTTTTCTTTCTTTTT | + | 6.34 | | SPI1 | MA0080.4 | chr8:21622922-21622936 | CACTTCCCCTTTCT | - | 6.22 | | SPI1 | MA0080.4 | chr8:21622585-21622599 | CACTTCCTCTTTCT | - | 6.51 | | SPIB | MA0081.2 | chr8:21622922-21622934 | CACTTCCCCTTT | - | 6.07 | | ZBTB7A | MA0750.2 | chr8:21623196-21623209 | GGCACTTCCGGGG | - | 6.54 | | ZNF263 | MA0528.1 | chr8:21622429-21622450 | TTTTCTCCTCCATCCTCCTCA | - | 6.42 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 21622717 | 21623235 | | chr8 | 21622132 | 21622625 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I021764 | chr8 | 21622141 | 21623686 |
|
Enhancer Sequence | CATTATTTGA TAAGAAAATA GATTTGGACA GAAATGCCCT CGCCTTGTCA CCCACCAGTG 60
ACCAGTCTGT CTCACCTGGA CATCCAGCTC TGCCTTCTCT CTGTTAGAAG GACCCAGCTC 120
CAGCCTCGCC AAAGGCTGCC CTGCCATGCG TGCTGGTGCA CGCCACATGG ACCCCATCCC 180
TCCTCACTTA TTGAAGACAT CACTCCTGAA ATCGCCCCTT CCTGCTTACA TCCTTCAATT 240
CCACCCTCTC TTGGGACCTT TCCCAACAGG TACAAATGTG CCACCATCAT TGCCTTTCTC 300
AAGACAGAAC AAAACCAAAA GCAAAGCCTT CCCTTGACCA CTACCCAGCC CCCTATTTCA 360
CTACTCCCCT TCCTAGCAAA GCTTGAAAGA GTAGATTTCT GGTTGCTGAT TTTACCTTCT 420
CCCTTCACAT TTTCTCCTCC ATCCTCCTCA CGTCAACATT CCAACCTCAC CCTCCAAGAA 480
GAATATTCTG GCAAGATCAT GGGTGACCTC CATGTCACTG AATCAGAAAG TCACTTCTCT 540
AAACTTCACT GGCTTGACTT CTGGGCTGCA TCTGACCAGG CTAACCACTT CCTCTTTCTT 600
TCTTTTTCTT TCTTTTTATT TTTTATTTAT TTATTTTTTT TGAGACATAG TCTTACTCTG 660
TCACCCACAC TGGAGTGCAG TGGCATGATC ACAGCTCACT GCCACCTTGA CCTCACGGGC 720
TCAAGCAATC CTCCCACCTC AGCCTCCTGG GTAGCCAGGA CCACCCGCAT GTGCCACCAT 780
GCCTGCCAGT TTTTGTGTAT TTTGTAGAGG TGGGGTTTTG CTATGTTGCT CAGGCTAGTC 840
TCGAACTCCT GGACTCAAGA GATCCACCCG CCTCAGCCTT CCAAAGTGCT GGGATTATAG 900
GTGTGAGCCA CTACACCTGA CCCACTTCCC CTTTCTTGAC ACTTCTACTT GACTTGGCTT 960
TTCTGACACA GCTGACTGAT TTCTCTCTCC CTCTCTGGCC CTAGTCTCAG CTGCCTTTGC 1020
TAGCTCTTCC TCCTCTACTT GGTGAGACCC AGCCTCACTC TCCTGACTAT ATACCCTCCC 1080
TCCATGACCT CATGGTTCCG TGGCTTTAAA CACTGTCTAT ATGCTAATCA CTCTCAATCC 1140
ATGTATCAAC CCTGACCTCT CCCCAGAATT CCAGGCCTAC ATCTAACTGT GTCCTTGGCA 1200
CTTCCGGGGG GAGATCTAAT TGGCAACTCC ACCCTAAAAT GGCCAATACA 1250
|
