| Tag | Content |
|---|
EnhancerAtlas ID | HS023-00990 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr1:57772510-57773690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr1:57773221-57773232 | CCACACCCTCT | + | 6.02 | | Klf12 | MA0742.1 | chr1:57773219-57773234 | GGCCACACCCTCTTT | + | 6.05 | | Klf1 | MA0493.1 | chr1:57773219-57773230 | GGCCACACCCT | + | 6.32 | | PHOX2A | MA0713.1 | chr1:57773024-57773035 | TAATTAGATTA | - | 6.32 | | PROP1 | MA0715.1 | chr1:57773024-57773035 | TAATTAGATTA | - | 6.14 | | Phox2b | MA0681.1 | chr1:57773024-57773035 | TAATTAGATTA | - | 6.32 | | SP4 | MA0685.1 | chr1:57773443-57773460 | TAGGCCACACCCCCTTT | + | 6.01 |
|
| | 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 |
| GH01I057306 | chr1 | 57772500 | 57778001 |
|
Enhancer Sequence | TTATGTGAGT GCAATCTTAC CTGGTGAGAA TTTCTAAAAG CTCCCAAGGG CCTTTCTGAC 60
ATTTCATCAT TAACTCCTTT TGCCTTCTCT GCAGGGTAGC AAAGGTGAGC TTGTGTAGGC 120
TTCAAGTGGA GGTTGAGGCC TGAGGCCCAA ACAACTCGCT TTCTCCACTC CACACTCACC 180
TCCCATTTAA CAGGAAGACA ACAAACCTTG TCAGAACATA GCAACAGTGA AAGGAAAGGA 240
TCTTGCAGTT TTTTAGGAGG GTCCCCTCGG GTCCCTCTTT GTGCACTCAT TTGACATTTC 300
CTTTCTAACA ACGACTGTCA TGGTTTGCCA AATACCTTCT CTTTTGTGCT TTCATTTCAT 360
CTTCATGGTG CTGTCCTCAT TTTACCATGG TTGGAGATGA TATAAGCCAC AGATTTTCCA 420
GCTAAATAGG ACTGGACTCC ATGCCTTTTG AGTCCAAGAT CTCTTCTGTA CCTTGTAAAT 480
ACCACCTGAC TTCTGGCTCT ATATTATGCT ACCTTAATTA GATTATCAGC CCTAGTACAG 540
GTACTGCCAC CCTGAATGAT AGTGAAAGAG CAGGACCTCT TGCTAGTAGG TGAGTTGCCC 600
ACAATCTTCC CCACTCCTCC CCAGCTGGTG AGACCACACC TCCTTCACCA TCTGTTGAAT 660
CTAGACCGCA CCTCCCAGAC CACACCTCCT TCTCCATCCG CTGAGTCTAG GCCACACCCT 720
CTTTCCCTTT CTGTTGAATC TAGGCCACAC TCCCTTTCCT GTCTGTTGAA TCTGGACCAC 780
ACCCCGTTTC CTGTCTGCTG AACCTAGGCC ACACCTTCTT TGCCTGTCTG TTGAATCCAG 840
ACCACATCCC CTTCCCTGTC TGTTGAATCT AGACTACACC CCCTTTCGTA TCTGTTGAAT 900
CTAGGCCACA CCTCCTTTCC TGTTTGTTGA ATTTAGGCCA CACCCCCTTT CCTGTATGTT 960
GAATATAGAC CATACTCTCT TCCCTGTCAA TTCAATCTAG ACCACACCTC CTAGACCACC 1020
TTCTTTCCCT AGCTATGGAA TCTAGATCAC ACCTCCCAGA CCAGGTCTCC TTCTCCATCT 1080
GCTGAATCTA GACTACACCT CCTGTCCAAT CTGTTGAATC TCTGCACCTT TGCCCAGCCA 1140
CCTGATGAGA GCTGTGGGGT CACTAACCTG AATAATAGTG 1180
|
