| Tag | Content |
|---|
EnhancerAtlas ID | HS017-21703 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr22:22439850-22441700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr22:22441143-22441158 | GTGCTGACTCAGCCA | - | 6.18 | | MAFF | MA0495.3 | chr22:22441143-22441158 | GTGCTGACTCAGCCA | + | 6.1 | | STAT1 | MA0137.3 | chr22:22441641-22441652 | TTTCTAGGAAA | + | 6.14 | | Stat4 | MA0518.1 | chr22:22441641-22441655 | TTTCTAGGAAAAGG | + | 6.34 | | ZNF263 | MA0528.1 | chr22:22440884-22440905 | GAATGAAGAGGGGAAGGGAGA | + | 6.42 | | ZNF263 | MA0528.1 | chr22:22441600-22441621 | TTCTCCTCCCCTCCGTCCTCA | - | 6.93 |
|
| | 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 |
| GH22I022085 | chr22 | 22440278 | 22440450 |
|
Enhancer Sequence | GCCTCAGCCT CCCAAAGTGC TGAGATTACA GGCTTGAGCC ACCTGCCTGG CTCCATATTT 60
ATATTTTCTA AACATCCTAC TTGGAGTGGC TGATCCTACC AGCTACCATG TTTCCACCTC 120
ACCTGGGATC AAACACTGAC AATTGGTAAT TTTATCTCTT GCAGTCTTCA AATATTGAGC 180
AAATTTGCCA TTTTTGCTAT TCAATAAAAA TGCTGGAAAG TTATTTGCCA TGCCACTGAC 240
TCTGTTCAGT GCTTGGAGGA CAGACTCCTA GGAGTGAGAA GTTGACCACA GCATCTGAAT 300
AGCTATTACC CCAAGTCTGT GGAAATTAGA GAACAAAATT TTACCAGAAA TGCCCCCCAG 360
AGCTTCTCCC CATAACCTCA CCACCCTTAG AGAAGAGAGC TCCTGTTCTC CTCAGCGCTG 420
CAGGGTCCAC AGAGGAGGAA GAGCTCTGGC CAGCAGGGAG GAGCCACAGA AGAAAGGACC 480
TGGTGTCTCC CGTGACCAGG GTAGTGAGTC ATGGGAACCA GTCACTGCTC TGGACTTGAC 540
CTGACCTAAG AGGACTTGGT ATAGAGTCAC CACTTCAGTC CTCACCAAGG AACATCCAAA 600
AAGCCCTGGA CAGATTCACC CTTAAGGAGA CCAGTAAAGC ATGAACTGCC CTGAGTTAAT 660
GAGAAGGTCA CAAAAAGGGT CTGTCTGGCC TGGTGCTGAG CCTGGGGGCA GTGATCAGAG 720
CAGGGGGAAT GCACAGCTGG CTCTGGGGAC ATCTGGTCAT CATGTCACAG GAGAGTGTGT 780
CTGGATGTGG ACACCTGGGG ACATGAAGGG CTCATTACCA AGTGATCTAG GGGAGATCAG 840
AGCTGCGATC AGCTAACTGC CTGCATGGTG CCCTCTGCTC AGTGATCACA GTGGTGAGCT 900
CCTGATGCCC CGGAACACAC AGTTTCACCC TTGCCTGTAT CCCTGATATC CACGAGAGGG 960
GCCTGACCCA AGGCCAGCGT GTCATCAGAA GGCTGGGGGG CTCTAATTTG CATGGATGGA 1020
CCCTCATTCT CAGAGAATGA AGAGGGGAAG GGAGAGATTT GGGGAAGCTC TGTCTCAGCT 1080
GTGGGCACAG AAGGAAGGCA GGACTCAGGA CAATCTCCAG CATGGTCTGG TTTCCTCTCC 1140
TCCTCACTCT CCTTGCACAC TGCACAGGTG ACTAGATATA AGGCCATGGC TAAAGCCCTA 1200
GGAAGCCCAT GGGCCCTGCT TTCTCCTTTT GTCTCTCAAC CCAGAATCAC CATGACTGTT 1260
TCTCTCCCAC TTCCAGGATC CTGGGCTCAG TCTGTGCTGA CTCAGCCACC CTCAGTGTCT 1320
TGGGCCACAA GGCAGAGGCT CACTGTCTCC TGCACTGGAA GCAGCTCCAA CACTGGGACT 1380
GGCTATAACG TAAACTGTTG GCAGTAGCTC CCAAGAACTG ACCCCAAACT CCTCAGGCAT 1440
GGTGATAAGA ATTGGGCCTC CTGGGTATCT GACCAATTCT CTGGTTCCAA GTCTGGCAGC 1500
TTGGCCTCCC TGGGCACCAC TGGGCTCTGG GCTGAGGACA AGACTGATTA TCACTGCCAG 1560
TCCCGTGACA TCTGCTGAGT GCTTGTACAG TGCTCCAGGC TTGCAGGGGA GTGAGACAAG 1620
AACCCCCTTC CTCCTTTCCC AGGAGGGTGA GTGCCCAGCA GCTACTGCAC AGGCCTGGCC 1680
TGTGGCTTCT GCAGTTGCTG TTTCCCCAGT GGGCCTGGGA GCATCCAGGG CCCCACCTGG 1740
GAGTAGATGC TTCTCCTCCC CTCCGTCCTC AGAGTCACCC ACAGCAGTCC CTTTCTAGGA 1800
AAAGGGCCTC CAGAAAACAG AATGTCCTGT ACCCTGCAAC TTGGGACACA 1850
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