| Tag | Content |
|---|
EnhancerAtlas ID | HS017-16956 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr19:48927660-48928800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr19:48928669-48928681 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr19:48928669-48928681 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr19:48928668-48928683 | TTCTATTTTTAGTAG | - | 6.57 | | ZNF263 | MA0528.1 | chr19:48928198-48928219 | TCTCCCCCTTCCCCCTTCTTC | - | 7.07 |
|
| | 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 |
| GH19I048424 | chr19 | 48927641 | 48929027 |
|
Enhancer Sequence | GGGACTACAG GCGCCCACCA CCACGCCCAG CTAATTTTTT GTATTTTTAA TAGAGACGGG 60
GTTTCACCGT GTTAGCCAGG ATGGTCTCGA TCTCCTGACC TCGTGATCCA CCCGCCTCAG 120
CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACCGCGC CTGGCTGGAA ATTACTTTTA 180
ATAATATATT TTACCTAACT ATGTCCAAAA TATTATTTTG ACACGTAATC AGTATAAACA 240
TGGGTGAGAC CGTTTACATA ATTTTTTTCC CCACACGCTG TCTTTGATAT CTGTGGCATT 300
TTACACTCAC AGCACATCTA GGTTCAGAGT GACCACATTT CAAGTGATCC ACAGCCCTAG 360
TGGCGTGTCA CTGCTGCACT GGACCGCCCA GGTCGACATC ACCCAAATGC AAAAAGTTTC 420
CTAGTCAACA TAATGAACAG AAAATATAAA AGGGCGCTGG CCGCCCCCCA GGACCCTGGG 480
ACTTTTTCAC TTCCTTACTC ACCCAGAGCA TTCTCCCCAG CCAGCCTGCT GACTCATCTC 540
TCCCCCTTCC CCCTTCTTCC GTTTTCTTCT CGCCAGCCCT TCCCTCCAGG AAGGACCCTG 600
AGAATTCCAG ATTCTCTCTT CTCTCTCTCT CTCTCTCTCT CACACAAAAC AGGGTGCCTT 660
TCCAGGCTGC CACCTCCCAC CTCTGCTTCA CTTGCGCCTT CCTCAGAAGG CAGGGATGGC 720
TGCAAACAGA ATCACTTTCC TCTTTTACCC CTTCAGGGAT ACCTCACACT GCCAGCCTGC 780
TCAGTCCTTG CAGTGGGAGA GCAAGAATTC AGAGACTCTC AGTGGGCGGG CGGGGGGGAT 840
CCCATTTTCT TTTTTTGAGA TGGAGTCTCG CTCTGTTGCC CAGGCTGGAG TGCAGTGCTG 900
CAATCTCGGC TCACTGCAAC CTCCGCTTCC CGGGTTCAAG CGATTCTCCT GCCTCAGCCT 960
CCCGAGTATT TGGGATTACA GGCATATACC ACCATCCCCG GCTAATTTTT CTATTTTTAG 1020
TAGACATGTG ATTTCACTAT GTTGGTCAGG CTGGTCTTGA ACTCCTAACC TTAAGTGATT 1080
CACCTGCTTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCGT ATCCAGCGGA 1140
|
