| Tag | Content |
|---|
EnhancerAtlas ID | HS136-09843 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr19:48927430-48928900 |
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 | GTGAGGCCAA GGTGAGAGGA TCACTTAAGA CCAGGAGTTC AAGACCAGCC TGTGAAACAT 60
AGTGAGACCC CCTTGACTCA CAAAAAAAAA AATTTTTTTT TTTTTTTTTT TTTTTGAGAC 120
AGAGTCTCGC TCTGTTGCCC AGGCTGGAGT GCAGTGGCAC AATCTCGGCT CACTGCAAGC 180
GCCGCCTCCC GGGTTCACGC CATTCTCCTG CCTCAGCCTC CCGAGTAGCT GGGACTACAG 240
GCGCCCACCA CCACGCCCAG CTAATTTTTT GTATTTTTAA TAGAGACGGG GTTTCACCGT 300
GTTAGCCAGG ATGGTCTCGA TCTCCTGACC TCGTGATCCA CCCGCCTCAG CCTCCCAAAG 360
TGCTGGGATT ACAGGCGTGA GCCACCGCGC CTGGCTGGAA ATTACTTTTA ATAATATATT 420
TTACCTAACT ATGTCCAAAA TATTATTTTG ACACGTAATC AGTATAAACA TGGGTGAGAC 480
CGTTTACATA ATTTTTTTCC CCACACGCTG TCTTTGATAT CTGTGGCATT TTACACTCAC 540
AGCACATCTA GGTTCAGAGT GACCACATTT CAAGTGATCC ACAGCCCTAG TGGCGTGTCA 600
CTGCTGCACT GGACCGCCCA GGTCGACATC ACCCAAATGC AAAAAGTTTC CTAGTCAACA 660
TAATGAACAG AAAATATAAA AGGGCGCTGG CCGCCCCCCA GGACCCTGGG ACTTTTTCAC 720
TTCCTTACTC ACCCAGAGCA TTCTCCCCAG CCAGCCTGCT GACTCATCTC TCCCCCTTCC 780
CCCTTCTTCC GTTTTCTTCT CGCCAGCCCT TCCCTCCAGG AAGGACCCTG AGAATTCCAG 840
ATTCTCTCTT CTCTCTCTCT CTCTCTCTCT CACACAAAAC AGGGTGCCTT TCCAGGCTGC 900
CACCTCCCAC CTCTGCTTCA CTTGCGCCTT CCTCAGAAGG CAGGGATGGC TGCAAACAGA 960
ATCACTTTCC TCTTTTACCC CTTCAGGGAT ACCTCACACT GCCAGCCTGC TCAGTCCTTG 1020
CAGTGGGAGA GCAAGAATTC AGAGACTCTC AGTGGGCGGG CGGGGGGGAT CCCATTTTCT 1080
TTTTTTGAGA TGGAGTCTCG CTCTGTTGCC CAGGCTGGAG TGCAGTGCTG CAATCTCGGC 1140
TCACTGCAAC CTCCGCTTCC CGGGTTCAAG CGATTCTCCT GCCTCAGCCT CCCGAGTATT 1200
TGGGATTACA GGCATATACC ACCATCCCCG GCTAATTTTT CTATTTTTAG TAGACATGTG 1260
ATTTCACTAT GTTGGTCAGG CTGGTCTTGA ACTCCTAACC TTAAGTGATT CACCTGCTTC 1320
GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCGT ATCCAGCGGA TGGCACTTTC 1380
CAAATCTACT TGGTTCCCAA GTTTTGGATA GCAAGTGGTG AGAATGTGAC TAGCAAGACA 1440
GACCAGCCCC ATCTCTCAAA ATGAACCTAA 1470
|
