| Tag | Content |
|---|
EnhancerAtlas ID | HS017-32741 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr8:145992180-145994490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr8:145992217-145992231 | TGATGACGTGGCTG | - | 6.1 | | FOSL1 | MA0477.1 | chr8:145992955-145992966 | CATGAGTCACT | - | 6.14 | | FOSL1 | MA0477.1 | chr8:145993074-145993085 | CATGAGTCACT | - | 6.14 | | ZNF263 | MA0528.1 | chr8:145993963-145993984 | CTTTCCCCTTCTTTCTCCCTC | - | 6.29 | | ZNF263 | MA0528.1 | chr8:145993960-145993981 | TCCCTTTCCCCTTCTTTCTCC | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr8 | 145993771 | 145994052 | | chr8 | 145993415 | 145993600 | | chr8 | 145992200 | 145993200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I144766 | chr8 | 145992150 | 145994409 |
|
Enhancer Sequence | CCCACACCCA CGTATTATTT CAGGGGTCAG TGACATTTGA TGACGTGGCT GCATATTTCA 60
CAAGGAGGAA ATGGATGCAT CTAGCTCTTC ACCAAAAGGC GGCTGGAGAA CTGTGGGAAC 120
TTGACCTGGC TGGGTAGGCT CTGCCCTCTC CCCTGCCCCT CTCCAGGCTC TCTGAGTACT 180
TCACTTGTTG AGAATGAGGG CAATTCCACA TCCTTTCTAG ACCTAGAAAC TAGACCCTTT 240
CTCCACGTGA CAGACCTGAG CTCCACAGGG AGGAAAGAGG CTGGGCCTGA GGTAGCCCCT 300
CTCTCCAAGT TCCCTATAGA TGTTGCACCA TGGAATTCCA CTCATGCTTG GCAGGACTTG 360
CTGTCTCCCC AGCATGATTT GGTATAGTCC TGATGAATCT GAATTTTTTT TTCTTTTCTT 420
TTCTTTTTTC TTTTGAGACA GGATTTCACT CTGTTGCCCA GGCTGGAGTG CAGTGGCACA 480
ATCATGGCTC ACTGCAGCCT CAACCTCCCA GGCTCAAGTG ACCCTCCCAC CTCTGCTTCC 540
CATGTAGCTG GGACTACAGG CACGAGCCAC CACGCCTGGG TAATTTTTTT GGTTCTTTGT 600
AGAGACAGGG TCTCACTCTG TTGCCCAGGC TGGTCTCGAA CTCCTGGGCT CAAGTGATCC 660
TCCTGCCTCA GCCTCCAAAG TGCTGGGATT ATAGGCATGA GTCATTGTAC TCAGCCAGAG 720
TCTGAACCGT ACAGGCATGA GTCATTGTAC CCAGCCAGAG TCTGAACCTT ACAGGCATGA 780
GTCACTGCAC CCAGCCAGAG TCTGAACCTT ACAGGCATGA GCACTGCACC CAGCCAGAAT 840
CTGAACCTTA CAGGCATAAG CCCCTACTCC CAGCCAGAGT CTGAACCTTA CAGGCATGAG 900
TCACTGCACC CAGCCAGAGT CTGAACCTTA CAGGCAGGAG TCACTGCACC CAGCCAGAGT 960
CTGAACCTTA CAGGCATGAG CACTGCACCC AGCCAGAGTC TGAACCTTAC AGGCATAAGC 1020
CCCTACTCCC AGCCAGAGTC TGAACCTTAC AGGCATGAGT CATTGTACCC AGCCAGAGTC 1080
TGAACCTTAC AGGCATGAGC CCCTACTCCC AGCCAGAGTC TGAACCTTAC AGGCATGAGC 1140
ACTGCACCCA GCCAGAGTCT GAACCTTACA GGCATGAGCA CTGCACCCAG CCAGAGTCTG 1200
AACCTTACAG GCATGAGTCA TTGTACCCAG CCAGAGTCTG AACCTTACAG GCATGAGCAC 1260
TGCACTCAGC CAGAGTCTGA ACCTTACAGG CATGAGCCCC TACTCCCAGC CAGAGTCTGA 1320
ACCTTACAGG CATGAGCACT TCACCCAGCC AGAGTCTGAA CCTTACAGGC ATGAGTCATT 1380
GCACCCAGCC AGAGTCTGAA CCTTACAGGC ATGAGCAGTG CACCCAGCCA GAGTCTGAAC 1440
CTTACAGGCA TGAGCACTTC ACCCAGCCAG AGTCTGAACC TTACAGGCAT GAGTCATTGC 1500
ACCCAGCCAG AGTCTGAACC TTACAGGCAT GAGCAGTGCA CCCAGCCAGA GTCTGAACCT 1560
TACAGGCATG AGCAGTGCAC CCAGCCAGAG TCTGAACCTT ACAGGCATGA GCACTGCACC 1620
CAGCCAGAGT CTGAACCTTA TAGGCATAAG CCCCTACTCC CAGCAAGAGT CTGAACCTTA 1680
CAGGCATAAG CCCCTACTCC CAGCCAGAGC CTGAACCTTA CAGGCATGAG CACTGCACCC 1740
AGCCAGAGTC TGAACCTCTT AATCACCTTG CACTCTTTTC TCCCTTTCCC CTTCTTTCTC 1800
CCTCAGCCAT GACTCACCCT CATCCCTCCC CACCCCGGAC ATAGTTTTAT CTTTAGAGCC 1860
CCTACCTATT CCACCATCCT GGGCCTTCCT ACCTGGTCCA GCTGAATCTC TCTGCCTGCT 1920
CTCTGCAGAC CGTAGGCTTT GGTTCTCAGC AGAAATGCAC GTGTTGTGTT TCCATCTCTG 1980
CCAGCAGAAT TTTCAGGCCT CAAACCTGAC CTGATCTTCT AGCTGGAGAG AGAGGAAGAG 2040
CCATGGCTGC CAGATGTTCC AGGGACTGAA AATACAGACA CACAGAGATG CTCCTTCCCA 2100
GGTGAGAAGA GGGAAGCAGT TCTGGAGGAG GCAGTAGTGG GATACATTAG GAGACATAAC 2160
CTGAAAAAAC AGAGCCAGGC GGCTGCGCGC GGTGGCTCAC GCCTGTAATC CCAGCACTTT 2220
GGGAGGCAGA GGCAGGCGGA TCACAAAGTC AGGAGACCAT TCCAGCTAAC ACGGTGAAAC 2280
CTCGTCTCTA CTAAAAATAC AAAAAATTAG 2310
|
