| Tag | Content |
|---|
EnhancerAtlas ID | HS176-41047 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr8:145992120-145994280 |
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: 4 | Chromosome | Start | End |
| chr8 | 145992156 | 145992543 | | chr8 | 145993771 | 145994052 | | chr8 | 145993415 | 145993600 | | chr8 | 145992200 | 145993200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I144766 | chr8 | 145992150 | 145994409 |
|
Enhancer Sequence | TAAAAAAAAA CAAAACTATT TTTGCCTTGT CTTAAATTGA TCTCTAGCAG TGCCTTTTTC 60
CCCACACCCA CGTATTATTT CAGGGGTCAG TGACATTTGA TGACGTGGCT GCATATTTCA 120
CAAGGAGGAA ATGGATGCAT CTAGCTCTTC ACCAAAAGGC GGCTGGAGAA CTGTGGGAAC 180
TTGACCTGGC TGGGTAGGCT CTGCCCTCTC CCCTGCCCCT CTCCAGGCTC TCTGAGTACT 240
TCACTTGTTG AGAATGAGGG CAATTCCACA TCCTTTCTAG ACCTAGAAAC TAGACCCTTT 300
CTCCACGTGA CAGACCTGAG CTCCACAGGG AGGAAAGAGG CTGGGCCTGA GGTAGCCCCT 360
CTCTCCAAGT TCCCTATAGA TGTTGCACCA TGGAATTCCA CTCATGCTTG GCAGGACTTG 420
CTGTCTCCCC AGCATGATTT GGTATAGTCC TGATGAATCT GAATTTTTTT TTCTTTTCTT 480
TTCTTTTTTC TTTTGAGACA GGATTTCACT CTGTTGCCCA GGCTGGAGTG CAGTGGCACA 540
ATCATGGCTC ACTGCAGCCT CAACCTCCCA GGCTCAAGTG ACCCTCCCAC CTCTGCTTCC 600
CATGTAGCTG GGACTACAGG CACGAGCCAC CACGCCTGGG TAATTTTTTT GGTTCTTTGT 660
AGAGACAGGG TCTCACTCTG TTGCCCAGGC TGGTCTCGAA CTCCTGGGCT CAAGTGATCC 720
TCCTGCCTCA GCCTCCAAAG TGCTGGGATT ATAGGCATGA GTCATTGTAC TCAGCCAGAG 780
TCTGAACCGT ACAGGCATGA GTCATTGTAC CCAGCCAGAG TCTGAACCTT ACAGGCATGA 840
GTCACTGCAC CCAGCCAGAG TCTGAACCTT ACAGGCATGA GCACTGCACC CAGCCAGAAT 900
CTGAACCTTA CAGGCATAAG CCCCTACTCC CAGCCAGAGT CTGAACCTTA CAGGCATGAG 960
TCACTGCACC CAGCCAGAGT CTGAACCTTA CAGGCAGGAG TCACTGCACC CAGCCAGAGT 1020
CTGAACCTTA CAGGCATGAG CACTGCACCC AGCCAGAGTC TGAACCTTAC AGGCATAAGC 1080
CCCTACTCCC AGCCAGAGTC TGAACCTTAC AGGCATGAGT CATTGTACCC AGCCAGAGTC 1140
TGAACCTTAC AGGCATGAGC CCCTACTCCC AGCCAGAGTC TGAACCTTAC AGGCATGAGC 1200
ACTGCACCCA GCCAGAGTCT GAACCTTACA GGCATGAGCA CTGCACCCAG CCAGAGTCTG 1260
AACCTTACAG GCATGAGTCA TTGTACCCAG CCAGAGTCTG AACCTTACAG GCATGAGCAC 1320
TGCACTCAGC CAGAGTCTGA ACCTTACAGG CATGAGCCCC TACTCCCAGC CAGAGTCTGA 1380
ACCTTACAGG CATGAGCACT TCACCCAGCC AGAGTCTGAA CCTTACAGGC ATGAGTCATT 1440
GCACCCAGCC AGAGTCTGAA CCTTACAGGC ATGAGCAGTG CACCCAGCCA GAGTCTGAAC 1500
CTTACAGGCA TGAGCACTTC ACCCAGCCAG AGTCTGAACC TTACAGGCAT GAGTCATTGC 1560
ACCCAGCCAG AGTCTGAACC TTACAGGCAT GAGCAGTGCA CCCAGCCAGA GTCTGAACCT 1620
TACAGGCATG AGCAGTGCAC CCAGCCAGAG TCTGAACCTT ACAGGCATGA GCACTGCACC 1680
CAGCCAGAGT CTGAACCTTA TAGGCATAAG CCCCTACTCC CAGCAAGAGT CTGAACCTTA 1740
CAGGCATAAG CCCCTACTCC CAGCCAGAGC CTGAACCTTA CAGGCATGAG CACTGCACCC 1800
AGCCAGAGTC TGAACCTCTT AATCACCTTG CACTCTTTTC TCCCTTTCCC CTTCTTTCTC 1860
CCTCAGCCAT GACTCACCCT CATCCCTCCC CACCCCGGAC ATAGTTTTAT CTTTAGAGCC 1920
CCTACCTATT CCACCATCCT GGGCCTTCCT ACCTGGTCCA GCTGAATCTC TCTGCCTGCT 1980
CTCTGCAGAC CGTAGGCTTT GGTTCTCAGC AGAAATGCAC GTGTTGTGTT TCCATCTCTG 2040
CCAGCAGAAT TTTCAGGCCT CAAACCTGAC CTGATCTTCT AGCTGGAGAG AGAGGAAGAG 2100
CCATGGCTGC CAGATGTTCC AGGGACTGAA AATACAGACA CACAGAGATG CTCCTTCCCA 2160
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