| Tag | Content |
|---|
EnhancerAtlas ID | HS104-03874 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:155138250-155140820 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:155140514-155140533 | TAGCGCCCCCTGCAGGCGT | - | 6.46 | | CTCF | MA0139.1 | chr1:155139983-155140002 | TGATGCCCTCTGGTGGCCG | - | 7.11 | | RAX | MA0718.1 | chr1:155139700-155139710 | GTTAATTGGC | - | 6.02 | | ZBTB18 | MA0698.1 | chr1:155139462-155139475 | AAACATCTGGCTT | - | 6.18 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 155138347 | 155140762 | | chr1 | 155138255 | 155139946 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I155165 | chr1 | 155138194 | 155141090 |
|
Enhancer Sequence | AAAAAAAAAA TGTGTTAATT TATCAAACGT AAACGTGCCT GTTTTTCTCA TTTCCAAGTG 60
TATCTGAAAC CTCCACAGAC AGTAGGGACC TAGACTTCTC TCCATCTTTC AGAAGTCGTG 120
TCTCCAAGGG AGCAGTTGCT GAGATCTGTG GGTCGTTTCC CACCCTGCCC CTGGCCCCCT 180
GCAGAGGCTG GGGTGGGAAC AGCTGGCTCT TCAAACCCTG CCCAAAGCTC TGAACTCTGC 240
CTCCTGCCAG TGGTCAGGCC TCCTCCACCT GACCCTTCAC CCGAGGTGAT GGGATGCCTA 300
ACCATAAGGC CAGCTGGGGG GCTTCTCTCT CTGCCTCTGC AGGAACTCAA CCAAATAGCA 360
TTTACAGAGC AACCTCTATG TGGCCAGCTG GCTTTCAGCC CTGGGGGTGG GAGGTGCGGG 420
AGTGGCTTTG GGAACCTGAT CCCGATCTCG GCACTGCCCC CTGAGAAACT TCCAGGCTGC 480
TGGGAGAAAA GCAAAGAAAG GTACCTAAAG CAGAGCTATT AAGTGCCCCA ACTGTGCCTA 540
TGTGAGAGTC CCACCATTGT TTGCTTGGGA GGCAGATCCT AGTAAGCCTA AGTCAAGGAG 600
GAGTGCGCAC AGGGCAGGCC AGCCCGGAGG TCCCTGAGGG CAGGGCCTCC AGGCTTCCCA 660
TTCTTTCGCA GTTCCCACAG CGCTCAGGCC CCACTGGGCT CATAATAAGC TTCAATGCCC 720
GCTTTTGACT GAACCTTCCC CTTTGTATCT GTCTCTGTGT CTCTCAGCAT CTCTGTCTCT 780
ACGGGTCTCT GGCTCTCTCT TGTTTCCCAA CATCCTTCCC CAGCCCCTGG GGAGCAGAGC 840
TGGGGGAGCC CGGCAGTGGG AACGGGACAG CGTCCTGTTC TCACCAAGGA CAATAAGGGC 900
CGGAAAGGGC TGGAGCCAAG GCCTGGCGCA GACTCCCCCT CCCTGCCTGC CCTGGGCGCC 960
CCCACCCTCC CGCCCTGACC CGCCAGCACG GCCTAAGTGC CAGTCCTCAG GGAGTCAGCC 1020
TCCTTGCCCT TGGTCTCACA TTCCTACTGC TCTCCCTTTT CTCTGGAGGC ATCCCTTCTG 1080
CCCCCAGGAA CCCGCAGAGC GAGCGCCCTC CCGCACTCCC CGCAGCCCCA TCCCCTGCAT 1140
TATTTACTCC TGTTTCCGGA GCTGGCTGCG GGCGCCGGCG GGTGTTAGGG CCACGTGTGA 1200
GGGAGCAGGA GGAAACATCT GGCTTCCCTC TGTCCCCCAG GGGCGGGGAC GCCTCTCTTT 1260
CCCTCAGGCC TACCGCCTCT CTCTCCCTCA GGCCTACCGC CTCCTCCGGG GTGGAACTGA 1320
GCCCCAGAAG TCCAGGGGCC AAGAGGTTAG CACCTTTGCC CTTCTCACCC TCAGGGCTCT 1380
GGCAGCCATG GAGTCCTCAC GCCCCCTTAC TTAATGATGG TGATTAGGTG GCTGTGATAC 1440
CCCTGCCAGG GTTAATTGGC AGGTCAGGTG CAGGCAGCCT GCAACCAGGC AGGGTGCAGA 1500
GCTGCGACGT TGGCGCCAAC CTGCCTTGTA AATGTACTCA TTCCCTGAGG AAGGCGTCAT 1560
TATTCCTGGG CCACATGCTG CCCATGGTGC CTACGCAGTG GGTGGCAGTA GGTGCTCAGA 1620
TCCCTTGGCA CTGCCCTGGC ACCTGCTCTC CGGCTCCTCC CCACCCTCCC CTAGCCATAG 1680
AGATGATGCT CGCTGCTGGT CCCCACCAAA GCCAGCTCTC GTTGTGGAAG GCATGATGCC 1740
CTCTGGTGGC CGGATCCCCA GTCTCCCCCC ATCCCGTCCC CCGCCACTCC CTTCCCCCCT 1800
CCCCGCCCTA GGCTGTGTCT GTGCTCACCT GGACTGGGAC CTGACCCTCT GCCCAGTGCT 1860
CCCACGGGTT AGGACAAAGT CGAGGTTTGA CAGTGAGACT TAGAGCCAAT CCAGCCTCCC 1920
TTTAGGCCCA GAGACCAACT TGGACAACCT CGTCCTCTCC CAGAGGGTCT CATATATCAC 1980
AACCCACCGC CCTCCCCAAC CATCAGTACG GGTGAGTCAG AGCCAGATCT TCTCAGGGAG 2040
GCTCTCTCTG GTCTCCACTG AACTTTCCGC CTCCACTCCC AGCCTAGGGG GAGAAGAGGC 2100
TTAATTCAGG ATTCAGTCCT TCCAAATGGA CCAGTCTTCC GAGTCTTCTA AGAAGGCTGG 2160
CTTCCACACT GACGGACCCA GCAGCAACTA ACGCCACTCC CGGCCCTCAG GGATAGCTTG 2220
CCTAGGAGGG TGCCGCTGGC TTCCAGGAGG CAGACGTGAG TCCATAGCGC CCCCTGCAGG 2280
CGTTTTGGAT AAACTGCCTA GCACATCCTC CTTGGGCAGG TTACGGAAGG GCAAGTGTTC 2340
TAGCCAAAGA TGGGAGTGGA GTGGGGTGGC CTCTAATCCC TGACCAAAAC TCCTCTACTC 2400
ACTTCTTCAT CTTCACTGAG TCTTATTCCC TAACTCAGGC ACCTATGGAC AGGATTTTGT 2460
TTGTCAGGGC AGGTTATTTC ATTCAACTAA CCCACCTTTT TTTTTTTTGA GACAGAGTTT 2520
CACTGTCGTT CAGGTTGGAG TGCAGTGGCG CAATCTCCAC CCACTGCAAC 2570
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