| Tag | Content |
|---|
EnhancerAtlas ID | HS187-11887 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:8640000-8642190 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr19:8640202-8640216 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 8640627 | 8640983 | | chr19 | 8641349 | 8641441 | | chr19 | 8640382 | 8641160 |
|
Enhancer Sequence | CCGAGGCTGT AGTGCAATGG TGTGATCTTG GCTCACTGCA ACCTCCGCCT CCCGGGTTCA 60
AGCGATTCTC CTGCCTCAGC CTCCCGAGTA GCTAGGATGA CAGGCATGTG CCACCACACC 120
CAGCTCATTT TTGTATTTTT AGGAGAGACG GGGTCTCACC ACGTTGGCCA GGATCGTTTC 180
TATCTCTTGA CTTCGTGATC TGCCCGCCTC GGCCTCCCAA AGTGCTAGGA TTACAGGTGT 240
GAGCCACCGC ACCCGGCCGG GCATTAGATT GTCATAAGCA GCATGCAACC TGGATCCCTC 300
GTGTGTGCAG TTCACAACAG GGTTTGCGAT CCTGTGATAA TCTAATGGCG CCCCCGAGAA 360
TCTGAGAGGA GGTGGAGCTC GGGCTTGCTT GCCTGCCACT CATCTCCTGC TCTGTGACCC 420
GATAGGGCTC ATGGTTTCTA ACAGACAGAC CATGGCCCGA TAGCAGTCCA TGACCCCGGG 480
GGTTGGGGAC CCTGTTGTAA AGGACTTCAG AAATACTGTT TCATTGAATC CTTCAGCGAT 540
CTTCCTGGCA TTCACCACTC CTCCAGGAAG ATTTCAGCAT CCCCAGACAG AGGTGGGTGT 600
CATTTTTTTC TCTTCTATCA TCCTCTGCGA TACGGGTGGC CCCTCCCAGA CCTTGTCTGC 660
CAAGCCGACT GTTGACTAAG CATTTTCAGA GGGCTTCCTT GGGGAGGGGT TGCCTTTCTT 720
TCAAGTAGCA AATCACTTCC TGTGTTCTTT TGATCAAAGC CCTGCCCATC CCAGGACCTG 780
AGCCTCCCTG GCTTGCTTCT CATCTTGGAA GAATTCCCAC CCCAACAGTC TCAGAGCTCC 840
AGCTGATGGT TTGGGTGTGA ATTCCGGGAT GCCCAATTTC TCATCAGCTT TCCTTTTTTG 900
AGACGGAGTG TGCTCTGTCA CCCAGGCTGG AGTGCAGCGG CAGGATCTCA GCTCACTGCA 960
CCCTCCGCCT CCTGGGTTCA AGTTATTCTC TTGCCTCAGC CTCATATGTA GCTGGGATTA 1020
CAGGCGTGTG CCACCACGCC CAGTTAATTT TTTGTATTTT TTAGTAGAGA CGAGGTTTCA 1080
CCACGTTGGC CAGGCTGGTC TCGAACACCT GACCTCAAGT GATCTACCTG TCTCAGCCTC 1140
CTAAAATGCT GGGATTACAG GCATGAGCCA CTGTCCCTGG CCCTCACTGG CTTCCTGAAA 1200
GAAGGTGTTG TCTCTCAGAC TAACACCACC TCTGCCTCTT GCCCTATGTC CCTGACTCCA 1260
CCCTAGTAAG CTGTACCTGC CAAGAATCCT GCAGTGGCCG CTGTCACAGC CACATGCTCT 1320
CATCCTCACT GACTGAATGA CGAGAAATGA AAGCTGAAGT GGTCTACACA GCAGAGAGCT 1380
GTGGGGTGGG GTCAGCCCTG GCCACCTCTT ACTTTGCGTC TTATGGTGGT ACGATACTGC 1440
TAGGAATAGC GCCATGATCA CGACAGTCTC CCCGTTGCTA TCATCGACAG ACCTCAGACT 1500
TGACAGGCAG CAACACCTCT GGCTGCCATC CTCCTCTTGG GATAAGGGAT GCCCACCAAA 1560
GGGTGGCATG GACGTATTCA GCCTCTCCTG CCTCTGCTGC AGCCATACCG CCCGTCACCG 1620
GCACAGGGAG GGCGTCAATC CACCCCATCG CTTGTTAGAC ATAGCTTCCC ATCTCAGCCG 1680
AGGACTCTGT GGCAGAACCC ACAGACCTTG AGAATGTTGC AACTGAAAGA CCCCTGAAGA 1740
GCAACTTCCG CATCTAGACG GATTTCCAAA TATGACATCT GTGGGAACCG GGGCCAAGAG 1800
AGGGGAAGTG ACTAGCCCAA GGCTACACAG GGAGACGAGA GACTGGGCTG GACTGGGAAA 1860
GGGCTCCCTT AATTTGCAAG CAAAGGAGGC TATGTCCTTG TCCCTGCAGA CTCTGTGATT 1920
CTCCCTGGGC CACCTTCTGT CTTCCAGGTC CTGCCCTATC CTTGGATCCA GGGATACCAC 1980
CCTGGCATCC CCACCACCTA CAGATGGGAG CTTGCTCCCT GGTAAGGGAT GCTGGAGGCA 2040
CCTGAGCTGC ACTGAGAGAC ACCCCACCCC CACAGAAGTC CACCATGCCC CTCCCCTCAC 2100
CCCAATTTCT GATGGTCATT TTTAGGACAC CTCCACCTGG CTGGTGTCCC TCCTCTTTCT 2160
TCTTCCAGAT CCCACCCTTG AAGGACTTAC 2190
|
