| Tag | Content |
|---|
EnhancerAtlas ID | HS188-10634 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr5:176074700-176077290 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP8 | MA0747.1 | chr5:176074834-176074846 | CCCACGCCCACT | + | 6.14 |
|
| | 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 |
| GH05I176649 | chr5 | 176076732 | 176078530 |
|
Enhancer Sequence | TGGGTGAGCG CGGGGTCTGC GCCTTGCCCT GTGCTGGGGG GTGGTGGGAG AGGGAGATTC 60
AGTCTTTTGC TGGGGGAGAC CACTCCCTGC CCCAAGAGTT TGGAGCTCGG GACCATCCCC 120
CCACTTCTGC CACACCCACG CCCACTTCCA GGACCACCCG AGGTAGCTAC AGAGGCCCGG 180
ATTGCTGGGG GCGGGTCCTA GCGACAGCGT GGGGTCGGGG TTGGGGTAGG GAGTCTCCCT 240
AAATAATCCC GAGGCCTGGT GGAGAAAGGG AAGGTGTTTC CTTGAAGACC CCAGGGGCGT 300
GCTAGGTGCA GGTTGCCCCC TCTCGCCCAG CCCTCCTTCC TACCCTGGGA TGTGGGATGC 360
GTGCCAAGCC CCACCCCTGG TTTAGCCGGT AAGGAGATTC TGGCGTGAAG GGAGCCGCCA 420
GGCCCCTTCC CCGGCCTCCT TTCCCTTCCA GTAGTACCTG GGTCAGGTGC CTCACCTTAG 480
GCTCCTGCAG AGTGGGGTGG GTCACAGTCC TCTGCCCACC CCAGTCCCGC ACAAGGAGGC 540
TGACCTGCCA GGAGGGGCAG GGAGGGACAA TGGCGAGTCC TTGGCGGCTG GGAGAGGATC 600
TCCCCGGTTG AGAGCCTGGG AGCTGGCCTT GGGGAACAGA ATTCAACATT CCACAGCTGA 660
CAAGCTGAGG CTCCTGGGCG GGTCTGCCCC TACCGGGGAA GGGAGCTACT AGTGCCCCTC 720
CCAGGGTGGC ATCTGTCCCC CTGGGCCCTG CCAGGTCATT TTTCCCATCT CTCCAAAGCC 780
GTGGCCCTCT GCAGTCTCTG CTCCTGAGGC CTTGGGTCAA GATGCCAGGC CTTTTCCCTT 840
GTGTTCAGCA AGACTCAGTG GCACTGCCCC CCACCCACGT GTCACCGAGC TCACTGGTGT 900
GGTGGGTGTC CTTGCACTGC AGCGCTAGGC TCTTGAGGGT GTGGGCAGTG TGTGGGAGCA 960
CTGGCAAAGA AGTCAGAAGG CCTGGCTGTA GCAGGCCTGG CTGGGACACC TTGGGCAAGT 1020
CATCTCTCCT CTCCGGGCCT CAGCTTGCCT GCCTGGGAGA CGACGATAAA GAATCTGCCT 1080
GTGAGGGCTG TTAGGCAGAT ACAATGAGTT CAATTTGTTG TATTCTCACA ACTGCCTTAT 1140
TATCTGCATT TTACAGATGG GGAAACTGAA GGAATAGACA CAGAGAAATT AAGTCACTTA 1200
CCTAGGGTCA CACAGCCAGA AAGTACAGAG CCAAGGTGAC GGCTTAGTGG GCAGAGGGTG 1260
GAGGTGAGGC AGAGCTGTGA GCAGAAGTAA CCTCAAATAC CGAGGGGGAG CAGGCGTGAG 1320
AGACCCGGGT TTGTTGCTGG GGCGGAGCGT GGGGTGTTAT GTTAAGGTGG CATGGAGAAG 1380
CGAGGGCTTC CAGTGATGGG TCTGATCTGG CTTCTGTTCT GGAGACCGCT TGCCTGGCTG 1440
CTGTGTGGAG GGTGGATGAG GGGCAGGGCC TGGAGGTTTG GAATGGGGGC AGGGCTGGGG 1500
CAAAGCTGGG ATGGTGAGGT GGGAAAGGTG AGGGAGGTTG CTGGGAAAGT CAAGAGGCTG 1560
AATTGACTGG GCTGGGTCAC TTGGGGGCTG GAGGGAGGAT TTCAGATTTG GGTTAAGGTG 1620
GCCTAAGGGA GGCTGCTTGT GGAACAGGCA CAGAGGTTTT CATGTTTAAT GTCAGGCAGA 1680
CCCTGGTGTT GTTCTGTTTG GAAACTGCTT GTGGTTTCCT TTTTTCTTTT TTCTTTTTTT 1740
TTTTTGAGAC AGAGTTTTGC TCTTGTTGCC CAGGCTGGAG TGCAATGGCA CGATCTCGGT 1800
TCACTGCAAC CTCCGTCTCC CAGGTTCAAG CGATTCTCCT GCCTCAGCCT CCCAAGTAGC 1860
TGGGACTATA GGTGTGTGCC ACCACGCCTG GCTAATTTTG TATTTTTACT AGAGATGGGG 1920
TTTCTTCATG TTGGTCAGGC TGGTCTCGAA CTCCTGACCT CAGGTGATCC ACCTGCCTTG 1980
GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCACG CCCGGCCATC CTGCTCGTGG 2040
TTTCTTACTG CTCCTAGAGT ACTGTCGGCC TCCAGGGCCC CGCGGGGCCG GGCTGTCCGC 2100
CCTTCAGTTT GTTCCTTGAA CTAGACGTGG TCTTGTGTCA GGGCCTCTGC CTGTGCCCTA 2160
CCCTCCTCCT GGAACAGGCT TTTCCCTCTT GCTCTTTTCA TCATTCAAAC CTCAGCTGAA 2220
ATGCCCCCAC CCTCCCTTCT GCCCTCTCTA AAGCTGGCGT CCAACCCCAG CATCCCCCAT 2280
CTCGTCGCCC CGCTCGATAT TTGTTAAGGG GTCTGTTTGC ATCTGAGGTT TCCTTGTCTG 2340
CTCACTGACT GTCCATCTCC CCTGCTGGAG TGTAAGCTCC GTGAGGGTCG AGTCCGTCCT 2400
ATTCACCAGC GAATCCCCGG CATGGCGGCG ATCAGTGCCG GTGGGTCGTG GAGGTGTTTG 2460
CTGCAGGCGG GTGGACGTAG GGGTGTGGGA CCAGCATGAG GTCTGGGTGG GGATCGGGAG 2520
ATGCCAGCGT CATGATGGGA TGGAAGACGA GCGTGAGGAG GAAGAACGGC AGAAGGCTGA 2580
GGCTGGAGGC 2590
|
