| Tag | Content |
|---|
EnhancerAtlas ID | HS188-00138 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr1:15294610-15296650 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr1:15296255-15296272 | TGGATTCCTAAAAAGAA | - | 6.19 | | RARA(var.2) | MA0730.1 | chr1:15295068-15295085 | AGGACACGTGAGGGTCA | + | 6.03 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26798 | chr1:15294684-15296104 | Esophagus | | SE_53292 | chr1:15293321-15296336 | Spleen |
|
| | 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 |
| GH01I014967 | chr1 | 15294172 | 15298701 |
|
Enhancer Sequence | ATGTAGAATC AGTGGGAGAC CTGAGCTTGT TTTCCTGCAA CTAGATGGTC CCATCTAGGG 60
GTGACGGGAG ACAGTGACAG ATCATCAGGC ATTAGATTCT AATAAGGAGC ACGCAACCTG 120
GATCCCTCAC ATGCGCAGTT CACAAGAGGG TTCGTGCTCC TATGAGAGTC TAATGCCATC 180
GCTGCTGATC AGACAGGAGG TGGAGCTCCG GCGGTAATGT GAGTGATGGG GAGCAGCTGT 240
AAATACAGAT GAAACTTCGC TCGCTCGCCC CTCACCTCCT GCTGTGCAGC CTGCTTCCTA 300
AGAGGCCAGG GACCAGTACC AGTCCATGGC CTGGGGCTTG GGGACCCCGT GTGAAGCCAC 360
TGCATTGTGT CACTTTGTTA CAACAAGAAT GGGAAACGAA CCAGGCCCTC TCTTTCCCTG 420
GACTTGGCAG CCCTAAACAC TGCCCTCTCT CAGGGCTTAG GACACGTGAG GGTCATCTGT 480
TTCCTTTAGA AACGCCTGCA GGGCACAGCA GCCAGCACGG GGCGGGTGGA GTTAGCTAGC 540
ACTGACTGAG CATGGAGCAG AAGAAAGGAT CCGGAGTTTC CTCTCCTTAC TGGAAGGACT 600
AAGGCCTGTG GGAGCCTTTT CCCTGCCACA GAGTGAGTCA CCTGCCTTAC ACTGAAAGAA 660
ACACAACTTT ATTATTTAAT TTGCTCATTC ACCAAATGTT CCCTGAAAGC TTCCCTACCC 720
CAAAGCTTGT GCCGATGCCT GTGGTTCAGA GCATTCCAGG CCCTGCTCAG AGTCTAGGGA 780
CATGCCTGAA ACCTACGACA CACTCAGTGT ACCTTACTTG AATCCTATTT TTCCAAGTGG 840
CCAACCAGGC CTGTAGATGA GAGTCTATCC CATAGGCATT CCTGCTTCAA GGAGTTCTAG 900
GCTGCAGAGA CTGTCTTAAG TCCAGCGGGG TCGGTGGGGC TGGAAGACTA AAGCTCCCAG 960
CAGGTGCAGC CATGCCCTGG CTGCCTTTGC AGATGTCACC AGGCCTGCAG ACAGTGGGGT 1020
AGTAGGTGGC CTGAGAGGCT GTTGAATAGA ACGATGTGTC ATCTGTGCTG GGGCGGCCAT 1080
GCCCACTTGC TTTCTTAGAC ACACATCCTT GTCACCACAG CACTGTGTGG GTTTGAAAAG 1140
CTACTTGATG TTTCCTGTGT CCCTTCCCAC ATCCGCACTC CATTCTTAGT CTCATTCCCT 1200
CCATCAAAGA CGTGTTCATC TTCTATGCAG TTCATCACCT GGGGTTGAAT GTGTATGTTC 1260
CTCTTTAGTA AATTCATACG CTTGAAGCTA CTGCTGTTTC TTTAGCCTGG TGGCTCTCGG 1320
GGCTGCTGCA GGGGGCCCAC CCTGAGCCAG CCCCTCGGTC CCACAGCCCT GACGTAGAAG 1380
ACTCTTTGCT GGTAAATCTC GGAACTCACT GGAAGCTTCC ACAAAGTTTA ACTCTACAGA 1440
CAGAATGTCT TCCTTACATA CTACCGGCTG CTTTTAAATA TTGTTAACAG ATCCCCCTTA 1500
AAGGCTTCTT AGACTCCACA TTTTGATCCA GTTGATAATA ATTGATGGTC AGGTGGAAGA 1560
ATTGCCCAGG CTCTGTTGTT GTTCTGTTAT AGTTGCCACT GGACCTGCTT TCAGCACCCT 1620
CACCCTGGCT GCTTCAGAGG GCAGCTGGAT TCCTAAAAAG AACCCATGCC CTAATGCACA 1680
AGTACTTTTT ATTTTATTTT ATATTATTTT TCGTGGGGGG ACAGAGTCTT ACTCTGTCGC 1740
CCAGGCTGGA GTGCAGTGGC ATGATCTTGG CTCACTGCAA CCTCTACCTC CTGGGTTCAA 1800
GCGATTCTCC TGCCTCAGCC TCCTGAGTAG CTGGGATTAC AGGCGCCCGC CACCACGCCC 1860
AGCTGATTTT TGCATTTTTA GTAGAGCTGG GGTTTCACCG TGTTGGCCAG GCTGGTCTTG 1920
AACTCCTGAC TTCAAGTGAT TCACCTGCCT CGGCCTCCCA AAGTGCTGGG ATTATAGGCA 1980
TGAGCCATGG TGCCTGGCCC ACAAGCACTT TTTAAAAATA ATTAATAATC ATCATCATTT 2040
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