| Tag | Content |
|---|
EnhancerAtlas ID | HS052-00313 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:15294090-15296350 |
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 | | NR2C2 | MA0504.1 | chr1:15294348-15294363 | AGACCTTTGACCTCC | - | 6.19 | | Nr2f6 | MA0677.1 | chr1:15294348-15294362 | AGACCTTTGACCTC | - | 6.3 | | RARA(var.2) | MA0730.1 | chr1:15295068-15295085 | AGGACACGTGAGGGTCA | + | 6.03 | | RREB1 | MA0073.1 | chr1:15294491-15294511 | GGTTGGGGGATGGTTTTGGG | - | 6.25 | | Rxra | MA0512.2 | chr1:15294348-15294362 | AGACCTTTGACCTC | - | 6.14 |
|
| | 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 | AAGGGCCCTT GAAAGTAGAA GGGGAGGCAC AAGAGAGAGT CAGAGGAGAT GTGACCGGAG 60
GAGCAGAGGC CAGAGGGATT CAATGTGGGG CCTTGACACA CCGTTGCTGG CTTTGAAGAC 120
ACAGGAAGGG GCTGCAAGCC AAGGAGTGCA GGCGACCTCT AGAAGCTGGG AAAGACAAGG 180
AAACAGGCTT TCCCCAGAGC CTCCAGAAGA AAGGCAGTCC TGCCAACACC AGGGTTTTAG 240
CCCGGTAACA CCCATTTTAG ACCTTTGACC TCCAGAACTA CTATAAGAAC ATTCATTTGT 300
ATTAAATTAA TTTGTATTAT GTTAGGCCAG CAGTCCCCAA CCTTTTAGGC ACCAGGGACC 360
GGTTTCATGG AAGACAGTTT TTCCACGGAC CAGGTGTCCG GGGTTGGGGG ATGGTTTTGG 420
GATGATTCCA GGGCATTACA TGCACTACAT TTCTTGTGCA CTAAATTTCT ATTATTATTA 480
CATTGTAATA TATAGTGAAA TAATTATACA ATTCACCCTA ATGTAGAATC AGTGGGAGAC 540
CTGAGCTTGT TTTCCTGCAA CTAGATGGTC CCATCTAGGG GTGACGGGAG ACAGTGACAG 600
ATCATCAGGC ATTAGATTCT AATAAGGAGC ACGCAACCTG GATCCCTCAC ATGCGCAGTT 660
CACAAGAGGG TTCGTGCTCC TATGAGAGTC TAATGCCATC GCTGCTGATC AGACAGGAGG 720
TGGAGCTCCG GCGGTAATGT GAGTGATGGG GAGCAGCTGT AAATACAGAT GAAACTTCGC 780
TCGCTCGCCC CTCACCTCCT GCTGTGCAGC CTGCTTCCTA AGAGGCCAGG GACCAGTACC 840
AGTCCATGGC CTGGGGCTTG GGGACCCCGT GTGAAGCCAC TGCATTGTGT CACTTTGTTA 900
CAACAAGAAT GGGAAACGAA CCAGGCCCTC TCTTTCCCTG GACTTGGCAG CCCTAAACAC 960
TGCCCTCTCT CAGGGCTTAG GACACGTGAG GGTCATCTGT TTCCTTTAGA AACGCCTGCA 1020
GGGCACAGCA GCCAGCACGG GGCGGGTGGA GTTAGCTAGC ACTGACTGAG CATGGAGCAG 1080
AAGAAAGGAT CCGGAGTTTC CTCTCCTTAC TGGAAGGACT AAGGCCTGTG GGAGCCTTTT 1140
CCCTGCCACA GAGTGAGTCA CCTGCCTTAC ACTGAAAGAA ACACAACTTT ATTATTTAAT 1200
TTGCTCATTC ACCAAATGTT CCCTGAAAGC TTCCCTACCC CAAAGCTTGT GCCGATGCCT 1260
GTGGTTCAGA GCATTCCAGG CCCTGCTCAG AGTCTAGGGA CATGCCTGAA ACCTACGACA 1320
CACTCAGTGT ACCTTACTTG AATCCTATTT TTCCAAGTGG CCAACCAGGC CTGTAGATGA 1380
GAGTCTATCC CATAGGCATT CCTGCTTCAA GGAGTTCTAG GCTGCAGAGA CTGTCTTAAG 1440
TCCAGCGGGG TCGGTGGGGC TGGAAGACTA AAGCTCCCAG CAGGTGCAGC CATGCCCTGG 1500
CTGCCTTTGC AGATGTCACC AGGCCTGCAG ACAGTGGGGT AGTAGGTGGC CTGAGAGGCT 1560
GTTGAATAGA ACGATGTGTC ATCTGTGCTG GGGCGGCCAT GCCCACTTGC TTTCTTAGAC 1620
ACACATCCTT GTCACCACAG CACTGTGTGG GTTTGAAAAG CTACTTGATG TTTCCTGTGT 1680
CCCTTCCCAC ATCCGCACTC CATTCTTAGT CTCATTCCCT CCATCAAAGA CGTGTTCATC 1740
TTCTATGCAG TTCATCACCT GGGGTTGAAT GTGTATGTTC CTCTTTAGTA AATTCATACG 1800
CTTGAAGCTA CTGCTGTTTC TTTAGCCTGG TGGCTCTCGG GGCTGCTGCA GGGGGCCCAC 1860
CCTGAGCCAG CCCCTCGGTC CCACAGCCCT GACGTAGAAG ACTCTTTGCT GGTAAATCTC 1920
GGAACTCACT GGAAGCTTCC ACAAAGTTTA ACTCTACAGA CAGAATGTCT TCCTTACATA 1980
CTACCGGCTG CTTTTAAATA TTGTTAACAG ATCCCCCTTA AAGGCTTCTT AGACTCCACA 2040
TTTTGATCCA GTTGATAATA ATTGATGGTC AGGTGGAAGA ATTGCCCAGG CTCTGTTGTT 2100
GTTCTGTTAT AGTTGCCACT GGACCTGCTT TCAGCACCCT CACCCTGGCT GCTTCAGAGG 2160
GCAGCTGGAT TCCTAAAAAG AACCCATGCC CTAATGCACA AGTACTTTTT ATTTTATTTT 2220
ATATTATTTT TCGTGGGGGG ACAGAGTCTT ACTCTGTCGC 2260
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