| Tag | Content |
|---|
EnhancerAtlas ID | HS091-30649 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr20:33154750-33156920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxa2 | MA0047.2 | chr20:33156180-33156192 | GCAAAGTAAACA | - | 6.27 | | NKX2-5 | MA0063.2 | chr20:33155536-33155546 | CTCAAGTGGT | - | 6.02 | | ZNF263 | MA0528.1 | chr20:33155623-33155644 | TCTCTCTCTCCCTCCTTCACC | - | 6.22 | | ZNF263 | MA0528.1 | chr20:33155582-33155603 | TCCTCCTTTGCTCCCTCCTTC | - | 7.29 | | ZNF263 | MA0528.1 | chr20:33155620-33155641 | CTCTCTCTCTCTCCCTCCTTC | - | 7.68 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65773 | chr20:33152428-33156266 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGTTAATACA GTGTGTCTTG AAACTACTGG GCTCAGGACA GCAGCCTTGT CCACCACCAG 60
GGCTGCAGAT TCCTAGAGAA GCAGGTGCTA TCACCCAGGC ATGTCCTGGT TCCCCAGGCC 120
TCCTGCTGCT GTTGGGGACA CAGACACTGA CATTTGACAG TCAGCCCACG CTGGGGGGAA 180
TGCATGTGGC CGTCACAGTT GGCAAAGTGC AGCAGCCTCT GCCCACCTGC CTGGGATCCA 240
GGAAGCTGGG AGGCAGAGGA GGCTGGCGGC CGACTGTGGA GCTGGACAGC ACTTTGGCGT 300
AACCTGGCAA CCCACAGGCC GGAGCGGACA TTATGTAGGA GGAAATGGTG GAGGAGAAAA 360
CTCCACCCTC CAGCTCTGAA GATGCAAAGT AACAAGTGAA ATCTCTGGAC CTCAGTGTCA 420
GGGTCTGAGA GGTCACAAGG TGAGACTGAG GATGAGGCTA CAAGTAACTG TCCCTTACAT 480
GGCACTTTTC ACTTACATGG CACTTTTCCC ACATTCAGTC CTCAAAACCA CCTTCCCAGT 540
TTGAGGAAAC TGAGGCCACC ACCACCTCCC CCAGATTTCA ACCTCCCCTA GCCTCGTCCC 600
TGGTGCCCTG GATGCCAGGC TCACACCTCT TACCTCTGCT CTTCCCAGCA GTGAGGTTTT 660
CAGAGCATGG ATCTGATCAC ATTTATCCTC AGCTCTTAAA GCCAAAGGTG CAGTCTGGAC 720
CTCTGCATAA GAGGCCCTTG AAGGCCTGTG GTCTGACCAC TGCTGTCTGA ATTGCCCTCA 780
TTCCCTCTCA AGTGGTACAG CCAGTCCCAC TGAGCTCCCA GCAGCACGGT GTTCCTCCTT 840
TGCTCCCTCC TTCCTCCTCT CTCTCTCTCT CTCTCTCTCT CTCCCTCCTT CACCCCCACC 900
CAGGTCTTGC TACCTAAAAT CATAGAACCC AGTTAGATCC TACCCATCCC TCAGGACCCC 960
ACTTAGAGGC CACCTTCCCC AGGAAGCCTC CTTAACAGCC CAGCTCTGGG CTCCCAGCTC 1020
GTCAGGCTGC CCTGTCCTGC CCATGTCTTT TCCTTTCTCT CCACAGACCG AGGGCTCCTT 1080
GGAAGTACAC CTCTGTCTCA TTCACCCCTC GCAGAGTGCC TGGTGAATAG TAGGAACCTA 1140
ATTAACATTT GCAAATAAAT AAATTAGCTT CCCAGGAGTT ACGGGATGTG CCTGAGGCCA 1200
GCGAGCCAGG ACAGACAGGG CTGGAGTCGC TATAGAGTTT GGGCTTCCAG AGCCCTGGCC 1260
TTCTGTGGCC TTTGTCCTGC TGTATGTAGC CTGGGCTCTT CCTGTCACTC TGGTTGTTGG 1320
GGAGGAGAAT AGGCTGGGAA GGGCCTGTGA GGGACAAGCT TGGGATGCTC AGTGCTGGAA 1380
GGACAAAGGA ATGAACTAAG ACCTTGACAG AATTACACTA GTTGGGAAAA GCAAAGTAAA 1440
CACGCACATC CAGCAGGATG AGGACAAGGG CTCCAGGTTG GCCACAGGCA CCGCATATCG 1500
GGAGCAACGA GCCTTCCCAC ACACAGACCT GGGATCTTGC ACAGCCCAGG CCACACACAA 1560
CCGGCAGGAA GAAACCTGAA ATGGGTCTCG AGCCAACCCC AAATGGGGGC TACACACCAC 1620
TCAGCCACTA ATGACCCACC CAACACGTCT CCAAGCATTT CCTCATAGGT CCCATTTCCC 1680
AGAATGACAC ACCAGGCCAA CTGAGAGGCA ACTCCGGGAG ACAGGATTGT GGTTTCACCT 1740
GTGTTGCAGT GAACAGTGAG TCCCAGGCAG GGGACAGGCA GCATGCAGGA GGTTGGTGTC 1800
AGACCTCGGG CTTCAGGCCT CACTCAAAAC AGAAAGGAGA ATGGCCAATG CAAGGCCAGC 1860
CCAGTATCTG AGGGTCTGCA GTACAGGGAG GGGTCAGGGC TGGCCCCTCA TGGCAAATAG 1920
GCAGTGGCTT GAGGAGTAGG GTTCCAGATG ATCCAGATCC TGCTTGGAAG GGTGGGTGGT 1980
TGGCCAGGTG CGGCAGCTGA CACCTGTAAT CCCAGCACTT TGGGAGGCTG AGGCAGGAGT 2040
TTGGCTTGAG CTCAGGAGTT CGAGCTCGTA ACAACATAGC AAGACCCTGT CTCTACCAAA 2100
AATTTAAAAA GTAGCCAGGT GTGGGGGTGT GCCTGTAGTT CTAGCTACTT GGGAGGCTGA 2160
GGTGGGAGGA 2170
|
