Tag | Content |
---|
EnhancerAtlas ID | HS040-02372 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:151916450-151918340 |
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 | chr1:151917016-151917033 | TGAATTTCTGGCAAGCA | - | 6.39 | Foxd3 | MA0041.1 | chr1:151918297-151918309 | AAACAAACAAAC | - | 6.32 | SPI1 | MA0080.4 | chr1:151918310-151918324 | AAAAAGCGGTAGTA | + | 6.16 | SPIC | MA0687.1 | chr1:151918310-151918324 | AAAAAGCGGTAGTA | + | 6.07 |
|
| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_00284 | chr1:151915786-151920328 | Adipose_Nuclei | SE_10113 | chr1:151911730-151920206 | CD14 | SE_23217 | chr1:151916497-151919851 | Colon_Crypt_1 | SE_35018 | chr1:151912751-151921049 | HeLa | SE_36600 | chr1:151916989-151920427 | HMEC | SE_64760 | chr1:151916770-151920379 | NHEK |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 151916929 | 151917142 | chr1 | 151916779 | 151917868 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I151940 | chr1 | 151912796 | 151920351 |
|
Enhancer Sequence | TCTTATGTGA TCCTCCCACC TCAGCCTCCC GAAGTGCTGA GATTACAGGC ATGAACCACT 60 GTGCCTGGCC CAGAATTATT TTTAAAAGTA ATCATGCTTG ACTTAGCCCT GTTAAGCCTC 120 CAAAATTCTG GTGAGGTCCC TTTGCTTGTA AATACTTAGA AAAACTGTAC ATGAGCAAAA 180 TAGAGAAGAA TTAGATAAAC ATGGCTTTGT ATATAGCAGT GTCCCAGTAA GTAAGCAAAC 240 TGATATTCCC TACATACCCT ATTTCAGAGG GCAGGCTGAG GGGCGCTCAG GCAGAAATAC 300 CGTAAGTTCA ACTGAATGGC AAGTTCTTTA ATCCAAGATT GAAGTGTGTG GCAAAACATG 360 CCAGGAACTC TTACAAGCAG TTGGCATGAA TTAACTTCTT TGATCCTCAC AGCAGCCCTA 420 AAAGTAGGAA ATATTTTTCT GTCCCTGTTA CAAGTAAGGA AACCAAAGGA CAGAGAGGGA 480 AAGTAACTGC CCAGTCACAC AGCTAGTAAA TGGCAGAGGT GGGGCATAGA TCCAGGCAGC 540 CTGAAGGTTG TACTCTGATG ATAAGATGAA TTTCTGGCAA GCACGTTTTG CTGACCTCTC 600 CAAGGCAGAC CTAATGTGGT GACAAAACCT ATCACACTTG CTTACTGTGG CACGATGCTT 660 TTGCGTTGTG ACACAGCATA GCTACAGTGC TTACAGCACA ATGCTGTGAG CCCAGAGGAG 720 CTTCATGTCA CCTTTAATGA CCCAAATTAG ACCTAAGAAA ATTGTTAGCC AACAATGACA 780 GCATCCTTAC ATCACGTCAG CGCTTTAAAA AGTGGTGAAA TTTAATACTC AGTTTGCTTT 840 TGAAATCAGG TTCACCCAAC CTCCACTCTT AGCTGTGCAT TAGATAAATG TAGAAATTGC 900 CTCCTTTTTC ATCTTGAGTC TCAAACAACA GCTCTGGACT CAGAGCTAAT AGACTTCCTG 960 AGTCCAACCA ATTCAAGCAG CCAATGAGGC ATCCTGGCAA ATGAGGACAT TTCTCCAGGG 1020 GATGAGGCTG TCCTTGGTGC CCTTGCTCCC CTCTGCCAGC AGGATAGGTT CTGTGAGTTA 1080 TGCTTCTGGT CACGTTGGTG GGTTTGTGCT GACCTGTCCC CAGTAGACTC TTTTGTGATG 1140 AGGGGTGGGA CTAATGAGAC GCCTGGCCAA AGTGGCAGAA TCTGTGACTG TGAAAGATGG 1200 TGACACTGCC AGGTATAAGG AAGGACTTAA GTTGATGGGC ACCAAACAGA GAACTTTCTC 1260 TATGCCTGTG ACTGGAACAT GTCCATCTTG GTAGCCAGGT CTCCACTACA CAATTCAGTT 1320 TTTGCTCCCT TAGCAGTTAA CTGTCAAATT AGAAATCCAT CCTGTTTTAG TCTTTAAAGC 1380 CTTGATATAA TTTAACTATA GTCAGCAGAA ACAAACAAAT GAACAAAATC CATCAATAAC 1440 TTGTGAGGCT CTTCCTTTCC TATAACCCGA GGTCATCAGA CATAATGGTT AAGGGTGTGG 1500 GTCCCTGGAA GAAGACTGCA TGGCTTGAAT CCTGGCCCTG TTACTCACCA GACACATAAC 1560 ATTAAGCTCT GGGTATCTCA GTTTCTTCAT CTTTAAAATA GGAATAATGA TAATTGAAGA 1620 CTAAGAGTGC CTCATAGTAA GACCTTAATA ATTACCACTA TCTCTGTTTC CAGTCATCCT 1680 CAGGTAGTTC AGTGTAATCT GGTAGAGACA TATCCTAGCT GTGAAGAAGT AATTATGTTA 1740 TTTTGGCTCT CCCCTTTTTC TCTTTACTTC TTGCACTGCT ATGTGACAGC TCTCGGGTGC 1800 CAAACAGCCT CTTCCTGTGA TTAAAGTTTC CAATTTATAA CAAACAGAAA CAAACAAACA 1860 AAAAAGCGGT AGTACTTACT CTAGCCACAC 1890
|