Tag | Content |
---|
EnhancerAtlas ID | HS147-03271 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:154993670-154995590 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr1:154994781-154994792 | AGCCACACCCA | + | 6.14 | TP53 | MA0106.3 | chr1:154993763-154993781 | ACCATGCCCTGGCAAGTT | + | 6.04 |
|
| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23265 | chr1:154995241-154996031 | Colon_Crypt_1 | SE_26626 | chr1:154993852-154994425 | Esophagus | SE_35099 | chr1:154994490-154995927 | HeLa | SE_41600 | chr1:154995264-154996095 | LNCaP | SE_52379 | chr1:154995118-154996014 | Small_Intestine |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 154993889 | 154993975 | chr1 | 154994223 | 154994276 | chr1 | 154994727 | 154994863 |
|
| Number: 3 | ID | Chromosome | Start | End |
GH01I155021 | chr1 | 154993853 | 154994425 | GH01I155022 | chr1 | 154994721 | 154994870 | GH01I155023 | chr1 | 154995340 | 154996090 |
|
Enhancer Sequence | TTCACTATGT TAGCCAGGCT GGTCTCGAAC TCCTGACCTT AAGTGGTCCT CCCGCCTCAG 60 CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACCATGC CCTGGCAAGT TTTTGTATTT 120 TTAGTAGAGA TGGAGTTTTG CCATGTTGCC CAGGCTGGTC TCGAACTCCT GGACTCAAGT 180 GATCGGCCCA CCTCGGCCTC CCAAATTGCT GAAATTACAG GTGTGAGCCA CTGTGCCCAT 240 CCCCCTACTT GATTTCATAT GTTTGGCTCT CCTGCTTTCT TGAGCCTCTC CCCTCCCTGT 300 CCCCTCCCAC TCTCCTGCCA TGCCCTCTGC CAGGATGATC TAGCTCATCC TCTCTCTTAC 360 AGTCTCTAAC TTAACCCCCC AAAAATATAC CTCCAGCCCG GATCCCTGCC CTTTTCTAAC 420 TGCCCCCCTG GGCATCTCCA GCTGGATGCC CTACAGACAC CTCAAAGATC TCAAACTGGG 480 CCAGTCGTCT TTCCCCAGAA CCTGTTTATC TTCCTGCCCT AACACCTGCC CAGGCCCAAG 540 CATAGAAATC CCAGTCACGC TCAGCACTTC AGTACTGAGG CCATCACGAA CTTCTCCTAG 600 ACTAAGACAA GCTTCTCTCT GACCTCCCTG CTCCTGCCCA ACCTCCACTC TGCCTTCTTT 660 GCTTATGGTC TTTTTTTTTT TTTTGGAGAC TGAGTCTCAC TCTATCATCC AGGCTGGGCT 720 GGAGTGCAGT GGTGTGATCT TGGCTCACTG CAATCTCTGC CTCCTGGGTT CAAGCAATTC 780 TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC TACAGGCATG CACCACCAAA CCCGGCTAAT 840 TTTTGTATTT TTAGTAGAGA TGGGGTTTCG CCATGTTGGC CAGGCTGGTC TCGAACTCCT 900 GACCTCAGGT GATCCACCCA CCTCGGCCTC CCAAAGTTCT AGGATTACAG GCATGAGCCA 960 CCGTGCCCGG CCCGCTTATG GTCTTAAAAG ACAAATATGA GCATATCACT TTCCAACCTA 1020 AGCTTTTCAA ATGACAAGTT AAGGTTCTTG CCCATCTCTT CCCACCTTGA CTTCCAACCT 1080 CATCTCCCAG CATTCTCTGA GGTCTCTACC CAGCCACACC CATCCCTTGG GCTCTACCCT 1140 TCTGAATGCC TCACATTCTC CAAACCCACA CAGGCCTCCC CTTGGAATGC TTTCCTCTAC 1200 TTCTCAGCCT AACAAACCAC CAAGTTGCCC CCAAAATCCA GCCCGTGGCC AGGCACCATG 1260 GCTCACACCT ATAATCCCAT AATCCCAGCA CTTTGGAAGG CCAAGGCGAG AGGATGGTTT 1320 GAGCTCAGGA GTTTGAGACC AGCCTGGGCA ACATAGTGAG ACCCCCGTCT CTACAAAATA 1380 ATAATAATAA CAAAATAATA ATAATAAGGC AGGTGTGATG GTGTTCCTGA CATCCCAGCT 1440 ACCCAGGAGA CTGAGGTGGG AGGATCACTT GAGCCCAGGA GGTCGAGGTT GCAGTGAACT 1500 GGGATTGCAC CACTGCATTC CAGCCTGGGT GACAGAGTGA GACCCTGTTT CAAACAAAAC 1560 AAAACAAAAC AAAAATCCAG CTCATGTATC ACCTCTTCTA TGAAGCCTTC ATTAATATGC 1620 CCCTTTTCCC AAATTGGCTG TTGTGTCCTC TGTGCTGTCC AGAGTGTACT TCACTCCTTT 1680 ATCAGGGTGC TGTCCACCCT GTTATCTATT CGATGTCACT CTCCCCAAGG GCATGGTGAG 1740 CTCCTCCTGG GCCACGGTGC TGACACAGAG CAGCCGCTTG GCAAACCTCA GTTACTTCCC 1800 CTCCCCTCAT GTCTGTTTCA AGCCCTGGCA AAGGTCCAGA CACCCAGGAA GGCCTTTGCA 1860 AATGGAACAG AACATGCTTA GGACTCACAA TTCCCAGGTG CCAACTCCTG CTTCCTGCTC 1920
|