| Tag | Content |
|---|
EnhancerAtlas ID | HS195-00421 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr1:154994460-154995590 |
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 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23265 | chr1:154995241-154996031 | Colon_Crypt_1 | | 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: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I155022 | chr1 | 154994721 | 154994870 | | GH01I155023 | chr1 | 154995340 | 154996090 |
|
Enhancer Sequence | GCCTCCCGAG TAGCTGGGAC TACAGGCATG CACCACCAAA CCCGGCTAAT TTTTGTATTT 60
TTAGTAGAGA TGGGGTTTCG CCATGTTGGC CAGGCTGGTC TCGAACTCCT GACCTCAGGT 120
GATCCACCCA CCTCGGCCTC CCAAAGTTCT AGGATTACAG GCATGAGCCA CCGTGCCCGG 180
CCCGCTTATG GTCTTAAAAG ACAAATATGA GCATATCACT TTCCAACCTA AGCTTTTCAA 240
ATGACAAGTT AAGGTTCTTG CCCATCTCTT CCCACCTTGA CTTCCAACCT CATCTCCCAG 300
CATTCTCTGA GGTCTCTACC CAGCCACACC CATCCCTTGG GCTCTACCCT TCTGAATGCC 360
TCACATTCTC CAAACCCACA CAGGCCTCCC CTTGGAATGC TTTCCTCTAC TTCTCAGCCT 420
AACAAACCAC CAAGTTGCCC CCAAAATCCA GCCCGTGGCC AGGCACCATG GCTCACACCT 480
ATAATCCCAT AATCCCAGCA CTTTGGAAGG CCAAGGCGAG AGGATGGTTT GAGCTCAGGA 540
GTTTGAGACC AGCCTGGGCA ACATAGTGAG ACCCCCGTCT CTACAAAATA ATAATAATAA 600
CAAAATAATA ATAATAAGGC AGGTGTGATG GTGTTCCTGA CATCCCAGCT ACCCAGGAGA 660
CTGAGGTGGG AGGATCACTT GAGCCCAGGA GGTCGAGGTT GCAGTGAACT GGGATTGCAC 720
CACTGCATTC CAGCCTGGGT GACAGAGTGA GACCCTGTTT CAAACAAAAC AAAACAAAAC 780
AAAAATCCAG CTCATGTATC ACCTCTTCTA TGAAGCCTTC ATTAATATGC CCCTTTTCCC 840
AAATTGGCTG TTGTGTCCTC TGTGCTGTCC AGAGTGTACT TCACTCCTTT ATCAGGGTGC 900
TGTCCACCCT GTTATCTATT CGATGTCACT CTCCCCAAGG GCATGGTGAG CTCCTCCTGG 960
GCCACGGTGC TGACACAGAG CAGCCGCTTG GCAAACCTCA GTTACTTCCC CTCCCCTCAT 1020
GTCTGTTTCA AGCCCTGGCA AAGGTCCAGA CACCCAGGAA GGCCTTTGCA AATGGAACAG 1080
AACATGCTTA GGACTCACAA TTCCCAGGTG CCAACTCCTG CTTCCTGCTC 1130
|
