| Tag | Content |
|---|
EnhancerAtlas ID | HS141-00546 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:43739780-43740930 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:43740829-43740850 | CTCCTCCTCTCTCCCTGCTTC | - | 6.23 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_03620 | chr1:43739796-43740322 | Brain_Angular_Gyrus | | SE_04220 | chr1:43739727-43741385 | Brain_Anterior_Caudate | | SE_05073 | chr1:43735842-43742135 | Brain_Cingulate_Gyrus | | SE_06984 | chr1:43736531-43741599 | Brain_Hippocampus_Middle_150 | | SE_24332 | chr1:43739623-43740635 | Colon_Crypt_2 | | SE_29457 | chr1:43738891-43741251 | Fetal_Intestine_Large | | SE_31961 | chr1:43739266-43741089 | Gastric |
|
| | 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 |
| GH01I043273 | chr1 | 43739327 | 43740786 |
|
Enhancer Sequence | CTCCTCAGTC AGGCCTGTGG TTTCTCCTCT TAGGTAGGGA GAGGACGGAG TGGATGCCAG 60
CCTTGGGAAG GTGGTCGGTT TCCAGTCCCA GGGAGAGGTG AGGGACCTGA GTCCTTCGCA 120
TTTGCTCACA TGCTAGTTCA ATATGAGGCC TTAAGTGTTT GGTGTTATCA GCTGGTTTCT 180
CTGGCAACTG CACCTCCCTT CGGTTGTGCC TCTTCAGCGG ATTCCCTGAG GGTGGTTGGG 240
AGGCTACATC TCCCTGCCCC ACCTCTGAAA CCAGAACATC CCACGTCTGG GCAGTGGCTG 300
CACCAGCTGG CCTGCTCTAG GTTCCTGGGC ATGGGAGAGG TGTTTCAAAT CCCCTAGGGT 360
GGTGAGAGTC ACTTCCTGCT TGGAGTCAGC CCTGGGAGGA TCTCCCCTCT GTAGCATGCA 420
GTGCCATTTC CTGGCTGATG GTGAGCCACG GGAAGCAGCA CTCAAGTGTT TCATCACTTC 480
CTGCTTCTCG AGGTGCAGAC TGCATGAAGC CCGTGGAAGA TGCCCAGAAA AGCAGGGAAA 540
TGAGACCTGT CTCCAAAGAA ACGTTACAGT AGAACTACAG AGGCTCTGAC AACAAAAAGT 600
TGGCTTTCAG CAGAAAAGGT CAAGGATGTC TCCTGGAGAA AACACGGGGC TGACAGATGA 660
GGGGAAGAGT GTTGCCAGTG GAGGGAGGGA ACAGCGTGAA CAGACCTGGG AGAGAAAGAC 720
AAGGCGTGTC CCAGAACGCC AAGGACAACA GAAATGGCTC CCCTGGGTGC TCCAAGGGTG 780
CCTCATACCC ACCATATTCA AAACTGACCC TGCTCCTCTC ATCTTGAATG AGCTCCTCTC 840
TCTCACCCGG AGGTGCCACG CTCAGGGGGC ATCTAGAGTA GAGACTCGGT GCAATGCTAG 900
TTGGCACCGT CACTGTCTCC TCACCCAAGT CCACTGACAA ATCACCAACT CCTCTGGTTT 960
CCCTCACACA GATTTGTCTG ACAATCCATA TCTTCATGCT CACTGCCCAG AAGGGACCCT 1020
CTTCATTCCT GCCTGAGTGG CACATCGGCC TCCTCCTCTC TCCCTGCTTC TGCTCTTTTC 1080
TCTTCATTCC CCTTCCCCCT GCCATGCACA CACACATCCC TTGAGCCAGA GTGATCATCC 1140
TAAAGCTAAA 1150
|
