| Tag | Content |
|---|
EnhancerAtlas ID | HS034-01067 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr1:44011050-44012380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF13 | MA0657.1 | chr1:44011456-44011474 | GAGCAACGCCCCTCTGTG | + | 6.49 | | POU4F2 | MA0683.1 | chr1:44011862-44011878 | CTCATTAATTATTCAG | - | 8.42 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_00616 | chr1:44009256-44025211 | Adipose_Nuclei | | SE_03403 | chr1:44004983-44011531 | Brain_Angular_Gyrus | | SE_03403 | chr1:44011667-44013233 | Brain_Angular_Gyrus | | SE_04240 | chr1:44003988-44015177 | Brain_Anterior_Caudate | | SE_05040 | chr1:44001099-44015486 | Brain_Cingulate_Gyrus | | SE_05962 | chr1:44000439-44020958 | Brain_Hippocampus_Middle | | SE_07193 | chr1:44003475-44015024 | Brain_Hippocampus_Middle_150 | | SE_08033 | chr1:44003431-44015175 | Brain_Inferior_Temporal_Lobe | | SE_23218 | chr1:44005985-44017477 | Colon_Crypt_1 | | SE_23829 | chr1:44009144-44011544 | Colon_Crypt_2 | | SE_23829 | chr1:44011550-44012644 | Colon_Crypt_2 | | SE_24870 | chr1:44006024-44012830 | Colon_Crypt_3 | | SE_26649 | chr1:44010798-44020559 | Esophagus | | SE_27645 | chr1:43995619-44017587 | Fetal_Intestine | | SE_28595 | chr1:44005404-44017604 | Fetal_Intestine_Large | | SE_31538 | chr1:44004919-44019003 | Gastric | | SE_41575 | chr1:44001646-44015303 | LNCaP | | SE_47657 | chr1:44011019-44012837 | Pancreas | | SE_50363 | chr1:44005822-44020588 | Sigmoid_Colon | | SE_52524 | chr1:44004832-44019377 | Small_Intestine | | SE_56987 | chr1:44011047-44012016 | VACO_400 | | SE_56987 | chr1:44012027-44012445 | VACO_400 | | SE_65452 | chr1:44004903-44018198 | Pancreatic_islets | | SE_69138 | chr1:44010309-44012639 | H9 |
|
| | 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 |
| GH01I043539 | chr1 | 44005459 | 44020850 |
|
Enhancer Sequence | CAGTCGAATC GTGACCCTGT CTTATGGGGC TGGGGTGAGA CCTGTCCTGG ATTCATGTGG 60
TCATTGTGTG ATGTGCGCGT GTGTGTGCTG TGTGCACTGT TGCAGATCTG TGCTGAAGGC 120
ACAGTGTGAG CTACAGCCAG GGGTCGGCAT GGGAATGGGG GGTGGCACGC AGGGCATGCG 180
TATGGATGTG TGCCCAGGAC GCGGGTGTGT CCATAGGCCC AAGGAGGGTC AAAAGCGGGA 240
GCCACCCATA GCTCTTCCCC TACGCTGGAC CCTCAGGATC CAAGTATGCA GATCTGAGCC 300
CCTCCTTCTC CTTTCATGGG GACCTTCTAG GCAAAGGAGC ATCCCCCCAC CCCAGCTCCT 360
CAGACCTGGA AATGGGGGGA AGATTGTGTT TGGCCGGCAG GAAGCTGAGC AACGCCCCTC 420
TGTGTGTGTT TGTGTTGGAG GGAGGTGGAA TTGTCCCCAT CCAGATCCAA CTCCGAACTT 480
TGGTCCCTTT CCTGCTGCCC TTCCCCCTGC CTGGCACTAT GAGACTGGCC TCAGCCCGCC 540
CCATCGCCAT GGTTACCACT CCTTGGTTAC TGGTGGGAGG CGGGGCACAG GGCAGATTTA 600
GCCAATCTGC AGGCTGAGGG GGAGGGGCGA GGTCGGAGCC AAGGTCCCTG GGGGAAGGGG 660
CCGTTCCCAG CCTGTCCAGA GCCCAGGGGT GATCCAGGGC CAACCCTGGG GTCAGCCCAC 720
GGGTCACCAG GCCATAGGGC TCCCCCACCT GCCTCCGTAT CTCTGGGTAC AGATCTCTCC 780
CCTTGCCCCA CCAGGGCTCT TTCTCCTAAT GGCTCATTAA TTATTCAGGA ACTGATTCTG 840
GAGTGGGGTG GGACTGGTGT GGTCCCGCCC TTTGTCCTCA AGTGCTGGGT CCTGGGTGGA 900
GCTAGAAGGG AAAGGAGAAG GGGCAGGCAT TCCCAAGGGG TGGGGCAAAG GGTCATGGGA 960
GCACCAGGTA CCAAAGAGAG GGCTGGGCAG GTGAGAGCAA GGAAAAAAGA CAGGTGGGGA 1020
ATCACATGGG GAAGTGGGGC AGGGGATCTC CAGGCCTGGC TGGAACCTGC AGGGGCAGGT 1080
TGGAGTAGAA AGCCTTATCA GGTGTGACCC ACATGGTTGG CAGGAAGGTG AAGGCTTGTC 1140
CACGTGTGGT CAGTAGCTCT TGGACATTGA AGTACTGTCC TTGCCCTCCC CGCCGACCCA 1200
ACCCCAGGCA CTTTCAGGGC CTTCAGACAG GAGCTCTAGG GCAGGGGAAG GATGGCCCAG 1260
TTGGGCTTCA ACAGATAACA CATCCTGGGA GAAGAGCTGC CCTCCTCCTC CTGCCTCAGA 1320
CCCAACGCGC 1330
|
