| Tag | Content |
|---|
EnhancerAtlas ID | HS134-01134 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:44010870-44012320 |
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 | GGTTGAAAGG TGGCATCCTT CCCAGCAGGA CTCTGGGATG GGGACAGACC GGCTACTAGG 60
AGAGACAGGG TGGCCAGAAA CCCTTTAGAC CTTCTGTCCT AGAGAGCCCC CACTGCTTGG 120
AGAGCCTCCT TCTAAGGAAT ACCTGGGTAC TTAGGAGCAT CTTTAGGCAC CAGAGCGGGG 180
CAGTCGAATC GTGACCCTGT CTTATGGGGC TGGGGTGAGA CCTGTCCTGG ATTCATGTGG 240
TCATTGTGTG ATGTGCGCGT GTGTGTGCTG TGTGCACTGT TGCAGATCTG TGCTGAAGGC 300
ACAGTGTGAG CTACAGCCAG GGGTCGGCAT GGGAATGGGG GGTGGCACGC AGGGCATGCG 360
TATGGATGTG TGCCCAGGAC GCGGGTGTGT CCATAGGCCC AAGGAGGGTC AAAAGCGGGA 420
GCCACCCATA GCTCTTCCCC TACGCTGGAC CCTCAGGATC CAAGTATGCA GATCTGAGCC 480
CCTCCTTCTC CTTTCATGGG GACCTTCTAG GCAAAGGAGC ATCCCCCCAC CCCAGCTCCT 540
CAGACCTGGA AATGGGGGGA AGATTGTGTT TGGCCGGCAG GAAGCTGAGC AACGCCCCTC 600
TGTGTGTGTT TGTGTTGGAG GGAGGTGGAA TTGTCCCCAT CCAGATCCAA CTCCGAACTT 660
TGGTCCCTTT CCTGCTGCCC TTCCCCCTGC CTGGCACTAT GAGACTGGCC TCAGCCCGCC 720
CCATCGCCAT GGTTACCACT CCTTGGTTAC TGGTGGGAGG CGGGGCACAG GGCAGATTTA 780
GCCAATCTGC AGGCTGAGGG GGAGGGGCGA GGTCGGAGCC AAGGTCCCTG GGGGAAGGGG 840
CCGTTCCCAG CCTGTCCAGA GCCCAGGGGT GATCCAGGGC CAACCCTGGG GTCAGCCCAC 900
GGGTCACCAG GCCATAGGGC TCCCCCACCT GCCTCCGTAT CTCTGGGTAC AGATCTCTCC 960
CCTTGCCCCA CCAGGGCTCT TTCTCCTAAT GGCTCATTAA TTATTCAGGA ACTGATTCTG 1020
GAGTGGGGTG GGACTGGTGT GGTCCCGCCC TTTGTCCTCA AGTGCTGGGT CCTGGGTGGA 1080
GCTAGAAGGG AAAGGAGAAG GGGCAGGCAT TCCCAAGGGG TGGGGCAAAG GGTCATGGGA 1140
GCACCAGGTA CCAAAGAGAG GGCTGGGCAG GTGAGAGCAA GGAAAAAAGA CAGGTGGGGA 1200
ATCACATGGG GAAGTGGGGC AGGGGATCTC CAGGCCTGGC TGGAACCTGC AGGGGCAGGT 1260
TGGAGTAGAA AGCCTTATCA GGTGTGACCC ACATGGTTGG CAGGAAGGTG AAGGCTTGTC 1320
CACGTGTGGT CAGTAGCTCT TGGACATTGA AGTACTGTCC TTGCCCTCCC CGCCGACCCA 1380
ACCCCAGGCA CTTTCAGGGC CTTCAGACAG GAGCTCTAGG GCAGGGGAAG GATGGCCCAG 1440
TTGGGCTTCA 1450
|
