| Tag | Content |
|---|
EnhancerAtlas ID | HS045-01551 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:44011040-44012450 |
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 | CAGAGCGGGG CAGTCGAATC GTGACCCTGT CTTATGGGGC TGGGGTGAGA CCTGTCCTGG 60
ATTCATGTGG TCATTGTGTG ATGTGCGCGT GTGTGTGCTG TGTGCACTGT TGCAGATCTG 120
TGCTGAAGGC ACAGTGTGAG CTACAGCCAG GGGTCGGCAT GGGAATGGGG GGTGGCACGC 180
AGGGCATGCG TATGGATGTG TGCCCAGGAC GCGGGTGTGT CCATAGGCCC AAGGAGGGTC 240
AAAAGCGGGA GCCACCCATA GCTCTTCCCC TACGCTGGAC CCTCAGGATC CAAGTATGCA 300
GATCTGAGCC CCTCCTTCTC CTTTCATGGG GACCTTCTAG GCAAAGGAGC ATCCCCCCAC 360
CCCAGCTCCT CAGACCTGGA AATGGGGGGA AGATTGTGTT TGGCCGGCAG GAAGCTGAGC 420
AACGCCCCTC TGTGTGTGTT TGTGTTGGAG GGAGGTGGAA TTGTCCCCAT CCAGATCCAA 480
CTCCGAACTT TGGTCCCTTT CCTGCTGCCC TTCCCCCTGC CTGGCACTAT GAGACTGGCC 540
TCAGCCCGCC CCATCGCCAT GGTTACCACT CCTTGGTTAC TGGTGGGAGG CGGGGCACAG 600
GGCAGATTTA GCCAATCTGC AGGCTGAGGG GGAGGGGCGA GGTCGGAGCC AAGGTCCCTG 660
GGGGAAGGGG CCGTTCCCAG CCTGTCCAGA GCCCAGGGGT GATCCAGGGC CAACCCTGGG 720
GTCAGCCCAC GGGTCACCAG GCCATAGGGC TCCCCCACCT GCCTCCGTAT CTCTGGGTAC 780
AGATCTCTCC CCTTGCCCCA CCAGGGCTCT TTCTCCTAAT GGCTCATTAA TTATTCAGGA 840
ACTGATTCTG GAGTGGGGTG GGACTGGTGT GGTCCCGCCC TTTGTCCTCA AGTGCTGGGT 900
CCTGGGTGGA GCTAGAAGGG AAAGGAGAAG GGGCAGGCAT TCCCAAGGGG TGGGGCAAAG 960
GGTCATGGGA GCACCAGGTA CCAAAGAGAG GGCTGGGCAG GTGAGAGCAA GGAAAAAAGA 1020
CAGGTGGGGA ATCACATGGG GAAGTGGGGC AGGGGATCTC CAGGCCTGGC TGGAACCTGC 1080
AGGGGCAGGT TGGAGTAGAA AGCCTTATCA GGTGTGACCC ACATGGTTGG CAGGAAGGTG 1140
AAGGCTTGTC CACGTGTGGT CAGTAGCTCT TGGACATTGA AGTACTGTCC TTGCCCTCCC 1200
CGCCGACCCA ACCCCAGGCA CTTTCAGGGC CTTCAGACAG GAGCTCTAGG GCAGGGGAAG 1260
GATGGCCCAG TTGGGCTTCA ACAGATAACA CATCCTGGGA GAAGAGCTGC CCTCCTCCTC 1320
CTGCCTCAGA CCCAACGCGC CCCAACCTGT ACCCCTCACT CTCATCCCCC AGCCTGCTGT 1380
CTTCCCGTGT TCTCTCCCGT GAAAGGCATT 1410
|
