| Tag | Content |
|---|
EnhancerAtlas ID | HS044-00322 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:44011080-44012330 |
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 | TGGGGTGAGA CCTGTCCTGG ATTCATGTGG TCATTGTGTG ATGTGCGCGT GTGTGTGCTG 60
TGTGCACTGT TGCAGATCTG TGCTGAAGGC ACAGTGTGAG CTACAGCCAG GGGTCGGCAT 120
GGGAATGGGG GGTGGCACGC AGGGCATGCG TATGGATGTG TGCCCAGGAC GCGGGTGTGT 180
CCATAGGCCC AAGGAGGGTC AAAAGCGGGA GCCACCCATA GCTCTTCCCC TACGCTGGAC 240
CCTCAGGATC CAAGTATGCA GATCTGAGCC CCTCCTTCTC CTTTCATGGG GACCTTCTAG 300
GCAAAGGAGC ATCCCCCCAC CCCAGCTCCT CAGACCTGGA AATGGGGGGA AGATTGTGTT 360
TGGCCGGCAG GAAGCTGAGC AACGCCCCTC TGTGTGTGTT TGTGTTGGAG GGAGGTGGAA 420
TTGTCCCCAT CCAGATCCAA CTCCGAACTT TGGTCCCTTT CCTGCTGCCC TTCCCCCTGC 480
CTGGCACTAT GAGACTGGCC TCAGCCCGCC CCATCGCCAT GGTTACCACT CCTTGGTTAC 540
TGGTGGGAGG CGGGGCACAG GGCAGATTTA GCCAATCTGC AGGCTGAGGG GGAGGGGCGA 600
GGTCGGAGCC AAGGTCCCTG GGGGAAGGGG CCGTTCCCAG CCTGTCCAGA GCCCAGGGGT 660
GATCCAGGGC CAACCCTGGG GTCAGCCCAC GGGTCACCAG GCCATAGGGC TCCCCCACCT 720
GCCTCCGTAT CTCTGGGTAC AGATCTCTCC CCTTGCCCCA CCAGGGCTCT TTCTCCTAAT 780
GGCTCATTAA TTATTCAGGA ACTGATTCTG GAGTGGGGTG GGACTGGTGT GGTCCCGCCC 840
TTTGTCCTCA AGTGCTGGGT CCTGGGTGGA GCTAGAAGGG AAAGGAGAAG GGGCAGGCAT 900
TCCCAAGGGG TGGGGCAAAG GGTCATGGGA GCACCAGGTA CCAAAGAGAG GGCTGGGCAG 960
GTGAGAGCAA GGAAAAAAGA CAGGTGGGGA ATCACATGGG GAAGTGGGGC AGGGGATCTC 1020
CAGGCCTGGC TGGAACCTGC AGGGGCAGGT TGGAGTAGAA AGCCTTATCA GGTGTGACCC 1080
ACATGGTTGG CAGGAAGGTG AAGGCTTGTC CACGTGTGGT CAGTAGCTCT TGGACATTGA 1140
AGTACTGTCC TTGCCCTCCC CGCCGACCCA ACCCCAGGCA CTTTCAGGGC CTTCAGACAG 1200
GAGCTCTAGG GCAGGGGAAG GATGGCCCAG TTGGGCTTCA ACAGATAACA 1250
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