| Tag | Content |
|---|
EnhancerAtlas ID | HS094-00885 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr1:44010920-44012440 |
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 | GGCTACTAGG AGAGACAGGG TGGCCAGAAA CCCTTTAGAC CTTCTGTCCT AGAGAGCCCC 60
CACTGCTTGG AGAGCCTCCT TCTAAGGAAT ACCTGGGTAC TTAGGAGCAT CTTTAGGCAC 120
CAGAGCGGGG CAGTCGAATC GTGACCCTGT CTTATGGGGC TGGGGTGAGA CCTGTCCTGG 180
ATTCATGTGG TCATTGTGTG ATGTGCGCGT GTGTGTGCTG TGTGCACTGT TGCAGATCTG 240
TGCTGAAGGC ACAGTGTGAG CTACAGCCAG GGGTCGGCAT GGGAATGGGG GGTGGCACGC 300
AGGGCATGCG TATGGATGTG TGCCCAGGAC GCGGGTGTGT CCATAGGCCC AAGGAGGGTC 360
AAAAGCGGGA GCCACCCATA GCTCTTCCCC TACGCTGGAC CCTCAGGATC CAAGTATGCA 420
GATCTGAGCC CCTCCTTCTC CTTTCATGGG GACCTTCTAG GCAAAGGAGC ATCCCCCCAC 480
CCCAGCTCCT CAGACCTGGA AATGGGGGGA AGATTGTGTT TGGCCGGCAG GAAGCTGAGC 540
AACGCCCCTC TGTGTGTGTT TGTGTTGGAG GGAGGTGGAA TTGTCCCCAT CCAGATCCAA 600
CTCCGAACTT TGGTCCCTTT CCTGCTGCCC TTCCCCCTGC CTGGCACTAT GAGACTGGCC 660
TCAGCCCGCC CCATCGCCAT GGTTACCACT CCTTGGTTAC TGGTGGGAGG CGGGGCACAG 720
GGCAGATTTA GCCAATCTGC AGGCTGAGGG GGAGGGGCGA GGTCGGAGCC AAGGTCCCTG 780
GGGGAAGGGG CCGTTCCCAG CCTGTCCAGA GCCCAGGGGT GATCCAGGGC CAACCCTGGG 840
GTCAGCCCAC GGGTCACCAG GCCATAGGGC TCCCCCACCT GCCTCCGTAT CTCTGGGTAC 900
AGATCTCTCC CCTTGCCCCA CCAGGGCTCT TTCTCCTAAT GGCTCATTAA TTATTCAGGA 960
ACTGATTCTG GAGTGGGGTG GGACTGGTGT GGTCCCGCCC TTTGTCCTCA AGTGCTGGGT 1020
CCTGGGTGGA GCTAGAAGGG AAAGGAGAAG GGGCAGGCAT TCCCAAGGGG TGGGGCAAAG 1080
GGTCATGGGA GCACCAGGTA CCAAAGAGAG GGCTGGGCAG GTGAGAGCAA GGAAAAAAGA 1140
CAGGTGGGGA ATCACATGGG GAAGTGGGGC AGGGGATCTC CAGGCCTGGC TGGAACCTGC 1200
AGGGGCAGGT TGGAGTAGAA AGCCTTATCA GGTGTGACCC ACATGGTTGG CAGGAAGGTG 1260
AAGGCTTGTC CACGTGTGGT CAGTAGCTCT TGGACATTGA AGTACTGTCC TTGCCCTCCC 1320
CGCCGACCCA ACCCCAGGCA CTTTCAGGGC CTTCAGACAG GAGCTCTAGG GCAGGGGAAG 1380
GATGGCCCAG TTGGGCTTCA ACAGATAACA CATCCTGGGA GAAGAGCTGC CCTCCTCCTC 1440
CTGCCTCAGA CCCAACGCGC CCCAACCTGT ACCCCTCACT CTCATCCCCC AGCCTGCTGT 1500
CTTCCCGTGT TCTCTCCCGT 1520
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