| Tag | Content |
|---|
EnhancerAtlas ID | HS101-09787 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:13327800-13330050 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIC | MA0161.2 | chr12:13328921-13328932 | TGTGCCAAGTA | - | 6.32 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_00070 | chr12:13322001-13329284 | Adipose_Nuclei | | SE_26715 | chr12:13324024-13328761 | Esophagus | | SE_26715 | chr12:13328797-13330070 | Esophagus | | SE_36302 | chr12:13324133-13329267 | HMEC | | SE_45692 | chr12:13323910-13328954 | Osteoblasts | | SE_55863 | chr12:13323889-13330257 | u87 | | SE_64909 | chr12:13324369-13329500 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 13329305 | 13329456 | | chr12 | 13329606 | 13329804 | | chr12 | 13329828 | 13329878 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I013171 | chr12 | 13324128 | 13329500 |
|
Enhancer Sequence | ACAGGCGTGC ACCACCATGG CAGACTAATT TTTTATATTT TTAGTACAGA CAGGATTTCA 60
CCACATTGGC CAGGCTGGTC TTGAACTCCA ACTCCTGACC TCAAGTGATC TGCCCGCCTC 120
AGCCTCCCAA AGTGCTGGAA TTACAGGCAT GAGCCACCGC ACCCAGCCCA TTTCCTTTTG 180
TTTTTAATCA ATTTAGAACT GAATTCTCAA GCTGCTGTTT GTTTTGATTC TAGGCATATT 240
TTGATATTCC AGTTAGTACC CAATTCAGTT TATATATGTA TAAAATTACA CACCCTGCAT 300
CAAAAACATC TTTACATATT TTTATACTTA AACCCAGTTC AAATTGATTT AAGGCTTAGG 360
AAAATAAGTT AGGTTTAGTT CAGTATGTGG TTTAGAAAAT GTGTACACTT TATTCTGGCT 420
TCCAACTAAA ACTGTGGTGT GTTTCTTGCC TCTGAATTGG ACAGATTTCT ATGTTTGGCC 480
TGTATTGTGG CAATGGTGTA TTATTTTGTT CTTGTCAGTT GCATTCATCA TTATTTTAAA 540
AAGATTCCAG AAAGCCTGGT GTTACAGTTA GCCCACCTTG ACCCTAAATG CTGCACTACT 600
GCATTTTGAC CAAGCATTGG GATCATAAAA ATTATCCACC TTCTGTTTCT AGGCTTTCCC 660
CACAGCTTGC AGCCCAGAGT CAGGAGAAAT GGCGTTTTAC TTCATGTGCT TCCCTAGAGT 720
GAGCAGGGCT ATCCAGACTG AAGGGAAATG GCATTTCTCC TTCTGCAACT CAGGACCCTA 780
CTGGATTAAT TCTTGCCTAA GAGGGCATCT CAGCCATGTG TTCTCCAGCT CATTAATCCT 840
CAGCAGTGAC TAACGCTGAA AACCCAACCC TTGTCTTTGG CTGCCAAGGG TGTAATTTCG 900
CTTGGAATGT TGCTTTCAGT TGACTTGTTC TCTACCTTTC TTTTCACCTG TCTGTTATGC 960
TTAGCTCTAC CCTCCTGCAC GTGTTAATTC TAATCCTTTG GTGATCTAAA CTAAAGAAAA 1020
TGCCTCAGGA ATAAACTTTT TATGGATAAG GTTTTTTTTG TGTGTGCTAT GACACCTATA 1080
CCTCTAATAT TAGTTTAAAT CTACCATTTC TCGAATGCCT ATGTGCCAAG TAACTTACAC 1140
GTATCACATT TGTTGTTACT AACAACCCAA TATAGTGTTG TCCCCATTTT TTAGATGAGA 1200
AAACTGAGGC TCAGAGAGTC TGAATGCCTT GCCCAAGGCC CTGCAGCTAG AAATCAGATT 1260
AAACCTCGTC TGTCTGACTC CAAAGTTTGT GCTTCATGGA CTTCCAGCTC TGGTTCATGT 1320
TACCCCAGTA GAGCCCTGTG ACTTCAAGAA TTTCTCAAAT GTCCAAAGCA ATCTATTTTA 1380
ATTCACTTTA TTAATAAAGA TAATAATTCC TGTCTGTCTC ACAGGTGGTA TAATGAAGTG 1440
AAAGGAAGCA GAAGAGAGTG TTATAGTTGG AAAGGTGGGA AATCACCCCC TCCATGCTGA 1500
AGGGAAGATT TCAGGTTCCA AATGACACGT TTCCCTCAGA ATGACTTTTG CTGTAGGTAT 1560
GTGAACCTGC CACCACCCTT TGAATTTGGT GGATTGATTT AACGCTGTAT CTGAACCTGA 1620
CTGAGGAGAT TCCTTCCTGG TTCATGACCC CGCTCTTGGA GATGCAGGAT CTTGAACCGG 1680
AAGACTCTGA GTGACAGAAT GAAGAGCTGG AGGAATCAGA GTGAGATACA AGAGGGTTCT 1740
AGATTTGTTC CTCATTTTAT CAGACAATTG AGTGTTGATC TTCCTTCTGG AACTTGTAAC 1800
AAGAGAGTGA ACGGCAAACA TGGACCGTTT ACCCTCAAGT TTGTTTTCTT GTGCATACCC 1860
CCTCTTCCTG ACACCTTGGA AGAACAGCCT CTCTTGACCA CCAGAGGACA AGCCTGTGTA 1920
GGCGTAGAGT AGATGCGTGG CTGAGTGCAT GTTTGCACCC TCATTTCACA TCCGTCTATA 1980
AAGCATTTGA GGCAGTTCAG ACAATAGCAT GATCACCAGC TGTGCTGCCA TTTCTTCCAA 2040
CAGTGACCAT GGATATCTTT GCTGTGTTCC TGAAACTCTG CAGACAGTCC TAAGGGATCC 2100
AGTGGGTCCT CTGATGGACC CCAATGCTGG AAGTCACGCA TATAGCTCTG AAGAGTTGTC 2160
ACAAGAAATG GCGTTTCTGG AGGATGCACA GGAAACTTTT CATTTGGCAT GAAAAAGGCT 2220
ATTGGATTTG CAAAGACTGC AGAGGAAGAG 2250
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