| Tag | Content |
|---|
EnhancerAtlas ID | HS114-00368 |
Organism | Homo sapiens |
Tissue/cell | Kidney |
Coordinate | chr21:45625890-45629060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr21:45627639-45627650 | GGATGACTCAG | + | 6.32 | | JUNB | MA0490.1 | chr21:45627639-45627650 | GGATGACTCAG | + | 6.14 | | Myod1 | MA0499.1 | chr21:45627865-45627878 | GGGGGCAGCTGCT | - | 6.03 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_00694 | chr21:45627172-45628515 | Adipose_Nuclei | | SE_03880 | chr21:45627327-45628971 | Brain_Anterior_Caudate | | SE_04775 | chr21:45626030-45629668 | Brain_Cingulate_Gyrus | | SE_05779 | chr21:45625585-45629669 | Brain_Hippocampus_Middle | | SE_06690 | chr21:45625851-45629031 | Brain_Hippocampus_Middle_150 | | SE_07737 | chr21:45627279-45628360 | Brain_Inferior_Temporal_Lobe | | SE_10305 | chr21:45623380-45628791 | CD19_Primary | | SE_11616 | chr21:45622912-45630050 | CD20 | | SE_24239 | chr21:45625900-45626559 | Colon_Crypt_2 | | SE_24239 | chr21:45626613-45628029 | Colon_Crypt_2 | | SE_24239 | chr21:45628152-45628712 | Colon_Crypt_2 | | SE_30176 | chr21:45627362-45628673 | Fetal_Muscle | | SE_31647 | chr21:45625794-45628702 | Gastric | | SE_33667 | chr21:45621645-45627097 | H2171 | | SE_40890 | chr21:45625813-45629023 | Left_Ventricle | | SE_42286 | chr21:45625817-45628837 | Lung | | SE_48538 | chr21:45625974-45628773 | Psoas_Muscle | | SE_50113 | chr21:45625833-45628971 | Sigmoid_Colon | | SE_51445 | chr21:45624818-45629069 | Skeletal_Muscle | | SE_52463 | chr21:45625843-45628782 | Small_Intestine | | SE_56643 | chr21:45626252-45630945 | u87 | | SE_59125 | chr21:45557380-45640832 | Ly3 | | SE_61237 | chr21:45557180-45641526 | HBL1 | | SE_61527 | chr21:45545883-45641600 | Toledo | | SE_62281 | chr21:45556124-45641130 | Tonsil | | SE_65639 | chr21:45625460-45628847 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH21I044205 | chr21 | 45625272 | 45628706 | | GH21I005055 | chr21 | 45625955 | 45628553 |
|
Enhancer Sequence | CTCAGGCAAC CTGCCTGCCT TGGCCTCCCA AAGTGCTGGG ATTGCAGGCG TGAGTCACCG 60
TGCCCAGACA AATTAAGGCT CTTGAGACGA GGTCATCCTG GGTTATGCAG ATGGACCCTG 120
AATCCGACAC TAGCACCCGT GTGGAAGGAA CGAGAGGGAG ATTTGGGGTC CGCAGAGGCA 180
AACCACAGGA GGACGGAGTC GGAGACTGGA GCACCGCGGC CTTGATCGGG GGACACCAGG 240
GCTGCCGGCT GTGCCAGAAG GGGCTGAGGC TGGACCGGAT TCTCTCCGAG TTCCCAGAAG 300
GAGCCAGTCC TGCCGACGCC TTGATGCTGG ACTCTGGCCT CCAGAAATGT GCGAGGACAA 360
ACATCTGCGG TTTCTAGGCC CCGCCTGTGG TCCTCTGTTG CAGCAGCCTG GACAGTCTGG 420
ACTGCCTGGA CAGCATGCAG ATGGGCTCTG CCCGCGGCTG CCCACGAGTT CCCACCGCCC 480
GCCCGTCCGT GGGAGAGCCA GTCCTCGTAT GTGAAGCGTA CCTGTATCCC TTTACTCCGC 540
GTACACAGGT GCCTTTGTCA CTTCTCCTTT GACCTGGCTG GCACATCTTA CCGGTTTCTG 600
CGCTAACAAT GAGTTGAAGG AAATCTTGAA CGCGCGTTCA TTTTATATCG GTATCAGAGT 660
CTGTTTATTT CTTGTTGACA CTAATCTTTG AGCATGAGTA GTTTAGTGAT TGTGAAACAG 720
AAACTTCTGG ATACAAAATC AGTCTCCTGG CTGTGACCCA ATCATCTTCG CAGTTCTGAT 780
TACCTGTGAT TAAGAAAATA AATAAGAACA CCCATTGGGG GAAGGCTTCC CTCCCCCGGG 840
CACAGCAGCT TTAAAACCGA AAGGGAAGTG GGTGCTGTGA GCAGCTCTGT TCAGGCCTAA 900
GGCCACGCAT GTGTGCCCCG TGGGGGAGAC ATGCACCAGC GAATCAGGAA ACAGTGGTGA 960
CAGCCGTTCC GGGAGGCTGA CTGGGGGTGC AGGGGTCACT TTTCTAATGT GGGTGGGTCT 1020
GTGTCCCCTG CAGGAACGTG GCTGCAGCAA AGCCGGTCAG CCAGCGGTCA GCTCCAGCCC 1080
CTGTCCAGGC CCTGTGGGTC CTGCTGACCA GGCTGCGGTT GTTCCCAAAC CAGTTCCCAG 1140
CCCCCGCTTG CCCTACTTCC TCTCACACCA GCTCCTTCCA CCCCCTCACA CCCACCTGCA 1200
GGCTCCCAGC CCAGGCTACT GACATCAATC ATGGCAATCG CTATTCCAGA GGTATACGCG 1260
GTGGGTGGGG TCCGGTATCG CCTGCCATGC CTCACTCACC GGGCACCCAG ATAACCTGAG 1320
GCCAGGGAGC AGCCACTCGC CCTGACCCAT GCTCCCCGGG CCCCTGAGGC ACCCAGGAGG 1380
ACCACCCGGC CGCTTCTGCT CAGAGCCCAG CACCCCCGAG TCTGTGAAGA GGTCACATCT 1440
GACCACGTTT CCAGGTGGCT GCCCAGGCGT GGGTTCATGG CCGCTTCCGG TTTCCTCCTC 1500
GAGCTGAACC ACACACCTGC TCTGTCCCGG GCTTTCTGGA GGGGTTTTCC GAAGTGAGAC 1560
TGTGGGCTCC CTCCAGGGCT GGGGGCAGGA GGACACACGG GGAAGGTGGG CAAGCAGCCC 1620
CAGGCTGAGG GAGGCCTCCC CTCTGCAGCG TTTGTTCATT CATTTGTTCA TCGCTAACAC 1680
TGTCTTGGGC ATCAGGGAAA ACAGGTGTCT CTGGTCCACA TGCAGAAGAG CCACCACCGT 1740
GGCACGACTG GATGACTCAG ACCCCGGGCG GGGGGTATGA TTTGGACACA GTCATTGTCC 1800
AGGGACACAA CTTTGCCTGG ACCAGAGCTT CTCACCCCCA GGCCATTTGA AACCCCAGGG 1860
GATACTCGAC AAAGTCCAGA GACATTTTGG GTTGTTCCTT TCCAGCCCCG GCGATGGTGG 1920
GGACGTGTCC ATGTCTGTGT CCCTCCGGTC ACTCTCTCTG GCCCTCTCCC TCCCTGGGGG 1980
CAGCTGCTCT CAGCCCTCCC TGCCCCCACA TCGCCATCCT GCCTGTCCTT CTGGGCCTGC 2040
ACGTTTGTTG TGTTTGGAAG GAGCCACCAA GGAGGAGGAT GTCAATGTGC AAGTTCTCAG 2100
GGAAGCAGGC CCCGCAGCCT CCGTCAGTGT CTTCCGTCCG CAGGAAGAAC CCAGGCCTGG 2160
GTGATTCATC GGGGCCTCAG GGCCGGGAGG CACTAAATCT TCTGCAGATG TGGTAAGATC 2220
CTATCACAGC AGAAAGGGAA GGGCTAGAGT CTCAGGGAAG GTTTTGCTAG GGAGACGGGC 2280
TTGGAGGGGG CTGAGGCTCA TGGGAGCTGC AAGGGTACAG GAGGGGAGGG GACCCCAGGG 2340
CAGGTGGATG GACACCTGGG TGGGTAAGAA AAGGGCCTCT CAGAGGGCAA GGGAGGGCCA 2400
GGGAGGGAGC AGTGAGCCCT GACTGACTGT ACAAGCTTAA CTGGCTGCCC TTGTCCTGCA 2460
GGTGGTGTGG GCTGTGTGGA TTTCGGATGT GGGCCCATAA CATAGCCACA CTGCTGCAAA 2520
GCAAGTGAGT CTGAGGCAAG AAGAAGGCCC AACCTTGGGA GGCTGACCTG GAGGGCAGGC 2580
AGAGGCAGGT GGTAAGGACC TGCCTTACCT GTTGAGGTGA CAGTGGGGGA CATATTGCAA 2640
GGAAGGAGGC CCTGGATCCT CAGGATGTGG ATGGTGGGTA GAAGGGTGAC AGCTAATGGA 2700
TGTCCACCTG CACAGATGCC CACCTGCATG AGTGCCCACC TGCATGAGTG CCCACTTGTA 2760
CCAATGTCCA CCTGTACAGA TGTCCACATG CAAATGCCCA TCTGCACTGA TATCCACCTG 2820
CACAGATGCC TACCTGCATG AATACCCACT TGCCTGAAAG CCCACCTGCA CCCATGTCCA 2880
CTGGCACAAA TGCCCACCTG CACCCGTGTC CACTGGCACA AATGCCCACC TGCACAGAAG 2940
CCCACCCACA CAAATGCCCA CCTGCAAAAA TGTCCGCCTG CACAGATGTC CACCTGCATG 3000
AATGCCCACC TGTGTCCACA TGCACGAATA CCCACCTGCA CAGATGCCCA CCTGCACGGA 3060
TGCCCACCTG TACAAAGGCC TACCTGCGTG AATGTCCACC TGCATGGATG CCCACCCGCA 3120
CGGATGCCCA CCTGCACAGT TATCCATCTG AACAGCCCTC TGGTGCCTCC 3170
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