Tag | Content |
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EnhancerAtlas ID | HS116-21773 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr21:45591150-45593310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT1 | MA0137.3 | chr21:45592181-45592192 | TTTCTGGGAAA | + | 6.02 | STAT3 | MA0144.2 | chr21:45592181-45592192 | TTTCTGGGAAA | + | 6.32 | Stat4 | MA0518.1 | chr21:45592181-45592195 | TTTCTGGGAAAGGG | + | 6.56 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00694 | chr21:45591173-45593356 | Adipose_Nuclei | SE_03880 | chr21:45591029-45594051 | Brain_Anterior_Caudate | SE_05779 | chr21:45589848-45594597 | Brain_Hippocampus_Middle | SE_06690 | chr21:45592076-45594516 | Brain_Hippocampus_Middle_150 | SE_09453 | chr21:45591770-45593805 | CD14 | SE_10160 | chr21:45592165-45598304 | CD19_Primary | SE_10883 | chr21:45590077-45601846 | CD20 | SE_24239 | chr21:45590332-45591498 | Colon_Crypt_2 | SE_24239 | chr21:45592747-45593467 | Colon_Crypt_2 | SE_30176 | chr21:45591845-45592759 | Fetal_Muscle | SE_31647 | chr21:45589420-45592073 | Gastric | SE_31647 | chr21:45592266-45593640 | Gastric | SE_33667 | chr21:45592179-45593627 | H2171 | SE_40890 | chr21:45590996-45593468 | Left_Ventricle | SE_42286 | chr21:45591020-45592054 | Lung | SE_42286 | chr21:45592108-45593377 | Lung | SE_48538 | chr21:45591030-45593646 | Psoas_Muscle | SE_50113 | chr21:45589527-45594430 | Sigmoid_Colon | SE_51445 | chr21:45590165-45593313 | Skeletal_Muscle | SE_52463 | chr21:45589655-45594316 | Small_Intestine | SE_53405 | chr21:45592140-45593505 | Spleen | SE_56643 | chr21:45592371-45593098 | u87 | SE_58720 | chr21:45552566-45596359 | Ly1 | SE_59125 | chr21:45557380-45640832 | Ly3 | SE_60477 | chr21:45556693-45597600 | DHL6 | SE_61237 | chr21:45557180-45641526 | HBL1 | SE_61527 | chr21:45545883-45641600 | Toledo | SE_62281 | chr21:45556124-45641130 | Tonsil | SE_65639 | chr21:45590102-45592103 | Pancreatic_islets | SE_65639 | chr21:45592304-45594095 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH21I005088 | chr21 | 45591653 | 45593652 | GH21I044169 | chr21 | 45589789 | 45597483 |
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Enhancer Sequence | CTGAGCACCT CTGCCCCAGG GTCTTTGCAC GGACCGTTCT GCCTGGAAAG TTCTTCCCGA 60 GATCTGCTGA GGCGGCTCCT CCTCGGCCGC ACGCTCCCTG AGGCTTCTTC ACCCGCGCAC 120 ACACGGGCAC CGCCTGCCTC CCGGTCTCCT CTCCCCAGAA CCTTAGCTCC AGGGTGCAGG 180 GACTCGCCCA CGTGGTTCCA GCCCAGGGCC TGGCCCGAGC AGGTGCTCCC TCTGTGCTTG 240 TTGAATGAAA GCGAAGTGAC CAACAGCACA GACTTTTTCC GAGGAAGAGA GAGAGCAGAG 300 AGCAAAGCAG AGGCCTGAGG GACCTTGTGA CCCCCAAGCC CACCTGGCTG GTTCCCTGCA 360 GACAGCCCTG GCTCCTGCAC TGCTGCTTTT CCCCGCCAGG GACCAGGCCC CCACCAGCCA 420 GGAGCCCGGG ACACGTCCAT GTTCTGGGAC TTGACCTTCG TCTCCCCACA GCCTGCATTT 480 CCACCCTGCC TGGCCGCAGC TCTGGTTGGT GGGAAGGGGC TCCAGGCGGC CCCGCTCTGC 540 TCCGGTACGT GCAGACATCT GGTGTGCAGT GACCTTCATC CCAAGCAAGG CCTAGAAAGG 600 GGGAAATCGA GGCAGCATAG AGAGCCGGCC CAGGGCAGCC TTCTGGGCTG GAGCATGGGG 660 GTATGAGGGG GCTGCCGGTG TGGTGTGGGT GGCCCGTCCC CTGGTGATGA GTGTGTGGGA 720 TGGCGCTCAG CCTCTGCCTC TGCGGCCTGC TCAGTGGGCC CTCCCACTCC CCTGGAGACG 780 TCTCTGTGTG CTTGTGTTAC CAGAAAGGAG TCCTGATCCA GACACCAAGA GAGGGTTCTT 840 GGACCTCACA CAGGAAGGAG TTCAGGGTGA GTCCAGAGAG TCAAGTGAGA AGTTTATTAA 900 TAGAGTAAAG GAATAAAGAA TGGCTACTCC AGAGGCAGTG CGGAGGGCTG GGCTGCTCAG 960 CTGAATATTC TTATGCTTAT TTTGGTCATT TCTTGATTAT ATGTTAAACA AGGAGTGGAT 1020 TATTCATGAA TTTTCTGGGA AAGGGTGGTC AATTCCCAGA ACTGAGGCTT CCTCTCCTTT 1080 TTAGACCGTG CAGGGTAACT TTCGGACGTT GCCATGGCAT TTGTGGACAT GGCGCTGGTG 1140 GGAGTGTCTC TTAGCAGCTA ATGCATTAGA ATTTGTGTAT AATGAGTGGC GAGCACGACC 1200 AGAGGTCACT CTAGTCACCA TCTTGGTTTT GGTGGGATTT GGCCACTTCT TTACTGCAAC 1260 CTGCTTTATC GGCAAGGTCT TCGTGACTTG TATCTTGTGC CAACCTCCTG TCTTGTGACT 1320 AAGAATGCCT TACCCTCCCG GGAACGCAGT CCAGCAGGCC CCAGCCTCAT TCCACCCAGC 1380 CCCTATTCAA GACGGAGTCG CTCTGGTTCA AACACCTCTG ACAGTTGGAC AAGTTGGTGA 1440 CAGCCAGGAG GGCCCGATGT GGACATGTGA CAGGCACCCT GTGGCCATCA GATTCTCAGG 1500 AGGAAGAAAT CCCCTTCTGA AATAAAGCAC CCTGAGAACC GGCGGGAAGG AGCGGGGACT 1560 CCGTCGGGGC TTTCCAGGGA AGCAGCCAGG GACTTGCCCT GATTTTGGTT TCTCCAGGTT 1620 GGAGCCGCCC CGCAGGCTGC CTCTGCCGGC GGGAGGAAGT GAGCAGCTCC TGCGGAACCT 1680 CTGGCTGGCA CAGAGCCCGG GGGCGGGGGA GCCCTCCCTG CCAAGAGAAG CCATCAGGTG 1740 CAGAGGACAG CACTGACTGG GCCAGTGGGG CGTTCTCCAG CTGGGTCAGC CGTGGCCCCC 1800 GCCTCGGGCT GGAGTCCGGC AGGCAACTGC TGCAGAAACG GAGGCAGAGG CAGGTGGAGG 1860 AGCCGCCTCC AGGCGGAGGA GCCCCAGCAA GATGGGGCGC TGGAGTTGAG CTCAGGCTGT 1920 CAGCCCCAGA ATCCAAGCTC CTTGCCCTCG TGCTAACCCA GCCTCACTAA CTGGCAGCTG 1980 GGGGCACCCT CCCAGCCTGC CAGGGACACC ACACTGGGCA CACACCACTT CGGCTGCAGG 2040 ACCCCATCCT CACTGGCTGT GGCGGGAGAC TGGTGAGCCG TCCTTGTAGA CCGGACTCCC 2100 CCTAGAGTCC TGAAGGACTG TCCTGGGGGC TGGGGAGCTG CTGGAGGCAG CAGCCTGGGC 2160
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