Tag | Content |
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EnhancerAtlas ID | HS197-13891 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr22:36741190-36743860 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr22:36742311-36742322 | AAAACAAAGAC | + | 6.14 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_00116 | chr22:36741927-36743611 | Adipose_Nuclei | SE_01541 | chr22:36741266-36744060 | Aorta | SE_05110 | chr22:36734537-36742108 | Brain_Cingulate_Gyrus | SE_05865 | chr22:36717131-36743101 | Brain_Hippocampus_Middle | SE_06839 | chr22:36722236-36742206 | Brain_Hippocampus_Middle_150 | SE_07886 | chr22:36734649-36742258 | Brain_Inferior_Temporal_Lobe | SE_09195 | chr22:36736566-36742350 | CD14 | SE_11020 | chr22:36722390-36744211 | CD20 | SE_17339 | chr22:36719961-36744102 | CD4p_CD25-_CD45RAp_Naive | SE_17788 | chr22:36723586-36741701 | CD4p_CD25-_CD45ROp_Memory | SE_18286 | chr22:36720347-36743699 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19119 | chr22:36737667-36742165 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19119 | chr22:36742859-36743596 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22328 | chr22:36734799-36741977 | CD8_primiary | SE_22328 | chr22:36743026-36744123 | CD8_primiary | SE_26521 | chr22:36741286-36744033 | Esophagus | SE_31378 | chr22:36743140-36743895 | Gastric | SE_35739 | chr22:36741281-36743900 | HepG2 | SE_36959 | chr22:36739003-36742325 | HSMMtube | SE_40597 | chr22:36741225-36743740 | Left_Ventricle | SE_42094 | chr22:36741259-36742861 | Lung | SE_42094 | chr22:36742947-36743899 | Lung | SE_45604 | chr22:36739365-36741767 | Osteoblasts | SE_45604 | chr22:36742174-36743331 | Osteoblasts | SE_47169 | chr22:36741730-36743037 | Panc1 | SE_47169 | chr22:36743215-36744104 | Panc1 | SE_50050 | chr22:36741267-36742026 | Sigmoid_Colon | SE_51217 | chr22:36740405-36741785 | Skeletal_Muscle | SE_52340 | chr22:36741307-36741997 | Small_Intestine | SE_52340 | chr22:36742067-36742912 | Small_Intestine | SE_52340 | chr22:36743068-36743836 | Small_Intestine | SE_53283 | chr22:36743045-36743808 | Spleen | SE_54489 | chr22:36741203-36743056 | Stomach_Smooth_Muscle | SE_58448 | chr22:36724049-36832686 | Ly1 | SE_62244 | chr22:36719186-36785326 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 36741870 | 36742041 | chr22 | 36742146 | 36742667 |
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| Number: 3 | ID | Chromosome | Start | End |
GH22I036346 | chr22 | 36742241 | 36742390 | GH22I036347 | chr22 | 36742860 | 36744123 | GH22I036321 | chr22 | 36717371 | 36741885 |
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Enhancer Sequence | ACTAAAAATA CAAAAAATTA GCCGGGTGTG GTAGTGGGTG CCTGTAGTCC CAGCTACTCG 60 GGAGGCTGAG GCAGGAGAAT GGCGTGAACC CGGGAGGCAG AGGTTGCAGT GAGCCGAGAT 120 CATGCCACTG CACTCCAGCC TGGGCGACAG GGCAAGACTC CGTCTCAAAA AAAAAAAAAA 180 AAAAAAGTTC CCATGGAATC CTCGCAGATG AGGAAGTGAG ACTCCACATA GCCATGTCTC 240 ATGGCCAGTA AGGGGCAGAG CTGGGATTTG AACCAGGTCC TCGAGGCTCC AACTATAGCA 300 CTTAAGGGCT CTGCTTTACT GAGCAGAGGC CATCTCAGCT TAGTGGCACA GCAGAGTGGG 360 TGTGACATAA GCTATAAAGC CTGCCAAGAG GAGCGCCTCC CAATCCCAGA CAGTGAGGCT 420 GCAGCTCCCA TGTCACCCCC ACAGACACAC TGTGCTTCCT TAAAGCACAG TCTGCCATTC 480 ATTTATTTGC AAGTCACTAA TTCTGAATTT CAGTGGTTAA TACTCCTTAG GGACAGGGGC 540 CTTTAATTTG GTCCACATGA TAATCTTATC AAGCAACAGA TGAGACACAA TAGGTCTGAA 600 AATCAGGAAC CCAAGTTCCA GCCTCAGCCT GGCCAACACC TGGCTGTGTG ACCCTGCTTA 660 AGTTCCTTGC TATCTCTGGG CCTCAATTCT TCCCACCTGC CATGTTAGAA GGCTGGGCTG 720 GGGCCGGGCG TGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGACG AGGTGGGCGG 780 ATCATGAGGT CAGGAGTTCC AGACCAGCCT GGCCAATATG GGGAAACCCC GTCTTTACTA 840 AAAATACAAA AATTAGCCGG GCATGCTGGT GGGCACCTGT AGTTGCAGCT ACTCAGGAGG 900 CTGAGGCAGG AGAATCGCTT GAACCCGGGA GGCAGAGGTT GCAATGAGCC AAGATGGCAC 960 CACACCACTG CACGCCAGCC TGGGTGACAA AGTGAGACTC CGTCTCAAAA AAAAAAAAAA 1020 AAAGAAGGCT GGGTTGTAAA GGAGACTGTT CCACATATCT ACTTGTTGAT AGGTCTTTGA 1080 TGAGCCAGGT TCATCCCCCA AAGGGTGGGC ATCGATGGCA GAAAACAAAG ACCTCGTTGT 1140 CACAGACTGA TTTAGCAATC AACAAGGAAA TGCAGTCCTA GTCAGGAGTT CCGGGCAAAT 1200 ACAATGGCCC ATGGCTCCCA TTGAAGGCTT TAGCACATTG CAGGGCACTC AGAAGCATGA 1260 GTCTACCTCG TAGAAATGTG CTTAAGTCTG TCTGAAGTCA CACAGAAAAT TAAACGGCTG 1320 ACCCTTTCAG AGCTGCTGTC TCTGTAACAG AATGAGCCTG CCACCACCTG CTTTTATTAC 1380 ATATGTGACC ATGAGCAAAA TCCCTCAGTC TGAAAGTTGG TCTTCCCATC TGTAAAGTGG 1440 GAAGGCCATA ATAATCTTTT TTCTTTTTTT TGTTTGAGAC AGGGTCTCAC TCTGTCGTCC 1500 AGGCTGGAGT GCAGTGGTGC AATCTCGGCT GACTGCACCC TTGACCCCCT GGGCTCAAGT 1560 GATCCTCCCA CCTCAGCCTC TAAGAAATAG CTGGGACTAT AGGCACGCCA CACTATGCCC 1620 ATCTAATTTT TTTATTTTTT TGTAGAGATG GGGTTTCACC ATGTTGCCCA GATTGGTATC 1680 AAACTCCTGA GCTCAAGCCA TCCTCTCGTC TTGGCCTCCC AAGGTCCTGG GATTGCAGGC 1740 ATGCACCACC ATGCCCAGCC TATAGTAACC TCTTCATGGC TTTTTTCCAC TAGGTCAAAA 1800 ACATTTTGAG GACTGTTTTA TTCAGCCCAA AGTTCAAGGT GGCTAGGGCA ACATAAAGAA 1860 ATAAAGAGCT ATTTTAGGAA TAATAACAAG CAGATATTTC TTTCCCACTG GGGACAAAAC 1920 CAGAAGGAAA TATCTTTGAG TTGAACAGAG GAATTTGGGG TTGATATTGG ACAGGACTTT 1980 GTGACCCCAG AGCCCGTTGC CTCTGGGATG CATAAATGCT CATCTCCCTG TCTCCTAACT 2040 TGGTGATGGA CTGCGTTTCT GCATTTTCTT TCTTGCCAGA AGAAAGAAAA TGACGCCCCT 2100 GATCTGCTGC ATGTGCTGGC CCTTTGCACA TGCTGCTCTC TGGACTCTCA ATACACTTCC 2160 CCTTGGTCAA GCCTGGCAAG GGACCAGCAC TAAAGTGCTG GACAGAGTCC CAGAGCAAGT 2220 CTTACTCTTG GTGGCTCACC TCTGCTCAAA GCACACTCCC TAGGGAAGTA ACCCACACCA 2280 ACAAGCATCC GTAAAGAACA AGATGGGCTG GGCACAGTGG CTCACGCCTG TAATCCCAGC 2340 ACTTTGGGAG GCCCAAGCAG AAGAATCACT TGTGCTCAGG AGTTCGAGAC CAGCCCTAGG 2400 CAACATAATG AGACCCTGTC TCTAATAAAA ATATTAAAAA TTAGCCAGGC GTGGTGGCAC 2460 AGGCCTGTAG TCCCAGCCAC CAGAGAGGCT AAGGTGGGAG GATCGCTTGA GCCTAAGAGT 2520 TTGAGGCTGC AGTGAGCTGT GATCATGCCA CTGCACTCCA GTCTGGGCAA CAGAGCTACT 2580 TTGGGAGGCT GAGGTGGGTG GATCACGAGG TCAGGAGTTC GAGACCAGAC TGGCCAATTA 2640 AAAAAGACCC TGTCTCAAAA AAAAAAAAAA 2670
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