Tag | Content |
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EnhancerAtlas ID | HS105-17628 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:11915000-11917760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr12:11915478-11915491 | CATTAATTAATTA | - | 6.46 | POU6F1 | MA0628.1 | chr12:11915479-11915489 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr12:11915479-11915489 | ATTAATTAAT | - | 6.02 | ZNF263 | MA0528.1 | chr12:11915903-11915924 | ACTCTTTCTCCTTCCTCCTCC | - | 6.9 | ZNF263 | MA0528.1 | chr12:11915909-11915930 | TCTCCTTCCTCCTCCTCCTCG | - | 7.36 | ZNF263 | MA0528.1 | chr12:11915906-11915927 | CTTTCTCCTTCCTCCTCCTCC | - | 8.38 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_01754 | chr12:11914419-11916329 | Aorta | SE_01754 | chr12:11916394-11918023 | Aorta | SE_09138 | chr12:11895682-11929433 | CD14 | SE_12874 | chr12:11915526-11916313 | CD34_Primary_RO01480 | SE_13315 | chr12:11914238-11920650 | CD34_Primary_RO01536 | SE_14048 | chr12:11914146-11917451 | CD34_Primary_RO01549 | SE_25354 | chr12:11914277-11930036 | DND41 | SE_25772 | chr12:11913943-11922646 | Duodenum_Smooth_Muscle | SE_30380 | chr12:11914693-11915878 | Fetal_Muscle | SE_30906 | chr12:11914521-11920257 | Fetal_Thymus | SE_32458 | chr12:11910093-11922451 | GM12878 | SE_39367 | chr12:11914420-11925956 | Jurkat | SE_43859 | chr12:11914295-11916262 | MM1S | SE_43859 | chr12:11917454-11920221 | MM1S | SE_46110 | chr12:11915046-11920204 | Osteoblasts | SE_49833 | chr12:11914096-11919206 | RPMI-8402 | SE_54656 | chr12:11914202-11920959 | Stomach_Smooth_Muscle | SE_58379 | chr12:11878906-11990784 | Ly1 | SE_58837 | chr12:11874923-11935776 | Ly3 | SE_59849 | chr12:11874575-11943335 | Ly4 | SE_61023 | chr12:11869475-11929777 | HBL1 | SE_61926 | chr12:11879670-11927640 | Toledo | SE_62748 | chr12:11877030-11934459 | Tonsil | SE_66238 | chr12:11914420-11925956 | Jurkat |
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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: 1 | ID | Chromosome | Start | End |
GH12I011761 | chr12 | 11914429 | 11925846 |
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Enhancer Sequence | CTGTTGAGCA TTTCCCTATG GTTCCTGTGA TTGAAATCGG GTTAATGCTT TTGTGGGATG 60 AGAACTGGTG CCAGCTCCTA GGCCTTGCAG GGCTTCTAAA GACTGTCCCT GCCACTCTTG 120 CCTTATGCTG GTTCCCAGGA CCTTACAGCC AGATCACAGG CCTGCTCCCC TGTTCTCATA 180 GCCCCCTTTC TGGCCTGAGA ATTGTCTGTG GCTTGGCCCT TTGCCCCATG CAACATGCAC 240 AGGTGTGGCT TCTGCTAACT ATCTACTTGA CCCCAACTGT GTGATTAGCG GCAATCCCCT 300 CTGCAACTCA AGGCGTGTTT GCCTTTCCTG TAACCTGTAA AAAATTTCAG TCTGCGTTTT 360 TCTCCCTCTG GAGATGGTAT CCACTGGGTT TTAGGCTTTA CAGAGCCAGC TGATCTGCGT 420 GGATGGGCCA CACTATCCTC CCTTAGCCGG CTCCGTAGCA CATGCACAAT TAATACTGCA 480 TTAATTAATT ATGGGAGAAA AAAAGCACAG TTGGCAAGGG AATGAAGGCT TTCAGCTTCT 540 AAAGTGAAGG CTTTGATGCT GAGCTTGAAA GTACATTTCC ATCCGCCTCA GCCAGCAGAG 600 AGAATCTGTG ACACTTATAC CATCCCCTGG GCATGAAAAC TCACACCCAA GGAAAGTATT 660 TCTAAATAGA GGCCCTCAAC TAGTTGCTGG AATCATCTAC TCATTGCCAT GGGCTGTGAA 720 AAGGGGGTGT AAGATTAGGG AGAAAAGACT CGCCCAAAGC AGCAGTGATT CGTGACCAAA 780 GCTGATGAGG GGTTTTATTT TTTCTCCTTA AGTAGCTCTT AAGTCACCAA CATCAGGAAC 840 TCTTTGTAGA GAAACAAATA TGAGTAAGTG ATTTGGTGCC AGCCCTCTTG AGGACATAAA 900 ATGACTCTTT CTCCTTCCTC CTCCTCCTCG CATGCCTTGC TTCAGGAAGG AACCCTAAGG 960 TGGTGCAGGT TCCCAAACCT GTTATTCGGA TGGGTTGGAA GGTTCATCTC TGTTAGGCAT 1020 GGTTTCCCAC TAGATATGAA CAAAGTCGGG GAGAAAATGC TTTCCTTTTT CATTCTGATT 1080 CCTTCACGCC ATTGTTCTTG AACTCCTCAG CTCCCACACT GACTCCTTTC ACTTCTCCTA 1140 TGAGGTGGTA GTGAAGCCAC CTCACAAAGT CCCCTCTCTG AACAGACGCA GTTCTCGTTC 1200 CCCTATTTAC AACTCTGTCA AGCATTTTTC GTGGGGGCTC TTGCTGACCT TAAAATTTGG 1260 CCGTGATTCA AATATTCATC CAGGTATCTG GGGTTTTATT AAAGGTCTTT TAGGAACACA 1320 AAAGTAGGAA TTCCCTGAGA GAGGTTTTCT TCACTTGAGA CTCATGGGTT ATAAATGAAA 1380 CTACTGGAAT GCCCTGACCA AGTGCTGAGA GGAGCTTCAG AGACCCACAA AAACCTAAAA 1440 AGATGTGAAA TTTGTCTCTG ATCAAATAGA TTTTGGACCT TATGAAAGAA AATAAGCTTT 1500 TCTTTTGATT CTTAGAGAAA AATTTTTGCT TCAGATGAAT CCAAGTGTGT GTGCACGCAC 1560 GTGCTTTCGT TGGGATCGTC TTATAGCTGT TATTCCAGAT ACCTGCTTCA CAAAGCTTCT 1620 GTGATTATTC CTACTACTGT GACGATTCCT GCCACCCCAG TGATCGGGGA AAAGAACTTG 1680 AAATACAACT GGGTATTGTA GCATTGGCAC TGTGCAGACG CTGTGTAGCT CTCTCATGTC 1740 TGGTACTTCT TTGTTTGCTA AAGGAGTATT GAGATTCAGA AAGTGGCTGC CTTCTAAACC 1800 TTTATTGTTC AGATAGCATT ACTTTGGACC CAGGACAGAG GGCTTATAGT TGACTGTGAA 1860 CGGGGTGAAT GTTATACTTA AGCAGGGAAT GTGGTCACCC AGTTGCAATG ATTTAGAGTG 1920 CTTTGAACAT AAATATCTCC CACGATGAAT GACCAGGGTG CCTGAAATTC CATTGTTGAG 1980 ACATTCCTTT TGGATCAGGC ATTATTTCCA CATAGCTCCA CTTTTAAAAG TAAATCATTA 2040 TGGCAGGAGA TAGTTATGGA GAGAGATAAT TAATACCTCA AGTCCCTAAT ATCTTAATGA 2100 AAATTAGCTT ATCAGATCTC CTGAATTTTT TGAAGTGGAA GGACCGTGGC CAGCACGGAG 2160 TGGGTAGAGT TGGAAATAAG CACTATAATT TGCTTAGGGC TGGCCTTCTC TGTGGATAAG 2220 ACAGATGGAA AACTAGATGG AAAATCCAGG CCTCCTGATT TAGACAAAAC ATTGTGAGCC 2280 TGGAGCTCTG AGGCCAGGAT GAGCAGTCTG CTACTTACTG TGCGTGGCCA TTGCTCTCAA 2340 GACATTGCCA TCATCAGTCT TGGCCAAAGA AGGTCAGGTC TCCTCTAGTA CACTGGCGAT 2400 TTGAGAATGT GCAAGTCATC TGCATTTCTT TGACAGGAGT AGTGAATTTG GGAGTATAAA 2460 TCTGAATCCT TAAGCCTTTC AACCATTCTC ACTAAATGTC TTTACTTCAG GGATGATCAC 2520 GTTTGATCGT AATGCCAAGA TCTTGCAGAT GTATAAAGGG CATGGTAATC CAAGTCTTGA 2580 GTTGAAGTAA GTGGTCAGGA AAATCTTGAC CCTTGGGGAA GGAGCTACCA GAGCTGGGTG 2640 GCCTATGTGT GTGTGACAGG GAGGAGGTGT GCAGAATTTG GGGGAAAGAT CCTTTGTAGT 2700 TCTCCATGTG GAATAATAAC TTCCATTTAT TGAGTGCTTA TGGTAGGCGC TTTTCACATG 2760
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