Tag | Content |
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EnhancerAtlas ID | HS098-58833 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:130861050-130863370 |
Target genes | Number: 33 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr9:130861276-130861291 | GTGTTCCTGAGAAGT | + | 6.34 | Tcf12 | MA0521.1 | chr9:130862583-130862594 | AACAGCTGCTG | + | 6.32 |
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| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_00502 | chr9:130859402-130866004 | Adipose_Nuclei | SE_01177 | chr9:130859439-130863274 | Adrenal_Gland | SE_02078 | chr9:130859356-130863981 | Aorta | SE_02461 | chr9:130859304-130863114 | Astrocytes | SE_08626 | chr9:130858493-130862947 | Brain_Inferior_Temporal_Lobe | SE_09846 | chr9:130858639-130861849 | CD14 | SE_13739 | chr9:130859872-130862337 | CD34_Primary_RO01536 | SE_23076 | chr9:130858917-130863198 | Colon_Crypt_1 | SE_23771 | chr9:130859824-130862455 | Colon_Crypt_2 | SE_24841 | chr9:130859798-130862587 | Colon_Crypt_3 | SE_24841 | chr9:130862748-130863210 | Colon_Crypt_3 | SE_25948 | chr9:130853911-130863239 | Duodenum_Smooth_Muscle | SE_26752 | chr9:130858869-130863439 | Esophagus | SE_27710 | chr9:130859695-130863223 | Fetal_Intestine | SE_28658 | chr9:130859472-130863226 | Fetal_Intestine_Large | SE_29715 | chr9:130859418-130863519 | Fetal_Muscle | SE_31462 | chr9:130859415-130863392 | Gastric | SE_37200 | chr9:130859386-130867552 | HSMMtube | SE_41771 | chr9:130860702-130862161 | LNCaP | SE_42378 | chr9:130858694-130866135 | Lung | SE_44311 | chr9:130858792-130863921 | NHDF-Ad | SE_44961 | chr9:130859352-130863261 | NHLF | SE_46195 | chr9:130858607-130863783 | Osteoblasts | SE_46747 | chr9:130859844-130863392 | Ovary | SE_47545 | chr9:130859779-130867121 | Pancreas | SE_48196 | chr9:130859594-130867368 | Psoas_Muscle | SE_49302 | chr9:130858827-130865482 | Right_Atrium | SE_51250 | chr9:130858612-130867152 | Skeletal_Muscle | SE_52155 | chr9:130859855-130862521 | Skeletal_Muscle_Myoblast | SE_53470 | chr9:130859373-130864872 | Spleen | SE_55063 | chr9:130858770-130863497 | Stomach_Smooth_Muscle | SE_63942 | chr9:130859841-130862657 | HSMM | SE_65681 | chr9:130859040-130867370 | Pancreatic_islets | SE_66839 | chr9:130859883-130862106 | 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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Enhancer Sequence | TTTGTTGAGT GAATGGCTGA GCATGCATGA ACCATCCCCC ACTGAGAGGA AAGAATGTCT 60 GAAATGTAGC AGTTTTTTCC CATTGCCATG CGGCTATGGC CGGCACGTGT ACGTCACAGG 120 AGTGACCGGT TTTCATGTGA CTTCCCAGGA AGGCTGGAAT TCCAGCGAAG GCTGTTGTGA 180 GAAATGGACT TTCAGAAAGG AAATTCCTTT TGCTGGAATG AGGGGGGTGT TCCTGAGAAG 240 TACAGAGCCA GAAAGGGACC TGGGGGGCAG GCCAGTAGTG CATGGGAGGA GAAGGCAGGG 300 AGGCCCAGGA GTTGAGGGTG CTGCGTGGTG GAGCTGCCCG TCCCTGGTGT GGGGGTGAGG 360 GAGCCTCCCG CCTTCTCGAC TCTCAGACAT CGCTGTGGAA CAGGGCCTGT GTCTGCCCTG 420 AAAGTGAGGA AGCCGAGCTG CAGAGTCCGG AGGCCCCTTG CCACCTCGGC TTCTCGGTTA 480 ATCAGTTTCC CTGCTACCCC CAGTGCCCAC TGTGCACCAA GGGGGATTTG CAGATCCAAG 540 GAAGGAGACA GAAGGAGGCC CAGGCCCTGT GAGGCAGAAG CAAGCACTTT GAGAATGCGT 600 TGAAGCCAGC TGCGGTGAGC ACACCCTCTG CTCTGGGTGT CTGCGACAGC ACCCACCCCA 660 GGGAGGCATG TGGCTCACCC TGGCAGCAGG CGGCTGGGTC CCAGAGGGCT CCATGCCTGA 720 TGTTCGCCTC CTGCCTAAAT GGCTTGTCCA CTCTATTTCC ATTCCTGTTA GAGATTTGGA 780 GCAGTCACCC TATAGGTGAT TTATGTCACT CTTGTCTGAG AGCACAGATG TCCACAGGAA 840 GTTAAATGTA ACCTCAGCAG ATAAAATATG TACCTGCATC TGTCCTACAT TCCAGCCACG 900 CCCCTCACAT TAGCCTTTTG ATCGCGCCAG GTCATGGGGT ATCTGTTCAG GCCTCCCTGC 960 CCCTGACACC TTTGGCAGCT GAGGAATCAC AAGGCGCTGT CAGTAGTGTG TCTAAGAGAG 1020 AGGCGCGGTG GTGATCCTTT GAGGACGCGA GCTAGCCAGT GGGCCATCCA TTTCCAAACC 1080 CCAGCTGGCT GTCAGTTGAT TTCTCCCAGT GAGAAATCCG GAGGACACAG GAAGACTATA 1140 CCATCTTCCT TGGGAGATTC TCGGTCCCAG TTTTGGGTTC CGGATTCAGG GCGTTGCTGA 1200 GTTGGGGTGA CTCACTTTCA TCCCCCATGT TCTGAAGGTT AGCCTTGAGG GTGGCGGCAG 1260 GATGTGCAGG GAGGCGGCTT GGGAGGACCA CGGCCCAACT TGCATCCCGC CCACCACTTC 1320 CCTAGCTGTC TGACCTTGTG TAAATGTTTA GGCTCTCGGA ACTCCTGTTT CCTTCTCTGT 1380 AAAATGGGGG AAATGACATT TCCTACCTCC TAGAGCTGTT TGCGAGGGGG GTAAGTGGGT 1440 TGCTAGAAGT AAAGCATTTG GCACGCCCTG CGGCCGGTGC TAGGTGCTGG GGAAATGTGT 1500 GCTCTCGTGG AGCTGTCCCA GTTGCCAACC ATTAACAGCT GCTGAACAAA GCCCACCTCC 1560 TGGGAGGCGG GGGCGGGGGG GGTTACTTTT GGAACCTCAT TGCCAAGGAA CAGTCTCTCA 1620 AAGCCTTCTT GGGACACTAA AGTGCTTTTC AGTGAGTGAG CGGGAGAGCC AGGGCAGCTC 1680 TATCACCTGG CTTCCCTGAG AGCAGGGACT GGCAGTACCA TCATACACAT GCCCTTGGCT 1740 CCTTACACTT CCCCGGCCTC GGGTGCTGTG GCAGAGTCTG GCTCTGCCCC CGATTTTCAC 1800 CTGCCCACCA AATTATTCTC GGACCAATGC CAGTTTTAGG AGAGAAACAG CGAGCTGCAG 1860 AGTTCCTGTC AGAAACTGGA CTCCATGGCC ATCCCCAAGT CTCAGCAGGG AGCATGTGTG 1920 GTTGAAGCCT GGGTCCAGGG ACCCAGGGAC GGCGCTGCAG CGAAGCCACC CTGCTCACCC 1980 TGGCTGTACG GCACGCAGGT CTTCAGACTG AGAAAGTGCC CAGCTGTCCC TGTCGGCCTC 2040 TGTCCGGAGG GCTCTTCCCA GGCTCCTTGT TTCCTCTCTG CTTGAGAGGG AGACAAGATT 2100 GGCCCTTGCC TGGGTTCTGG CCAGCACCTG GGGTTCTAGG TGGTGGCTCT GGCATGTAAG 2160 TCGATTGCCA TGGTGGCTCT GAGAGTGGAG CAGAAGCATC TTGGGTCCTT GGGGCCAGCT 2220 CTGCTCGCAA TTAGTGAAGT CATTGCCTGG GGATGGGGCC CCACAAGGGA CAAGGAAAGG 2280 CTGGTCCAGG AGCCAAAAGA CAAAATGTTA CCTTTCTTTT 2320
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