Tag | Content |
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EnhancerAtlas ID | HS085-00612 |
Organism | Homo sapiens |
Tissue/cell | Heart |
Coordinate | chr11:73034420-73037030 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr11:73036844-73036854 | GGGGCGGGGC | - | 6.02 | MEF2B | MA0660.1 | chr11:73034791-73034803 | GCTAAAAATAGT | + | 6.11 | RREB1 | MA0073.1 | chr11:73036254-73036274 | GCCCAAACCTCCCCCACCCC | + | 6.39 | ZNF263 | MA0528.1 | chr11:73035002-73035023 | TCCTTCTCCCTGTTCTCCTCC | - | 7.07 | ZNF263 | MA0528.1 | chr11:73034824-73034845 | GGTGGAGGAATAGGAGAAGGG | + | 7.19 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_01582 | chr11:73030301-73037752 | Aorta | SE_02882 | chr11:73031862-73036852 | Astrocytes | SE_04339 | chr11:73031975-73037551 | Brain_Anterior_Caudate | SE_06140 | chr11:73030318-73037316 | Brain_Hippocampus_Middle | SE_26016 | chr11:73031691-73037258 | Duodenum_Smooth_Muscle | SE_27041 | chr11:73031604-73037579 | Esophagus | SE_30618 | chr11:73031986-73036224 | Fetal_Muscle | SE_32060 | chr11:73031782-73037392 | Gastric | SE_39001 | chr11:73031680-73037276 | IMR90 | SE_40817 | chr11:73031658-73040101 | Left_Ventricle | SE_42282 | chr11:73031638-73037644 | Lung | SE_44364 | chr11:73031680-73037150 | NHDF-Ad | SE_44992 | chr11:73031717-73036952 | NHLF | SE_45900 | chr11:73031646-73037694 | Osteoblasts | SE_46937 | chr11:73031963-73034697 | Ovary | SE_46937 | chr11:73034753-73035669 | Ovary | SE_46937 | chr11:73035818-73036170 | Ovary | SE_46937 | chr11:73036224-73036621 | Ovary | SE_48721 | chr11:73031870-73037646 | Right_Atrium | SE_49552 | chr11:73034776-73036223 | Right_Ventricle | SE_50607 | chr11:73031699-73037502 | Sigmoid_Colon | SE_53958 | chr11:73031625-73037049 | Spleen | SE_54638 | chr11:73017438-73040151 | Stomach_Smooth_Muscle | SE_60317 | chr11:73022596-73047103 | Ly4 | SE_65783 | chr11:73032656-73036525 | Pancreatic_islets | SE_68363 | chr11:73017636-73046660 | TC32 |
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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 |
GH11I073319 | chr11 | 73030584 | 73039310 |
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Enhancer Sequence | TGGTAGGTCC ACAGGCAGGC ATCCTTGCCA GCAGCCCTCG TGGTGGGTCC TGTAGTCAGA 60 GACAAAGAAC CTTGTGATAT TTGTACCCTA GATCCTGAGA CCAGTGCTAT TCTGTGGCCC 120 CGCAGCCCTG GAGGCCTTCC TGAAGAAGAG GAGAGCCGCG CTTTAGGGAG AGGAGTGCCT 180 CACACTGGGG GCCTGAGCGG AAAGCCTGCT TCCCTGTCAG ATGCCTGAGC GCCCTCCCAG 240 CTCCTGCCGC TCCTGGGCCC CTCCTCCCCT CTGGCCTGGA CCCGCCACTT CCAGGCTTCT 300 CCCCAAGGCC AGCGGGGGCG TTGCCTGGGG CGGGTGAGGA ATTTCCGAGG GAATGGCTAA 360 ATTCAGCCCC AGCTAAAAAT AGTCCCGGGC CTGGCCCCAA GGCTGGTGGA GGAATAGGAG 420 AAGGGTGGGC CCGGCCTGCC CCATCTCATC ACCTGGACGT GGTGCCTGGG CAGTGGAGGG 480 TCTCTGCTGG TCCCCTGGGC ATCTGTGTCT TTGTTCCAGC CACTCGCACC AGGACTTCCT 540 CTCATGGAGG CTCCCTGCTT TCTTCTCTCC TTCTGTCCTC TGTCCTTCTC CCTGTTCTCC 600 TCCCTGGGTC TTGCTCCTCT TCCTGTCTCT CATCTCCTCT GACCATCTGT GTCACCCTGC 660 CTCCCTTTAG AGAGCCAGAC AGAGACCCCT GGCCAGGGAC TGGTCTTAGG AAAACGGCCG 720 TGTAGGGCAG AGTCCCCCTC AGCTTCCCAG CCCAGGTGTC AGGAACCGCC TCTGTCCCAG 780 GATACACAGT GATTGCAGCT CCTCTCTGCT TCGGAGGTAA CAGACCTCTA AGGCTCTGGG 840 ATGTGGAGAT GTGGGTGGGA GCCCCCAGTT TGCCCCGTGA CCCAATGCTT GATTCTGGTC 900 GGGTGGATCC ACCCATGCCA AGCCCTCCTG TTCCTGGCAC GAGGTGGAGC CTGGGTACAC 960 GTTTATTAAA TAAATAATGT GGGGGAGGCA GGAGGAGGAC AGCTGAGCCC TGCCCTGGGG 1020 GAGCGCCCAG GCTCCTCTCA GCTCCCCTTA CCACCCATGC CTATGCCTAG CCCTATGTTG 1080 CTGCTGTCCT GGGGACCAGG CAGGTGGAAG CTGGCAGATG GGCAAAGGGT GCCGTCCCGA 1140 GTCGGCACTG ATTGGGGGTG GGATGGGAAG CAGACACAGG CCCAGAGAAG GTGAGGGTGC 1200 TTAGCTCAGG TCACAGAGCC CAGAAAGAGA GAGGTGGTAT TCAAACCAGG ATAGTCTCAC 1260 TGGGTTGGAG TTCAGACCCA GATGGTCTGG CTCCAGAACC CGTGCTTAGG CCCCTGGCTT 1320 TCAGGACTGC CTGAGTTGGG GGCAGTGCCA TCATCAAGGT GGGCACAGAA AGAAAGGGTG 1380 GATTTTGCTT TGGACATAGT GATCCTACTG GATTCACAGT CCATGGTCTG AGTCCCAGGA 1440 ACCAGCACAT AGTAGTTGCT CAGTAAATAT TAGTTGAATG GCTCAGTTGC ACTTGAGAGG 1500 CCCTTGGGGA GTGGGAGGAG GTGACAGGCA CAGAAGGAAT GAGTGTTTCC TCCCTTTATG 1560 GGCCCAGGGA CCCTTCTCTT GGTGCTGGAA AGCAGCTGAG GTGGGTGCTG GGCTTTCTGC 1620 TGGCGGAGAG AACTCAGCCC AGGAGTTTGG GAAGGTGGAG AGATGGGCCA CGGGCAGGTG 1680 AAGGGGAGAC AGGCAGGCCA GGCAGTGCAG TGCAGTCCCG TTTGCAGTAT CTGGAAAGCA 1740 GATCTCTTGG GCCATGGCCG GCGTGACTCA AATGGAGACA AAAAAACCTT CCATATTTGG 1800 ACAAAGAGCC CAGAGAGGCC CAGACCCGCA GCCAGCCCAA ACCTCCCCCA CCCCCAGCCT 1860 CCTGCCCTGT CTCCCTCTGG GCCCCTAGCC CTGAGTCCTG TCCCATGAGT TGAACTCTTG 1920 GGCCTCAGTC ATCAGGTCGC TTCCTGTGTG GCCAGGCCTG GGCTGTGGGT GCTGGGGAAG 1980 AAATTTCGTT CCAGGGCTGG GCCCTGTGCT TGGGCTGGAG ATGTAGAGAG GAGCCCTGCT 2040 GGAGCCTGCG GGCTGGAGGG GAGCACACTG AAACCAACAG TTCCCACACT GTGGGGTAAG 2100 CTGACAGCAA ACCCCCACCC ATCTCAACAC AGGCAAAGCT TGAGGAGCAT CGCATATAGG 2160 CATTGTACAC ACACACTCTC TCTCTCTCTC TCACTTTCTC ACTTTTCAAT CCCCAGCAGA 2220 TTTCCATACC CACAAAGACA TCTGTACAGA TATCAGGAGT GAGGACCGAG CCTGAGACCT 2280 TCCCTGGAGC AAGCTTTGAT GACAGCAAAG TTGGAGTAGA TTGGGGCAGC CAGATGTCAA 2340 CAAGTAACAT AAACAGGCAT TATCCATCTG GAGAGATGTG AACAGAGCAA TTTGCTCCTG 2400 TACCACCCTC TGAGTGTCCA GCAAGGGGCG GGGCTGGGCA GTGGATGCCA GAGCCTGGTG 2460 AGTGGGGAGA GGGCCTAGGC CGCTTCCTGC CTGGGAGCAG ACCTTGCTCC CATGGGACAG 2520 CCCAGCCATT TGACTGAGAA CCGGGGTGTT CACTGTCATT GGTGGATTGA CTGAGCCCTG 2580 ACTGCACAGA TGCTTCTACC TTTTCTAACT 2610
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