Tag | Content |
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EnhancerAtlas ID | HS094-02485 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr1:154391350-154393480 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:154391457-154391478 | GGGAGAGGGGGAGAGAGAGGG | + | 6.21 | ZNF263 | MA0528.1 | chr1:154391432-154391453 | AGAGCAGGGAAGAGGAGAGGA | + | 6.23 |
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| Number of super-enhancer constituents: 38 | ID | Coordinate | Tissue/cell |
SE_00437 | chr1:154390273-154397370 | Adipose_Nuclei | SE_01040 | chr1:154390266-154394476 | Adrenal_Gland | SE_06653 | chr1:154390374-154394420 | Brain_Hippocampus_Middle | SE_09117 | chr1:154392451-154392745 | Brain_Mid_Frontal_Lobe | SE_09189 | chr1:154388527-154398657 | CD14 | SE_14719 | chr1:154390449-154393846 | CD4_Memory_Primary_7pool | SE_16173 | chr1:154390869-154392998 | CD4_Naive_Primary_7pool | SE_17632 | chr1:154390245-154394418 | CD4p_CD25-_CD45RAp_Naive | SE_18405 | chr1:154389059-154394421 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19165 | chr1:154390146-154394423 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_24531 | chr1:154390928-154392675 | Colon_Crypt_2 | SE_24531 | chr1:154392681-154392974 | Colon_Crypt_2 | SE_26130 | chr1:154390648-154394176 | Duodenum_Smooth_Muscle | SE_26877 | chr1:154390381-154397107 | Esophagus | SE_32086 | chr1:154390256-154393099 | Gastric | SE_32086 | chr1:154393209-154394222 | Gastric | SE_36673 | chr1:154390756-154393680 | HMEC | SE_41139 | chr1:154390423-154394426 | Left_Ventricle | SE_41647 | chr1:154390541-154393000 | LNCaP | SE_41647 | chr1:154393206-154394159 | LNCaP | SE_42431 | chr1:154390433-154394432 | Lung | SE_43544 | chr1:154384840-154394484 | MM1S | SE_44716 | chr1:154390741-154394024 | NHDF-Ad | SE_47983 | chr1:154390623-154393036 | Pancreas | SE_48261 | chr1:154388323-154397557 | Psoas_Muscle | SE_48934 | chr1:154390514-154394206 | Right_Atrium | SE_50453 | chr1:154390541-154394239 | Sigmoid_Colon | SE_51380 | chr1:154389216-154394408 | Skeletal_Muscle | SE_52880 | chr1:154390698-154393024 | Small_Intestine | SE_52880 | chr1:154393210-154394221 | Small_Intestine | SE_54278 | chr1:154390562-154394244 | Spleen | SE_54618 | chr1:154390203-154397361 | Stomach_Smooth_Muscle | SE_59139 | chr1:154375857-154394038 | Ly3 | SE_62668 | chr1:154357227-154415486 | Tonsil | SE_64458 | chr1:154390429-154393143 | NHEK | SE_64458 | chr1:154393145-154396883 | NHEK | SE_65390 | chr1:154390491-154396964 | Pancreatic_islets | SE_67236 | chr1:154384840-154394484 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 154392646 | 154393050 | chr1 | 154391539 | 154392211 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I154417 | chr1 | 154390221 | 154396888 |
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Enhancer Sequence | TGGCGCTGAC CCCCCCTTGT GCACACCCCT CAAGCCTCAG CATTCCCTTC CCTGGGCCTC 60 TGAAGGGTGG AAAGATGTGA GAAGAGCAGG GAAGAGGAGA GGAAATTGGG AGAGGGGGAG 120 AGAGAGGGTG GTGGGGAGCC CAGAGAAGGG AGCTGGGGGT GGAGCATGGA GAGGTACCTG 180 GGCCAAGTAG AGAGAGGCTT TGGCCAGGCT CATCTGGGTC CAGCGTGGAT TCCCTCATGC 240 ATGAGCTGTG TGAATTTGGG CAAGTTCCCT AACTTCTCTG ATCTCTTGTT GCCTCAACAA 300 TGAAATGGGG ACAAGACTTC CTCCCTGGCA GACTTTTTGT GAGTAGTGTG CTCTTAGGGA 360 AAGCCCAGGG CGCAGGGTAA GTGTCCCAGT TGCTAATGAT TGTTATGGTT ATTATCACAT 420 CAAAGCCAGG AGCCAGTCTC AGTCCAAAGA TGGAGAATGC AAGAACAGGT GACCAAGAGC 480 ACTGGGACTT GTCCTAGCCC TCGTGGGACC AAATTCTATA CTTGTTTCCA TGTGGACACA 540 AGGTGTCCAC AGGCTTCTCC TGGAGGCTTC TCAGCACCCA CCTACTTTTA GATCAAGACC 600 ATTATTGCTG ACAGGGGACC TTTGTTTCCT CTGTAGCCCC TTCTGAAATC CTATGCCTTT 660 GCAACCCAAG AAGCTGGGTT AGGCTGGGGG CCTCCTGTGC TGCCAGCTGG CCTGGGCAGC 720 GGGGACCTGC GTCTCTGCTC AGAAACTGGG GTGGTGAGAT GGGATTAGCA GGCACGAGCC 780 AAGCCTGTGT CCTCGGTGGC AGGCCAGGCA GCTGGTTCAC CGCTTACATA AACGGGGCCA 840 GGAAGCTGAA CTTGTTTTTG CTGGCAAGAG CTGCGGCAAG CTGCAAGAGA GTTGAGAAAT 900 ATGTGTCTCC GTGTGCGTGT TTTTCTCTGG TTATTGACAT TTGCAAGTTT ACTTGAAGAG 960 GGGGAAAAAG TAGAAAAACA ACAAAGCTGT TTGGATTCCT GGCACCCAAA CTTAGGTCCC 1020 AACTGGGGAG GAACCCCACT TTCCCAGAGC TGTGCTGCAG GGTCCCCAGA CCAAAGGGTG 1080 TCTGGGCCAT GGTGGGGGTC CCAGTGTCCC TGGGAGGGGG AATCCTAGGC CACCGGGGCA 1140 GGGAGATATG GGCTTGCTTG TTGGGAGTTA CTAGGACCTA AACTCTCTTT CCCTTGAGGA 1200 ATGGGAGGCA AGGGAGGTTG TGGGAATTTT CCCTCCCCTA GAGCTCTCCA GGGAGAAAGA 1260 AGCATTTTTC TGAGGGCACT GGGATGATCT GGTCATCATC CTTCTCCCAA AGCCATCAAC 1320 TATTAAATAA TAAATCCATA GATTCATTAT GTGTTTTCAA GCTGAGTATT GTTTGCTTCC 1380 TGCCCTCTGA GAGCTAATGA TTGGGCGCCA TGGGATGCTA GACCGCAGGA GTGGGGGCCT 1440 GTGGGGGATC TACAGGTCAC AGTCTGAATC CTCATTTCAC AGAGAAGGCC AGTGGGCTCT 1500 GCCAGGGGCG GTGACGTGCC CATGGCTGCC TGTGAGTCAT CACAAGACCA GGAATAGAAC 1560 TCAGGTCACC TGACAGCACA GAGCTGTTTC CTCTACACCA AGGGGCCTCC TGCTTGTGGA 1620 GATGTACTTT ATTTTATTTT ATTTATTTAT TTATTTATTT ATTTATTTTC AAGAAGGAGT 1680 CTCGCCCAGG CTGGAGTGCA GTGGTGCAAT CTCAGCTCAC TGCAGCCTTC GACTCACTGC 1740 AGCCTCTGCC TCCCGGATTC AAGCGATTCT CATGCCTCAG CCTCCTGAGT AGCTGGGATT 1800 ACAGGCACAC ACCACCAAGC CTGGCTAATT TTTGTATTTT TAATAGAGAC AGGGTTTCAC 1860 CATGTTGGCC AGGCTGGTCT CGAACTCCTG ACCTCAAGTG ATCCACCCGT CTCAGCCTCC 1920 CAAAGTGCTG AGATTACAGG CGTGAGCCAC TGCACCCTAC TGAGATGTAC TTTATATTAA 1980 AGAACAAATC AAGGCAGACT GTACGTTTGT GTCAGCCCAA CCCCACACAA TTAATAGTCA 2040 GTGATTAAAC TGACCAGACC AGACCAGACA CCAACACTGA CTGTTGAGGA GGAGCTTGGG 2100 GGTTTGTTTT CGGGAGGCAA TACTGCCTCC 2130
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