Tag | Content |
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EnhancerAtlas ID | HS042-02747 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:154391100-154392960 |
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: 35 | 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 | chr1:154391732-154391926 | Brain_Mid_Frontal_Lobe | 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_36673 | chr1:154390756-154393680 | HMEC | SE_41139 | chr1:154390423-154394426 | Left_Ventricle | SE_41647 | chr1:154390541-154393000 | 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_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_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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I154417 | chr1 | 154390221 | 154396888 |
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Enhancer Sequence | AGCCTGCGGC CTTGCCTCTT CCTGGACAGT GGCCGAGGGT GCCCTCTGAA ATGTTAAGGA 60 GAAATGAATG GGCCCAGATG GTGGGGTGAC TTGGGGAGGA CGCGAGATTT GGAGTCCAAG 120 GGGAGGCAGT TTTAGGCTCT AACTCATCCT ATACACGCTG CGGCTGTGGG GGAAGGGAGA 180 GAAAGGCCAA GGGCACGACT CCTGGCTCCT GAGAGTCCCC AGTGCCCCAT TAGGTTGGCA 240 GCTGCAGTGA TGGCGCTGAC CCCCCCTTGT GCACACCCCT CAAGCCTCAG CATTCCCTTC 300 CCTGGGCCTC TGAAGGGTGG AAAGATGTGA GAAGAGCAGG GAAGAGGAGA GGAAATTGGG 360 AGAGGGGGAG AGAGAGGGTG GTGGGGAGCC CAGAGAAGGG AGCTGGGGGT GGAGCATGGA 420 GAGGTACCTG GGCCAAGTAG AGAGAGGCTT TGGCCAGGCT CATCTGGGTC CAGCGTGGAT 480 TCCCTCATGC ATGAGCTGTG TGAATTTGGG CAAGTTCCCT AACTTCTCTG ATCTCTTGTT 540 GCCTCAACAA TGAAATGGGG ACAAGACTTC CTCCCTGGCA GACTTTTTGT GAGTAGTGTG 600 CTCTTAGGGA AAGCCCAGGG CGCAGGGTAA GTGTCCCAGT TGCTAATGAT TGTTATGGTT 660 ATTATCACAT CAAAGCCAGG AGCCAGTCTC AGTCCAAAGA TGGAGAATGC AAGAACAGGT 720 GACCAAGAGC ACTGGGACTT GTCCTAGCCC TCGTGGGACC AAATTCTATA CTTGTTTCCA 780 TGTGGACACA AGGTGTCCAC AGGCTTCTCC TGGAGGCTTC TCAGCACCCA CCTACTTTTA 840 GATCAAGACC ATTATTGCTG ACAGGGGACC TTTGTTTCCT CTGTAGCCCC TTCTGAAATC 900 CTATGCCTTT GCAACCCAAG AAGCTGGGTT AGGCTGGGGG CCTCCTGTGC TGCCAGCTGG 960 CCTGGGCAGC GGGGACCTGC GTCTCTGCTC AGAAACTGGG GTGGTGAGAT GGGATTAGCA 1020 GGCACGAGCC AAGCCTGTGT CCTCGGTGGC AGGCCAGGCA GCTGGTTCAC CGCTTACATA 1080 AACGGGGCCA GGAAGCTGAA CTTGTTTTTG CTGGCAAGAG CTGCGGCAAG CTGCAAGAGA 1140 GTTGAGAAAT ATGTGTCTCC GTGTGCGTGT TTTTCTCTGG TTATTGACAT TTGCAAGTTT 1200 ACTTGAAGAG GGGGAAAAAG TAGAAAAACA ACAAAGCTGT TTGGATTCCT GGCACCCAAA 1260 CTTAGGTCCC AACTGGGGAG GAACCCCACT TTCCCAGAGC TGTGCTGCAG GGTCCCCAGA 1320 CCAAAGGGTG TCTGGGCCAT GGTGGGGGTC CCAGTGTCCC TGGGAGGGGG AATCCTAGGC 1380 CACCGGGGCA GGGAGATATG GGCTTGCTTG TTGGGAGTTA CTAGGACCTA AACTCTCTTT 1440 CCCTTGAGGA ATGGGAGGCA AGGGAGGTTG TGGGAATTTT CCCTCCCCTA GAGCTCTCCA 1500 GGGAGAAAGA AGCATTTTTC TGAGGGCACT GGGATGATCT GGTCATCATC CTTCTCCCAA 1560 AGCCATCAAC TATTAAATAA TAAATCCATA GATTCATTAT GTGTTTTCAA GCTGAGTATT 1620 GTTTGCTTCC TGCCCTCTGA GAGCTAATGA TTGGGCGCCA TGGGATGCTA GACCGCAGGA 1680 GTGGGGGCCT GTGGGGGATC TACAGGTCAC AGTCTGAATC CTCATTTCAC AGAGAAGGCC 1740 AGTGGGCTCT GCCAGGGGCG GTGACGTGCC CATGGCTGCC TGTGAGTCAT CACAAGACCA 1800 GGAATAGAAC TCAGGTCACC TGACAGCACA GAGCTGTTTC CTCTACACCA AGGGGCCTCC 1860
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