Tag | Content |
---|
EnhancerAtlas ID | HS045-03852 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:154391290-154393090 |
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 |
|
| 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 |
|
| 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I154417 | chr1 | 154390221 | 154396888 |
|
Enhancer Sequence | GGGCACGACT CCTGGCTCCT GAGAGTCCCC AGTGCCCCAT TAGGTTGGCA GCTGCAGTGA 60 TGGCGCTGAC CCCCCCTTGT GCACACCCCT CAAGCCTCAG CATTCCCTTC CCTGGGCCTC 120 TGAAGGGTGG AAAGATGTGA GAAGAGCAGG GAAGAGGAGA GGAAATTGGG AGAGGGGGAG 180 AGAGAGGGTG GTGGGGAGCC CAGAGAAGGG AGCTGGGGGT GGAGCATGGA GAGGTACCTG 240 GGCCAAGTAG AGAGAGGCTT TGGCCAGGCT CATCTGGGTC CAGCGTGGAT TCCCTCATGC 300 ATGAGCTGTG TGAATTTGGG CAAGTTCCCT AACTTCTCTG ATCTCTTGTT GCCTCAACAA 360 TGAAATGGGG ACAAGACTTC CTCCCTGGCA GACTTTTTGT GAGTAGTGTG CTCTTAGGGA 420 AAGCCCAGGG CGCAGGGTAA GTGTCCCAGT TGCTAATGAT TGTTATGGTT ATTATCACAT 480 CAAAGCCAGG AGCCAGTCTC AGTCCAAAGA TGGAGAATGC AAGAACAGGT GACCAAGAGC 540 ACTGGGACTT GTCCTAGCCC TCGTGGGACC AAATTCTATA CTTGTTTCCA TGTGGACACA 600 AGGTGTCCAC AGGCTTCTCC TGGAGGCTTC TCAGCACCCA CCTACTTTTA GATCAAGACC 660 ATTATTGCTG ACAGGGGACC TTTGTTTCCT CTGTAGCCCC TTCTGAAATC CTATGCCTTT 720 GCAACCCAAG AAGCTGGGTT AGGCTGGGGG CCTCCTGTGC TGCCAGCTGG CCTGGGCAGC 780 GGGGACCTGC GTCTCTGCTC AGAAACTGGG GTGGTGAGAT GGGATTAGCA GGCACGAGCC 840 AAGCCTGTGT CCTCGGTGGC AGGCCAGGCA GCTGGTTCAC CGCTTACATA AACGGGGCCA 900 GGAAGCTGAA CTTGTTTTTG CTGGCAAGAG CTGCGGCAAG CTGCAAGAGA GTTGAGAAAT 960 ATGTGTCTCC GTGTGCGTGT TTTTCTCTGG TTATTGACAT TTGCAAGTTT ACTTGAAGAG 1020 GGGGAAAAAG TAGAAAAACA ACAAAGCTGT TTGGATTCCT GGCACCCAAA CTTAGGTCCC 1080 AACTGGGGAG GAACCCCACT TTCCCAGAGC TGTGCTGCAG GGTCCCCAGA CCAAAGGGTG 1140 TCTGGGCCAT GGTGGGGGTC CCAGTGTCCC TGGGAGGGGG AATCCTAGGC CACCGGGGCA 1200 GGGAGATATG GGCTTGCTTG TTGGGAGTTA CTAGGACCTA AACTCTCTTT CCCTTGAGGA 1260 ATGGGAGGCA AGGGAGGTTG TGGGAATTTT CCCTCCCCTA GAGCTCTCCA GGGAGAAAGA 1320 AGCATTTTTC TGAGGGCACT GGGATGATCT GGTCATCATC CTTCTCCCAA AGCCATCAAC 1380 TATTAAATAA TAAATCCATA GATTCATTAT GTGTTTTCAA GCTGAGTATT GTTTGCTTCC 1440 TGCCCTCTGA GAGCTAATGA TTGGGCGCCA TGGGATGCTA GACCGCAGGA GTGGGGGCCT 1500 GTGGGGGATC TACAGGTCAC AGTCTGAATC CTCATTTCAC AGAGAAGGCC AGTGGGCTCT 1560 GCCAGGGGCG GTGACGTGCC CATGGCTGCC TGTGAGTCAT CACAAGACCA GGAATAGAAC 1620 TCAGGTCACC TGACAGCACA GAGCTGTTTC CTCTACACCA AGGGGCCTCC TGCTTGTGGA 1680 GATGTACTTT ATTTTATTTT ATTTATTTAT TTATTTATTT ATTTATTTTC AAGAAGGAGT 1740 CTCGCCCAGG CTGGAGTGCA GTGGTGCAAT CTCAGCTCAC TGCAGCCTTC GACTCACTGC 1800
|