Tag | Content |
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EnhancerAtlas ID | HS134-04509 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:204419190-204420590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SCRT1 | MA0743.1 | chr1:204419193-204419208 | AAGCAACAGGTGGCC | + | 7.45 | SCRT2 | MA0744.1 | chr1:204419193-204419206 | AAGCAACAGGTGG | + | 7.34 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_00064 | chr1:204417530-204422553 | Adipose_Nuclei | SE_01898 | chr1:204418618-204421334 | Aorta | SE_03975 | chr1:204420278-204421359 | Brain_Anterior_Caudate | SE_04850 | chr1:204419076-204421220 | Brain_Cingulate_Gyrus | SE_05834 | chr1:204414554-204422838 | Brain_Hippocampus_Middle | SE_06778 | chr1:204419046-204422484 | Brain_Hippocampus_Middle_150 | SE_07775 | chr1:204417757-204421412 | Brain_Inferior_Temporal_Lobe | SE_10255 | chr1:204419836-204423398 | CD19_Primary | SE_10905 | chr1:204414650-204438582 | CD20 | SE_25125 | chr1:204417816-204422942 | Colon_Crypt_3 | SE_26688 | chr1:204416875-204421560 | Esophagus | SE_28866 | chr1:204417158-204423024 | Fetal_Intestine_Large | SE_30246 | chr1:204418561-204421552 | Fetal_Muscle | SE_31610 | chr1:204417780-204422694 | Gastric | SE_34711 | chr1:204415846-204421729 | HeLa | SE_37407 | chr1:204418938-204421997 | HSMMtube | SE_40776 | chr1:204417564-204421617 | Left_Ventricle | SE_42225 | chr1:204417746-204421550 | Lung | SE_48201 | chr1:204414946-204421702 | Psoas_Muscle | SE_48746 | chr1:204417807-204421419 | Right_Atrium | SE_49909 | chr1:204419158-204422984 | RPMI-8402 | SE_50149 | chr1:204415315-204422829 | Sigmoid_Colon | SE_51536 | chr1:204417745-204423045 | Skeletal_Muscle | SE_52421 | chr1:204416678-204422949 | Small_Intestine | SE_58430 | chr1:204415099-204506026 | Ly1 | SE_59794 | chr1:204415680-204491493 | Ly4 | SE_62377 | chr1:204415291-204492168 | Tonsil | SE_65868 | chr1:204418691-204420865 | Pancreatic_islets |
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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 |
GH01I204445 | chr1 | 204415101 | 204423341 |
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Enhancer Sequence | TTCAAGCAAC AGGTGGCCCA GGAAGTCAGG CTGAGGCTGA GGCTGAGGAT ACAGCCTCCC 60 TCTCAGGGTT CAGACATACT CCCTGAGGAA GCCCTCCTCC TGCAGAACCA GGAGAGGTCC 120 CAAACTAGGC AAAACCCCCA CTGGATGTTC CCAGAAGCAC AATGTGGTGT CCTTGGAGCT 180 TTGCAGTAGA GTGAGGCGAA CATCCCGATT TTGAAGCTAC CCGTGGTGCC TGGACAGAAC 240 TTGCTTAGCA GAGCCACCTC GGAGTTCAGG TGATGACACG TCCCATGTTG TCAGCCTTGC 300 TCCTTTCCTT GTTTTAGGAT TTCCGCAGAG GGTCCGCAAA GCTACTCCTT TTGTCCTCCT 360 TTTCCATTTG ACAGTCTCCA TCCCTCCCCC ACTTCTTGCT GCTGAGAGCC ACCAGGAAGA 420 AGCACCATGT TCTCTGCCCT CGGTTCACCC TCCCCCACAG CCCTCTCACT TGTCCTCATA 480 GGAGTCCCCT TCACCTAGCC CCAGGGACAC ACACTGGGTT TTTCTCACCC CCACCCCCAA 540 ACAGCTTCAA AGCCAAAGGG ACAAAGAGGA GGGGTTTCTC CAAGTACCCC AGTGGTGAGA 600 AAGCCAATGG CAGGGCCAAG AGAACTGAGA CACATAAGCC CCACCACTAT TCAAGCCCAT 660 AAGTTCTCTC CAGGTCCCTC AGTCTGAATC ACACCTAGCC ACTCCCTCTA AGCTCAGGAT 720 AAGGAACTGC TGGGTGGGGT GAAGTACACA GGGGAGGGGA GCTGTGGAAA GGCAGGGAGG 780 ACCCACGTTA CCTTTCGGGG AAGCTGTCCC TGGGCCAAAG TCCATACTGT CACACCCTCC 840 TGGCCAGCCC AGGGCCCAGC AACTTCTATG CCAGAGGGCG CAGAGGCAGG GCGGCCACCC 900 CCAAGGTTGG CAGTTTCATG ATAAAGCAGC CTGCCTCCAC CGCTGTCCTC CAGAGGAATC 960 TCCACCTAAG TGAGGCACTC CCTCCAGCCC ACCACAGACT GGCAGAGCCC TGCTCTGTCC 1020 CAGCTGCCTC TACCCTGGGG GCCCACAGCT ATAATTAGGG CCCCTCCAGC AGCCAGCAGA 1080 CATGCCAGGC CAGGGCTTGG CTGGAGGTGA CAAAGCACGG CTGCTGAGCC TATTTTGAGA 1140 GTTAGCTGAT CCCTGGACCG CTACAGTGGG GCAGAGAATC AGCTGACCCC ATAGCAAAGG 1200 GGAGAGGGAG CTGGTCCTGA GCCCTTTCTT TTCACCCAAG GAAGAAGCTT CCAGCTTCGT 1260 GTCTTAAGGA AAAGGGGAGT GAGAAGACTT TATGAGTGAA ACCAGAGCCA GCCAAGGCCC 1320 TCTTCCCTTC AGTCCTTGGG TATATCTGGT ATTCCACAAC CTCTCCCACA GATCTTCACC 1380 CAGGGCTGGT CAGGATAACC 1400
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