Tag | Content |
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EnhancerAtlas ID | HS102-02256 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr1:204419150-204421020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIC | MA0161.2 | chr1:204420987-204420998 | TGTGCCAAGTA | - | 6.32 | 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: 2 | Chromosome | Start | End |
chr1 | 204419536 | 204420687 | chr1 | 204419200 | 204419532 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I204445 | chr1 | 204415101 | 204423341 |
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Enhancer Sequence | GAGGACAGGA AGTCAAATTA GGAGGGGCCA CTCCTGTGGC TTCAAGCAAC AGGTGGCCCA 60 GGAAGTCAGG CTGAGGCTGA GGCTGAGGAT ACAGCCTCCC TCTCAGGGTT CAGACATACT 120 CCCTGAGGAA GCCCTCCTCC TGCAGAACCA GGAGAGGTCC CAAACTAGGC AAAACCCCCA 180 CTGGATGTTC CCAGAAGCAC AATGTGGTGT CCTTGGAGCT TTGCAGTAGA GTGAGGCGAA 240 CATCCCGATT TTGAAGCTAC CCGTGGTGCC TGGACAGAAC TTGCTTAGCA GAGCCACCTC 300 GGAGTTCAGG TGATGACACG TCCCATGTTG TCAGCCTTGC TCCTTTCCTT GTTTTAGGAT 360 TTCCGCAGAG GGTCCGCAAA GCTACTCCTT TTGTCCTCCT TTTCCATTTG ACAGTCTCCA 420 TCCCTCCCCC ACTTCTTGCT GCTGAGAGCC ACCAGGAAGA AGCACCATGT TCTCTGCCCT 480 CGGTTCACCC TCCCCCACAG CCCTCTCACT TGTCCTCATA GGAGTCCCCT TCACCTAGCC 540 CCAGGGACAC ACACTGGGTT TTTCTCACCC CCACCCCCAA ACAGCTTCAA AGCCAAAGGG 600 ACAAAGAGGA GGGGTTTCTC CAAGTACCCC AGTGGTGAGA AAGCCAATGG CAGGGCCAAG 660 AGAACTGAGA CACATAAGCC CCACCACTAT TCAAGCCCAT AAGTTCTCTC CAGGTCCCTC 720 AGTCTGAATC ACACCTAGCC ACTCCCTCTA AGCTCAGGAT AAGGAACTGC TGGGTGGGGT 780 GAAGTACACA GGGGAGGGGA GCTGTGGAAA GGCAGGGAGG ACCCACGTTA CCTTTCGGGG 840 AAGCTGTCCC TGGGCCAAAG TCCATACTGT CACACCCTCC TGGCCAGCCC AGGGCCCAGC 900 AACTTCTATG CCAGAGGGCG CAGAGGCAGG GCGGCCACCC CCAAGGTTGG CAGTTTCATG 960 ATAAAGCAGC CTGCCTCCAC CGCTGTCCTC CAGAGGAATC TCCACCTAAG TGAGGCACTC 1020 CCTCCAGCCC ACCACAGACT GGCAGAGCCC TGCTCTGTCC CAGCTGCCTC TACCCTGGGG 1080 GCCCACAGCT ATAATTAGGG CCCCTCCAGC AGCCAGCAGA CATGCCAGGC CAGGGCTTGG 1140 CTGGAGGTGA CAAAGCACGG CTGCTGAGCC TATTTTGAGA GTTAGCTGAT CCCTGGACCG 1200 CTACAGTGGG GCAGAGAATC AGCTGACCCC ATAGCAAAGG GGAGAGGGAG CTGGTCCTGA 1260 GCCCTTTCTT TTCACCCAAG GAAGAAGCTT CCAGCTTCGT GTCTTAAGGA AAAGGGGAGT 1320 GAGAAGACTT TATGAGTGAA ACCAGAGCCA GCCAAGGCCC TCTTCCCTTC AGTCCTTGGG 1380 TATATCTGGT ATTCCACAAC CTCTCCCACA GATCTTCACC CAGGGCTGGT CAGGATAACC 1440 ATTATGTTGG CTGCAGCCCT TACCTTCCTC CCTGAGAAGC CCCTCTCCTT CCTGCAGCCC 1500 ATTCAACAAC CTCATATCAC ACAGGCTGCC TCCTCCAGGA AGGATTCCTG GAATGTGCTG 1560 GTTGGCTCCA GTCCCGGTTC TGCCACTCAC AATCCTGGGC AACTTAATTC CCATCTCTGT 1620 GCCTCAGTTT CTCATCAGGG AAAAGGGGAA CATAGCTTCA CTTGCATGAT GTGTGTGCAG 1680 ACTGTGTACT TTTTGCTATG TGATGCTGTG GTTACTGCAC TGGCACTGGC TTATACAGAT 1740 AGTATTTTCA TGCGCACGTA TCCCCATGTA TCAGCCAGTC TGTCAGTCAC TTGGAACAGA 1800 GAAACCAAAA CCAAGAGGGC TCCCCAGCTA AGAAGCCTGT GCCAAGTACT TTATTTACAG 1860 TGTCCTAACT 1870
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