Tag | Content |
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EnhancerAtlas ID | HS045-08802 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr10:81005110-81006900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr10:81006421-81006442 | CCTCCCTCGCCCTCCTTCCCC | - | 6.22 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00967 | chr10:81001368-81009228 | Adrenal_Gland | SE_03471 | chr10:81003517-81009089 | Brain_Angular_Gyrus | SE_04037 | chr10:81003322-81010914 | Brain_Anterior_Caudate | SE_04933 | chr10:81003306-81010402 | Brain_Cingulate_Gyrus | SE_05772 | chr10:81003225-81012196 | Brain_Hippocampus_Middle | SE_06946 | chr10:81000453-81011029 | Brain_Hippocampus_Middle_150 | SE_07838 | chr10:81003278-81011875 | Brain_Inferior_Temporal_Lobe | SE_09148 | chr10:81000344-81011517 | CD14 | SE_11725 | chr10:81000940-81015628 | CD20 | SE_13540 | chr10:81006262-81010999 | CD34_Primary_RO01536 | SE_24559 | chr10:81006244-81006967 | Colon_Crypt_2 | SE_26499 | chr10:81003581-81010248 | Duodenum_Smooth_Muscle | SE_26661 | chr10:81000438-81010326 | Esophagus | SE_31588 | chr10:81000983-81010356 | Gastric | SE_40721 | chr10:81000448-81010508 | Left_Ventricle | SE_42200 | chr10:80994761-81011639 | Lung | SE_43896 | chr10:81001261-81011164 | MM1S | SE_45787 | chr10:81003300-81009657 | Osteoblasts | SE_47007 | chr10:81004855-81007671 | Ovary | SE_47703 | chr10:81004825-81007483 | Pancreas | SE_48707 | chr10:81002884-81010544 | Right_Atrium | SE_50353 | chr10:81000694-81011674 | Sigmoid_Colon | SE_52824 | chr10:81002323-81010454 | Small_Intestine | SE_53282 | chr10:80994962-81011321 | Spleen | SE_54575 | chr10:81000811-81010193 | Stomach_Smooth_Muscle | SE_59543 | chr10:81001388-81026785 | Ly3 | SE_61092 | chr10:80988661-81027750 | HBL1 | SE_62376 | chr10:81000995-81055642 | Tonsil | SE_66905 | chr10:81000728-81010383 | H2171 | SE_67368 | chr10:81001261-81011164 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 81005366 | 81005598 | chr10 | 81006414 | 81006827 |
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Enhancer Sequence | CCTTGATGCC AGTGGGCTCC CTGAAGGCAG GGACCACGTG TTTCTCATCA CCGTATGCCC 60 CAGTGCCAAC TGTGGTGCCT GGCGGATGGT GGGTGCCCAG TGGCTGCTGA ATGATGATGG 120 CACGAGTGGA AGGCTGGTTG GGTGTGTTTT CCCCATTGGA GTTGGGACGG GGTCGGGGGG 180 CAGAGGGATT GAAAGAGCAC TTCCAGATCT CAGTCTGCAT TGGTTGAGCA CCCAGTCCAT 240 GCAGTCCCTG GGAACTCTGA GATGAGTCCC TAGTCTGGAG TCAGGCAGCT AGAGGGAGAA 300 AGGTGCTTCC ACAGAGGTTC TGCGGAAGTC CTGCCCGGGG CTTCCTGAAT GTTGCCCCAG 360 GGAGTAAGGA GTGACTGAGC TGGGTCTAAG ATGACGCCAT TCAGTACAGT AGCCACTGGC 420 CACATGTGGC TGTTTGTGAA TTTCAATTAA TTAAAGGGAT GAGTTAAGCT TATCCTTGGC 480 ACTAACCACA TTCAAGCACT CAGTAGCCAC CGAAGGCTGG TAGCCGCCTT GTTGGGCAGC 540 TCAGACTCTA GAACATGTCC ACCACAACAG GAAGCTCCAT GGACGACAGA CAGCGCTGTC 600 CAGGAGGATA GACTTAAGAC AGAGGTGCAG TGAGGACACT AGCTCAGAGC CCACAAGTGT 660 AACAGTGCAG GCGAGTCTGT TAGATAAAGA GACCTCCTGT TTCTCTAGCA TTTGTTTTGT 720 GGCAGCCTGC TGCGGGGAAG GAGTAGACCA GCCAGGCATT CCCATTTAAC ACAGGAGAAA 780 ACTGAGGTTC ACTTTTGCCC AAGGTCATCC AGCAAGAGGG TGGCATGAGT CCCAGGTCTC 840 CAACCCCTTG GCCAGCACTC TGTCATCCAG CAGAGGTCAG CCAGGGGGCA CGAGTGGGCA 900 GCGGTCCCAG GAGCAGCCTC AGACCTCCCT GAGGGACAGT CTTGGTGCCA GTAGGCGTCA 960 GTCCCTGTGA AGTCATCCAT TGATCGGGCG GGAGCGCCAG CTCAGCCTCG GGTCCTCAGG 1020 AACAGAGAGT TCTGTGCTGG CAGAGCTGGA AGGAGCGGGC GCGAGGCTCT CTGGGCAAGG 1080 GAGGTGTTTA CCTTGAGCGA TGCGGCATGG GTCCCTCGGG AGAGGCTGGC TCCTCCATGG 1140 GGAAGGAACT CCTCAGTGGG GCCTGTGGCT GGGATCCTTA GCACCACCTC AGAGAGAGGG 1200 GTACAGGCCC GAACCCAGCA GGGAGAAGGA TTTCGGGACC TTTGACTGGT ACAGAGTGCA 1260 CCTCACCCTT GCTCTTGCCC CGCCACACCG TGTCACAGAG CATCTGCTGG GCCTCCCTCG 1320 CCCTCCTTCC CCAAGCCTCG GCTGCAGGAG GAAACTCTCC CAGGGCCTGG CAGAGCAGCA 1380 GCTGCCTCAC GAGGGAGCCT GCAAAGGGAA AAACAAGGCC TCCACCCTCG AAGCACTTCC 1440 AGCTTCCCAG GGAGCTCCCT GGCCAGACAC CACAGGCAGG GAAGGAAGGC CAGCCCACTG 1500 GCCGGAGGGC CGAAGGGACT TCCTGCCCCA AGGTCACATG GCAGGAGAGG CCATGGATGG 1560 AGCCAATGCC CTCTCCCAGC CCACTGCAAA TCCCAGTCTC CCAGTGGGAA CGTGTGGTTT 1620 ATGATTTCAT TGTGCCTGCT GCCTGGTTTC CTGCTCCAGC CCTGAGGTGA GGGTTAGCTT 1680 CCTGTGGCCT TGTCCCTGTG TCCTGAGGTG CCCACTCCCC CAGCAGCAGG CCTTGCTGCC 1740 GCCTCCAGCT CCCATGGCCC TGACCTGACT GAAGTGGGAG GTCTGAAAAT 1790
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