Tag | Content |
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EnhancerAtlas ID | HS045-00280 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:8471940-8473350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr1:8472704-8472715 | AATAAACAATG | - | 6.02 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_00045 | chr1:8465614-8485937 | Adipose_Nuclei | SE_02022 | chr1:8471864-8473073 | Aorta | SE_02685 | chr1:8471679-8473108 | Astrocytes | SE_03407 | chr1:8472178-8472509 | Brain_Angular_Gyrus | SE_03947 | chr1:8466807-8473327 | Brain_Anterior_Caudate | SE_04978 | chr1:8472168-8473408 | Brain_Cingulate_Gyrus | SE_07042 | chr1:8471442-8473593 | Brain_Hippocampus_Middle_150 | SE_07921 | chr1:8471677-8473585 | Brain_Inferior_Temporal_Lobe | SE_11329 | chr1:8466472-8473455 | CD20 | SE_23717 | chr1:8471892-8473171 | Colon_Crypt_1 | SE_25808 | chr1:8466353-8473444 | Duodenum_Smooth_Muscle | SE_27457 | chr1:8471373-8473141 | Esophagus | SE_28078 | chr1:8471067-8473500 | Fetal_Intestine | SE_29095 | chr1:8467196-8473478 | Fetal_Intestine_Large | SE_29887 | chr1:8471530-8472949 | Fetal_Muscle | SE_31622 | chr1:8471348-8473131 | Gastric | SE_37218 | chr1:8470307-8473795 | HSMMtube | SE_40658 | chr1:8471226-8474591 | Left_Ventricle | SE_41679 | chr1:8471818-8472621 | LNCaP | SE_42166 | chr1:8471250-8473174 | Lung | SE_44612 | chr1:8466766-8473359 | NHDF-Ad | SE_45170 | chr1:8471272-8473290 | NHLF | SE_45677 | chr1:8466378-8473709 | Osteoblasts | SE_47251 | chr1:8465934-8485673 | Panc1 | SE_48103 | chr1:8466858-8473292 | Psoas_Muscle | SE_48600 | chr1:8471253-8473209 | Right_Atrium | SE_50481 | chr1:8471784-8473126 | Sigmoid_Colon | SE_51176 | chr1:8466318-8473509 | Skeletal_Muscle | SE_52016 | chr1:8471071-8473292 | Skeletal_Muscle_Myoblast | SE_52725 | chr1:8471316-8473303 | Small_Intestine | SE_54752 | chr1:8471019-8473384 | Stomach_Smooth_Muscle | SE_58576 | chr1:8455425-8501956 | Ly1 | SE_60758 | chr1:8454848-8500160 | DHL6 | SE_62661 | chr1:8450826-8509851 | Tonsil | SE_63725 | chr1:8470591-8473292 | HSMM |
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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 |
GH01I008406 | chr1 | 8466449 | 8473883 |
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Enhancer Sequence | GGCCTATTTC CTTTAGAACT TAATCCTATT GTTCCACAAA TTACAGATTC TCGCCAAATG 60 AAAACACCTC CCTCGACAAC TTAAGGCCAC AAACCTCTGA CATAATTCAA TGTGTGTCAT 120 TAGCACATTT CCAAAACAGA GCACTTGTGG GAAGAAGAAC CAAGTTCTGA TCTTAGAAGC 180 CCTGTGCCTA AGTCAATAAC CACCAAATCC CAAAGGTGCT GGACAGATGC TGCTCCGGCC 240 CCGAAAATAA TCAAACACAC AAAAGTTACT ATTAATATTT CTTGCCAAAC AACAATCAAA 300 AAAATCCAAC TCCTGCACAT GGGAACAAAG CGACAATGGC AGCAGCTGCA AATACATAAG 360 CGAAGCATCA CTGAAGAAAG TCTCCAGCTT AATATTGCTC CCGACACCCT CTGTGGTGGT 420 TCACTCATAC AGCAAAGACA CGGGATAAAA AATTCCACAG ACTGTTTTCA AGATAATAAA 480 ATGGCATATG ATGATGACTC ACTAACAGAC TAAAAGGAAA AAATATCCGT CAACAGTCAT 540 AGGAAGCTTA CAAAGCTGCA GAGATCTGGC ACCACTAAAG CTCCTCCACC TCCCCTGGCT 600 CTCACCTCCA GTACACACAT GTATGTGGGA CATACAAAGT GTGTGTGTTC ATGTGCACAC 660 CCTTTAGGGA TTAATTTGAA GCCAAGTTGC AATTGGCTAA TGGCTTACTC TACTGCTTAA 720 GACAGTATTT TATTCTTGAC TGGCTCAATA AACCTGCTGA GAAAAATAAA CAATGGATTT 780 CAATCTTATA AATAATCTAG AACACAGAAC CGCTGCGCAA ACAGGAGAGT TGATTTACTG 840 CGCACAATAA ACAGAACAGG AAGGACCAGT GTGGCAGAGT GAACCCCAAG TCCTAGACCC 900 ATTGTCCTGG GACAGTAGAG TTCACAGGGG TTTTCTGTCT ATTACACAAA GTCTAAGGCC 960 TGGGATATCC AGGTTTCAAA CTGGTCTTAA AAAGAGCATT TCAAAGCAGA TCAGGTGGAG 1020 AAGCTTTGGT GGTGCCAGAT CTCCGAAGCT TTGTAAGCTT CCTATGACTG TTGATGGATT 1080 TTTTTTTCCT TTGGTCTGTT AGATTTTGCT CACACTGAAG AGCAAAAGAT GAGGAAAATG 1140 TTCGTTTAAA AACAATGAAG AGTTTTCACG TCTTAGGACC ATTAATTATC TACCCATGAT 1200 TACAATGTAT TTCGAACCTA TTATTTATAC ATGCGTGAAC ACACACACAC ATACTTCATT 1260 TTAAGCAAAT AAAAAGTAAG GGCTGTTACA GGACTCTAAG GGTGCCATAA AGAGGTATTA 1320 AAATGAGGTC CCTGCCCAGA AGGCTTTATA TTCTATATAA ATACATATAT GCATTCATGC 1380 ACACATGTGT GCAGAGTAAA AATGCATGGA 1410
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