Tag | Content |
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EnhancerAtlas ID | HS122-00036 |
Organism | Homo sapiens |
Tissue/cell | LoVo |
Coordinate | chr1:8471760-8473440 |
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 | ATATTTATAG TTTTAAGCCA GTAAATTACA TATACTAAAA GGTTTTGGTT TTTAGAAATT 60 TATTTAAAAG TTTTAGGGTT TTTCTTTTTA GGCTCACATT ATCCAAAACG TGTAGTTTGC 120 CCCCAGTTCA CTGGCTCTGT GCTTTACTTT GCGAAACTAG CCATCTATAC AGATTCATCG 180 GGCCTATTTC CTTTAGAACT TAATCCTATT GTTCCACAAA TTACAGATTC TCGCCAAATG 240 AAAACACCTC CCTCGACAAC TTAAGGCCAC AAACCTCTGA CATAATTCAA TGTGTGTCAT 300 TAGCACATTT CCAAAACAGA GCACTTGTGG GAAGAAGAAC CAAGTTCTGA TCTTAGAAGC 360 CCTGTGCCTA AGTCAATAAC CACCAAATCC CAAAGGTGCT GGACAGATGC TGCTCCGGCC 420 CCGAAAATAA TCAAACACAC AAAAGTTACT ATTAATATTT CTTGCCAAAC AACAATCAAA 480 AAAATCCAAC TCCTGCACAT GGGAACAAAG CGACAATGGC AGCAGCTGCA AATACATAAG 540 CGAAGCATCA CTGAAGAAAG TCTCCAGCTT AATATTGCTC CCGACACCCT CTGTGGTGGT 600 TCACTCATAC AGCAAAGACA CGGGATAAAA AATTCCACAG ACTGTTTTCA AGATAATAAA 660 ATGGCATATG ATGATGACTC ACTAACAGAC TAAAAGGAAA AAATATCCGT CAACAGTCAT 720 AGGAAGCTTA CAAAGCTGCA GAGATCTGGC ACCACTAAAG CTCCTCCACC TCCCCTGGCT 780 CTCACCTCCA GTACACACAT GTATGTGGGA CATACAAAGT GTGTGTGTTC ATGTGCACAC 840 CCTTTAGGGA TTAATTTGAA GCCAAGTTGC AATTGGCTAA TGGCTTACTC TACTGCTTAA 900 GACAGTATTT TATTCTTGAC TGGCTCAATA AACCTGCTGA GAAAAATAAA CAATGGATTT 960 CAATCTTATA AATAATCTAG AACACAGAAC CGCTGCGCAA ACAGGAGAGT TGATTTACTG 1020 CGCACAATAA ACAGAACAGG AAGGACCAGT GTGGCAGAGT GAACCCCAAG TCCTAGACCC 1080 ATTGTCCTGG GACAGTAGAG TTCACAGGGG TTTTCTGTCT ATTACACAAA GTCTAAGGCC 1140 TGGGATATCC AGGTTTCAAA CTGGTCTTAA AAAGAGCATT TCAAAGCAGA TCAGGTGGAG 1200 AAGCTTTGGT GGTGCCAGAT CTCCGAAGCT TTGTAAGCTT CCTATGACTG TTGATGGATT 1260 TTTTTTTCCT TTGGTCTGTT AGATTTTGCT CACACTGAAG AGCAAAAGAT GAGGAAAATG 1320 TTCGTTTAAA AACAATGAAG AGTTTTCACG TCTTAGGACC ATTAATTATC TACCCATGAT 1380 TACAATGTAT TTCGAACCTA TTATTTATAC ATGCGTGAAC ACACACACAC ATACTTCATT 1440 TTAAGCAAAT AAAAAGTAAG GGCTGTTACA GGACTCTAAG GGTGCCATAA AGAGGTATTA 1500 AAATGAGGTC CCTGCCCAGA AGGCTTTATA TTCTATATAA ATACATATAT GCATTCATGC 1560 ACACATGTGT GCAGAGTAAA AATGCATGGA AAAGAGGAAT CAGAGTCAAG TCCAAGAATA 1620 AAATAAAATA AATTTTAATT TTGTTTTTTG TTGTTGTTGT TGTTTTTGAG ACTACTCTGT 1680
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