Tag | Content |
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EnhancerAtlas ID | HS091-02979 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:154398920-154401670 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:154399000-154399021 | AAAAAAAAAAAGAAAGAAAAG | - | 6.41 | POU2F2 | MA0507.1 | chr1:154399204-154399217 | TGAATTTGCATGT | + | 6.05 | TCF7L2 | MA0523.1 | chr1:154400148-154400162 | CCCCTTTGATGTCT | - | 6.14 | ZNF263 | MA0528.1 | chr1:154401281-154401302 | TGAGGAGGAGAGCGAGGGGAG | + | 6.42 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00437 | chr1:154399481-154401751 | Adipose_Nuclei | SE_01040 | chr1:154399528-154400582 | Adrenal_Gland | SE_01040 | chr1:154400681-154401626 | Adrenal_Gland | SE_06653 | chr1:154399347-154403450 | Brain_Hippocampus_Middle | SE_09189 | chr1:154398672-154408855 | CD14 | SE_16173 | chr1:154399945-154400671 | CD4_Naive_Primary_7pool | SE_18405 | chr1:154399517-154407766 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19165 | chr1:154401205-154402489 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_24531 | chr1:154399580-154400359 | Colon_Crypt_2 | SE_26130 | chr1:154399302-154401704 | Duodenum_Smooth_Muscle | SE_26877 | chr1:154399516-154400662 | Esophagus | SE_26877 | chr1:154400694-154402391 | Esophagus | SE_32086 | chr1:154399571-154400607 | Gastric | SE_32086 | chr1:154400656-154401897 | Gastric | SE_41139 | chr1:154399325-154402156 | Left_Ventricle | SE_41647 | chr1:154399531-154400535 | LNCaP | SE_41647 | chr1:154400745-154403911 | LNCaP | SE_42431 | chr1:154399355-154400656 | Lung | SE_42431 | chr1:154400696-154402137 | Lung | SE_47983 | chr1:154399591-154400258 | Pancreas | SE_47983 | chr1:154400922-154401243 | Pancreas | SE_48261 | chr1:154399318-154401864 | Psoas_Muscle | SE_48934 | chr1:154399344-154402194 | Right_Atrium | SE_50453 | chr1:154399516-154401315 | Sigmoid_Colon | SE_51380 | chr1:154399138-154401914 | Skeletal_Muscle | SE_52880 | chr1:154399518-154401631 | Small_Intestine | SE_54618 | chr1:154399097-154409137 | Stomach_Smooth_Muscle | SE_62668 | chr1:154357227-154415486 | Tonsil | SE_65390 | chr1:154399323-154400849 | Pancreatic_islets | SE_65390 | chr1:154400868-154402476 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 154399696 | 154400530 | chr1 | 154399716 | 154400696 | chr1 | 154400830 | 154400990 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I154427 | chr1 | 154399576 | 154401508 |
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Enhancer Sequence | CAGGAGGTTG AGGATGCAGT GAGCCGAGAT CGCGCCATTG CACTCCAGCC TGGGTGATAG 60 AGCGAGATTC TGTCTCAAAA AAAAAAAAAA AGAAAGAAAA GAGAAAAGCA TATCACAGCA 120 GAAGACTATA TTCAAACCAT TTATATGAAG CTCAAAAATG AAGCAAAGTT AAGAAAAATG 180 TAGGGATGTA TGGGTAGTGA AAGTTAGGTT GGTGGGCTTT CCTGGGTATT TTATGCTTCA 240 TAAATTAACT TTTATGTATG TAGCTTTTAC ATACATTATA TATATGAATT TGCATGTATT 300 CAGTATTATG TAATACATTA AAAACAATGT TCGCAATGCT AAAAATATAT TGTTGAAGAT 360 TCTGTGTGAA AGCTATACTG TAGTTGTGGC TTTTTATAAC CCTTTCAAGC CCTCTGGGCA 420 GTAGCAGTCC ACCCCTTATT GCCCTCAGTG GACTTCACCT TCTAGGGACT CAGAATTTTT 480 TTTTTTTTTT TGAGACGGAG CTTCGCTCTT TTTGCCCAGG CTGGAGTGCA GTGGCGTGAT 540 CTCGGCTCAC TGCAAGCTCC GCCTCCCTGG TTCAAGCAAT TCTCCTGCCT CAGCCTCCCA 600 AGTAGCTGGG ATTACAGGAG CCTGCCACCA CGCCCAGCAA ATTTTTTGTA TTTTTAGTAG 660 AGACAGGGTT TCACCATGTT GGCCAGGATG GTCTCGATCT CTTGACTTGT GATCCGTCTC 720 GCCTCGGCCT CCCAAAGTGC TGGGATTACA GGTGTGAGGC CCAGCTGGGA CTCAGATTTT 780 GCTGAGGACC AGGACAGTAC TGTGTGCTGT GTCCTGGCCT TGCAGCAGTG AATGTGTCTC 840 CCGTTTCTCA AGGGCAGGTC TCTGGGATGC CTGACTGTGT CTTCCTTGCC AGTGCCTGGC 900 TGCTGCAGCC TCCTCAAATG TTTATCAAAC ACAGGACTTG CCCACCGTGG GAGAAAGTAA 960 GGCCATAGGT GTCTCAGGAA CCTGCCCAAA CTCGCCTGGC TGCACGGTGA CAATTCAACC 1020 AGCTTTCTTA CCCAAGGTCT GTTGGTGACC AGAGAAAACC TTAGATGACC GGCTGCCATG 1080 ATGGCCTTAT ATCTGTCCCT TTTCTGCCAG CCTTGAGGTA GAGGGTGCCA GGGAGGAGGA 1140 CTCTGGCTCT AGGTGTTAAA GTGAGAGGGA AGTGTGAAGG GTATCTGTAT AGCTAGACAG 1200 GGCTCAATGC CAGGCAGAGC TGTCTCCGCC CCTTTGATGT CTATGTCTCT GTCCCTGGAC 1260 TGTGGCCAGT AGCCAGTGTG GACTCCAACC TCACCAGCTT TAGGGGTGTT ATCTGCCTGG 1320 GAGTCACTGA TCCTTACTCC CTCCTCTGAC AGCCACCTTG GATGGGGTGA AAGGAAGGAC 1380 AGCCTGCCAA GTATGAGATA AAAACGCCTC ATAAACAAGA AGGGATTTGC AGGCCAGGCA 1440 GAGAGCCTTG TGCTGCTTCT GAGTCCCAGG AGCATGGGCG AGGAGGTGAG GTCAGGCACT 1500 CAGCAGCTGC TGGTCCTCTC TGAAATCTTT GGCCAGATTT ATTGCTACTG CTTGCTAATA 1560 AATGGTTATG CATTTGGTTC AAAGGACCAA GTGTGCTTAC ATGAAAACTG GCTGTGTTCC 1620 CTGGCCTCTG TTTCCTTAGC TGGTTGGACT AATTTGATTG GTTAATAAAT GAGTCCAAGG 1680 TGGTTGGGCT AATTTTTATC TTAGATTCTA TGACTCTATA ACTGCTACTC AAAAAAAGTG 1740 TACTTGTTCC TTTAATCTTT AATCTTATTT TTCTTGAGTA GTAGAATACA CCCAATTTTT 1800 TTCAAGGGGT AGAGAATGCA TTTTTTTTTT AACCTTCCAG TTTGGTCCCT AGAGTAAACA 1860 CAGCATTGCT GTAGTAGATG TAGGGTACTG GAGGGAGCAT GGAACAGGGA ACCAGAAGCC 1920 CTGGTTCCTA CCCCAGCTGG GCATCTGGGC CAGTCTCTTG ATTCCTCTGT GCCTCAGTTA 1980 CCAACTATAT AACGGGCATT CTGCCATGAA TACCCTGCGA TTTGGAAACC TCCTGTGTAC 2040 GTGTGCACTT GGGTGCCTGG CATTCATTCC TAATGGCATC CATTCGTTCA CACATTCATC 2100 CAGTACTCAG CAGACTCCTG CCATGGGCCA GGCAACGTCC CGGGCACTTG GAATATAATG 2160 GAGAACAAAG CAGGGTGCCT ACTTCTGTGG TGCTTGGAGT CTTGAGGGGA AGAGAGACAC 2220 GGAATTCGTA ATTACATGGC AGCGTGTGGG TGACGTATTG CAGAATGAGG GCCTAGTGGA 2280 GCTGGGGGAC CGGAAACGAT GTTTAGGCCG AGACCTGGAA TAGGAGGAGT TGTCGTGGGG 2340 ATGATGTAGG AAGAACGAGT GTGAGGAGGA GAGCGAGGGG AGTTGAGGGG AGGGCTCCAC 2400 ACCTTCTAAG GAGTGGGGAG AGATGAGGCC TCCAAGGACA GAAGGGCCCT GCAGGCCACG 2460 CTGAGGAGCT TGGACTTCAT CTTGTGGATG GTGGCAGGCC CTTGAAGGGT TTTCTAATCC 2520 AGGGAGTGGG GTGGCTGGAT CATGGCTTCA GAAGGCTCTC CCAGGCAGCT GGATGGTGAA 2580 GACCAGGTTG GGGAGGTCAC CAGGAGAATG CTGCCCTAAT CCAGGCAGAG GTGACGGTAG 2640 CCTGGGCCAC TTCATCATTA TCACTGAGGC CTCTCGTGGC TTCCTCAGAC CAGAACGAAG 2700 CCCCCTTCTT CAGTGGCTGT GGGCTCACCA AGTGTCTTCT CCCTCCTCCA 2750
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