Tag | Content |
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EnhancerAtlas ID | HS122-04558 |
Organism | Homo sapiens |
Tissue/cell | LoVo |
Coordinate | chr14:55573240-55576100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr14:55575108-55575119 | GATGAGTCACC | - | 6.32 | JUND | MA0491.1 | chr14:55575108-55575119 | GATGAGTCACC | - | 6.62 | ZNF263 | MA0528.1 | chr14:55575036-55575057 | GGAGGAGGGCGAGGGGAGAGG | + | 7.74 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_00244 | chr14:55563236-55576350 | Adipose_Nuclei | SE_00820 | chr14:55574748-55575102 | Adipose_Tissue | SE_02600 | chr14:55573844-55576160 | Astrocytes | SE_09388 | chr14:55568067-55576360 | CD14 | SE_23110 | chr14:55574129-55575416 | Colon_Crypt_1 | SE_23790 | chr14:55574594-55575269 | Colon_Crypt_2 | SE_24786 | chr14:55574109-55575428 | Colon_Crypt_3 | SE_26013 | chr14:55573672-55575878 | Duodenum_Smooth_Muscle | SE_26711 | chr14:55573567-55575917 | Esophagus | SE_27630 | chr14:55573899-55576071 | Fetal_Intestine | SE_28543 | chr14:55573873-55576230 | Fetal_Intestine_Large | SE_31668 | chr14:55574018-55575868 | Gastric | SE_33558 | chr14:55572184-55573676 | H2171 | SE_33558 | chr14:55573897-55579764 | H2171 | SE_34039 | chr14:55574107-55575498 | HCC1954 | SE_34802 | chr14:55573592-55576155 | HeLa | SE_36310 | chr14:55573891-55575863 | HMEC | SE_37768 | chr14:55573433-55575974 | HSMMtube | SE_41170 | chr14:55573962-55575665 | Left_Ventricle | SE_42472 | chr14:55573658-55575611 | Lung | SE_44570 | chr14:55573874-55576148 | NHDF-Ad | SE_45117 | chr14:55573558-55575933 | NHLF | SE_46036 | chr14:55573692-55576091 | Osteoblasts | SE_46880 | chr14:55574151-55574573 | Ovary | SE_46880 | chr14:55574627-55575401 | Ovary | SE_49010 | chr14:55574074-55575920 | Right_Atrium | SE_50181 | chr14:55574075-55575919 | Sigmoid_Colon | SE_52430 | chr14:55573656-55575984 | Small_Intestine | SE_56717 | chr14:55573869-55576081 | u87 | SE_57551 | chr14:55574279-55575356 | VACO_503 | SE_64542 | chr14:55574036-55575714 | NHEK | SE_66903 | chr14:55572184-55573676 | H2171 | SE_66903 | chr14:55573897-55579764 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 55574264 | 55575347 | chr14 | 55574465 | 55575376 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I055097 | chr14 | 55563775 | 55576469 |
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Enhancer Sequence | CTCCCAAAGT GTTGGGATTA CAGGCATAAG CCATGGCATC CAGCTTCAGT GGTCTTAATA 60 ATTCACTTTG AAAGTTAAAA AACGTTCTGG TATTCCTTTT CCAAATTGGA TCAGTTTTAA 120 GATGAGATAA ATGACAAGGC AAGCTGTTTT TAAATATGTG TTTATCTTTT GCAACTAAAA 180 CAATATGAAG TAAATTAAAT GCTGAGCTTG ATAAAAGATT GCAATGGTTA TGCCTGTATT 240 ATTTCAAATT TTGGTGTTCA TCAAAATGGT AATTTTTCTC ATAGATTGAC TTTATGAGAA 300 GTGAATGCTA AATGAATTTT AACTTAAATG TAGATTCATA AATTATTTCT TTTGTGTTTT 360 TATCTTTTAT TGTTTTTTGA GACAGAGTCT CACTCTGTTG CCCAGGCTGG AGTACAGTGG 420 CTTGATCTCG GCTCACTACA ACCTCCACCT CCTGGTTCAA GTGATTGTCC TGTCTCACCC 480 TCCCCAGTAA CTGGGATTAC AGGCGCCCAC CACCACACCC AGGTAATTCT TGTGTTTTTG 540 TAGAGGTGGG GTCTCGCCAT GTTGTCCAGG CCGGTCTGGA ACTCCTGGCC TCAAGCGATC 600 TGCCCGCCTC AGCCTCCCAA AGTGCTGGGG TTACAGGCGT GAGCCACTGC GCCCGGCCTC 660 CTTGGTATTT TTATGTCTAT TTTTTTAGAT GGAGTCTCGC TCTGTCCCCC AGGCTGGAGT 720 GCAGTGGCGC GATCAGCTCA CTGCAACCTC CACCTCGCGG GTTCAAGCAA TTCTCCTGCC 780 TCAGCCTCCT GAGTAGCTGG GATTACAGAC GTCCATCAAC ACGCCCAGCT AATTTTTGTA 840 TTTTTAGTAG AGATAGGGTT TCACCATGTT GGCCAGGCTG GTCTTGAACT GCCTACCTCA 900 GGTGATCCAC CCACCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCGTAAG CCACCTGCGC 960 CTGGCCGGTA TTTTTAAATT AGAGTTCTTC TAAGATTTAT CTGAAAAAGT TACACTACTA 1020 AAAAATTTGC AACCCACACC CAAGGACATA ATTTGTCTGG GCATAGAGAC TTGATGGCAC 1080 TTCAAGTAGC TGGATGAGCT TCTCTTAACA TGCGATTTCT CTCAGGTTTA CATTCTTCTT 1140 GACTGCCCTT GTTCCTTTCC TATTCTATTT GAAGCAAAAT GGTTAACGTT CTTCCACTTT 1200 CACCAGGACA GCCCTATTTG CCCCTTCCTT GTCCTTGTTA GCCTGGTTTT ATAAAGCCTC 1260 TTTTGCAGGG GTCGGAACAG TTAATAGCAT TGGGGATTGT CGCTTGTTCC CTGTAGATGA 1320 AAAGTATTTT TCTATTGTTT AAAAAAAAAT CGAGGTCATT CTCCAAAGTA ATTTCCTGAA 1380 ATAAAGCGTG GGAGGAAGTC ATGGGCATGA GGATGAGTCA TCAGGCAGCA GCACGAGGCT 1440 GCAGGCGTGA GCTGGGGAGC CCTGGCTCAG TCCTCCGCAG GCTTGGATCC CTGAGCGGAG 1500 CAGGCCACTG GGGCCTTCTG CCGTGAGAAG AGACCTACTG AGAGGCGGGG AGTGGGGGTG 1560 GGAGTGGTTG CTTCTGACCT GTAGGACAGT GGTCAGCGTG GGCGGGTGGA GGCACAGGAG 1620 AAGGCCGACA GGCCCTGGGT CCTAGGGCCA CTCAGCTGCT GGAAAATGAA GTTCAGAGTT 1680 GTTTGGACTG TCTGAAGTAG GATAGAACCA GCCTTAGCCC TAGTTAGGTA ACACATGGCA 1740 GAGGCACCTG AGCAAAGACG TGAGCTGGAC CATGGGCTTC CTGGCAGGAC TTCCACGGAG 1800 GAGGGCGAGG GGAGAGGAGC AAGGGAGCAG AAGGCAGCTT GCCGTCCACG AAGCCTCCTG 1860 AGGCCCCAGA TGAGTCACCA GACAACAGCC TGTCTACTTA AAGCAACTGC TGGGCAACTG 1920 CTGAGTAGAA CAGTCCCTAA CCACATGAAC ACTGGGGAGG AGGTTCTGAA AGACGCTGCT 1980 GGGTGCAAGG TCCCTAACTA GGGTAATCCA ATTTCACTCC AGGCTAACAT GAGAAATTAT 2040 GACTCCAGCA GCCAATCCTG TGGGCCGTGA GAGAGTGGGA GAGGGATTTT CCAGATATAA 2100 GTCCCACTAG AGCTTCTTTT TTTTTTTTTT TTTTGATACG GAGTCTCACT CTGTTATCCA 2160 CGCTGGAGTG CAGTGGCACC ATCTCGGCTC ACTGCAAGCT CCGCCTCCCG GGTTCAAGCG 2220 ATTCTGTTGC CCCAGCCTCC TGAGCAGATG GGACTACAGA TGTGCACCAC CATGCCCAGC 2280 TAATTTTTGT ATTTTTAGTA GAGACAGGGT TTCACTATGT CGGCCAGGCT GGTCTCGAAC 2340 TCCTGACCTC ATGATTCTCC TGCCTTGGCC TCCTAAAGTG TTGGGATCAC TGGCATAAGC 2400 CACAGCTTCC GGCTGAGTCC CACTAGAGCT TCTAAGAAGA AATTAGGGAA GCAGGATTAT 2460 GAGAGGCCTG GTCCCACTCA CAGTGTGCGA CATCACTGAT GACTATGCTT GGTTACCTGC 2520 CTTGTTATTT GCTACCTTTG TTATTGTCTA TTTCTTGGTA ATTAGTAGTA CACTATAGTG 2580 ATTAGGAGTG ATCAAGAAGA TGCCTGGCTT CATATTCCAA CTTTGTCGTT TACTAACTGT 2640 GAACTTGGCC GAGTTTTTTT TTTTTTGCTT GTTTGTTTTG TTTTGAGACA GGATCTCTCT 2700 CTGTCACCCA GGCTGGAGTG CAGTGGCGTG ATCTCAGCTC ACTGCAACCT CCACCTCCTG 2760 GAATCAAGGG ATCCTCCCAC CTTAGCCTCC CAAGTAGCTG AGATACACGT GTGCACCATC 2820 ACACCTGGCT AATTTTTGTA TTTTTTGTAG AGATGGTGTT 2860
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