Tag | Content |
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EnhancerAtlas ID | HS101-03695 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:204282210-204285150 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:204282214-204282232 | CCCTCCCTCCTTCCCTCC | - | 6.84 | EWSR1-FLI1 | MA0149.1 | chr1:204282210-204282228 | CCCTCCCTCCCTCCTTCC | - | 7.12 | EWSR1-FLI1 | MA0149.1 | chr1:204282218-204282236 | CCCTCCTTCCCTCCTTCC | - | 8.7 | EWSR1-FLI1 | MA0149.1 | chr1:204282222-204282240 | CCTTCCCTCCTTCCTTCC | - | 9.09 | EWSR1-FLI1 | MA0149.1 | chr1:204282230-204282248 | CCTTCCTTCCTTCCTTGC | - | 9.25 | EWSR1-FLI1 | MA0149.1 | chr1:204282226-204282244 | CCCTCCTTCCTTCCTTCC | - | 9.72 | ZNF263 | MA0528.1 | chr1:204282222-204282243 | CCTTCCCTCCTTCCTTCCTTC | - | 6.67 | ZNF263 | MA0528.1 | chr1:204282210-204282231 | CCCTCCCTCCCTCCTTCCCTC | - | 6.82 | ZNF263 | MA0528.1 | chr1:204282218-204282239 | CCCTCCTTCCCTCCTTCCTTC | - | 7.92 | ZNF263 | MA0528.1 | chr1:204282214-204282235 | CCCTCCCTCCTTCCCTCCTTC | - | 8.14 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_23313 | chr1:204283017-204284108 | Colon_Crypt_1 | SE_24138 | chr1:204282905-204283426 | Colon_Crypt_2 | SE_28816 | chr1:204282582-204285217 | Fetal_Intestine_Large | SE_31690 | chr1:204282936-204283957 | Gastric | SE_31690 | chr1:204284323-204285125 | Gastric | SE_33663 | chr1:204282160-204285331 | H2171 | SE_37243 | chr1:204283266-204291796 | HSMMtube | SE_50227 | chr1:204282848-204284237 | Sigmoid_Colon | SE_52903 | chr1:204283402-204284220 | Small_Intestine | SE_65374 | chr1:204282543-204284287 | Pancreatic_islets | SE_65374 | chr1:204284470-204285135 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 7 | Chromosome | Start | End |
chr1 | 204283200 | 204283400 | chr1 | 204283400 | 204283800 | chr1 | 204282475 | 204282632 | chr1 | 204282931 | 204283054 | chr1 | 204283310 | 204283744 | chr1 | 204283748 | 204283921 | chr1 | 204284052 | 204284136 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I204313 | chr1 | 204282903 | 204286933 |
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Enhancer Sequence | CCCTCCCTCC CTCCTTCCCT CCTTCCTTCC TTCCTTGCGT TGCCCAGGCC AGTCTTGAAC 60 TCCTGGCTTC AAGAGGTCCT CCCACCTCAG CTTCTCAAAG CACTGGAATT ACAAGTGGGA 120 CCAACTGTGC CCAGCCCTTA GCCCATTTCC AAAGCTCAGC TCCAAATCCC AGGATGGTTC 180 CTGACTAATC GCCCTGTTGG AGTTCACCAT CTTAGTGATG CACTTCACAC AATAGTCAGG 240 CCTCCCCACA CAGCTCATCT TTTCAACCTA ACTTACAGGG TGCTGGAAAA ACACCGGGTT 300 GTCCTCCACT CCAGGATGCC TACCTCCAGA AACATGCACA TTCCTGGGCT CATCTGGCCT 360 CGGGGACTCC CTGAACATAG GGATGACCTC CCCATTTCTC AAGAGCACAA ACCACAGCCA 420 GGAGTTCAGA GCTCACACAA GATGTTACTA TTGAAGAAAG AAGCTGACCT TGAGGCTACT 480 GCTTCTCTTC TCAGTCCCTG GGGAGAAAAT TCTCTTGTTG GCAGTCTATA TTCCATATTA 540 GCCCAAGGAA ATCATATGAT TCTCCACCTC CATGCCCCCA TCCTCAGGTG GCTGTCTTTG 600 AGATTTTCAC CTGACATTCT GCAGCTAACC ACCTTTCTAT CTGTCATCTC CCTGGGAGAC 660 ATGGTCATTA GCAGAGAGCA CCATGTAGGT GTCTAATTAA GCAAGCAGCA GCAAATGCAG 720 AAACCTGTTC AAGCCACCCC ACAGAGCATC TCCCCGGGGA TCCTCTTACA GGCAGCTCCC 780 TCCCCCGAGC TTCCTGGAAA GGTCTCTATT GTTTGCCTAG AACACAGAAA AGTGTCCGAT 840 TCTGCCCTCC TACTTATCTG CTGGCACAGA CTTCCTGGCC TCTGCACAAC CCCAGGGGGT 900 ACTATTCCCA TATAGCACAA TGTGAACGGT GCCCTCAGAA TTGTGGGACA CAGCAGCACT 960 GGTGGGTGGG AAAGTGAGGG TCCCCAGATG GGGAGGGACA GGATCTTCTG AGGGATGTCC 1020 TCTTACCTGT CTTCCTTAGG GGTCCCAGAG CCATATCCTG CCATCCTAGC ATCTTGAGAT 1080 CAGGGCACAG GAAGCAAGGT GCCCTCAAAC AGATTGATAA TAAGATGGCA GAGACAGAGG 1140 TGGACAGCAT GAGTGGCTCA GCCACTCCCT CAACCTGTGT CTCAGAGTCC TGTTGTCTGA 1200 ACTGTAGCTC ACCTGTTCCT GTTTCACCCT TCAAATGGAA TGTTCCACTT CCCCTGTGAG 1260 CCCGGGGAGA GAAATAAATT CCCTGTTCTA GAAAAGCTTT CTTCTTTAGA GACTGAAGTC 1320 TCTGGAATTT CATCTAATAC TCCTGCAGAC GACAATGGAG TGACTGGGCC AACAGTAAGT 1380 GCAGAGAAGG ATCCTGGAAC GACAAGACTG ATCCTAACTG GCCACCACTC CCCCTGGCCT 1440 GGGGATGGTC TAACCAAGGA GACTGGAGGG GAATAGACAG ACACCTGCTG CCTCTGTAGC 1500 TCCTGGCGGA CCTCACTCTC AGGTGTCAGA TGAGTATCCC AACCAAGCTG GGGCGAGAAA 1560 TAGCAGAATC CTCCTTAACT TCTTCTCCTG TGCCCTTCCC TGAGTCAAGC TTGTCTTTCT 1620 TCTAGGCCCT TATCTCCCTG CCTCAGAGAC CTTTATCCAC TTCATCTCTT ACCTCCACAA 1680 TGGCGCAGGG GCGGTAGAGA TGCTGGTATG GATGCCCACA AGCTTTTCAC AGGGACAGCA 1740 TGTATGCTGG TATTTGGGGA GTAGGGAATA GTACTCAGGG ATGGATCTAG GTCTTCTAAT 1800 TCCACAGGGG CTTCAGTGAC TCCAAATCCA ACCCCTAGAG GTATCAATGT AGGCCTCGGT 1860 GCCCTCATGT GATCCAGAGC TCTGCCAGCT TGGCTCGGAA CGCTGGCACA CACTCCTGCA 1920 CCACACCAAG ATATGTGGGT TCACTCTGGC AGAAATGGGA GAATGACAGC CCTGTCCAGC 1980 TGTTTTCCAG TTCCTGTGAG ACAAACTGGA CTTTGATTAC AGCAGGAATG GTTTAGGTTA 2040 GATAGTAAGA ATCACTTGAA ATGGGTGATA AGAGGACATT TAGGACTCTG TCCTTGGCCT 2100 TTAAAATTAA AGCCAATTTC CCCTCCACTG GCTATGGCTC AATACCTGTT TCATCATGTG 2160 ACTCTCTTGC TCAGAAATCC TCAGTGGTTA CCCCTCCCCT GCCTGCTACA TAAGGGTCCA 2220 CCTCCACGGT TTGGCATCCA AGGCCCACTG CGGCACGTCC CCACTCATCT TTCAAACGTC 2280 ATATTCTATG GCTCCATGTG TAAGTTTTCT AGTTCAACCT GACTGAACTT TGCAACATTT 2340 CCCCGAAAGG CCTTAGGCAT TCCTGCTCTG GCAGCGTCAT TCCCCTTCCC TCTCCCCCAG 2400 ATGCCTGTTA AATCCAAATC TCCCAGGGGA AGGCAGGTGG ACACCGTGTT AGGGCTGAGC 2460 TCAAATGCCA CCTCTTCCAG AAAGCTTCAG TTAAACACCC CCAGCCCACA GAAAACCCCC 2520 TCCGCCGTGA AGTTGTAGGC ATATGTTAGC CAGTCATTCC CTAGAAATGT CCTGAGCATG 2580 ACAGTGCTAG AGACTGAGCA GAGATGTGGT CCCCACCTTC AAGGAAACCC TAATCTAGAG 2640 AGTGGATACA GATAAAAGCA AACCAACAAA ACCATCCTCC CGTGACAGGC AGCCTGGGAT 2700 GAGGGCAGCG TGAGTGGGGA GCCGGGGAGA TGCCCAGGGG AGGCCACAGC ATGGAGACGA 2760 CAGCATGAGA GGAGGAGGCT GGGCGTTTTA GAGGGAGTCA CATTAAGGAG ACGGGAGATT 2820 ACTGGGGTAC CTGGACTAGG TAAAGGTTCG TGTTGGGAAG TAACGATAAT TCTATAAACA 2880 TTTACTGTGT GTTTACTATG GACACTGTGG GAATGCTTCC TATTTATAAG CTTGCTTATT 2940
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