Tag | Content |
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EnhancerAtlas ID | HS101-02442 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:120332460-120334770 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GSC | MA0648.1 | chr1:120334360-120334370 | GCTAATCCCC | + | 6.02 | NR2F1 | MA0017.2 | chr1:120333275-120333288 | CAAAGGTCAACAG | + | 6.78 | Sox3 | MA0514.1 | chr1:120333588-120333598 | AAAACAAAGG | - | 6.02 | TEAD1 | MA0090.2 | chr1:120334176-120334186 | CACATTCCAT | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28136 | chr1:120329260-120335053 | Fetal_Intestine | SE_29167 | chr1:120332279-120334918 | Fetal_Intestine_Large |
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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 |
GH01I119789 | chr1 | 120332320 | 120334689 |
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Enhancer Sequence | CGGCTCACTG CAACCTCTGC CTCCCGGGAT CAAGCAATTC TTGTGCTTCA GCCTCCCAAG 60 TAGCTGGGAT TACAGGTGCC CACCACCACA CCTGGCTAAT TTTTGTATTT TTAGTAGAGA 120 CGGGGTTTCA CTATGTTGGC CAGGCTAGTC TCGAACCTGA CCTCAGGTGA TACACCTGCC 180 TCAGCCTCCC AAAGTGCAAA TTACAGACAT GAGCCACTGC ACCCAGTCAC ATCCTTCTAG 240 ATTATCAGAT TCTAGACCTG TTCATTGTCT TAATTCTATC TTCTGAAGTT TTTGGAAGCA 300 ATAATAGTTT TAAATAAGAT ATGATCAATC AATCATGTAT TTACTATTGA CTATGAATTT 360 ACTATGACAT AATACTCTAT TCTAGAACCT TAAAAAGGTT TAAAGTCAAA GTCATTACTC 420 CCAAATCCAG GATTCCACCT GCAGATTTCT TTTTGCTCCA CCTTGTCCCT AAAATTTCCT 480 CTCCAGCTGT CTTCATGGGG TCCTTGGGCT GCAGGGCAGG GCCTTGAGGT TGCTCATAAA 540 CTTCTACTTT CATAACCTGC TTATATGTCT GTACTGTCTG TTCCTTGGTT CCAAGATAGC 600 CTGAAATGAC TGTCCTCAAG TAGGATACAT ATCTGATCCA CTATTATTGT GCATACTCTT 660 TTGTTTCATA TTCACTTACT TTTGTAAAAG TTCTCAGTGA CTTTAGAGAC TGATTCTTGA 720 CTTAGGGAAG TACACGATCC AGATATAAAC AGAACAAGAT AATGCTGGAG CTGGAAGGGA 780 TTGTTTATTC CAGGGTTGTC AACTGGCCCC GTGGGCAAAG GTCAACAGAC CTGCTTTGTT 840 TGGCTCTCAT ATGGTTGAAA GAAATTGATT TCCGAGCTCA TTTCCCAGTT CAAATTGCCC 900 TACAAGAGAC CACTCCACTT ATTCACATCT AACTAAACCC TATAAGCGTT GGGATTTAGT 960 TTAAGGCCCC CATTTTATAG ATAAACTGTG GTTTGGAAGA GAGACATATA TTCGCGATCA 1020 CAAAGATTTA AAATGGAGAC AATAACATTT GCTAAGCATT TATGGCAGGC CCCATTCCAA 1080 ATGCATCACA TATCTTAACT AATTTAATCC TCAAATCCCG GAGAAAAGAA AACAAAGGCT 1140 CTGACACTGT AGGCTAAATG TCACCCAGCC AGTTTGAGGC AGAGACAGCC AGTTCTAGTG 1200 TGGCTTAACT CTTAACCCTT TGCTCTTCCC ACCATAATAA ACTGCCATGA GCCGTGGCTG 1260 GAGTCATATA AACGGGCACA TCTCAGGAAA CAACATTTAC CTGAATTTTC TCTTGCATCA 1320 GATGCTTCTC TAGTCTCAGT TGAGACTCCT GGTTCTAAAT TATTGCAGTA AGGCCTTAGG 1380 ATAAAATTTC CCAAAGCGTG GTCCTTGGTC CCCTGGGTTG AGAACCACTC TGCCCTACTG 1440 CCCTTTCATG TACAGTGGGC CACAGAATAA GACTGTCTAG TTTGTGCACT GCACAAAGGC 1500 ACACAACTAA GAGGACAAGA AAGGGCTAAA TTCCAGCCTG TCTTGATTCT GAGAGACCGT 1560 GGGGCTATGT TTTCTTACAA AGAAGGGGCA TCTTTTTTTT TTCAATTTCT ACAAAGCCAC 1620 CACATGGGTG AGAAGTGGTT CTGTCCTTCA GGTGAAGCTG CGTAAATTCC TGGGCTCTAG 1680 AGGAGTTACA GGTGATGACT TAGCTAAGTT AATCATCACA TTCCATCCTC CTCGCTACCT 1740 TAATCTGTTG GAGAATGAGC ACATAACTCA TGTAGGGCCT TTCCTGGCCA ATGGGGCTTA 1800 ACTTGGAGGC TCCTGTTTAA GGGTTGTGGA TCTCTTTCCT GGTAGAGGTG AGGCTGGACC 1860 TGCTTCAGCC ACCTTGCATT AGACGGGGCC AGAAAATGAA GCTAATCCCC AGCAAAAAAT 1920 AGCCACAAAA TAGAGGAAAC TCCCGTCTGG TAACTTTGTT GAGCTGTTGG TCAAGTTATA 1980 CCTGAAGCTC AAATATACTT ATGGAGTGTG GAGTGACACA AACCTATACA TTTTTTTTAA 2040 TGGTGAAACA GTCTGGCTGT CAGTTGTGAC CAAAGGAGGA GGGGAAGCAT AGCACCTATT 2100 CCATACACAC TCCAACACAT CCCTGTTCCC TGTGCCCCTT GCTGGCTTTA TGTTTTCACC 2160 ACAGCTCTTG TCATCCTCTC ATACTATGTC CTTTACTTAT TTAGTTTGTT GTTTGTCTAC 2220 ATCCTCTCCC CATCCGTGAT GAAATGGATA CTCTATGATT GCAAGGAATT TTATCTATTT 2280 TGCTCACTGA TGGATTCTCA GCTTCTAAAA 2310
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