Tag | Content |
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EnhancerAtlas ID | HS196-00792 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr1:44014600-44017400 |
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) |
KLF5 | MA0599.1 | chr1:44016018-44016028 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:44015762-44015772 | GGGGCGGGGC | - | 6.02 | Myog | MA0500.1 | chr1:44017053-44017064 | GACAGCTGCAG | + | 6.62 | SP1 | MA0079.4 | chr1:44015760-44015775 | GAGGGGCGGGGCCTG | - | 6.22 | Tcf12 | MA0521.1 | chr1:44017053-44017064 | GACAGCTGCAG | + | 6.14 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_00616 | chr1:44009256-44025211 | Adipose_Nuclei | SE_04240 | chr1:44003988-44015177 | Brain_Anterior_Caudate | SE_04240 | chr1:44016899-44020669 | Brain_Anterior_Caudate | SE_05040 | chr1:44001099-44015486 | Brain_Cingulate_Gyrus | SE_05040 | chr1:44015834-44021066 | Brain_Cingulate_Gyrus | SE_05962 | chr1:44000439-44020958 | Brain_Hippocampus_Middle | SE_07193 | chr1:44003475-44015024 | Brain_Hippocampus_Middle_150 | SE_07193 | chr1:44016119-44020709 | Brain_Hippocampus_Middle_150 | SE_08033 | chr1:44003431-44015175 | Brain_Inferior_Temporal_Lobe | SE_08033 | chr1:44015878-44020741 | Brain_Inferior_Temporal_Lobe | SE_23218 | chr1:44005985-44017477 | Colon_Crypt_1 | SE_23829 | chr1:44013362-44015343 | Colon_Crypt_2 | SE_23829 | chr1:44015459-44017409 | Colon_Crypt_2 | SE_24870 | chr1:44012836-44017627 | Colon_Crypt_3 | SE_26649 | chr1:44010798-44020559 | Esophagus | SE_27645 | chr1:43995619-44017587 | Fetal_Intestine | SE_28595 | chr1:44005404-44017604 | Fetal_Intestine_Large | SE_31538 | chr1:44004919-44019003 | Gastric | SE_41575 | chr1:44001646-44015303 | LNCaP | SE_41575 | chr1:44015364-44020400 | LNCaP | SE_47657 | chr1:44013015-44015395 | Pancreas | SE_47657 | chr1:44015425-44018793 | Pancreas | SE_50363 | chr1:44005822-44020588 | Sigmoid_Colon | SE_52524 | chr1:44004832-44019377 | Small_Intestine | SE_56987 | chr1:44014752-44017377 | VACO_400 | SE_65452 | chr1:44004903-44018198 | Pancreatic_islets | SE_69138 | chr1:44014239-44017340 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 44015731 | 44016125 | chr1 | 44016660 | 44016751 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I043539 | chr1 | 44005459 | 44020850 |
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Enhancer Sequence | GCTGGACCCC TACAGCCTCC CTGGGAGGTG GTTGCAGCCC CCTTCCTCCA GCCAGTTCCA 60 CTTACTCCTT TCTTAGGCCA CTTCCTCCCA CCCTGCATGG GCTTGGTGGC TCGAGAATGT 120 TGCCGTCCAT ACCCCGGGAG CTGTGCTGAA AGGGCTGTGC GGCCCCCGAC CACTGTGTGT 180 GTCAGGGAGG GGGCACGCTC TCGTGGGGTG TCAGGCCAGG TGGCAGTGGG TAACTGGCAG 240 AAAGGCCCTC CTGGTGTGCT CTGGTGGCAC CCTGTTGACC CAGTCTCAGA AGTTGTGTTC 300 CGACCCTCAC TGAACACCAG CTGTGGGTCA GGCACGGGGC AGAGTAGTTC AAGTAGCTTG 360 GTTTGCTGCC TGCCTGGGGA CCTGACACTG TGGGATCTGG TCAGTGCTGG GATGGGAAGC 420 TCTGGGCACC TCAGGCCATG GGACACAGAG CAGGCTCCTA CAGCAGCTTG GCTGGGTGGG 480 ACATGAGAGA GGGGCTGGGC TGGGCACACT CAAAGGCAGG GAGGAGTCTG AGGGCCTGGC 540 CTGTCAGGGT GGCCTAGGTG GTGGGTCCAA GCTGTGTGCT CTGCACAGTG CTAGGCCTGT 600 ACTATAGTAG GTGCTCAAAA AATACTTGTT GAAAGAGTAA AGAAGCCGGG TGTGGTGGCT 660 CATACCCGTA ATCCCAACAC TTTGGGAGGC CAAGGCAGGT GGATCGCCAG AGCTCAGGAG 720 TTTGAGACCA GCCTGGCAAT GTGGTGAAAC CCTGTCTTTA CCAAAAATAC AAAAAATTAG 780 CCAGGCATGG TGGTGTGCAC CTGTGGTCCC AGCTACTCGG GAGGCTGAGG TGGGAGGATT 840 GCTTGAGCCT AGGAGGTGGA GGCGGAGGTT ACAGTGAGCT GAGATTGTGC CACTTGTACT 900 CCAACCTGGG TGACAAAGTG AGACCCCCCT CTCAAAAAAA AAAAAGACTA AAGAAAAGTG 960 AGCCTGAGAG CTTAGGAGGA GCACATTTCA GAGGGGAACG GAGAGAGGAA CATCAGGCCC 1020 GTTGGTAGCT GAGGAGAGGT GCGGTTAGAT CTGTGCTCCC CAAAGATCCT CTGCTGAACA 1080 TAAGGGGCAA CGCCTTGTCT CCTGTGCTGT GTCCTGCGGG TGGAGGTGGA TTGGAGGGAA 1140 GCGGAGGGCG AGGCCTGGTT GAGGGGCGGG GCCTGCCTGT CTGGTCCCCC GGGCTGCCTT 1200 GGGCCAGCTT GGCCTAGTCT GTTGGGTGGG CGGGCAGGGT GCAGGCTCCT CTCCAGCCTC 1260 CAAGGGAGGG GAGTTGTTCT GCCTCCTCGA TAGCCCCAGG CCTTGGGCAC AGCCCAGCCT 1320 CCCACGGCTC TTGGGCCCTC CTCCTTCCAG GCCGCCGGTG ACCCACACCT GGCTCTCCTC 1380 CCCGGCGTCT CCTCTCCGCT TCTTTGTTTG GAGCGGAGGC CCCGCCCCAC CCCGCCCCCA 1440 GGCGCACTCG CCCGGCCATT CCGGTTCAGC CGGTTCCAGC CCCCAGTTTC TGCCGCTGCA 1500 GGTCCCGGCA GGAGCTGGAG GGGCACTTTC TCCCTGGGTT TCTCTTCCCT GGTGCAGCAG 1560 GGGCCGCGGT CCTCATCCTC CTGGTTCCTC AGTTCGGTCC TTCTTTCATT CTCCACCCCT 1620 GGGTGCCAGG AACTGGGTCA GACACTGGGA CAGGAATCCA GACAGGCATG CTATCTGCCC 1680 TGCCCAGGGT TATGTTCTAG GAGGGGAAGC AGCCATTAAT CAAACACCAA AAATGTGGAA 1740 AAGTAATAAT CTCACACGTG TGCATAATAA ACTGTGAGTG AAAGTTATAA GCTCGGCAGG 1800 TAGGTAATAA GCTAGGAGCA GTGCTGTGGG AGGCAAGGGA GTTACCCGGG AGTTTCAAAC 1860 TAGGAACTGA GCTCATAGGT TGGGGGCAGG GGGACTGGAG AAGGCAGTGA TACTTAAATG 1920 GAGAGCAGAA GGATGAATGG AAGTTAGAGT GTATGGCGGA GGTTGGCAGA AGCAGCAGCT 1980 TATGCAAAGG CCCTGTGGCT GCAGGGAACA TGACGTTGCT CTTTAGAGGA GCCAAAGCTG 2040 GGGCTCTGGG GAGAGCAGCT GGGTCAGACC CCGCGGCTTT GTCTGCCATA ACAGGTGTTT 2100 GGAGAGTGAT TCGGCAGGTC TTTGGAGGGT TTTGATAGGG CGGGGTGTCG GGGGAGGCTG 2160 TCAGCTCACT CTGGACACTG AGTAGAGAAC AGACGGGAGG CGTGGGGCAG GCCTGGAGGC 2220 AGGGGCTTCC GCGTGTTAGG CCAGTGGAGT GCCAGTCAAG GGAAGGTGGT ATCTGGACTA 2280 GGGTGTGGCA GCGCAGGTGG AGAACCCTGA GCTGCTTTGT GGAGGGCTTC AAGTGTGGGG 2340 GAAGAGTGCA CGGTATGGGG GTGGGGGACA GGAGACACCC CCAGTGGAGC CTGAGCAGGA 2400 GAGTCGTGTC TGAGAGGGTC TGTCTGGAAG GCGCAACAGA GGCCAACTTT GCAGACAGCT 2460 GCAGTCGGGA GAGCCTGGAG CCTCCTTCAA AGGGCATTCA GGGGAAGGGC AAGGCACGCT 2520 GGGGGGTTCT GGACCTTCTG TGGTGTCTTC TTGTCTTTCT GGTCCCTACA GCCTCCCTGA 2580 GCTGGCTGCC CGAGCCTGCC CTAGGCACTC TAAGAACATA GTCAGTCCCA AGGTCTCCCT 2640 CCAGGGAAGG CCGTAGGTGA GCTTAGGAGT GAGAAGGCTG GATCAAAGCC TGGCTCCATG 2700 CCTGCATCCC TCTGACTTGC CAGTCATTTC ACCCTCCGAG CCTCTATTTC CCCACCTCTT 2760 AAATGGGGAT AATAATACTA CCTACCTTAT GGGATTGCGG 2800
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