Tag | Content |
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EnhancerAtlas ID | HS136-00474 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr1:43445560-43447050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr1:43445814-43445829 | TCAGGGCAAAGTCCA | + | 6.17 | Hnf4a | MA0114.3 | chr1:43445815-43445831 | CAGGGCAAAGTCCAGC | + | 6.4 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_23189 | chr1:43445347-43446703 | Colon_Crypt_1 | SE_29267 | chr1:43445257-43447456 | 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 |
GH01I042979 | chr1 | 43445295 | 43447259 |
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Enhancer Sequence | GACAGGGCAG GTAGCTCAGC AAGTGTGAGC ACCTCTCAGT GTAAGAGCTG AGGTGGGAGA 60 GGGGCAGATG GGCTGTGGAG CTGGCCACAC TAAAGGCAGC TGTGTGTTTG CAGGGCTCAG 120 GACCAAAGGG AGGCTGAGTC AGGAAGGCAC TCCTGGGCTT CTGGCTTGAG CAGGCTCAAA 180 GTCAACAGAT GCAGCTGCAT CTGTGTCTAG CGATTGGGAA GGTCCACAGC AGGACTCCAG 240 CTCATACCTG GGAGTCAGGG CAAAGTCCAG CCTAGGGAAG AGCCCCCAAG AGCCAGGCTG 300 GGTGTCAGGT GGGGCCCTTG TCCTGAAGGG AGAAGAGACT ACAAGGTAGA GCACCAAGCA 360 CACCTGGCTC TGGCACCTTT ACGTCTCTGG CCACTTCTCT CTTATGGCTC CCTGTAACAA 420 TGAGATACGG ACACCTGGAG GCACCTGGGG CTAGTTTCTT CCTCATACCT GCCCCGCTCC 480 GATGAGGCTC CCTCCAGGCT CCGCATCTTG ACTTAGTTAC AACCTGATCC TGAGCTGGGA 540 CCCAAGGGTG TCCTGCTCCT GGCTCCAATC TCCTGGTGAG GATGAACTTT GGTTTGGCTC 600 CACCTGCTCA AGTGCCTTCG GAAGTGTGCC CACCTTGCCA GCCTCGTCAG AATGCAGTCT 660 CAGGATGATG AAAGAGTTCA GGAAATGCCA CCCCAAGGTA CGTCACTTTG GACTTCAAAC 720 TGAGAGCATT TGAGGAACAG CAAATGCAGG GAGGGACTTT CTCTGAACTT CCCTTATCTG 780 CTTCAAGATA AATCCTCCAA AAGGAACTCA ATGGTTATAA CTCCCCTCCC CAGGAACCTC 840 ATCAACCAGA GAAGAGTAAA CTCAGATCAC AGGACAGGAG ACTGGGGGTC AACACCACCC 900 CCAGACAGAC TTTATCACAT ATCACCTATT CTTCTGAAGG CCCATTCATC TTTCCTCCAA 960 ATCATTTACT CTCTCCTAAG TTGCCTGAAC CCTCCCTCCG CTCACCCCCT TTAAGAGGTA 1020 TATATGCTCT CACTGAGGTT TAGGACATTT GCTTTTCTTT CATGTGATGC CCCCATGCAT 1080 GTAGTATATT TGTGTACCTT TTCTTCTGTA ACTCTTTCTT CTACTGTCAG TTTATTTCAT 1140 AGAGTCAATT ACCGAACCCT CAGAGGGTAG AGGGGAAATC TTCCCTCCCC TGCAGTGATG 1200 CTCTGGGACT GCCAGACACC TGGTGTCTAA TAGACACCAG AACTCACTCC CAACAGCCCA 1260 TTTGGGCAAT TAGTCGCTCA TATGATAAAC ATTTTTTTAA ACCCCCAAAG TGTACCAGTC 1320 CTTGGACTGA AAGCTGGATT TACAAGGTCA AATCAGATTC AGTCCTTGTG ATAGAAGAGT 1380 TCATAATACA GTGGAGCCAA ACGCATGAAA CATAACACAG CCTATTACAA CACAACGCGA 1440 CATGACAGCT TCACACATCC CAACACAGGA TACAAGGGCT CAGGTCTGGT 1490
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