Tag | Content |
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EnhancerAtlas ID | HS182-18091 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr5:156927920-156929140 |
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) |
CDX2 | MA0465.1 | chr5:156929061-156929072 | AGGCCATAAAA | + | 6.02 | NR2F1 | MA0017.2 | chr5:156928763-156928776 | CAGAGGTCACAGG | + | 6.19 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_10243 | chr5:156923470-156935115 | CD19_Primary | SE_10863 | chr5:156909781-156978888 | CD20 | SE_36955 | chr5:156928580-156930722 | HSMMtube | SE_50178 | chr5:156926964-156930388 | Sigmoid_Colon | SE_52470 | chr5:156927667-156928980 | Small_Intestine | SE_53856 | chr5:156927915-156930322 | Spleen | SE_60866 | chr5:156904542-156937373 | DHL6 |
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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 |
GH05I157500 | chr5 | 156927218 | 156937080 |
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Enhancer Sequence | ACCCCATTCC ACAGACAGGG ATGCTGTGGC TCAGGCAAGT CCAGTAGCTG GCCGAGGGAC 60 ACACCTGCTG AATTCAAGTC AGGTCTGCCT GAGGCCTACC TCATGTTTAT CAACCTTATA 120 CCCCTAACTG TCCAGGGCTC TAGCATATTG GAGAGCCACA TCCCATCCCC TGACCACAGA 180 CACCTGTCCA CCTGTCTCCC CTAAGAGAAG GAATAGAACA CTTTCCTCCC ATTATTCTCC 240 CACCATGTTG GGCTCCAGGA AGACCTGTAT TCCTGCCTTC CTAATGTACC ATATTTCTTC 300 CCACGAAGGC ACAGGCTCCC CTTCCACCTG AAATGTGCCT TCCCTCCTGC GTGCCTCACT 360 AACTCCTAAT GCAGCCTTCA GATATGGGCT CCAGGTCACC TCCCACACAA GCAAGGAGGT 420 TCCCCCTCAC ATTATATATG TTCAGAGCAC TGTGTCATTT GTCTTCCTAG CACTTGCCAT 480 GGACTGTACA TATATTCTTT TGCAATTATT TCAATATGTG TTTCTCCCAC TAGACTATCA 540 GCTCCCCAAG GACAGGAACT ATGTCATTTT TGCCACTCAT CCTAACCCTA GGACCAGACA 600 CAGTAGCCCA CACTCAGTGT GCCTGTTGAA TGAGCAACTG CTCAGAACCT AAGCCAACTG 660 GCCATGCCCA CTCTCAGGCC ATTCCTCAAC CCCAGTGGCC CTCCATGTTC ATACCACTCC 720 CTCCTTTCTG ATGGGTCTGT GTTGATCTCT CTGGGCTCAT GGTGGTGGGG GTGGCATCCT 780 TGACTAGTTC TTGTTTTATT CTGAAAGTGA CATACTGGCA TTAAAAAAAG AAAAATCACA 840 TCACAGAGGT CACAGGCAGG GTGCGGTGGC TCACGCCTGC AATCCTAGTG CTTTGGGAGG 900 CCGAGGTGGG TGGATCATCT GAGGTCAGGA GTTTGAGAAC AGCCTGGTCA ATGTAGCAAA 960 ACTCTGTCTC TGCTAAAAGT ACAAAAAAAA AAAAATTAAC CAGGTGTGGT GGCACACACC 1020 TGTATTCCCA GCTACTCAGG AGGCTGAGGC AGGAGAATCG CTTGAACCCT GGAGGTGGAG 1080 GTTGCAGTGA GTGGAGATCT TGTCACTGCA CTCCAGCCTG GGCAACAGAG TGAGAGAGAG 1140 AAGGCCATAA AATCAGATTT TTTTTTCCAT TTATACAGAA CCTCAGTCTC ACCCCCATAA 1200 TTTACTGTTA CTTGTTATCT 1220
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