Tag | Content |
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EnhancerAtlas ID | HS182-13786 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr20:32404670-32406080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RELA | MA0107.1 | chr20:32404996-32405006 | GGGAATTTCC | + | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_09929 | chr20:32397565-32406597 | CD14 | SE_43506 | chr20:32399042-32408837 | MM1S | SE_55016 | chr20:32404569-32406043 | Stomach_Smooth_Muscle | SE_67148 | chr20:32399042-32408837 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 32404913 | 32405110 | chr20 | 32405158 | 32405492 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I033816 | chr20 | 32404570 | 32406043 |
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Enhancer Sequence | GTTAATTTAG GTTTAGCTGA GAATGTCTGA TGGATGCATA GAGGCCAGAA GCTCACAAGA 60 GATATATCTT CATTAAGTTC TGCTCATTGC TGGAGTGAGG GTGGTTTTCT CATGTTTAAT 120 AAAGTCTCTC TCAAACATGA GCATATGTGA AGACACTGTA ATAAGTTTAT AGTCTTATGA 180 GACAAAGAAC GTGGCTCTTT GGTTCTCTGG AATCAAGATC TCAGGTTGAA AAGCACAGTG 240 TCTTAATGGC GCATGTGCCA GCAGTATCTC TTATCCCAGA GGCCCAGGGA TAGAAAACTC 300 GAAATCCACC CAGGGAAGTG AGCAGTGGGA ATTTCCCTCA GTGACGCTTA AGTTTCTTGT 360 TTGGAAAAAT GGTTGGCTAG ATTGAGTTTG GTTTACTTCC TAAGACAGAT GGAGTACCAG 420 AGGCCCTATG TGTTGGCTAT CCAAACACAC TGGTTCCTTT AATTCAAATG ACAAATCCTT 480 ATTTTGCCCC ATTTGGCAGG GAGATTAGAT ATTTTTAATT GCCTGCCAGA GTAGGTTTAT 540 AATGTGATTT GTAACTCAAG ATAGATTTTG TTTGGAAGTT TAACTAAACG TGAAGACCTG 600 TGAGCAGGAC TGTTTTGCTT GGAGAAACCT TGAGTTGTCC AGAGTTGGGT TTGAGTGTGG 660 AGCGAGGTCT TGGAGAGCAT CCTATGAAGA TGTGTGCGAG CCAGCCATCT CCGAGGCGTA 720 AAGCCAGGAC CTAATTTGTT TACAGTGGTC CAGAGCCTTG ACATGAAGCC AGAGCCCACC 780 AGGAGGAGGG GCAGAGCTCT TGGGGCCTTG AGGAATTTCT TATGAAAACT TAGTCTTCTT 840 GCTCAGAATT ATTTTGGGTT GTGCCACTGT CTTTAAGAGT GTGAGAGAGA GGATATTAGA 900 AAACAACTTT AGTTGGTCAT TTTGCAGATG GATGATTATA TTTAGAAGGG GAAAATCTGA 960 GCATAGCAAT GGGAAACTAC AGATCTAGCT GTTTGTAGTA CTGGCCTGTT TTTAAGCTGT 1020 TTGGCTCAAG TCAGCAATCA TTTATTACGT TTCTTCTAGG TGGAAGGTGT GGTGATGTGG 1080 GCAAAAGATT CCCAGTTTGA ATGCAGCTTT ACCTTTCATC AGTAGTACCT TGGTAGTTAC 1140 TTATATTTCT CTGAGTCTCA ATTCCCCACT GTGTGAAAAG GGAAATACTA CCAATACTTA 1200 CTTGTTAGGG CTCTTATGAG GATGTGGAAT AAGTTGATGT ATGTAGAGTG CCTGCCAGAA 1260 TGCCTGGCAA ATAGGCGAGA TGAAACTGTT TCCTTGGCTT CCCAGGGATA GTCTTAGGGA 1320 CAGTAAGGCT ATAAAGATGG ATGAGACACT GCCTTCTCCC CACAAGGGCC CACACAGTTC 1380 ATCGAGGAAG ACACACAGGT AAAAGTAACT 1410
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