Tag | Content |
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EnhancerAtlas ID | HS182-12604 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:99131250-99132500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr2:99131760-99131775 | TGCTGACTCATGCTC | - | 6.66 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09236 | chr2:99127825-99136975 | CD14 | SE_43508 | chr2:99130420-99132423 | MM1S | SE_67159 | chr2:99130420-99132423 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 99131378 | 99131974 | chr2 | 99131481 | 99132241 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I098514 | chr2 | 99131200 | 99133262 |
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Enhancer Sequence | ACACACGTGT GGTCCCAGCT ACTCAGGAGG CTGAGATGGG TGGATGGCTT GAGCCCAGGA 60 GTTTGAGGCT ACAATAAGCC TGATGTCATT GCACTCCAGC CTAGGAGACA GAACAAGACC 120 CTGTCTCTAA AAGCTGGAAA AAAAAAAAAG TACAAAACCC CAAAACTCCA AAGGACTGAG 180 TTCTGGGAGC TTTTGGATAG CTGAGCATGC AGAGGTTCCC GGAGAGTGGC ACATAGGGCG 240 GGCAGGGCAG CTCCACGCCC TTCCCACATG CCTTGCTCTG TGCACCTCTT CCAGCTGGAG 300 GTTCATCCGC ATCCTTTGCA GTATCCTTCC TGTCTGTCTG CAGGAAGGTG ATATTTGTCT 360 TTCTGAGGTT ATTATTAATA GTAACTTTCA GTGCCAGTGA ATGGTGTGAC ACCTCACTGA 420 TCTATGATTT TAGCTGTCTT GGATTTGGGG TTTCTGAGAG TAAGTCCTTT CCTCTTTCTG 480 CCCCTCTAAA GTAGCCTCTT TCTTAGAGGC TGCTGACTCA TGCTCAGCTT CATGCCAGCC 540 TTTCATTTTA CTTTCTCTCT TGTGCTGCCT GTGTTTGGAG AGCAGAGGCA CAGTGAAGCT 600 TCTCAGCCCA TTTGCTGCCA CAGTGACAGC AATAGGCTGT GGTGGGGTAG GACGGGGGTG 660 GGGTAGGACG GGATCCGGTG GGTGGGGCAG GGAGAGGGGC CCCCATTGCA CTTGGGCTTT 720 TTCTTTGGGT TGATAACGAT AGTTCATATT TCATCTCCAT GTGACCTTGA AAAAAATCAC 780 TCTGAGCATC CGTGACCTCA TCCGTGCAAC TCCTTTTAAA AATTATTCTT AGAAGAACCC 840 CAGTGAATAA GCAAAAGTGG AGCTCTGATG TGTTAATCCT CACCCCTCAA CTCCAGCTCC 900 GGGGAGCCTG AGAGGTTCCT GAGGTGGAGG GACCTGCAGT ACTCCCGCTA GGCCTCTGGC 960 AAACGTTTCC CAGGACTGCT GCTGAAGGCC TTGCCACCTC ACTAGTCCTG TGTGAATCCT 1020 AACACCCCTC CCGTCCTGCC AGTGCCCTCT CCACCACCCC TTTCCCTGCC CCCCATGGCT 1080 GGAAGGGACA TCATGGGAAG TGGGATAGAA CCTCAGGGTT TACTGTCCAC TTGATGGCCT 1140 GCCGCCTCTT GTCGGAGGGG TCACATGAGT GCGCAGAGTG AGGAATGGGA GCTGCTCACT 1200 TCATGGGTTA TTGCTTCTTT TTTCTTGACC CCAAGAAAAA ATTCCAGCCC 1250
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