Tag | Content |
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EnhancerAtlas ID | HS182-03318 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:940100-941360 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr11:940384-940405 | TTTCACTTTCTCTTTTCTCTG | + | 6.09 | IRF1 | MA0050.2 | chr11:940378-940399 | GTTTCATTTCACTTTCTCTTT | + | 6.65 | Nr2f6(var.2) | MA0728.1 | chr11:940172-940187 | TGAACTCCTGACCTT | - | 6.04 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_29414 | chr11:939725-945422 | Fetal_Intestine_Large | SE_53986 | chr11:939885-941185 | Spleen |
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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 |
GH11I000939 | chr11 | 939465 | 943793 |
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Enhancer Sequence | TGTGCCACCT GTCTGGTTAA TTTTTGTGTT TTTTGTAGAG ACGGGGTTTC GCCATGTTGG 60 CCAGGCTGGT CTTGAACTCC TGACCTTAAG TGATCCACCC GCCTTGGCCT CCCAAAGTGC 120 TGGGATTACA GCCGTGAGCC ACTGCGCCGG CCCGTGTCTG AAATTTTAAG ACGATGTGCC 180 CAAGTGTGGC ATTTGGTGGC CTTATTCAAT CTGGAAACTT ATGTCTTTTG GGCTCTAGTG 240 GAAAATATTC TTGTTGTATT TTGTTGCTAA CCTCTTCTGT TTCATTTCAC TTTCTCTTTT 300 CTCTGTATTT CTCTATGGTA GTTGAAATTA TACCTCCTGG TGTAGATTTT CCTGCCTTTC 360 TGCCTTTCGC GTTCTGTTTC CACGACTCTC AAGTTTGTCC TCTAGCCCTT GTTTTGCATT 420 TTTAATTTCT GCTGTCAGTT TTATAGCTTG AGAGCTTTCT CATGACCCAA GTGCCCCTTT 480 TTTGGTGGCA TCTGTTTCTT TAAGCTGTAT TTTATCTCGT CTGTGTAAAG GTGTTTCCTT 540 TGGCGTTTCC TTCTGTGCAT TGTCTCATTG CTTTGAATGC CTTTTGTGTA GGTTTGTTTG 600 GTCTCTGGCC CATGCTGTGA GGTTCTGAGC TCTCACTTTG TGCTTGGTGG CTGGTGGCTG 660 TCCACCCATG TGTACCAGTG CCTGCCAACC TGAAGGGCTT TGGCAGGGGC CTTCGCTGCA 720 GGGTGAGGTC TGAGGAGGAG CCTGAATGCT GGTTCAGTTC TTCCAGAGGA CTCTCGACTC 780 TCTTCTCTTG CTTGGTGAGC AGGTGGGTGT TGTGAGCCCG GCTGCCATCA TTCTGGGATG 840 GGGCATCTCA CCCCTCGGGG AGTCTGTCAC TGCGCTGTGC TGCTCTCACG AGGCCCCTTG 900 CTCCACACTC CGTGGAGCTC GGAGCTTTTG TGTTCTCACT TTTCCAGCTT GTCTTTTTCT 960 GAGATGGGGG CCGAGGGGCC TGCCTGGCTG CAGGGTCTCA TGGCAGGGAT CTGCTGCTCT 1020 CTGTATAGAC TTGAAGCCCA TCCTCCTGAC ATCGGTCTCC TGAGGTTCCT TTCATTCCCA 1080 AGCCTTTTCG GGTTCTCTGT TCGAGACGGT TTGCTTCTTA ATTTGTCTTC CCTCCTGCAG 1140 GTAGCTGGGG TGCAGCTTGC TCTCCTTGGC TGAGTCAGTT ACTGCTTGAC CATTGCTTGG 1200 CAATGTCCAG GATTGTGATA ACTCTATTGT CCTTGATGAC TGATTGTTTC TACACACATG 1260
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