Tag | Content |
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EnhancerAtlas ID | HS182-22384 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:140559750-140562910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr9:140561342-140561353 | GTTTTAATTAA | + | 6.14 | Lhx3 | MA0135.1 | chr9:140561346-140561359 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr9:140561350-140561363 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr9:140561347-140561360 | AATTAATTAATTA | - | 6.78 | POU6F1 | MA0628.1 | chr9:140561348-140561358 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr9:140561352-140561362 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr9:140561348-140561358 | ATTAATTAAT | - | 6.02 | POU6F1 | MA0628.1 | chr9:140561352-140561362 | ATTAATTAAT | - | 6.02 | RARA(var.2) | MA0730.1 | chr9:140561844-140561861 | AGGCCATGTGGAGGTCA | + | 6.38 | RREB1 | MA0073.1 | chr9:140562773-140562793 | CCACCCACCACTCACCCACC | + | 6.02 | RREB1 | MA0073.1 | chr9:140562777-140562797 | CCACCACTCACCCACCCACC | + | 7.06 | ZNF263 | MA0528.1 | chr9:140561887-140561908 | TACTCCTCCTCCTCCTCCCCG | - | 6.21 | ZNF263 | MA0528.1 | chr9:140562728-140562749 | TTTTCTTCCTCTTCCTCCATT | - | 6.39 | ZNF263 | MA0528.1 | chr9:140561881-140561902 | TCACTCTACTCCTCCTCCTCC | - | 6.55 | ZNF263 | MA0528.1 | chr9:140561878-140561899 | GCCTCACTCTACTCCTCCTCC | - | 6.56 | ZNF263 | MA0528.1 | chr9:140561884-140561905 | CTCTACTCCTCCTCCTCCTCC | - | 8.31 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_11232 | chr9:140561146-140563373 | CD20 | SE_32833 | chr9:140558964-140562778 | H1 | SE_41929 | chr9:140559711-140561304 | LNCaP | SE_58494 | chr9:140551343-140601094 | Ly1 | SE_62965 | chr9:140561512-140658488 | Tonsil | SE_68889 | chr9:140558888-140562343 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr9 | 140562371 | 140562671 | chr9 | 140559752 | 140562041 | chr9 | 140561000 | 140562084 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I137664 | chr9 | 140558495 | 140562715 |
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Enhancer Sequence | TGTAAGAAAT TTGGAGCTGG GGTGGGCATA GGAGGTGATG TTTAGGAGCA GCCTGAGTGT 60 GGGGAGACTG CTGTGCTCGA ACCTGCGTCG TGCAGGTGCG TCCTGGAGCT ACTCCTTGTG 120 GCAGAAGCAT TGCCCTGAGA CCCAGCCCTG GTATGCTTGG CACTGGGACA GGAGCTCCGG 180 TGGGAGGTGC GCATTGCGAG CTGGTGTTTT CTGTTTGCTT TCCTACCCAC TGTCATGTTG 240 TGGGCTCTTG GCCCCAGAGG TAAAATGTCT CTGTGAGTTG AGTTCCTTGT GAGAGGGCTG 300 GTCCCCAGAT TCCATGTCTA GGTTTTTGTT AGTATTTTTT CAACAGAGCT AATCCTGAGA 360 GGCCCTACGA GCAGTGATTG CTTTGTGGGA TGAGCTGTGT TGATGGTTTC TGTGGAGGGA 420 CCCTTCACGT TTTAGGGTGA AAACAATAAA TGTCTCGTTA AATGGTTTCC ATCTGAGAAC 480 ACTGATTGTT TTAAAATGGT TGTGAATGCG AGGGTTTAAG CAGCTTCCGA GGAGGCCTGG 540 AGGTGCCTGG GCGGCCGCGT GCAGCTCTGG AATCCTGCCG CTGGGGCAGC CTCCATTTCG 600 TGAGATGGCT CTGGAGCATG CCCAGTGCGT GGAGCTTTCA GAGGGAGCCG CCGAGCTGGG 660 CTACTGTGAT TTCTCTGCAG TTGGCCGCAG TCAACAATTG CACTAAGACA GGAGGAAAAA 720 AGTGATGGGG TACAAGCAAG AAACGTGGTA TTTGGTACTT TTTTTCTTTT GCTTAATCCC 780 TCTTTCTTTT ACATTGGTGC TTCTAGGCTG GGGCCAGGGC CTGCAGAGCA GGGACGCTTG 840 CTGTGATGGT GGGGACACCT CCTTGTCCTC CATGCCGCTT GCCTGCCAAA ATAACCCTGT 900 TTTGCTCTCT GGTCACCCAC CATGTGCACT TTCTTGGGAG TGGGATGGGA GGTCCCCTCC 960 AACTGAGGGT ACTGAGAACA GCTCAGGCCC GTTCCACATT TGCTGGTAGC AGGAGGAACT 1020 CTGACCTTTT TCAGTTATGC TGATGATAAA CCAGGACTTT TTCCCTTGTT TGAACATTTA 1080 TAAAGAGCGT GCTTGAACTT TTTTGCTGAC TAGCAGTGTT TTCCTGTTTT ATTCTCCTAC 1140 CTGCCCCCAT GGCAGCCTCA GTGGTGGAGG GAGTGAGGCT GGGAAGGGAT GACACTGCCA 1200 GGTGAGCAGG AACCAGGGAC CCTGGGACCA GAGGCCAGGC TGTGCAGGGC AAGGGCTGGC 1260 CGTGCCACGG TGCAGCTGGC TCTTTGCCAT GCAGGCTGCA GAAAAGGAAA TCTGTCCGCC 1320 TTGGCTGTGA GGATGGCATT GACCACTCAT CAGGAGAGCT GGGAACAGAG CCTCCCCCTC 1380 GGAGCCTGTG TAGTCCCCGT CCACACGTGT GGGTTGTGTG ATGATCCTGT CTGCGTGTTC 1440 ATTGGGAGAC TCCATTTTCC GTGGAATGGT GAGGAGGGTA GAGAGGCAGC AGAGTCTCCA 1500 CTTGGATTTT CTAAGCAATT CCACAGAAAA TAAGACGTTG CTCAAGCAAG TGCTGGGCAC 1560 ATCTTAGGGA GAGACCTAGT GAGGAGGGCT GTGTTTTAAT TAATTAATTA ATTGTAAATA 1620 ACAGGATTAG AGCAGATTGG TTCATAGCTG CCTGTTCTAG AACCGTATTC TTCGAACAAA 1680 AGGGTGGGGG ATGGTAGGCT TCTCTCCTAG CTCTGAGGAA ACTCCAGCTC AGCGCACAGC 1740 ATGAGGAGGA CGAGGGAACA ATAGGGCGTT CCTTTGTGCC TGCCCTTGAA ACGCGGTGGA 1800 GGCCACTCAG TGAGCCCGGG CAGTGCCATC GCTCACGTGT CCCCAGCAGC AGTGGCGTCT 1860 GTGGGGATGC TGTGCACTGG AAATTGGCAC TGTTTTGGGT AGTGGTTCTG AGAGGAACTG 1920 TTTAACCAGG TATGCAAATG TGCTGATGCA GGAATGTTTT TGAACACCTG TGATGTAAAT 1980 TTTAACGGTG GTTAATGTTA GCAGCTCCAC CTGGGTTAGC TCAACCCTTA GAGATTATTT 2040 GTTCTCATCT CTTTGGAGTT GAAAATGTTG TACTTTTCTA GGAGCCATTT CCCCAGGCCA 2100 TGTGGAGGTC AGGTATCTGC TGGTTCTGGC CTCACTCTAC TCCTCCTCCT CCTCCCCGCT 2160 CTGTGGAGAG GGTGGCTTGA AGGAGACGGG CAGCAGGTGT GTGACTGCAG TCCTGGGGCA 2220 CGGGCAGAGG CTGGCATGTG GGGAAAGCAG GACCCGGGAG GCTGTAGCTT AAGTAGACAT 2280 TTGTTTTTTA TTTGAAGAGA ATTTTAGAGA TGGGGTGGTG GTGGATTTTA GCATTAGAGA 2340 TTTCTGGCTT CTGCTTGAAG CACTGTGAAT AGGGGACAAA AAAATAACCA AGAGGAAAAG 2400 TTCATGTAAA GTAGAAGTTT TGGTGTGTTT TCTTGAAAGG AAATTGTCTA CAGTGAAAGC 2460 GTTGTATTTT TAGAGAACTC GGGGAGGAAA ACGCTGTTGT GCTGCTTATC ACACGGGTCT 2520 GGCCTTTTTG ACATCTGAAA TCTTATAGGA ATTTGTCTTT TTGAGAGTGT ATGCTGCTTA 2580 TTTGGTTTCG TGGAATCCAG AAAAGAGCCT ATCCAAATTA TCTTTACCTT CAGGGTAAAT 2640 TACCTTTTAG AATTGTGGCA GATGGCACAT AGGACCTCTC AGAGGGACTG CACCTTGTAC 2700 AAGAAGAAAA GTGAGAGGGT GTTGCAAAGG AGAGCTTCCA CCTCCTTTAT AGACTTTTGC 2760 AGAACAGCTT TCTTCCTTTC GACCTTGGAG AAGAGGCAGG ACCAGTGGGG AGGCAGACAA 2820 GTAGGTGAAG GAAGACAAAA GGAAGAAGGG ACGCACTGAT CGAGAAGACA AGGAGTGCTG 2880 ATGGCTTTGG GCGCCAGCTG TCTACTCCAG AGAGTCTAAC TGACCTGGGA CTTGCAGGAT 2940 CCTGCTAGAA GAAAAATCCT TGCTTCCTTC TCCTCCTGTT TTCTTCCTCT TCCTCCATTC 3000 TCCTTCCTCT CCCTTCTATT CACCCACCCA CCACTCACCC ACCCACCACC TGGCACATAC 3060 ACCCACCCAC TCATCCATCC ATCCATCTAC TGTCTACTAT CCACCTCACC ACCCACCCAT 3120 CCATTTATTT ACCCACCTAC TCATCCATTC ACCTGTCCAC 3160
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