Tag | Content |
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EnhancerAtlas ID | HS018-00138 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:9739390-9742470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:9741478-9741490 | GTTTGTTTGTTT | + | 6.32 | Lhx3 | MA0135.1 | chr1:9741294-9741307 | CATTAATTAATTA | - | 6.46 | Lhx3 | MA0135.1 | chr1:9741297-9741310 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr1:9741301-9741314 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr1:9741298-9741311 | AATTAATTAATTA | - | 6.78 | Lhx3 | MA0135.1 | chr1:9741302-9741315 | AATTAATTAATTT | - | 6.92 | Nr2f6(var.2) | MA0728.1 | chr1:9741678-9741693 | TGAACTCCTGACCTC | - | 6.22 | POU6F1 | MA0628.1 | chr1:9741295-9741305 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr1:9741299-9741309 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr1:9741303-9741313 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr1:9741295-9741305 | ATTAATTAAT | - | 6.02 | POU6F1 | MA0628.1 | chr1:9741299-9741309 | ATTAATTAAT | - | 6.02 | POU6F1 | MA0628.1 | chr1:9741303-9741313 | ATTAATTAAT | - | 6.02 | RARA | MA0729.1 | chr1:9741675-9741693 | GCTTGAACTCCTGACCTC | - | 6.52 | ZNF263 | MA0528.1 | chr1:9741215-9741236 | AGAGAAGAGGGGAGGGGAGGG | + | 6.07 | ZNF263 | MA0528.1 | chr1:9739752-9739773 | CTCTTCTCCTCCTCCTCTTCT | - | 6.35 | ZNF263 | MA0528.1 | chr1:9739749-9739770 | TGCCTCTTCTCCTCCTCCTCT | - | 6.66 | ZNF263 | MA0528.1 | chr1:9741222-9741243 | AGGGGAGGGGAGGGGAGGGGG | + | 6.82 | ZNF263 | MA0528.1 | chr1:9739755-9739776 | TTCTCCTCCTCCTCTTCTTCC | - | 6.88 | ZNF263 | MA0528.1 | chr1:9739758-9739779 | TCCTCCTCCTCTTCTTCCTCG | - | 7.09 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_09834 | chr1:9740222-9742309 | CD14 | SE_11127 | chr1:9736110-9752785 | CD20 | SE_17476 | chr1:9739282-9742251 | CD4p_CD25-_CD45RAp_Naive | SE_19640 | chr1:9741692-9742222 | CD4p_CD25-_Il17p_PMAstim_Th17 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 9739426 | 9739466 | chr1 | 9741635 | 9741787 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I009679 | chr1 | 9739283 | 9742309 |
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Enhancer Sequence | GCTGGGATTA CAGGCGTGAG CCACCGCGCC TGGTCTGGGG GAAATTTCTA TAGAGGATGA 60 GAAGTCAGGG ATGTTGACTT CTCATGCTGG GCCTCAGGTG CTTGAGACCA GTCAGGCTCT 120 CCCTGTGAAA TTAGCAAGAA CTCACCCTTT GGCCAAGTAG GCTGAGCGCC CCACACCCAC 180 ATCGCCTGTT TACCTCTCAA TATTCTCCCA GGCCTTGGTT AGCCGCCCTT AGCCCATGTC 240 CTGTTTCTCA GGCATGAAGA AGGCCCCTGA TGTCAGCATC ACAGAGCTCT CCCAGCCCTA 300 CAGGTGGCCA GCCTTCCTGG AGACCACTCC TGGTGCCATT CCTTGGGCAC CAGTGACTTT 360 GCCTCTTCTC CTCCTCCTCT TCTTCCTCGT CATGTTTTAG CATAAGAAGC TTTATTGAGC 420 TAGAATTCAC ATACCATACA ATTCATTTAA TGTGCACAAT GCAATGGTTT TTTGTTGCTG 480 TTGTTGTTAT TGTTTTCGTT TTTATTTTTG AGATGGAGTT TCACTCCTGT CACACAGGCT 540 GAAGTGCAGT GGCGTGATCT CGGCTCATTG CAACCTCTGC CTCCCGGGTT CAAGTGATCC 600 TTCTGTTTCA GCCTCCCGAG TAGCTGGGAT TACAGGCGCC CACCACCACA CCGGGCTACT 660 TTATGTATTT TTAGTAGAGA TGGGGTTTCA CCATGTTGGC CAGCCTGGTC TCGAACTCTT 720 AACCTCAGGT GATCCACCCG CATTGGCATC CCAAAGTGCT AGGATTACAG GCATGAGCCA 780 TCATGCCTGG CCTAATGGTT TTTATTTTTA TTTTTAAATT TTTTGTAGAG ATGGAGTCTT 840 GCTATGTTGC CTAGGCTGGT TTCAAACTCT TGGTGTCAAG TGATCCTCCC ACCTCGGCCT 900 CCCAAAGTGC TAGGATTACA GGTGTCAGTC ACCAAACCCC GCCTCAGTGG TTTTTAGTAT 960 ATTCACAGTT ATGCAACCAT CAGCATCATA AATTTTAAGC TGTGCATGGT GGCTCATGTC 1020 TGTAATCCAA GCACTTTGGG AGGCTGAGGC TGAACTCACT TGAGCCTAGA AGTTCAAGAC 1080 CAGCCTGGGC AATATAGTGA GACCCTGTCT CTATTAAAAA AAAAAAATTA AAACATTTTC 1140 ATCACTCCAA AAAGAGATTT CACACCATTA GCAGTTACTC TCTACTTTTC TTCCATCTCT 1200 CAGCCTCTGG CAACCACTAA TCTGCTTTCT GTCTCTATGG ATTTGCCTGT TCTGGACATT 1260 TCATATAAAT GGGATGATAC ACTATGTGGT CTTTTGGGGT TGAGTTTGCA CCTTAGCATA 1320 TTGCCTTTAG AAACCTGTCT GCCTCATACC ATTACAGAGG AGCTGTTGTT TGTACTGACC 1380 ATTTAGTCCA TCACAGGTAT TGATGGAGCC TCTAAGCATG GAATAGTGCT GGCCCCACAG 1440 CAGGAACGCG GCAGCCATGG GTGGCGTATT AGTTACTGGT TGCTGTTTAA CAAATCACGC 1500 CAACACTTGG CAGACTGAAC AGCAAGCATT TATGATCCCG TAGTTTCTGT CAATCAGGAA 1560 TACAGGAGCC GCTTCGTTGG GTGGTTCCGG TCCAGGGTCT CATGAGGCTG CCATTGAGCT 1620 TTCAGTGGAG GCTGCAGGTG TCTGGGGCTG GAGGTACCTG CCACAGCGTG GTTGGCAGGC 1680 TCAGTGACTG GCTGGCTGTT GGCCAGATAT CTCAGTTCCT CTTCATGTGG GCTTCTTCAT 1740 AGGGTGGCTT GAGTGTCCTT ATAGCATGGC CACTGGCTTA CCCCAGAGCA AGAGATGAGA 1800 GCACTGGAGA GAGACAGAGA GAGAGAGAGA AGAGGGGAGG GGAGGGGAGG GGGTGTATAA 1860 GCCCAAGACT GAAGCCCCAG TGATGTTTCA TAACCTAATT TTTTCATTAA TTAATTAATT 1920 AATTTTAGAG ATAGGGTCTC TGCTGCCCAG GCTGAGGTGC AGTGGCACAA TCAGAGCTCA 1980 CTGCAGCCTC CAGCTCCTGG GCTCAAGCAA CCCTCCAGCC TCACCCTCTC AAGCAGCTGG 2040 GACTACAGGT ATGCATCACC ATGCCTGGCT GCTGCTGCTG CTTTTTTTGT TTGTTTGTTT 2100 GAGACGGAGT CTCACTCTGT CACCCAGGCT GGAGTGCAGT GGCGCAATCT CGGCTCACTG 2160 CAACCTCCCC TTCCCGGGTT AAAGCGATTC TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC 2220 TACAGGCGTG CGCCACTAGT TTCTGTATTT TTAGTAGAGA TGGTTTCACC ATGTTAGCCA 2280 GGCTGGCTTG AACTCCTGAC CTCAGGCAAT CTGCTCGCCT CCCCGCCTCG GGCTCCAAAA 2340 GTGCTGGGAT TACAGGTGTG AGCTACCAAA CCTGGCCCGG ATTCTTTTAT AATCTAATGT 2400 TAAAGGTGCT ATCCCATCAC TGTGCCATAT TCTTTAGGTC ACATTGACTG TGAATGTGGG 2460 TGGGGGCTAC ACAACGGTGA GAATCTCAGG ACGGAAGTAA CTGAATGTAG TTTCATATGG 2520 AGAGTGATCC AGCTTGTTCT GGAAGGGACT GCAGTCTCCC CGGGACTTAG CTTTGGAGAA 2580 TGAGCCAGCT TGTTCTGGAA GGGATTTCAG TCTGCCCAGG ACTTAGCTTT GGACCAGCTA 2640 TGAGTTCTCT GTGATGAAAT CTCAGCTTTT CCCAACTGCA GCTTCAACCT CCTGAGTTCA 2700 AGTGATCTTG TTGCCTCAGC CTCCTGAGTA GCTGGGACTA CCACCACGCC TGGCTAATTT 2760 TTGTATTTTT TGTAGAAATA GGGTTTTGCC ACGTTGGCCA GGCTGGTCTC CAACTCCTGA 2820 GCTCAAGCGA TCTGCCTGCC TTGGCCTACC AAAGTGCTAG GATTACAGAC ATGAGCCACC 2880 ACACCTAGCC AAGGCTGCGT TTTTATTTTT TATTTTATTA TTAGTATTAT TTGAGACAGA 2940 GTTTCACTCT TGTTGCCCAG GCTGGAGTGC AGTGGCGCCA TCTCAGCTCA CTACAACCTC 3000 CGCCTCCAGG GTTCTCCTGT CTCAGCCTCC TGAGTAGCTG GGATTACAGG CATGCCACTA 3060 CACTTGGCTA ATTTTTGGTA 3080
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