Tag | Content |
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EnhancerAtlas ID | HS190-00020 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr1:2186140-2188960 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr1:2187603-2187614 | TTCTTATCTGT | + | 6.14 | Gata1 | MA0035.3 | chr1:2187603-2187614 | TTCTTATCTGT | + | 6.62 | NR3C1 | MA0113.3 | chr1:2186846-2186863 | TGGAACACTGTGTCCTG | + | 6.06 | NR3C1 | MA0113.3 | chr1:2186846-2186863 | TGGAACACTGTGTCCTG | - | 6.14 | NR3C2 | MA0727.1 | chr1:2186846-2186863 | TGGAACACTGTGTCCTG | - | 6.28 | NR3C2 | MA0727.1 | chr1:2186846-2186863 | TGGAACACTGTGTCCTG | + | 6.35 | ZNF263 | MA0528.1 | chr1:2187877-2187898 | TTCTTCTCTGCCCCCTCCCTC | - | 6.04 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_03761 | chr1:2186951-2187914 | Brain_Angular_Gyrus | SE_03761 | chr1:2188272-2188982 | Brain_Angular_Gyrus | SE_05718 | chr1:2186119-2189208 | Brain_Cingulate_Gyrus | SE_07454 | chr1:2186119-2189367 | Brain_Hippocampus_Middle_150 | SE_08491 | chr1:2185789-2189149 | Brain_Inferior_Temporal_Lobe | SE_08969 | chr1:2187324-2187728 | Brain_Mid_Frontal_Lobe | SE_08969 | chr1:2188435-2188720 | Brain_Mid_Frontal_Lobe | SE_11007 | chr1:2184548-2192323 | CD20 | SE_12005 | chr1:2184665-2189009 | CD3 | SE_15942 | chr1:2185651-2188669 | CD4_Naive_Primary_7pool | SE_16427 | chr1:2185351-2189136 | CD4_Naive_Primary_8pool | SE_17042 | chr1:2184540-2189098 | CD4p_CD225int_CD127p_Tmem | SE_17322 | chr1:2181525-2189193 | CD4p_CD25-_CD45RAp_Naive | SE_17845 | chr1:2181649-2192081 | CD4p_CD25-_CD45ROp_Memory | SE_18345 | chr1:2184333-2191921 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19191 | chr1:2185876-2189148 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20071 | chr1:2184982-2189278 | CD56 | SE_21247 | chr1:2185434-2188617 | CD8_Memory_7pool | SE_21558 | chr1:2185341-2189061 | CD8_Naive_7pool | SE_21979 | chr1:2185169-2189317 | CD8_Naive_8pool | SE_22376 | chr1:2182855-2189180 | CD8_primiary | SE_41586 | chr1:2184798-2187019 | LNCaP | SE_41586 | chr1:2187683-2188254 | LNCaP | SE_46124 | chr1:2186130-2189227 | Osteoblasts | SE_62490 | chr1:2120386-2191742 | Tonsil |
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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 |
GH01I002253 | chr1 | 2184631 | 2191030 |
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Enhancer Sequence | ACAGTCTTGG CCAGACTGTG GTCACTGCGT GCGTGTGTGT GTGTGTGTGA TGCGCAGGGC 60 ATTTGCTGGT GGAATAGCAC GGGCCATTGG CATTTGCACC TGAGGCGTGC AGCCCCCCTG 120 CTGCACACCT ATGGGGTCCC TGCGGTCAGG TGAGCTCTGG GGGGTTTCTG AGGGTGGAGA 180 CAGCCACAAC AACACTTCTT TCCTCCAAAT GCCTGTGCTG TGCACTTGGG TGCAGGTGGC 240 TTTTAGGGGA CATGGCTGGG CACTGCCCCA CAGTGTCACC TCTGTGTCCT GTGGTGCGTG 300 CTGTGGACTG GCACCACACC CCACGTGCTT GTTAGGCCAG TTTCTCTCAG GTGTCGGTCA 360 CCCTACCATG CGGCCTTTCT TTTGTCTTTT ATCTTTAGCT AAGGAGTCCA TGGCATACCA 420 AAAGCTGAAT GATGACAGCC AGTGTCCCCA TCCTGTCCTC CCCAACTTTC CACAGGCAGG 480 GACGCTCCCC ATTCTTGCTG CATAGTCTTC TGTTGACCCC ATGTACCTGA GTGACCCCCA 540 CGTACCTGAG TGTGACAAGC ACTATGGTGC TTGACCTCAG TCCAGCTGCT TAGACCTGTA 600 CCTGCCACAG CCCCACGTGC TGACACCTTG CGTCTTGAGT TTTGATAAAT CTATCCTTTG 660 GCTGATTAAT ATGACTGAGT GGTGTCTTCT GACCCCATTT CTTATCTGGA ACACTGTGTC 720 CTGACTTCAT TTCCTGTCTG GAGCACACTG TCCTGACCTC ATTTCCTGTC TGGAACACAC 780 TGTGTCCTGA CCTCATTTCC TGCCTGGAGC TCTCTGTGTC CTGACCTCAT TTCCTGTCTG 840 TGCCGCTCTG TCCTGACCTC ATTTTCTGTC TGTGCCACCC TTTGTCCTGA CCTCATTTCC 900 TGTCTGGAAC ATGCTGTGTC CTAACTGCAT TTCCTGTCTG GAGCTCTCTC TGTCCTGACC 960 TCATTTCCTG TCTGGATCTC TCTATGTCCT GACCTCATTT CCTGTCTGGA ACATGCTGTA 1020 TCCTGATATC ATTTCCTGTC TGTGCCACTT TGTCCGGACC TCATTTTCTG TCTGGAGCAC 1080 TCTGTATCCT GACCTCATTT CCTGTTTGTG CCACCCTTTG TCCTGACCTC ATTTCCTGTC 1140 TGGAACATGC TGTGTCCGGA TTGCATTTCC TCTCTGGAGC TCTCTCTGTC CTGACCTCAT 1200 TTCCTGTCTG GAGCCAGTGA CCTCATTTCC TGTCTGTGTC ACTCTGTCCT GACCTCATTT 1260 CCTGTCTGTG CCACTCTTTG TCCTGACCTC ATTTCCTGTA TGCAACACAC TGTGCCCGGA 1320 CTGCATTTCC TGTCTGGAGC TCTCTCTGTC CTGATCTCAT TTCCTGTCAG GAGCACTCTG 1380 TGTACTGACC TCATTTCCTG TCTGTGCCAC TCTTGTGTCC TGACCTCTTT TCCAGTCTGT 1440 GCCACTCTGT GTCCTGACCT CATTTCTTAT CTGTGCCACT CTGTGTCCTG ACCTCATTTC 1500 CTGTCTGGAG CACTCTGTCC TGACCTCATT TCCTGTCTTG TGTCCTGACC TCATTTCCTG 1560 TCTGGAGCTC TCTGTGTCCT TACCTCATTT CCTGTCTGTG CTGCTTTCTG TCTTGGAGTT 1620 GCGTGCCTGA CCTCATTTCC TCTCCACTGT GTGTTCCTGG AGTTAGGCAT CATCTTGGTT 1680 TTTACTCCCT TGCTTGGTTT TCTCAGGATC TCTGGCTGCT CCGTCCTTGC TCCAGCGTTC 1740 TTCTCTGCCC CCTCCCTCTG TGGTCCAGAG GCCGATGGCC AGCTGGCCCT CACCTGCCCG 1800 CCCTGGGTAT TTCTGTGCTC TTCCTGGTGA GGGATTCTAG GGGTTCCCCT CCTGGGTTCA 1860 TCCTTACCTG AGTAGCCACA GCACACTGTG CAGTTGGGTG CCTGGGAGGC ACGTGCTTTG 1920 GGTGTTGCAT GGCTGACCTG GTAACTGGGC ACCCGTGTAT GGAGGGCTGG AACAGAACAC 1980 TTGTCGGCGC TCCTCAGCGT CTTGCCTCTG GTGTCCCCAT GGCGAAGTCC CCTGCCATCT 2040 GCTTTGGGCT CTGACATGTG ACCTGACTGT GCCCTTCAGG AGCTTTCAGA ACCTCCTCTT 2100 AGATCTGGCA TTCAAAATGT CTTGTCAGAC ACCTCGAGGC GGCTTGTGTT TGGCCCTGTG 2160 TTGGGCGCCT ATTGGGCCCT TGTCAGGTTT TTGTTGCCAG GAGGCTCGCG CCCCGATCTT 2220 CGGGATGGTG CCCGTGGCAT CTTCTGCTCG GTGCTCCCTA GGGCTGGACG TTGGTCCTCC 2280 TGGCACTGGT GCTCCGGTTG CTGTGGTCTC CCTGCTGTTC CCTTGTGGCT CAGGATTACT 2340 CTCTGGAGGT CTCCGCCTTA TCATGAGCAC TTTCTTTGTT GGCTACTTTT AGTTTCATGA 2400 TTTCATTTTC GTTTCTAAGA TATCTATCTC TTTGTAAAAG CTCCCACCTT TTGTGACTTG 2460 TGGATGCTGT ATCTTTCTCC TGTTGCTGCA GACATTAATG ATGTTTTTCT TGACAGTTTG 2520 TCCTGCTGGT TTCCTCTGCA TTCCTTTGGT TGGTTTCAGA CCTCGGCTTT AAAGGGGCAT 2580 TTCCCCACAT TGCCAATTCT TGACCATCTG GTCACGTCAA GGCTGACGTG CCAATGGCTG 2640 CAAGGGGGAG GGCACCTGGG AGCCCGCGGA TGGCTCTTAT GCAGACGTGC GGGCCAGCCC 2700 CGATCCTGCT TCTGCAAGGC CTCCCCTCCC ATGGTGGCGC TTTGGTGCCA GAGCGCGTCG 2760 GCGTGGCTCC CTAGCGTCTG CCTCTGCAGC TGCTTGGCCC CCAGCCGCCT CCTCCCAGCT 2820
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