Tag | Content |
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EnhancerAtlas ID | HS098-59285 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chrX:13002260-13003830 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chrX:13003044-13003055 | GGCCACACCCT | + | 6.32 | POU2F2 | MA0507.1 | chrX:13002333-13002346 | ATATGCAAATGTA | - | 7.12 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_11864 | chrX:13001713-13003980 | CD3 | SE_14440 | chrX:13002315-13004022 | CD4_Memory_Primary_7pool | SE_15419 | chrX:13002153-13003939 | CD4_Memory_Primary_8pool | SE_15857 | chrX:13002125-13004273 | CD4_Naive_Primary_7pool | SE_16331 | chrX:13002047-13004066 | CD4_Naive_Primary_8pool | SE_16908 | chrX:13003109-13003778 | CD4p_CD225int_CD127p_Tmem | SE_17382 | chrX:12984499-13005297 | CD4p_CD25-_CD45RAp_Naive | SE_17855 | chrX:12999184-13004354 | CD4p_CD25-_CD45ROp_Memory | SE_18339 | chrX:12984154-13005741 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19260 | chrX:13002067-13004118 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20114 | chrX:13002378-13003986 | CD56 | SE_20864 | chrX:13002839-13003872 | CD8_Memory_7pool | SE_21563 | chrX:13002429-13004056 | CD8_Naive_7pool | SE_21967 | chrX:13002172-13004182 | CD8_Naive_8pool | SE_22410 | chrX:13002195-13004199 | CD8_primiary | SE_25447 | chrX:13001225-13004218 | DND41 | SE_28103 | chrX:13002326-13004084 | Fetal_Intestine | SE_29081 | chrX:13002246-13004220 | Fetal_Intestine_Large | SE_30940 | chrX:13002725-13003803 | Fetal_Thymus | SE_31989 | chrX:13002645-13004135 | Gastric | SE_32462 | chrX:13001645-13005810 | GM12878 | SE_38726 | chrX:13002477-13004145 | HUVEC | SE_49904 | chrX:12999012-13003870 | RPMI-8402 | SE_50189 | chrX:13002556-13003781 | Sigmoid_Colon | SE_52563 | chrX:13002534-13003726 | Small_Intestine | SE_58417 | chrX:12964783-13034394 | Ly1 | SE_58905 | chrX:12964721-13049077 | Ly3 | SE_62231 | chrX:12964510-13049336 | 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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Enhancer Sequence | TATAACCCTG AATTTGTCAT TTCAAATATC ATTGATAACT TGAGCTAGGA AGGTGAGAGC 60 ACCGTGAGTT CATATATGCA AATGTAAATT CTCAAAGCCA TACGTGCATG CCTAAGGCAT 120 TCCTCTAAGG TTCCACTGAC TTTCTCTGTA TAAGCTCCGT GTTATAACAG GTGTATAAAT 180 ATACATGCAA CATGCATCGA GAACAAACAT ATTGGCATCT AATGTTTGGA ACCTTCCGCC 240 TATCAGGGCT TCTTTTCTGA AATAAGTCAT GAAGTTTCCC AACAGGAGAG ATGGATACCA 300 AAAATAAAAT CCATTTAAGT CCTCAACCCA TTCAAATAAT AAATCCTTCA GATTAGAAAG 360 AGGTGAGGTC AATTGAATCT AACATAGACA TTAAGAACTA TCTGCCCCAA AGAAGGCTAC 420 TCCACACTTT TGACCATATT CCTTTGAAAC AGGGAGGATT CATGTTCTCT CTCCTCTCCT 480 GGAAGCTGAC AGATACCCAT GTATGATGTT GACATTTATG TATGTCTAGA ATGCCTAAGG 540 CATTTGGCTT GGCCAAGGCC GGTTGTGACT TGGCCCCCTG CCACCATTCT TTGTACCACA 600 GGTGTTTCCA AGTAGGATCT CATTCGAGTT GGGAGGGTGA GTTAGGGCTT TAGACCACAG 660 GAGCAGCTGA GGGAAAACTG TAAGGGGCCA GGCTTAGCCA AGAAAAGAAG GCTGAGAAAG 720 ATCCAAACCA GACAGCTGGC TACCATTCTA ACCTCTATCC CCACCCCAGC GCTACCACAC 780 TTCAGGCCAC ACCCTACCCA GAGTGTGGTT TTCAAACCAC AGGCTGTGTC GTAGGAAATC 840 AATTTATTGA TTCTTGCCAG CATTGAAAAC AAAAATTAAA AAAAAAAAAA GACAAAATAA 900 ATCACTAAAA AGAAATCAAG CAAGAATTTT CAGAACTCCC CAGCATGGTA AGGGTAACTA 960 TTGTTTATCA AACTTCTGTT TGAGTTATTT ATGAGGGGGA GAGATGACTG ATCTGTGATG 1020 TACAATGTTT CTTTCAGTGT GAGTCAGACT CACACTTGTC AAGACTTCCA TCCCCCAGCC 1080 TCCTGCCTGC TTATGGCCTC AATTCCTTTC TTTTCTCTGT CTAGCTTCGA CTCCTAATCA 1140 CTCACTTCAG ATTGATTTTA AACCCTTTCC TCCCCATGTC CAGCTGAAGT CTTCCTTCAT 1200 GCCCCAGTCC TGAATCCACT CCAAGAACCT GTTTGCCATT TTTTCACCCA GGCTCCCAAG 1260 TACTAACAGA TAAAATATAC ACTTTGCCAT GCTGTCACCT CAAAATTTGT CACTTGTTCC 1320 TGGTCAACTT ACTATTAGCT GTGCCACCTT CAGAAACTTC GTAACTTCTA TGAGCTTCAC 1380 TCTTCTCACC TGCCTAATGT GGAAGGGGAT GGCCATGACA CATGGGGTTG CTGTGAGAGT 1440 TGAAGGAAAT ATGTACATTG TAGGTGCTCA GTATATGGTC TCCTTTATTA TTACAACAGC 1500 CTCTTAGTTC ACAAATCAAT GCACTATTAT TACATGAAAT ACTTCTTGAC CTCTTTGTAG 1560 CCTTGTGTGT 1570
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