Tag | Content |
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EnhancerAtlas ID | HS187-03213 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr10:43912860-43914590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr10:43913162-43913174 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr10:43913162-43913174 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr10:43913160-43913175 | CTACTAAAAATAGAA | + | 6.57 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_09734 | chr10:43912641-43917359 | CD14 | SE_10623 | chr10:43912638-43914246 | CD19_Primary | SE_11214 | chr10:43912353-43917550 | CD20 | SE_12056 | chr10:43913205-43914045 | CD3 | SE_13492 | chr10:43912282-43914892 | CD34_Primary_RO01536 | SE_14443 | chr10:43912394-43914909 | CD4_Memory_Primary_7pool | SE_16431 | chr10:43913186-43914135 | CD4_Naive_Primary_8pool | SE_17415 | chr10:43913090-43914701 | CD4p_CD25-_CD45RAp_Naive | SE_17860 | chr10:43912840-43914763 | CD4p_CD25-_CD45ROp_Memory | SE_18657 | chr10:43913105-43914472 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19328 | chr10:43913319-43914177 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20103 | chr10:43912381-43914849 | CD56 | SE_20790 | chr10:43912421-43914846 | CD8_Memory_7pool | SE_22430 | chr10:43912466-43914826 | CD8_primiary | SE_31584 | chr10:43913415-43914052 | Gastric | SE_34525 | chr10:43913256-43914208 | HCT-116 | SE_35537 | chr10:43913177-43914585 | HepG2 | SE_39974 | chr10:43912333-43913374 | K562 | SE_39974 | chr10:43913481-43914689 | K562 | SE_42749 | chr10:43913453-43914065 | Lung | SE_50654 | chr10:43913269-43914199 | Sigmoid_Colon | SE_52516 | chr10:43913361-43914041 | Small_Intestine | SE_53392 | chr10:43912598-43914661 | Spleen | SE_55568 | chr10:43913511-43913934 | Thymus | SE_60870 | chr10:43890659-43924046 | DHL6 | SE_61921 | chr10:43875798-43952058 | Toledo | SE_62633 | chr10:43890313-43917519 | Tonsil | SE_66483 | chr10:43913295-43914480 | Jurkat | SE_68378 | chr10:43890703-43916925 | TC32 | SE_68633 | chr10:43891049-43916828 | TC71 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 43913618 | 43913796 | chr10 | 43912989 | 43914489 |
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Enhancer Sequence | TAGAAATGAT CCCTGAAAGC CGCCTAATTT TTGAATGATA AAATATTTCT AAATTGGTCA 60 GGCACAGTGG CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCTGAGGAGG GTGAATCACC 120 TAAGGTCAGG AGTTTGAGAC CAGCCTGGCC AACATGACGA AACCCCTTCT CTACTAAAAA 180 TACAGGCCGG GTGCGGTGGC TCACGCCTGT AATCCCAGCA CTATGGGAGG CTTGAGGCAG 240 GTGGATCACC TGAGGTTAGG AGATCAAGAC CAGCCTGGCC AACATAGTGA AACCCGGTGT 300 CTACTAAAAA TAGAAAAATC AGCTGGGCGT GGTGGCACAC ATCTGTAATC CCACCTACTC 360 GGGAGGCTGA GGCAGAAGAA TTGCTTGAAC CCAGAAGGTG GAGTTTGCAG TGAGCCGAGA 420 TGGCTCTACT GCACTCCAGC CTGAGCCACA GAGCGAGACT CCTTCTCAAA AAAAAAAAAA 480 AAAAAAAAAA CAACAAAAAA CCTGAAGATA ACTTTATATA GTCAGTGGGG AGTATTGAAG 540 TTTCAGGATC AGAGATTTAA TAAAATTTGT GGCCCTTTAG GTAAATATCT TTAAAGAATA 600 TTGTTTCAGG CAACGTAGTT TGTGTGTGGG TGTGTGCTGT CTTGACTTAG ATTTTAGGCT 660 CTGGCTAAAA GCCAGTTAGT TCCTCTTCTT GAGCTGCCGA TTATGTCTGC ACCCCCAACC 720 ACCTCTGTTA TCAGGCTCAA ACACTCGGGA CCATTATACA CCGTAATCAC TCCAGGGCCA 780 GTTACCAGAC AACTAGGGCC AGCCCCATGC CCCTGAGCCC CCGGAAATTA CTCAAATTAG 840 CCAATCCCAA ACCTGTTGGC CTTGCCTAAC CCTTCTCTTC CTGCAAAAAC CACAACAAAG 900 GCTCTTCTGC AGTTCCCCCC TCACTCCCTC TGCCTAGTGA CCCCTTCTGC TCCTGCTGAG 960 TGGCCTTGTG TGAAGCCCCA GGGAAATGAG AGTACAAAAC TAAAACTTGG GCCAACGTGG 1020 TGGCTCACGC TTGTAATCCC AGCACTTTGG GAGGCAGAAG CAGGCAATCA CTTGAGGCCA 1080 AGAGTTCAAG ACCAGCCTGG CCAACATGGT GAAACCCTGG CTCTACTAAA AATACAAAAA 1140 TTAGCTGGGC ATAGTGGCGC GCACGCCTGT AGTCCCAGGT ACTCGGGAGG CTGAGGAGGG 1200 AGAATCGCTT GAAACCGGGA GGTGGAGGAG CAACCTCCTC TGGGAGGCTG GAGCTCCACT 1260 ACTCTCCAGC CTGGGTGACG GAGTAAAAGA CTGTCTCAAA CAAAAAACAA AAACAAAAAC 1320 TGTAAAACTG GTTTGTAACT CCTGTGCTGC ATCTAATCTC ACCATACCTC ACCCAAGGTA 1380 AACTGTTTTG TTTGTGTTTT TGTGTTTGAG ACAGAGTCTG GCTCTGTTAC CCAGGCTGGA 1440 GTGCAGTGGC TCGATCTTGG CTCACTGCAG CCTCCACCTC CTAGATTTAA GCAATTCTCC 1500 CGCCTCAATC TCCCAAGTAG CTAGGATTAC AAGCATGTGC CACCAAGCCC AACTAATCCT 1560 TGTATTGTTA GTAAAGATGG GGTTCCACCA TTGGTTGGCC AGGCTGGTCT CAAACTCCTG 1620 ACCTCAAGTG ATCCACCTGC CTCAGACCCC CAAAGTGCTG GGATTACAGG CATGAGCCAC 1680 CGTGCCTGGC CAAATCTGAG CTTTTTATAA AATCTTCATC ATAATGGTTC 1730
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