Tag | Content |
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EnhancerAtlas ID | HS051-02678 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr10:3798710-3800990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr10:3800097-3800109 | TCTATTTATAGC | - | 6.62 | MEF2B | MA0660.1 | chr10:3800097-3800109 | TCTATTTATAGC | - | 6.52 | REL | MA0101.1 | chr10:3800613-3800623 | GGAAATCCCC | - | 6.02 | ZNF263 | MA0528.1 | chr10:3798726-3798747 | TCCTCCTCCTCTTCCTCCTCC | - | 11.79 | ZNF263 | MA0528.1 | chr10:3798729-3798750 | TCCTCCTCTTCCTCCTCCGCC | - | 6.64 | ZNF263 | MA0528.1 | chr10:3798762-3798783 | TCTTCCTCTTCTTCCTCTTCT | - | 6.72 | ZNF263 | MA0528.1 | chr10:3798735-3798756 | TCTTCCTCCTCCGCCGCCACC | - | 6 | ZNF263 | MA0528.1 | chr10:3800863-3800884 | CTTTCCTCTGCCTCCTCCTTC | - | 7.25 | ZNF263 | MA0528.1 | chr10:3798759-3798780 | TCTTCTTCCTCTTCTTCCTCT | - | 7.41 | ZNF263 | MA0528.1 | chr10:3800860-3800881 | TCCCTTTCCTCTGCCTCCTCC | - | 7.59 | ZNF263 | MA0528.1 | chr10:3798720-3798741 | TCTTCCTCCTCCTCCTCTTCC | - | 8.28 | ZNF263 | MA0528.1 | chr10:3798711-3798732 | TTCCTCTTCTCTTCCTCCTCC | - | 8.49 | ZNF263 | MA0528.1 | chr10:3798717-3798738 | TTCTCTTCCTCCTCCTCCTCT | - | 8.69 | ZNF263 | MA0528.1 | chr10:3798714-3798735 | CTCTTCTCTTCCTCCTCCTCC | - | 8.88 | ZNF263 | MA0528.1 | chr10:3798723-3798744 | TCCTCCTCCTCCTCTTCCTCC | - | 9.83 |
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| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_11200 | chr10:3798685-3804931 | CD20 | SE_11875 | chr10:3798779-3801509 | CD3 | SE_14379 | chr10:3799388-3801036 | CD4_Memory_Primary_7pool | SE_16288 | chr10:3799097-3801280 | CD4_Naive_Primary_8pool | SE_17806 | chr10:3798581-3801753 | CD4p_CD25-_CD45ROp_Memory | SE_18262 | chr10:3796480-3802324 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19173 | chr10:3797327-3802134 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20046 | chr10:3798736-3801374 | CD56 | SE_20738 | chr10:3798911-3801449 | CD8_Memory_7pool | SE_22385 | chr10:3798615-3801536 | CD8_primiary | SE_26609 | chr10:3799312-3801220 | Esophagus | SE_31554 | chr10:3799999-3800908 | Gastric | SE_35818 | chr10:3798751-3801211 | HMEC | SE_47115 | chr10:3796594-3801122 | Panc1 | SE_52398 | chr10:3799254-3801156 | Small_Intestine | SE_53372 | chr10:3799886-3801109 | Spleen | SE_62321 | chr10:3783568-3829344 | Tonsil | SE_64224 | chr10:3798877-3801326 | NHEK | SE_65716 | chr10:3799988-3800437 | Pancreatic_islets | SE_65716 | chr10:3800569-3801421 | Pancreatic_islets |
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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: 2 | ID | Chromosome | Start | End |
GH10I003756 | chr10 | 3798734 | 3798856 | GH10I003757 | chr10 | 3798893 | 3801187 |
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Enhancer Sequence | CTTCCTCTTC TCTTCCTCCT CCTCCTCTTC CTCCTCCGCC GCCACCGCTT CTTCTTCCTC 60 TTCTTCCTCT TCTTCTCTTA CTTCTTCCAT AAAGTTGAAG TCCCAGGTTG AGTGAATAAA 120 TGCTTTTTGT TCCTTTGAGA GGTTCCCCTA AAAAATGAAA ACAGAATTCT CTAACATCTT 180 GCATGAACAA AAGAACACCT ATTTACAAAA AAGCAAACAG CACATCCAGC ATGCTGCTAT 240 GCACCTCACT TCTAGGGTGC AAACTCTCAT AACTGTCCGA GGAGAAGCCA ATTCCCCTTC 300 ACAGGTGAGG GCCAGTGAGG TGCTTCCTCA GGTCTCTTGG TCTAAGGAGA ACAAGGCTGG 360 TCTTGACTTC CTTAAGGCAT AGCCATTTCC AACAGCGAAG CATATTGAAA AATTCTGGAG 420 TCAAGTTGGC TTTTCAAAAC CCACACCCCA AGAGAATGGC AAAAGAGAAA TCAGCTGCTG 480 CATTGCTGTT CAGTTTTGCT GTTATTGAAG CTATCTGTTT TAATTATTTC AATCAATGGT 540 GTTCTTATGT GTACTCTTTG GAACTTTAAG CAAATGGAAT AATGTAGAAA ATCCAATAAA 600 TAAGTAAAGG GAGATGAAGA ACAGAGAACA CTGTGTTTTT CAGGGAAAAG AACAATAGCA 660 GCAGTGGTGT CAACAGAGAC TCCTCTTCTC TGTGGCCTTG CTGGCTTGTG CTGCAGAGAT 720 ACTGGCTCAG TTCTCTTGGC CTTGTCACCT AAGGTCAACA CCAGTCTCTC TTCTGTTATT 780 TGGACTTCTT TAAGTAGCTA AAGGTCTCCC TGTGGCTGCT TAATTTCAGC CATCACTACA 840 GTGCTTCTGA GCGACATCAT GGTCCTACAG ATGTCACTTA TGTGTGTAAA CCACAGATCT 900 GCACCTGGGC AAACTGGTCC TCATGGAACC ACGTCTTGCC GAGACAACCC TACAAACAGG 960 AAACTCACCT GTGTTTATAA ACACCATCTT ACTTAGCGAT GGGTCAAGAT TCCCGGGCAG 1020 TCCTAGGAGC AAAGTCCCAG AGATTCCTGC ATCGTCGAAT CTTATTTGCC CTGAAAACAA 1080 CAAATTACAT TACTAAGTGA AGGGAATACA CTCAAATTAT CTCTAAAAGT GTAATTTGTC 1140 ATCATTAGCA GAAAAAGGTG ATTCAAAGAA ACATTGTAAA AATCACCCTA AGGACATCTT 1200 CTCGGAATCT TAGAGAACAA GATGACTCAC CTTTCCTGCC TTAACCAGCA ACCTGTCTGG 1260 GCCTTGCTCA GAGCTCATCT CGCACCAGAA CAGCCTCCCC GCTGCCTCCC TCTTCCTAGA 1320 GGCCATGCTG TTGCCATGTG GTTTAAATCA TAGCTGATGC CTATGCGGTC CTACCATGTC 1380 CAGAACTTCT ATTTATAGCG TCTCATGTAA TTTTTATTTA TTAGATAAGT GCAATAATCA 1440 CCGGATGAAA AGAGGCACAG ATGACCCTGT CCAGGAGCAA AGTGGTGGCA GGACTGGACC 1500 CATGCCAGGT CCCAGCCAGT CCGTTCCTCT CCGCATGGCC CAGCCGCTGG GCTCTGGAAG 1560 CTGCAGGCAG GGTCCCTTGC AAGCCGGTGG CCTCAGCCCC ATCTCTTTAC TTCTCTGCAA 1620 CTTGTTTTCT CTATGTGCAA GCTGTGACTA ATCACACCTC CCTTCAGGGG ATTTTCACAG 1680 GTTTCATAAG TGAAGTAAGT GCCTATTTTC TTTCTTTCCC TGTGTGTACC TTGTATACCA 1740 CAGATGGACA CGTGTCTAAA ATACCTATTT TGTCAGTCTT TTCCTCCAAC TCAGAAACAC 1800 CGAGAGCCCT CCCCAATCCC AGCATTTCTA TCAGGAAAAG GCTAACATGC CACCGGCAGC 1860 AAAGAGCTCA GTGTCACCAG ACATCATTTT GCAGATAAAG AAAGGAAATC CCCGGGTGGC 1920 TGAAAATCTC CCCAAGTATG GGCCCAGGGA CCTTGATGGG TCAGGTCTCA CTGCATCCTG 1980 TCCCACTCTG TCCCAGCAAA CTTTCTTCTC CAGTCAAAAC TGGTCTCACT CTCTGAGGAA 2040 CACCTGTGCC GACACTCAGG CACAGCCTAT GGGGAACACT GCTCCCTGCC CTCTCCCACC 2100 CAAATCAACA CACCTTCAAA GGAACAGAAC ACTTCTGCGC CTGGCAAGGC TCCCTTTCCT 2160 CTGCCTCCTC CTTCACAGAG ACTTTGGGAT TGTCCTCTGA TGACAGAGTG CCCTGCCTCC 2220 TGATGGAGTG ACGCTGGGAT TAGAGGTGGG ATGGAGGATG CCTGCTCACA CCTCCCAGAT 2280
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