Tag | Content |
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EnhancerAtlas ID | HS098-04765 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:206752680-206754340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:206754168-206754186 | CCTTCCTTCCCACCTTCA | - | 6.75 | HSF1 | MA0486.2 | chr1:206753661-206753674 | GAAGCTTCTAGAA | - | 6.28 | HSF1 | MA0486.2 | chr1:206753666-206753679 | TTCTAGAATTTTC | + | 6.71 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_09327 | chr1:206745188-206758382 | CD14 | SE_10603 | chr1:206747310-206756416 | CD19_Primary | SE_11004 | chr1:206727079-206757887 | CD20 | SE_11917 | chr1:206750311-206757762 | CD3 | SE_14503 | chr1:206746009-206758997 | CD4_Memory_Primary_7pool | SE_16490 | chr1:206750757-206757114 | CD4_Naive_Primary_8pool | SE_16959 | chr1:206748089-206757504 | CD4p_CD225int_CD127p_Tmem | SE_17411 | chr1:206724289-206760065 | CD4p_CD25-_CD45RAp_Naive | SE_17843 | chr1:206723887-206758306 | CD4p_CD25-_CD45ROp_Memory | SE_18269 | chr1:206723684-206769868 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19128 | chr1:206746389-206766399 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20034 | chr1:206746357-206757932 | CD56 | SE_20823 | chr1:206746904-206757454 | CD8_Memory_7pool | SE_22080 | chr1:206746077-206757652 | CD8_Naive_8pool | SE_22390 | chr1:206744356-206757869 | CD8_primiary | SE_25703 | chr1:206752909-206754508 | DND41 | SE_27304 | chr1:206752644-206753579 | Esophagus | SE_27304 | chr1:206753679-206754504 | Esophagus | SE_31229 | chr1:206751813-206754781 | Fetal_Thymus | SE_39708 | chr1:206752855-206753614 | Jurkat | SE_39708 | chr1:206753678-206754514 | Jurkat | SE_50667 | chr1:206747343-206754765 | Sigmoid_Colon | SE_53261 | chr1:206746644-206756568 | Small_Intestine | SE_53552 | chr1:206746429-206757806 | Spleen | SE_55221 | chr1:206752840-206754343 | Thymus | SE_59167 | chr1:206727342-206757447 | Ly3 | SE_62534 | chr1:206724532-206763666 | Tonsil | SE_65624 | chr1:206752745-206755870 | Pancreatic_islets | SE_66615 | chr1:206752855-206753614 | Jurkat | SE_66615 | chr1:206753678-206754514 | Jurkat |
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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 |
GH01I206573 | chr1 | 206746529 | 206757654 |
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Enhancer Sequence | CTTGGGCCAC CCCAAGAGGC AAAACTGTCT GCTTGGTTTC TCGCTTTGTA CCCGTGGACA 60 GATCCTTAAG AATCTGGCAG GTGAATAGGA ATCAGAGTCT TTGTCTTATC CTCTGAAGAT 120 TGCTATAGTA TCGATCTCGC TCTCATGGCA GATAGTGCCT GTTAGGTAAA CCTTTGGGGT 180 GTTTGTGTGT TTCTTGGCAC CAAGTGTTAA TTCAGCAGCT GGATGAAGAC CCTTGAGGTC 240 TGGAATTGTT GTGAGGGGTC TGTCTATTTC AGTTCTTTTC GAATGTTGCT GCGAATTAAA 300 ATCAACTAGG AGATTTTTAA AATTCCCATG CCCAGACTGC ACCCCAGACC AATTAAATCA 360 GAATCTCCAG GGATGAAGCC CAGGCAGCTA AGTTTCTAAA GATCCCCCAG ATGATTGCAC 420 TGTGCAGACA AGTTTAAGAA CCACTGGTCT GGATTATACG CCATCTCTTG GGTGGAAAAA 480 GGATCCGTGA GCCCTCGTGG CTGTGGCTGG CTGGCCTAAT TCAGGAGGTG ATTCATTTGG 540 TCCATGGGTC ACATCTTGTC TGCCAGATAT TTTTGTGGGC AGCAGCCATC CCAGACCTGG 600 GTGCTGGCAT TCCATGGCTG TGACATTCGT AGTGTTGGCT ACACACGGGG CTCCTGGCAC 660 TCCCAGACAG GGCTTCCCAT CACCAGCCAG AGGGCCAGGC CTCAGAATGG TGAGGTCAGG 720 GCTGCTGTCT TTTGAGTCAG CCCTGGAAGG CAGAGGTGCC TGTGGCCACT TGCGTCACTT 780 CCCCGCGTTT GTGGTGGGAA GGGGAGAGAT AGATGGGTCT ATCTGCTGAA GAAAGGGGAA 840 CAGGAAGAAG AAACCCTAGG CTAAGGCAGC TTTGCTTCTC ACTGTATTCA AAATCAAGCC 900 TTTGAAAGCC ACAGCACAGC TGCCTTTTCT TACGGGGAAA TGGCTCTAGC TTGATTGGAA 960 ACTATGAGAG GAGATCTTTC CGAAGCTTCT AGAATTTTCT TTCCATTACT TATTTTTTAT 1020 AGACAAGTAT GAGAAAGCTA TTACCTCCTG AGGAGCAATA GCCTACATGC GTCAGAGACA 1080 GAGTGAGTGT ATAATAGTAA CCAGACAACG GGGTCTTTCT AATTAGAAGC TCCCAGCGGG 1140 AAGGTATAGG GGTAGGGCCA GGGTCAGGCA CATCTGGTCC CATAGACATG TGCTCAGCTG 1200 GCAAGGACTG AGGATGGGGA GCTCTGGGAG CTACCCAAGG GAAGGGATGA GGAAAATGAG 1260 AGGCTTCACT GTGAGAGTCC CCGGGTTAAT GGACTGACAG TGAATGAAGA GAGTCTGTGA 1320 GGCTCACACT ACTTGCTACT CACCTCCGGC AAGTGGGAGA TGGCCAGAGC TGCTTGCCCT 1380 TGGGTGGTCT GCAACAGAAT CAAGGTTCAG TTCCAGAGAC CTGGGAAGGC ACACAGGAGA 1440 AGGCTGGGCC CTGCATCCTG GTGGCTGCAT CTCACTTGAG TTAGAAGTCC TTCCTTCCCA 1500 CCTTCACAGG TGACATGGTG CCTCTGGGGC CTGACCCGCT GCTTAGACTC ATCTTAGATG 1560 AACATTTCAC AGATCAGGTA ACTTACAGGC TTTGGTTTAA CAGCTGCTCA TCCCAGCCCC 1620 GCAGCACAGA GTTTCAGTGA TCATTATGGG TGTGGCAGGC 1660
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