| Tag | Content |
|---|
EnhancerAtlas ID | HS041-02523 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:206748120-206750420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr1:206749069-206749080 | ACAGATAAGGA | - | 6.14 |
|
| | Number of super-enhancer constituents: 28 | 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 | chr1:206746090-206750296 | CD3 | | SE_14503 | chr1:206746009-206758997 | CD4_Memory_Primary_7pool | | SE_16490 | chr1:206747976-206750712 | 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 | chr1:206746359-206750220 | DND41 | | SE_27304 | chr1:206748233-206749980 | Esophagus | | SE_31229 | chr1:206747597-206750097 | Fetal_Thymus | | SE_39708 | chr1:206748495-206749981 | Jurkat | | SE_50667 | chr1:206747343-206754765 | Sigmoid_Colon | | SE_53261 | chr1:206746644-206756568 | Small_Intestine | | SE_53552 | chr1:206746429-206757806 | Spleen | | SE_55221 | chr1:206748265-206748685 | Thymus | | SE_55221 | chr1:206748689-206750305 | Thymus | | SE_59167 | chr1:206727342-206757447 | Ly3 | | SE_62534 | chr1:206724532-206763666 | Tonsil | | SE_65624 | chr1:206748409-206749787 | Pancreatic_islets | | SE_66615 | chr1:206748495-206749981 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 206748926 | 206749451 | | chr1 | 206748306 | 206750240 | | chr1 | 206748515 | 206748888 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I206573 | chr1 | 206746529 | 206757654 |
|
Enhancer Sequence | AAGGCCCCAT AGGGATTCCT CTTTCTCATT TGGTTGAGAC CATCACAAAG GGACCAATGA 60
CTTTTTTTTT TTTTTTTTTT TTTTGAGATG GAGTCTCGCT CTGTCATCCA GGCTGGAGTG 120
CAGTGGCGCA ATCTTGGCTC AATGCAACCT CTGCCTCCCA GGTTCAAGCG ATTCTTCCGC 180
CTTAGCCTCC CGAGTAGTTG GGATTACAGG CGCACGGATA ATTTTTTTGT TTTTGTTTTT 240
GTTTTTTTTT TTAGAAGAGA CAGGGTTTCA TTATGTTGCC CAGGCTGGTC TTGAACTCCT 300
AACCTCACCT TTGAATGCGG TTTGGACATT GAGCAGGGTA TTTCAAATCC AGCCCAGATA 360
GATGGGTGTC TGCCCCTTGC CTGCAGACGT TCCCATCTAG GGCAAGCACA ACAGAAGCAC 420
CGGGTGTTTG GGGTGTGGAA GGCAGCTGCA GATGGACATT CTCCTGTAGG AGGGGCCTGA 480
GGCTTTCCTC CCTGACTTAA GCCTGGAGAT GGCTTCCTTC CAAGGGGTGA AAGAATTGCT 540
GCTGACAGAT TTGCTAAGAG CTGAGAAAGA GGAAATGTGG CAAAGGCTCA TGGTGAATGG 600
CTTCCGGGGT ATTTTTTGTT TTGTTTTCTT GAGTTGTGTG TGTTAAGAAT GCGTAGACCG 660
GCTTGGGCTT GGCTAAGATA GAGTCTTGCT GACAATAGAG AAAAGTGGTG AGCAGTGAAA 720
AAGTAAAGTC GTGGCGGTTA GAAATGTTCT TTGTGCTCCT TTAGATTGGT TATTCCTGCT 780
GCCATTCAGC CATGCTAGCT AGCCTCCAAG AGGCCCCCAT CTCCACACCC AATTCTCTGA 840
AATAGAAGAG GAAGCAATGA TGAGAAAAAA ACACCACCCT ATCTTATGTG TAAAATCTTA 900
GTCCTGCGAA GGGGCCCTTA GAGCTTCTCC AGTATCACTT CATGATTTCA CAGATAAGGA 960
AACTGAGGCC CTGAGAGGGG AAGTAGCTCC CCAGACGTCA CAGGTCATTT GATGGTCTTG 1020
CATTTGTTCT CATCAGCTAG CTGCCAAGAG CTGAGCCACA CGGCTAACGC CAAAGTCCAA 1080
AGCCTGGTGT GTGTTCTTGG TATCAGACCC TCAGGGTGCA GCTGAGTGTG AGGTGCTCCT 1140
GGACCTAGGG GTCTGGGGTG GGCTCTGGCC TGAGACTCCC CAGGCTGTCT TGCCCTCCCC 1200
TGCCACCCAA TCAACAGGTA TTTATCTGAC ACCTACTTAA AGTTTGGCCC AGGTTTCAGC 1260
CAAGCGGGGT GCCAAAAAGC TTAGGCACCA AACTAATGTC TGCCTCCATC CAGAGAGCAT 1320
CTCACTGGGG AGATGGGATT AACATGTGAA ACAATCATTA AACAATAAAA GGCAGCATAT 1380
AATTAGATGC CAGCTGTAGC CACACAGGCT CTGAAATCAC CTCTATAGGC TCTTGCAGTA 1440
TGGATTTAAC ATTAGCCAGC AGCTGCAGAG ATCTGTGACG ATGGTAATTT GTACTTTTGC 1500
TGCAATGGGA ATCTGAGGCT TTGAGGCCAT GGGGCTGGTG TTTGGGAGCG AGTCACAGAA 1560
CCAGGGAGTG AGCCTAGCTG TCTACCTCCA TCCCTACCCC AGCCAGCTTT GTTGCCTCCT 1620
CATTGCAGAA TGGAGTAAAG TGAGCAAAAT CCAAGGAAGT GCCCAAGCCT TTGTCTTCTT 1680
GTGAAAAGTG TCCATGAAAT GAGAGTGAAG TTACAAAGGC CCATTAACTG GTGGTGTGAG 1740
GAAATACACA GGAAACATAG GAAGTATGAT TCAGGAGAAA GAGAGACCAG GACAAAACTG 1800
TGATTACCTT TCTCCATGTG GGAATCAAAA TGCCAGGGAT CTGGTACATT AAGAGAGCAG 1860
AGGATGGAGA GATGGCTATA GACTGGAGAA ATTGCATTGG GAAACTACAT AGAGAAGGTG 1920
GAACTAGGGC TAATAGTGTT CTAGGCAGGA GACTCTGCAC AAACAACAGC ATAGAGCAAA 1980
CTACTGCACA TGGCCAGGTT CCATAAATAA AGTTTGTTTT GTTTTTGAGA CAGGGTCTTG 2040
CTCTGTCACC TAGGCTGGAG TGCAGTGGCA CAATCACGGC TCACTGCAGC CTTGAACTCC 2100
TGGGGGCTCA GGTCATTCTC CCACCTCAGC CTCCTGAGTA GCTGGCACTA CAGGTGCACT 2160
TCACTGTGCC CAGCTAATTT TTGTATTTTT TTTTTTTTTG TAGAGACAGG GTCTCACTAT 2220
GTTGCCCAGA CTGGTCTCGA ACTCCTGGGC TCAAGCGATC ATCCTGCCTT GGCCTCTCAA 2280
AGTGCTGGGA TTGTAGGTGT 2300
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