| Tag | Content |
|---|
EnhancerAtlas ID | HS064-01237 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr1:206748260-206750310 |
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 | AATGCAACCT CTGCCTCCCA GGTTCAAGCG ATTCTTCCGC CTTAGCCTCC CGAGTAGTTG 60
GGATTACAGG CGCACGGATA ATTTTTTTGT TTTTGTTTTT GTTTTTTTTT TTAGAAGAGA 120
CAGGGTTTCA TTATGTTGCC CAGGCTGGTC TTGAACTCCT AACCTCACCT TTGAATGCGG 180
TTTGGACATT GAGCAGGGTA TTTCAAATCC AGCCCAGATA GATGGGTGTC TGCCCCTTGC 240
CTGCAGACGT TCCCATCTAG GGCAAGCACA ACAGAAGCAC CGGGTGTTTG GGGTGTGGAA 300
GGCAGCTGCA GATGGACATT CTCCTGTAGG AGGGGCCTGA GGCTTTCCTC CCTGACTTAA 360
GCCTGGAGAT GGCTTCCTTC CAAGGGGTGA AAGAATTGCT GCTGACAGAT TTGCTAAGAG 420
CTGAGAAAGA GGAAATGTGG CAAAGGCTCA TGGTGAATGG CTTCCGGGGT ATTTTTTGTT 480
TTGTTTTCTT GAGTTGTGTG TGTTAAGAAT GCGTAGACCG GCTTGGGCTT GGCTAAGATA 540
GAGTCTTGCT GACAATAGAG AAAAGTGGTG AGCAGTGAAA AAGTAAAGTC GTGGCGGTTA 600
GAAATGTTCT TTGTGCTCCT TTAGATTGGT TATTCCTGCT GCCATTCAGC CATGCTAGCT 660
AGCCTCCAAG AGGCCCCCAT CTCCACACCC AATTCTCTGA AATAGAAGAG GAAGCAATGA 720
TGAGAAAAAA ACACCACCCT ATCTTATGTG TAAAATCTTA GTCCTGCGAA GGGGCCCTTA 780
GAGCTTCTCC AGTATCACTT CATGATTTCA CAGATAAGGA AACTGAGGCC CTGAGAGGGG 840
AAGTAGCTCC CCAGACGTCA CAGGTCATTT GATGGTCTTG CATTTGTTCT CATCAGCTAG 900
CTGCCAAGAG CTGAGCCACA CGGCTAACGC CAAAGTCCAA AGCCTGGTGT GTGTTCTTGG 960
TATCAGACCC TCAGGGTGCA GCTGAGTGTG AGGTGCTCCT GGACCTAGGG GTCTGGGGTG 1020
GGCTCTGGCC TGAGACTCCC CAGGCTGTCT TGCCCTCCCC TGCCACCCAA TCAACAGGTA 1080
TTTATCTGAC ACCTACTTAA AGTTTGGCCC AGGTTTCAGC CAAGCGGGGT GCCAAAAAGC 1140
TTAGGCACCA AACTAATGTC TGCCTCCATC CAGAGAGCAT CTCACTGGGG AGATGGGATT 1200
AACATGTGAA ACAATCATTA AACAATAAAA GGCAGCATAT AATTAGATGC CAGCTGTAGC 1260
CACACAGGCT CTGAAATCAC CTCTATAGGC TCTTGCAGTA TGGATTTAAC ATTAGCCAGC 1320
AGCTGCAGAG ATCTGTGACG ATGGTAATTT GTACTTTTGC TGCAATGGGA ATCTGAGGCT 1380
TTGAGGCCAT GGGGCTGGTG TTTGGGAGCG AGTCACAGAA CCAGGGAGTG AGCCTAGCTG 1440
TCTACCTCCA TCCCTACCCC AGCCAGCTTT GTTGCCTCCT CATTGCAGAA TGGAGTAAAG 1500
TGAGCAAAAT CCAAGGAAGT GCCCAAGCCT TTGTCTTCTT GTGAAAAGTG TCCATGAAAT 1560
GAGAGTGAAG TTACAAAGGC CCATTAACTG GTGGTGTGAG GAAATACACA GGAAACATAG 1620
GAAGTATGAT TCAGGAGAAA GAGAGACCAG GACAAAACTG TGATTACCTT TCTCCATGTG 1680
GGAATCAAAA TGCCAGGGAT CTGGTACATT AAGAGAGCAG AGGATGGAGA GATGGCTATA 1740
GACTGGAGAA ATTGCATTGG GAAACTACAT AGAGAAGGTG GAACTAGGGC TAATAGTGTT 1800
CTAGGCAGGA GACTCTGCAC AAACAACAGC ATAGAGCAAA CTACTGCACA TGGCCAGGTT 1860
CCATAAATAA AGTTTGTTTT GTTTTTGAGA CAGGGTCTTG CTCTGTCACC TAGGCTGGAG 1920
TGCAGTGGCA CAATCACGGC TCACTGCAGC CTTGAACTCC TGGGGGCTCA GGTCATTCTC 1980
CCACCTCAGC CTCCTGAGTA GCTGGCACTA CAGGTGCACT TCACTGTGCC CAGCTAATTT 2040
TTGTATTTTT 2050
|
