| Tag | Content |
|---|
EnhancerAtlas ID | HS045-05148 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:206748060-206749930 |
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: 2 | Chromosome | Start | End |
| chr1 | 206748926 | 206749451 | | chr1 | 206748515 | 206748888 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I206573 | chr1 | 206746529 | 206757654 |
|
Enhancer Sequence | GGTCTGTGGA GTCCATTTCA GAACACAGGC CTTCGAAGAC CTGGGAGGGG GCCCTGCAGT 60
AAGGCCCCAT AGGGATTCCT CTTTCTCATT TGGTTGAGAC CATCACAAAG GGACCAATGA 120
CTTTTTTTTT TTTTTTTTTT TTTTGAGATG GAGTCTCGCT CTGTCATCCA GGCTGGAGTG 180
CAGTGGCGCA ATCTTGGCTC AATGCAACCT CTGCCTCCCA GGTTCAAGCG ATTCTTCCGC 240
CTTAGCCTCC CGAGTAGTTG GGATTACAGG CGCACGGATA ATTTTTTTGT TTTTGTTTTT 300
GTTTTTTTTT TTAGAAGAGA CAGGGTTTCA TTATGTTGCC CAGGCTGGTC TTGAACTCCT 360
AACCTCACCT TTGAATGCGG TTTGGACATT GAGCAGGGTA TTTCAAATCC AGCCCAGATA 420
GATGGGTGTC TGCCCCTTGC CTGCAGACGT TCCCATCTAG GGCAAGCACA ACAGAAGCAC 480
CGGGTGTTTG GGGTGTGGAA GGCAGCTGCA GATGGACATT CTCCTGTAGG AGGGGCCTGA 540
GGCTTTCCTC CCTGACTTAA GCCTGGAGAT GGCTTCCTTC CAAGGGGTGA AAGAATTGCT 600
GCTGACAGAT TTGCTAAGAG CTGAGAAAGA GGAAATGTGG CAAAGGCTCA TGGTGAATGG 660
CTTCCGGGGT ATTTTTTGTT TTGTTTTCTT GAGTTGTGTG TGTTAAGAAT GCGTAGACCG 720
GCTTGGGCTT GGCTAAGATA GAGTCTTGCT GACAATAGAG AAAAGTGGTG AGCAGTGAAA 780
AAGTAAAGTC GTGGCGGTTA GAAATGTTCT TTGTGCTCCT TTAGATTGGT TATTCCTGCT 840
GCCATTCAGC CATGCTAGCT AGCCTCCAAG AGGCCCCCAT CTCCACACCC AATTCTCTGA 900
AATAGAAGAG GAAGCAATGA TGAGAAAAAA ACACCACCCT ATCTTATGTG TAAAATCTTA 960
GTCCTGCGAA GGGGCCCTTA GAGCTTCTCC AGTATCACTT CATGATTTCA CAGATAAGGA 1020
AACTGAGGCC CTGAGAGGGG AAGTAGCTCC CCAGACGTCA CAGGTCATTT GATGGTCTTG 1080
CATTTGTTCT CATCAGCTAG CTGCCAAGAG CTGAGCCACA CGGCTAACGC CAAAGTCCAA 1140
AGCCTGGTGT GTGTTCTTGG TATCAGACCC TCAGGGTGCA GCTGAGTGTG AGGTGCTCCT 1200
GGACCTAGGG GTCTGGGGTG GGCTCTGGCC TGAGACTCCC CAGGCTGTCT TGCCCTCCCC 1260
TGCCACCCAA TCAACAGGTA TTTATCTGAC ACCTACTTAA AGTTTGGCCC AGGTTTCAGC 1320
CAAGCGGGGT GCCAAAAAGC TTAGGCACCA AACTAATGTC TGCCTCCATC CAGAGAGCAT 1380
CTCACTGGGG AGATGGGATT AACATGTGAA ACAATCATTA AACAATAAAA GGCAGCATAT 1440
AATTAGATGC CAGCTGTAGC CACACAGGCT CTGAAATCAC CTCTATAGGC TCTTGCAGTA 1500
TGGATTTAAC ATTAGCCAGC AGCTGCAGAG ATCTGTGACG ATGGTAATTT GTACTTTTGC 1560
TGCAATGGGA ATCTGAGGCT TTGAGGCCAT GGGGCTGGTG TTTGGGAGCG AGTCACAGAA 1620
CCAGGGAGTG AGCCTAGCTG TCTACCTCCA TCCCTACCCC AGCCAGCTTT GTTGCCTCCT 1680
CATTGCAGAA TGGAGTAAAG TGAGCAAAAT CCAAGGAAGT GCCCAAGCCT TTGTCTTCTT 1740
GTGAAAAGTG TCCATGAAAT GAGAGTGAAG TTACAAAGGC CCATTAACTG GTGGTGTGAG 1800
GAAATACACA GGAAACATAG GAAGTATGAT TCAGGAGAAA GAGAGACCAG GACAAAACTG 1860
TGATTACCTT 1870
|
