| Tag | Content |
|---|
EnhancerAtlas ID | HS047-02933 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:206748510-206749900 |
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 | TCCCATCTAG GGCAAGCACA ACAGAAGCAC CGGGTGTTTG GGGTGTGGAA GGCAGCTGCA 60
GATGGACATT CTCCTGTAGG AGGGGCCTGA GGCTTTCCTC CCTGACTTAA GCCTGGAGAT 120
GGCTTCCTTC CAAGGGGTGA AAGAATTGCT GCTGACAGAT TTGCTAAGAG CTGAGAAAGA 180
GGAAATGTGG CAAAGGCTCA TGGTGAATGG CTTCCGGGGT ATTTTTTGTT TTGTTTTCTT 240
GAGTTGTGTG TGTTAAGAAT GCGTAGACCG GCTTGGGCTT GGCTAAGATA GAGTCTTGCT 300
GACAATAGAG AAAAGTGGTG AGCAGTGAAA AAGTAAAGTC GTGGCGGTTA GAAATGTTCT 360
TTGTGCTCCT TTAGATTGGT TATTCCTGCT GCCATTCAGC CATGCTAGCT AGCCTCCAAG 420
AGGCCCCCAT CTCCACACCC AATTCTCTGA AATAGAAGAG GAAGCAATGA TGAGAAAAAA 480
ACACCACCCT ATCTTATGTG TAAAATCTTA GTCCTGCGAA GGGGCCCTTA GAGCTTCTCC 540
AGTATCACTT CATGATTTCA CAGATAAGGA AACTGAGGCC CTGAGAGGGG AAGTAGCTCC 600
CCAGACGTCA CAGGTCATTT GATGGTCTTG CATTTGTTCT CATCAGCTAG CTGCCAAGAG 660
CTGAGCCACA CGGCTAACGC CAAAGTCCAA AGCCTGGTGT GTGTTCTTGG TATCAGACCC 720
TCAGGGTGCA GCTGAGTGTG AGGTGCTCCT GGACCTAGGG GTCTGGGGTG GGCTCTGGCC 780
TGAGACTCCC CAGGCTGTCT TGCCCTCCCC TGCCACCCAA TCAACAGGTA TTTATCTGAC 840
ACCTACTTAA AGTTTGGCCC AGGTTTCAGC CAAGCGGGGT GCCAAAAAGC TTAGGCACCA 900
AACTAATGTC TGCCTCCATC CAGAGAGCAT CTCACTGGGG AGATGGGATT AACATGTGAA 960
ACAATCATTA AACAATAAAA GGCAGCATAT AATTAGATGC CAGCTGTAGC CACACAGGCT 1020
CTGAAATCAC CTCTATAGGC TCTTGCAGTA TGGATTTAAC ATTAGCCAGC AGCTGCAGAG 1080
ATCTGTGACG ATGGTAATTT GTACTTTTGC TGCAATGGGA ATCTGAGGCT TTGAGGCCAT 1140
GGGGCTGGTG TTTGGGAGCG AGTCACAGAA CCAGGGAGTG AGCCTAGCTG TCTACCTCCA 1200
TCCCTACCCC AGCCAGCTTT GTTGCCTCCT CATTGCAGAA TGGAGTAAAG TGAGCAAAAT 1260
CCAAGGAAGT GCCCAAGCCT TTGTCTTCTT GTGAAAAGTG TCCATGAAAT GAGAGTGAAG 1320
TTACAAAGGC CCATTAACTG GTGGTGTGAG GAAATACACA GGAAACATAG GAAGTATGAT 1380
TCAGGAGAAA 1390
|
