| Tag | Content |
|---|
EnhancerAtlas ID | HS175-02709 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr1:206748450-206749520 |
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 | GAGCAGGGTA TTTCAAATCC AGCCCAGATA GATGGGTGTC TGCCCCTTGC CTGCAGACGT 60
TCCCATCTAG GGCAAGCACA ACAGAAGCAC CGGGTGTTTG GGGTGTGGAA GGCAGCTGCA 120
GATGGACATT CTCCTGTAGG AGGGGCCTGA GGCTTTCCTC CCTGACTTAA GCCTGGAGAT 180
GGCTTCCTTC CAAGGGGTGA AAGAATTGCT GCTGACAGAT TTGCTAAGAG CTGAGAAAGA 240
GGAAATGTGG CAAAGGCTCA TGGTGAATGG CTTCCGGGGT ATTTTTTGTT TTGTTTTCTT 300
GAGTTGTGTG TGTTAAGAAT GCGTAGACCG GCTTGGGCTT GGCTAAGATA GAGTCTTGCT 360
GACAATAGAG AAAAGTGGTG AGCAGTGAAA AAGTAAAGTC GTGGCGGTTA GAAATGTTCT 420
TTGTGCTCCT TTAGATTGGT TATTCCTGCT GCCATTCAGC CATGCTAGCT AGCCTCCAAG 480
AGGCCCCCAT CTCCACACCC AATTCTCTGA AATAGAAGAG GAAGCAATGA TGAGAAAAAA 540
ACACCACCCT ATCTTATGTG TAAAATCTTA GTCCTGCGAA GGGGCCCTTA GAGCTTCTCC 600
AGTATCACTT CATGATTTCA CAGATAAGGA AACTGAGGCC CTGAGAGGGG AAGTAGCTCC 660
CCAGACGTCA CAGGTCATTT GATGGTCTTG CATTTGTTCT CATCAGCTAG CTGCCAAGAG 720
CTGAGCCACA CGGCTAACGC CAAAGTCCAA AGCCTGGTGT GTGTTCTTGG TATCAGACCC 780
TCAGGGTGCA GCTGAGTGTG AGGTGCTCCT GGACCTAGGG GTCTGGGGTG GGCTCTGGCC 840
TGAGACTCCC CAGGCTGTCT TGCCCTCCCC TGCCACCCAA TCAACAGGTA TTTATCTGAC 900
ACCTACTTAA AGTTTGGCCC AGGTTTCAGC CAAGCGGGGT GCCAAAAAGC TTAGGCACCA 960
AACTAATGTC TGCCTCCATC CAGAGAGCAT CTCACTGGGG AGATGGGATT AACATGTGAA 1020
ACAATCATTA AACAATAAAA GGCAGCATAT AATTAGATGC CAGCTGTAGC 1070
|
