| Tag | Content |
|---|
EnhancerAtlas ID | HS061-02006 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr1:206748410-206749850 |
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 | TTGAACTCCT AACCTCACCT TTGAATGCGG TTTGGACATT GAGCAGGGTA TTTCAAATCC 60
AGCCCAGATA GATGGGTGTC TGCCCCTTGC CTGCAGACGT TCCCATCTAG GGCAAGCACA 120
ACAGAAGCAC CGGGTGTTTG GGGTGTGGAA GGCAGCTGCA GATGGACATT CTCCTGTAGG 180
AGGGGCCTGA GGCTTTCCTC CCTGACTTAA GCCTGGAGAT GGCTTCCTTC CAAGGGGTGA 240
AAGAATTGCT GCTGACAGAT TTGCTAAGAG CTGAGAAAGA GGAAATGTGG CAAAGGCTCA 300
TGGTGAATGG CTTCCGGGGT ATTTTTTGTT TTGTTTTCTT GAGTTGTGTG TGTTAAGAAT 360
GCGTAGACCG GCTTGGGCTT GGCTAAGATA GAGTCTTGCT GACAATAGAG AAAAGTGGTG 420
AGCAGTGAAA AAGTAAAGTC GTGGCGGTTA GAAATGTTCT TTGTGCTCCT TTAGATTGGT 480
TATTCCTGCT GCCATTCAGC CATGCTAGCT AGCCTCCAAG AGGCCCCCAT CTCCACACCC 540
AATTCTCTGA AATAGAAGAG GAAGCAATGA TGAGAAAAAA ACACCACCCT ATCTTATGTG 600
TAAAATCTTA GTCCTGCGAA GGGGCCCTTA GAGCTTCTCC AGTATCACTT CATGATTTCA 660
CAGATAAGGA AACTGAGGCC CTGAGAGGGG AAGTAGCTCC CCAGACGTCA CAGGTCATTT 720
GATGGTCTTG CATTTGTTCT CATCAGCTAG CTGCCAAGAG CTGAGCCACA CGGCTAACGC 780
CAAAGTCCAA AGCCTGGTGT GTGTTCTTGG TATCAGACCC TCAGGGTGCA GCTGAGTGTG 840
AGGTGCTCCT GGACCTAGGG GTCTGGGGTG GGCTCTGGCC TGAGACTCCC CAGGCTGTCT 900
TGCCCTCCCC TGCCACCCAA TCAACAGGTA TTTATCTGAC ACCTACTTAA AGTTTGGCCC 960
AGGTTTCAGC CAAGCGGGGT GCCAAAAAGC TTAGGCACCA AACTAATGTC TGCCTCCATC 1020
CAGAGAGCAT CTCACTGGGG AGATGGGATT AACATGTGAA ACAATCATTA AACAATAAAA 1080
GGCAGCATAT AATTAGATGC CAGCTGTAGC CACACAGGCT CTGAAATCAC CTCTATAGGC 1140
TCTTGCAGTA TGGATTTAAC ATTAGCCAGC AGCTGCAGAG ATCTGTGACG ATGGTAATTT 1200
GTACTTTTGC TGCAATGGGA ATCTGAGGCT TTGAGGCCAT GGGGCTGGTG TTTGGGAGCG 1260
AGTCACAGAA CCAGGGAGTG AGCCTAGCTG TCTACCTCCA TCCCTACCCC AGCCAGCTTT 1320
GTTGCCTCCT CATTGCAGAA TGGAGTAAAG TGAGCAAAAT CCAAGGAAGT GCCCAAGCCT 1380
TTGTCTTCTT GTGAAAAGTG TCCATGAAAT GAGAGTGAAG TTACAAAGGC CCATTAACTG 1440
|
