| Tag | Content |
|---|
EnhancerAtlas ID | HS043-03672 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:206748210-206749460 |
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 | GAGTCTCGCT CTGTCATCCA GGCTGGAGTG CAGTGGCGCA ATCTTGGCTC AATGCAACCT 60
CTGCCTCCCA GGTTCAAGCG ATTCTTCCGC CTTAGCCTCC CGAGTAGTTG GGATTACAGG 120
CGCACGGATA ATTTTTTTGT TTTTGTTTTT GTTTTTTTTT TTAGAAGAGA CAGGGTTTCA 180
TTATGTTGCC CAGGCTGGTC TTGAACTCCT AACCTCACCT TTGAATGCGG TTTGGACATT 240
GAGCAGGGTA TTTCAAATCC AGCCCAGATA GATGGGTGTC TGCCCCTTGC CTGCAGACGT 300
TCCCATCTAG GGCAAGCACA ACAGAAGCAC CGGGTGTTTG GGGTGTGGAA GGCAGCTGCA 360
GATGGACATT CTCCTGTAGG AGGGGCCTGA GGCTTTCCTC CCTGACTTAA GCCTGGAGAT 420
GGCTTCCTTC CAAGGGGTGA AAGAATTGCT GCTGACAGAT TTGCTAAGAG CTGAGAAAGA 480
GGAAATGTGG CAAAGGCTCA TGGTGAATGG CTTCCGGGGT ATTTTTTGTT TTGTTTTCTT 540
GAGTTGTGTG TGTTAAGAAT GCGTAGACCG GCTTGGGCTT GGCTAAGATA GAGTCTTGCT 600
GACAATAGAG AAAAGTGGTG AGCAGTGAAA AAGTAAAGTC GTGGCGGTTA GAAATGTTCT 660
TTGTGCTCCT TTAGATTGGT TATTCCTGCT GCCATTCAGC CATGCTAGCT AGCCTCCAAG 720
AGGCCCCCAT CTCCACACCC AATTCTCTGA AATAGAAGAG GAAGCAATGA TGAGAAAAAA 780
ACACCACCCT ATCTTATGTG TAAAATCTTA GTCCTGCGAA GGGGCCCTTA GAGCTTCTCC 840
AGTATCACTT CATGATTTCA CAGATAAGGA AACTGAGGCC CTGAGAGGGG AAGTAGCTCC 900
CCAGACGTCA CAGGTCATTT GATGGTCTTG CATTTGTTCT CATCAGCTAG CTGCCAAGAG 960
CTGAGCCACA CGGCTAACGC CAAAGTCCAA AGCCTGGTGT GTGTTCTTGG TATCAGACCC 1020
TCAGGGTGCA GCTGAGTGTG AGGTGCTCCT GGACCTAGGG GTCTGGGGTG GGCTCTGGCC 1080
TGAGACTCCC CAGGCTGTCT TGCCCTCCCC TGCCACCCAA TCAACAGGTA TTTATCTGAC 1140
ACCTACTTAA AGTTTGGCCC AGGTTTCAGC CAAGCGGGGT GCCAAAAAGC TTAGGCACCA 1200
AACTAATGTC TGCCTCCATC CAGAGAGCAT CTCACTGGGG AGATGGGATT 1250
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