Tag | Content |
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EnhancerAtlas ID | HS190-08567 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr22:30705400-30706770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB3 | MA0638.1 | chr22:30705634-30705648 | GTGCCACGTCATGG | + | 6.42 | FOXF2 | MA0030.1 | chr22:30706443-30706457 | CAATGGTAAACAAA | + | 6.23 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00207 | chr22:30696033-30714616 | Adipose_Nuclei | SE_01017 | chr22:30705323-30706234 | Adrenal_Gland | SE_01933 | chr22:30704755-30709496 | Aorta | SE_03076 | chr22:30705469-30707709 | Bladder | SE_06187 | chr22:30705172-30707851 | Brain_Hippocampus_Middle | SE_11435 | chr22:30693586-30712890 | CD20 | SE_12307 | chr22:30699489-30707598 | CD3 | SE_15119 | chr22:30704052-30707762 | CD4_Memory_Primary_7pool | SE_16208 | chr22:30700645-30707378 | CD4_Naive_Primary_7pool | SE_18199 | chr22:30696796-30709288 | CD4p_CD25-_CD45ROp_Memory | SE_19840 | chr22:30703973-30709406 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22773 | chr22:30696696-30709496 | CD8_primiary | SE_23721 | chr22:30705436-30708802 | Colon_Crypt_1 | SE_25730 | chr22:30696761-30709491 | DND41 | SE_26571 | chr22:30696437-30709562 | Esophagus | SE_31521 | chr22:30703991-30709477 | Gastric | SE_34216 | chr22:30705635-30709402 | HCC1954 | SE_39484 | chr22:30705418-30707852 | Jurkat | SE_41271 | chr22:30705407-30708762 | Left_Ventricle | SE_41665 | chr22:30705417-30707947 | LNCaP | SE_42270 | chr22:30703944-30709448 | Lung | SE_47044 | chr22:30705465-30707545 | Ovary | SE_47736 | chr22:30705437-30707875 | Pancreas | SE_48841 | chr22:30705238-30708514 | Right_Atrium | SE_50213 | chr22:30703979-30709498 | Sigmoid_Colon | SE_53095 | chr22:30703979-30707919 | Small_Intestine | SE_55187 | chr22:30705437-30706850 | Thymus | SE_63164 | chr22:30696999-30708171 | Tonsil | SE_66498 | chr22:30705418-30707852 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I030300 | chr22 | 30696534 | 30717414 |
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Enhancer Sequence | GACGGGGTTT CACCATGTTG GCCAGGATGG TCTCAATCTC TTGACTATGT GATCCACCCG 60 CCTCAGCCTC CCAAAGTGCT GGGATGACAG GCATGAGCCA CCGCACCCGG CCAGGGCAAT 120 CTGCCATTTG CTGGCAACCC CAGCTTCTGA GGAGGAAAGG CTCAGAGGAG ACAAAGGTGG 180 CACCTAATCA CAGATCTTGT CAGGCTCCTG GACTGGAACA GGCTTAGCCA TGCTGTGCCA 240 CGTCATGGTC CAAGGCAGCA GTGACACTCT GCTGACCCCA TTCTCTGTAG GTTCCCAGTT 300 TCCTAGCGTT CTCCCAAAAC CCAGAGGCTT GAGGCTTCCA AAAGTTCAGA AGGACAAGAC 360 TGCTTCCCAG GCTACTGAGA CCAAGGGCTG GGGTTCTCTC TTCCCTTGTC CTTCTAGACA 420 TCTGCTTTCT GCCCAAGCAC ATCTCAGCAC CTCTGGCTAG GCAGGTTCAG CAAGGGCAGT 480 GTCCATGCTC ATCACCTCCT TATCCTAGCC TGTCGTGGGA GATAAATCTT GATACCAAGG 540 AACCCGTCTA AACCCTCCTC CAAGCCTCAC TCCCTGAACC AGCCCAAACA AAGAGAAATA 600 CACCCTAAGC AGAAAGTCTG AGGTCACAGA CCACAGGACT GATCCTCCTC TCACCCATAG 660 GGGAAACCAG GTGGGGTGTA GGGGAGAATA AATAGAGTGG GGACTTGAAG TTAGCTGAGC 720 TAGGTACTCC AGTTCTGCCA TCTACTAACT GGGAGACCAT GTGCAAAAAG TGACAACTTC 780 TTCATCTTTC AGTGGGGTCA TAACGCACAC CTCATCTCTT ATAGGGCTGC AATGAGGAAT 840 AAATGTGTAC AAGGGCCCAG CCTGGTGGGT GGCCAGCAAA TGGTAGCTAT TAGGTGACTG 900 GTATTTGCGG CTTAACTAGC AATTTCACAT CTCTTTTCTC ATCTGACTGG TCCCCATACA 960 CAGGCCTTTG AGGAAGGCAG GGCATGATTA CCACCATTTT ACTCATGAAG CAATTGAGGC 1020 TCTGAGAGAT TACTTAATTT GCTCAATGGT AAACAAATTC TAACTCCTGG CCGCTGATCC 1080 AAGCTCTACC GCTTTACAGC TGTGTGAAAC AGGGCTGGCT GCTTTGCTCT CTGAGCTTCC 1140 AGTTCCTCAT CTGTAACCCA GGAGGAATGC CACCTCCTCA GAGAACATTG GTAAACATGA 1200 TGTGAGGCAA TTAAGAGCTG ACACTTTCAT GCGCTGGCCG TGTACTAGCT CTGCCAAGCA 1260 CTACACAGGC ACACAATCCC CCAAGGAAAT AGCTTTAATT ATCTCCATTT AATAGACAAG 1320 AACACTAAGA TTCAGCACAG TGGAGTAATA TGCCCAAGGT TACATAGCCT 1370
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