Tag | Content |
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EnhancerAtlas ID | HS060-23069 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr22:30705380-30706750 |
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 | ATTTTTGTAT TTTTAGTAGA GACGGGGTTT CACCATGTTG GCCAGGATGG TCTCAATCTC 60 TTGACTATGT GATCCACCCG CCTCAGCCTC CCAAAGTGCT GGGATGACAG GCATGAGCCA 120 CCGCACCCGG CCAGGGCAAT CTGCCATTTG CTGGCAACCC CAGCTTCTGA GGAGGAAAGG 180 CTCAGAGGAG ACAAAGGTGG CACCTAATCA CAGATCTTGT CAGGCTCCTG GACTGGAACA 240 GGCTTAGCCA TGCTGTGCCA CGTCATGGTC CAAGGCAGCA GTGACACTCT GCTGACCCCA 300 TTCTCTGTAG GTTCCCAGTT TCCTAGCGTT CTCCCAAAAC CCAGAGGCTT GAGGCTTCCA 360 AAAGTTCAGA AGGACAAGAC TGCTTCCCAG GCTACTGAGA CCAAGGGCTG GGGTTCTCTC 420 TTCCCTTGTC CTTCTAGACA TCTGCTTTCT GCCCAAGCAC ATCTCAGCAC CTCTGGCTAG 480 GCAGGTTCAG CAAGGGCAGT GTCCATGCTC ATCACCTCCT TATCCTAGCC TGTCGTGGGA 540 GATAAATCTT GATACCAAGG AACCCGTCTA AACCCTCCTC CAAGCCTCAC TCCCTGAACC 600 AGCCCAAACA AAGAGAAATA CACCCTAAGC AGAAAGTCTG AGGTCACAGA CCACAGGACT 660 GATCCTCCTC TCACCCATAG GGGAAACCAG GTGGGGTGTA GGGGAGAATA AATAGAGTGG 720 GGACTTGAAG TTAGCTGAGC TAGGTACTCC AGTTCTGCCA TCTACTAACT GGGAGACCAT 780 GTGCAAAAAG TGACAACTTC TTCATCTTTC AGTGGGGTCA TAACGCACAC CTCATCTCTT 840 ATAGGGCTGC AATGAGGAAT AAATGTGTAC AAGGGCCCAG CCTGGTGGGT GGCCAGCAAA 900 TGGTAGCTAT TAGGTGACTG GTATTTGCGG CTTAACTAGC AATTTCACAT CTCTTTTCTC 960 ATCTGACTGG TCCCCATACA CAGGCCTTTG AGGAAGGCAG GGCATGATTA CCACCATTTT 1020 ACTCATGAAG CAATTGAGGC TCTGAGAGAT TACTTAATTT GCTCAATGGT AAACAAATTC 1080 TAACTCCTGG CCGCTGATCC AAGCTCTACC GCTTTACAGC TGTGTGAAAC AGGGCTGGCT 1140 GCTTTGCTCT CTGAGCTTCC AGTTCCTCAT CTGTAACCCA GGAGGAATGC CACCTCCTCA 1200 GAGAACATTG GTAAACATGA TGTGAGGCAA TTAAGAGCTG ACACTTTCAT GCGCTGGCCG 1260 TGTACTAGCT CTGCCAAGCA CTACACAGGC ACACAATCCC CCAAGGAAAT AGCTTTAATT 1320 ATCTCCATTT AATAGACAAG AACACTAAGA TTCAGCACAG TGGAGTAATA 1370
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