Tag | Content |
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EnhancerAtlas ID | HS176-25088 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr22:30707240-30708530 |
| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_00207 | chr22:30696033-30714616 | Adipose_Nuclei | SE_01017 | chr22:30706695-30709458 | Adrenal_Gland | SE_01933 | chr22:30704755-30709496 | Aorta | SE_03076 | chr22:30705469-30707709 | Bladder | SE_03076 | chr22:30707877-30708390 | Bladder | SE_06187 | chr22:30705172-30707851 | Brain_Hippocampus_Middle | SE_11435 | chr22:30693586-30712890 | CD20 | SE_12307 | chr22:30699489-30707598 | CD3 | SE_12307 | chr22:30708349-30709320 | CD3 | SE_15119 | chr22:30704052-30707762 | CD4_Memory_Primary_7pool | SE_15119 | chr22:30707987-30709532 | CD4_Memory_Primary_7pool | SE_16208 | chr22:30700645-30707378 | CD4_Naive_Primary_7pool | SE_16208 | chr22:30708123-30709338 | 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_41665 | chr22:30707972-30708489 | 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 | chr22:30707128-30707691 | 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: 2 | Chromosome | Start | End |
chr22 | 30707929 | 30708500 | chr22 | 30708168 | 30708313 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I030300 | chr22 | 30696534 | 30717414 |
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Enhancer Sequence | GCTGTCAGGA CTGGGAAACC TATGAGATCA TGCAGTGAGG CCATCCCCTC CCCAGAAGGT 60 AAGCGGTCTG CCTGACGCCA CACACTCTGT GAGTTGGTAG GAAAAAGGAA GAGGGTCTGC 120 AGCAGCCTGG CACTCCCTTC TGGGGCCCGG CCACCCCTGC CTAGGAGCCG GCTGGCAGTG 180 TCCAGGCTCC CTGTCTGAGT GAGAGAGTCT GGCTTGCTTC ACTCTCCCTC CTTCCCAATG 240 CAGGCTAATT CTGGGGCTGC CTGTCTTTCC CATGAGGAAT TCCCTGGCTC TGCTCCTTCT 300 AGTGCTGGGT CAGTGCACAA TGGTAAACAG GTTCTCTCCA CCCTTCACTG GCCTTGGTGC 360 CCTGGACCTC TGCCCAGCTC TCTACTCTGC TCAGCTCCAC CCTACTCAGT GTGAGAAATG 420 GTTCCTTTAG CACTAGCCTT GCTGGCTCCC AAAAAGAAAA ACCAAGGTAT CTACCTTCCT 480 CTGATGCACT CATCTAGGGA AGGGCGTAGA CCACAGAGAA ACTCCCAAGC AGCTCTCCCT 540 GACAACTGCA GAAAGGTATT AGATAGGGTC TTGCTCTGTC GCCCAAGATG GAGTGCAGTG 600 GCATGATCTC GGCTCACTGC AGCCTCCGCC TCCTGGGCTT AAGCCATCCT CCCACCTCAG 660 CCTCTCGAGT AGCTGGGACC ATAGGCTCAT GCTACCATGC CCCACTAAGT TTTGCATTTT 720 TTGTAGAGAC AAGGTTTCAC CGTGTTGCCC AGGCTAGTCT CAAACTCCTG GGCTCAAGTG 780 ATCTGCCTGC ATCAGCCTCC CAAAGTGTTA GGATTACGGG TATTAGTGAC TGAGTGCCGC 840 CTGAGACTAT TCTCAACAGA AGACATCTTT TCTCCAAATC CCAGCTCCTA CCAGGCAGAG 900 TGCTGCTTGA AATTCCCTTG CTGGTGACTG AGTCCTTGGA TCACAATCTC ACTGCAGGCA 960 CCCAGGGGCC ACCCTGACTC ATCCTTACCA AACTGCTAGA TCTCATTGAT AGATCTTACC 1020 AAAATTAGTC TTGACTCACT GTTTATATAA GGCCCCTCCT CTGCCCAGAC TCGTCCATGG 1080 CTCCCTACTG CCCTCATTAT CCAACAGAAA CCTCAGACCC TGTAGCTGGG CATTACGGCA 1140 CACGCCCTGT CATCCCAGCT GCTCGGGAGA CTGAAGTGGG AGGATCACTT GAGCTCAGGA 1200 GTTTGAAGCT GCAGTGAACC ATGATTGTGC CACTGCACCC TAGACTGGGC CACTGGGTCA 1260 CAGGGCAAGA CCTTTTCTCA AAACAAACAA 1290
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