| Tag | Content |
|---|
EnhancerAtlas ID | HS092-12353 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:65072690-65074460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6 | MA0677.1 | chr12:65074141-65074155 | TGTCCTTTGACCTT | - | 6.13 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_01804 | chr12:65070462-65076201 | Aorta | | SE_11789 | chr12:65048359-65079116 | CD20 | | SE_11913 | chr12:65070474-65077295 | CD3 | | SE_14822 | chr12:65070642-65076199 | CD4_Memory_Primary_7pool | | SE_15696 | chr12:65070818-65075403 | CD4_Memory_Primary_8pool | | SE_15988 | chr12:65070665-65076127 | CD4_Naive_Primary_7pool | | SE_16487 | chr12:65072270-65076245 | CD4_Naive_Primary_8pool | | SE_17278 | chr12:65072138-65074488 | CD4p_CD225int_CD127p_Tmem | | SE_18102 | chr12:65070476-65080258 | CD4p_CD25-_CD45ROp_Memory | | SE_18758 | chr12:65058416-65080356 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20172 | chr12:65070690-65076242 | CD56 | | SE_21231 | chr12:65070985-65075772 | CD8_Memory_7pool | | SE_21679 | chr12:65070577-65080045 | CD8_Naive_7pool | | SE_22024 | chr12:65070479-65080200 | CD8_Naive_8pool | | SE_22370 | chr12:65057844-65080308 | CD8_primiary | | SE_26327 | chr12:65072914-65076107 | Duodenum_Smooth_Muscle | | SE_32113 | chr12:65072597-65073011 | Gastric | | SE_32113 | chr12:65073037-65074387 | Gastric | | SE_35199 | chr12:65071647-65075559 | HeLa | | SE_41405 | chr12:65070412-65078188 | Left_Ventricle | | SE_41811 | chr12:65073243-65074347 | LNCaP | | SE_43200 | chr12:65070897-65072927 | Lung | | SE_43200 | chr12:65073005-65076216 | Lung | | SE_49372 | chr12:65071770-65074615 | Right_Atrium | | SE_50736 | chr12:65070547-65076106 | Sigmoid_Colon | | SE_54802 | chr12:65070368-65077942 | Stomach_Smooth_Muscle | | SE_57296 | chr12:65073149-65074315 | VACO_400 | | SE_63011 | chr12:65051055-65082906 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I064664 | chr12 | 65058182 | 65079989 |
|
Enhancer Sequence | AGTAACTTGC CTCTGGTCAC GCAGCTAGAA TGTGGCAGAG CTGTGTGATT TTAGACCTAA 60
GTATGTCTAA ATCATAGTCC ACAGGCCGTC ACTAAGCTAA AGTAGAGGAA ATGATAGGGC 120
CACATTCACC TTCTCTCTTT TGAACAGTCA CTCGTTTTTT GAAGCGGGGG TGGGGACAGA 180
GTTGCTGTGT TGTCCAGACT GGAGTGCAAT GGCACGATCT CAGCTCACTG CAACCTCTGC 240
CTCCCAGGTT CAAGTGATTC TCCTGCCTCA GCCTGCTGAG TAGCTAGGAT TACAGGTGTG 300
CCACCACACC CAGCTAATTT TTGTATTTTT TGTAGAGATG GGGTTTCACC ATGTTGGCCA 360
GGTTGGTCTC GAACTCCTGA CCTCGTGATC CACCCACCTT GGCCTCCCAA AGTGTTGGGA 420
TTACGGGCGT GAGCCACCGC TCCCAGCCTG AACAGTCACT CTTAATTGCA CTATGTTTAT 480
TTGGGCATTT TGTTATGTTT TTATGTTTTT AATTTTGATA TAATTTCACA GTTATAGAAA 540
AATTAACCAA AAGAGTATAA ACAATTCTCA GACCCTTTAC TGAGATTTGT TGGGACATAT 600
TCTTAGAAAG TCTGAGTTGT GAGCCTGTGG GATTGGGCCG CACTTCTTGA GTAGAGCCTG 660
GGTCATGCTA CCCGAGAACT CCTGGGTGCC TGTGAGGTTG GGTGTGTCCC ATCTGAGAAA 720
GTTCGCTACT GAAAAACAGT GACGTAACCC CACCCAGGAA CTGAAGTGAG CCTGAGAGCA 780
GCTCTCCAGG GCTTGCTGGC TGGAAACAAT GAGGGAAGAG TCTAGGATTT ATGAAATATT 840
TTTTTGTGGA AGAACTCTTC CTCTGAGAAA CTGCTGGAGG GTTTGGGGAA TACAAAACAA 900
AACTGACTTA TGAAAAGATG ACTTGTAACT CACCAAGCAG ACGCTCTCAG GCGTGGCATG 960
ATGCCCTCAC TGGCTGCCAA GAACAATAAC TGACACATTA TCCACAGACG GCTGCGCCCC 1020
ATGCCATTTC CTCTCCTGCC ATCACAATGA AAGACCAGGG TTGACACTTG GTATTGTATC 1080
TATTCCACGT CCGCTGCACC ATTTTCTTTT AACCCTTCTT TCTTGCTCTC ACCCCTTTAC 1140
CTGTTGGAGC TACTATGCCC CTCCTGGGTT TCGTTTTCTT CTCTTCCTTT TTCCTGGGCA 1200
TACAGCTGCG TTCCTAGAAA TTGTGGTTCT GATTCATAAT CATTGTATGT GGAGGAAGGG 1260
GCAGGATTCT ACTCTGTGAG GGGACGGGAG GGTCTTTTTT AAAGGGGTAA ACAATTGGAA 1320
AGTTTTTAGA GTTAAGGGTC TTTCTCTGAT GCTAAATGAA ACCACTGTCC TCTGTTCCAA 1380
GGCCTGAGCT TATATCTTCT TTGCTATGAG ACCCAGAGAA ACAGTGCTTG GGGGCCATTT 1440
TGGAAGCAGC TTGTCCTTTG ACCTTCCCCA CTCCACTTGT GCAGACACCA CGCCCCGTGA 1500
GGACGGGCGT GGTGTCTGCT GCTGAGCCTG ACTGCCCCAC ACTTAGGCAG GTACCTGGCA 1560
CATGGCAGAA GCTCAGCAAA TATTTGCTGA ATGATGAGGC CTTGGTGTAT GATTGCTACA 1620
TTTTTGGCTT AAAAAGTACA GCATCAGGGC CCTTGGGGTT TTACCTGCTT TTCTGGGATA 1680
TACTTTCCAG CTGATCTTTG TTTTTTTTTG TTTTTGTTTT TGAGACAGAG TCTCGCTCTG 1740
TCGCCCAGGC TGGAGTGCAA TGGCGTGATC 1770
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