| Tag | Content |
|---|
EnhancerAtlas ID | HS149-00205 |
Organism | Homo sapiens |
Tissue/cell | NKC |
Coordinate | chr11:35103210-35106200 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr11:35106056-35106068 | CCAATCACTGCA | + | 6.44 | | IRF1 | MA0050.2 | chr11:35103734-35103755 | AAAATAAAAGCAAAACAGAAA | - | 6.03 | | IRF1 | MA0050.2 | chr11:35103728-35103749 | AAAATAAAAATAAAAGCAAAA | - | 6.81 | | KLF4 | MA0039.3 | chr11:35105982-35105993 | CCACACCCTGC | + | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr11:35103502-35103517 | GAGGTCAGGAGTTCA | + | 6.22 | | ZBTB18 | MA0698.1 | chr11:35103828-35103841 | CTTCCAGATGTGC | + | 6.17 | | ZNF263 | MA0528.1 | chr11:35103412-35103433 | TCCCTTTTCACCTCCTCCTTT | - | 6.31 |
|
| | Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
| SE_10718 | chr11:35103651-35106244 | CD19_Primary | | SE_11615 | chr11:35103176-35107063 | CD20 | | SE_12205 | chr11:35103452-35106884 | CD3 | | SE_14966 | chr11:35103246-35107086 | CD4_Memory_Primary_7pool | | SE_16067 | chr11:35103332-35106798 | CD4_Naive_Primary_7pool | | SE_16834 | chr11:35103458-35106781 | CD4_Naive_Primary_8pool | | SE_17248 | chr11:35103634-35106575 | CD4p_CD225int_CD127p_Tmem | | SE_18923 | chr11:35103259-35107250 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19832 | chr11:35103417-35107078 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20601 | chr11:35103628-35106266 | CD56 | | SE_22911 | chr11:35103621-35106842 | CD8_primiary | | SE_30479 | chr11:35103583-35110787 | Fetal_Muscle | | SE_36037 | chr11:35103058-35106758 | HMEC | | SE_44354 | chr11:35103454-35106871 | NHDF-Ad | | SE_46152 | chr11:35103257-35106758 | Osteoblasts | | SE_52114 | chr11:35103627-35106397 | Skeletal_Muscle_Myoblast | | SE_56204 | chr11:35103121-35108206 | u87 | | SE_62613 | chr11:35051325-35112817 | Tonsil | | SE_63905 | chr11:35103613-35106477 | HSMM |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr11 | 35103730 | 35105993 | | chr11 | 35103883 | 35104400 | | chr11 | 35103874 | 35105511 | | chr11 | 35105542 | 35105874 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I035081 | chr11 | 35103199 | 35111026 |
|
Enhancer Sequence | GCCTGCCTCT GCCACTAGAA TGGAGGCTCC ATGAGGTCAG GAGCCTGTTG TCTTCATTGC 60
TGTCCCCTCA ATCTTTAAAG CAGAGCTCGG TACTTAGTGG TTACTCACAT CATATTGACT 120
AATTAAACAA ATGAATGTTC CCAGCTCCCA CCAGCCCCTC CTACCTGTTA TGGTCAATAT 180
CATGTCTTCT CTCCCTCAAG GCTCCCTTTT CACCTCCTCC TTTTCCTGGC AAAGCAAACA 240
CAACAAACAA AAATCTGCAA GATGCTGGGA GGCCAAGGCA GGTGGATCAC TTGAGGTCAG 300
GAGTTCAAGA CCATTCTGGC CAACATGGTG AAACCCTGTC TCTACTAAAA ATACAAAAAT 360
TAGCCAGGTG TGGTGGTGCG CGCCTGTGAT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA 420
ATCACTTGAA CCTGGGAGGT GGAGCTTGCA GTGAGCCAAG ATTCCACCAC TGCACTCCAG 480
CCTGGGTGAC ACAGTGAGCC TCCACCTCAA AAAAAAAAAA AATAAAAATA AAAGCAAAAC 540
AGAAAAACCT GCAAGATGCC ATAGTGCTCC CTTCTCAACT TCATGGAAAT TCTGAAATAT 600
ATATGGGATT CATTTTTCCT TCCAGATGTG CGATTTGGAG GGTGGAGTGT CAAAGGAAGA 660
GAACTGGGGG AATTCTTGAC CTGGCTGGGC TCTTCTTTGG CCCCAGCTCC CCGTTCATCC 720
TTCACCTCCC TCCCATCCTG GCTGCTCACA TTCCTATGTG GTGAGTTCTG CTCCTCAGCA 780
GTGGAGCAGG GGCTGGACTG GGCAGGGGAG AGTCGCAGGC TCCATGTGTC CAGCCTGCCC 840
TGGTGGACTG ATGGTGTTGC CCAGGAAAGG CGTGCGAGGC CACGGCTTCT GACAGCCGCA 900
ATCTGGAGTT GCTGTTAGGT CTGATTGAAT GATTGACACA CCACAAGCAG AAATCTAGAA 960
CTCCAGAACG GGTCTGGTGG AAGGAGCCAA CTCTGTTTGC AGTTTCCTCT TCTCACCACA 1020
GCACAGTGTC GGGTTACCAC GGAGATAGGG AGGAACCTTC TGAGACCTCT CCAATGGTGG 1080
GTGGCAGCCA CAGTCAGCCA GGGAGGACTA CACCCAATCC TTGGCTCCGC CCCTCCTCCC 1140
ACACCCCAAA AGAAGCCACA CAGCTAGCCA GAGAGGGGCT GCCTCTGGAA TGCACACCAG 1200
GGCTTGTCCA CACACACTCC CCGGCCCTCT GCGCCTCTTT AGGGAGGTTC CTGCTGCTGG 1260
ATCTGCTGCC TTCTTCACCT TGAGAGTGCA TTTATGTAAC AAGAAAACAC CTGGGTGTTT 1320
TCACAGGTAG GAAGAGATTG GCGGCTGAGC TGTTCTCTCA TTTGGATGCA AGGCTGTGAG 1380
ATGGGGCCTC TGTTGGCCTA GAGGTCCCGA GAAATTGGGA GGAGAGGTGC CAGTAGCAAG 1440
CCCCAAGGTC GGGGTTCCTC CTCTAACCTC TCTGTGGGGT GGAGGCATCC ACACCAAACC 1500
TTAAGAGGGA GCAATGGGTC TAACTGCTAA TTCTGAAGGT GAGCAGGCCC GTTTCCACAT 1560
GCCAATGTCA AAATCCAACC ACAGTTTGAC AAGCCTTTGG GAACATCCAG TAATTACATA 1620
ATAGCACTCC CAAACATGAC AAGTGCTTTC ATCTTTACAA AGACTGTCGT GTTTGTTCTC 1680
ACTCTCCTCC CCATATGAGT TGCTTCTCTT TCTTTCCCCT ATTTTGCAGA TAAGAAGGTG 1740
GAGGCTCAGG AAGGTAGAGT GACTTTCTAC TACTAAAGAA CTAGCAGGAA AGTATTTCAA 1800
ATTCAAGTCT CATGACCCTA AATGCAGGGT ATTTCCCAGT GGCTCATGGT AAATGAGTTC 1860
CTTAAAAATG AGCCACGCTG AGGCCTGAAA CTACAGGGCT TACTGATGTG GCTGCAAGCT 1920
GCAGCTCTAA GCCAGAAAGG GGACAAGCTA AGGAGAAGAG GAACCACCTT TGCACTGGCG 1980
GACTTCAGCG TGTCTCACGC ATGCCGAATG TTTACATGTG TTCCCCACTT GGTATCCATA 2040
GCAACTGGCA GAGGTGCAAA AATGCTTCAT TGGTATTTGT AAGAGGATGA GAAGAAAGCC 2100
CTCCAAGATC CTCTTTCTCC CAGTGGGCAG GGCTATTTCC ATCCATGGCT TCGTGACTTC 2160
TCCCAGCAGC CGTTTGGCAT GAGGATTTCA AACAGCAGGG AGCCAGTGAG TCCACCGGAT 2220
AGGTATTTGA AATGTACTGA ATGGAAAGCC CTCATCTCCT GCTCCCTCTT CCAGGCAATT 2280
ATTCATGGAG TCAGGAGAGG ATTCTGTTAT TCAAGGAGTC TCCATAGTAA GGGGCTGAGA 2340
GATTGTGGTT TCTAGTCTTT AACCACAACA TTTAAGGCGT GGCTCCATTT TTCTTATAAT 2400
TTCCAAGTGT ACATCATTAC CTAATTCTCC CTGAAGAATC GAAATTGCTT TATGATGCAT 2460
ATGTATTAGT GATGTGAGCT GAGGTTCGGA GCCAGCAAAC ATCTTTCTCA GAAACCTCCC 2520
TCTTGTTCTC CTCTCCCATG TTGCCCCTTG AAGTTACTCC TTCTACCAGA GATGCTCAAA 2580
GGTTCTTGGT CAGAAAGTCT ATATTGCAGC AATTAAAACT GGGGTTCAAC TCAACATATG 2640
TGTAGCAGAA TATTTTATCT CTCAGCATCT CAATTTGTGA CTTAAATGAT TCATGAGATG 2700
TTTGTTAGTG CATTATGGTC AAAAGCACCT TTCTAAGTGC TTTGAGAGAA ACAAGAATAA 2760
AAGCATTCCT AACCACACCC TGCCCCCTGC AATCCCACCA AGGATCTTAC AAAACCCATT 2820
TGGCTAAGCT CTTATATAGC ATTGAACCAA TCACTGCACA CTCAGCATGT GACCAACACA 2880
TATATTGAAG CCCACGTGAA AAACTGAGCA CCTATTCAAG TTTCCCAGGC AGGGCTAGAT 2940
TCATGGGCAG GTAACCAGTG CAGTTGCACA GGGACCTCTG CTCAGAAGGC 2990
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