| Tag | Content |
|---|
EnhancerAtlas ID | HS111-02865 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr2:43385420-43386970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:43385486-43385507 | CCCTTCAGCTCCTCCTCCTCA | - | 6.59 |
|
| | Number of super-enhancer constituents: 42 | ID | Coordinate | Tissue/cell |
| SE_03102 | chr2:43384671-43387327 | Bladder | | SE_09287 | chr2:43383934-43388379 | CD14 | | SE_10736 | chr2:43385270-43387369 | CD19_Primary | | SE_11722 | chr2:43384536-43388438 | CD20 | | SE_11879 | chr2:43384841-43388354 | CD3 | | SE_14384 | chr2:43384968-43390226 | CD4_Memory_Primary_7pool | | SE_16107 | chr2:43385039-43388515 | CD4_Naive_Primary_7pool | | SE_16655 | chr2:43385030-43387619 | CD4_Naive_Primary_8pool | | SE_16950 | chr2:43385153-43387343 | CD4p_CD225int_CD127p_Tmem | | SE_17323 | chr2:43384367-43390308 | CD4p_CD25-_CD45RAp_Naive | | SE_17875 | chr2:43384151-43389961 | CD4p_CD25-_CD45ROp_Memory | | SE_18565 | chr2:43384470-43389555 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19552 | chr2:43384838-43388407 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20209 | chr2:43384383-43388430 | CD56 | | SE_20901 | chr2:43385124-43387775 | CD8_Memory_7pool | | SE_22349 | chr2:43384494-43388457 | CD8_primiary | | SE_23059 | chr2:43384055-43387389 | Colon_Crypt_1 | | SE_23724 | chr2:43384477-43387342 | Colon_Crypt_2 | | SE_24685 | chr2:43384340-43387340 | Colon_Crypt_3 | | SE_25333 | chr2:43383856-43391948 | DND41 | | SE_26374 | chr2:43384543-43388739 | Duodenum_Smooth_Muscle | | SE_26557 | chr2:43384020-43387372 | Esophagus | | SE_27617 | chr2:43384083-43393474 | Fetal_Intestine | | SE_28536 | chr2:43383866-43393674 | Fetal_Intestine_Large | | SE_30898 | chr2:43384773-43387387 | Fetal_Thymus | | SE_31392 | chr2:43384365-43391297 | Gastric | | SE_34919 | chr2:43383855-43388500 | HeLa | | SE_38828 | chr2:43385030-43386643 | HUVEC | | SE_43203 | chr2:43384366-43387389 | Lung | | SE_47826 | chr2:43384619-43386674 | Pancreas | | SE_47826 | chr2:43386793-43387270 | Pancreas | | SE_49954 | chr2:43384504-43386643 | RPMI-8402 | | SE_50052 | chr2:43384264-43393423 | Sigmoid_Colon | | SE_52337 | chr2:43383845-43392633 | Small_Intestine | | SE_53288 | chr2:43384755-43387396 | Spleen | | SE_55101 | chr2:43384949-43387332 | Thymus | | SE_56731 | chr2:43384774-43386703 | VACO_400 | | SE_56731 | chr2:43386712-43387326 | VACO_400 | | SE_58412 | chr2:43352450-43425007 | Ly1 | | SE_61450 | chr2:43354337-43468354 | Toledo | | SE_62203 | chr2:43354169-43468733 | Tonsil | | SE_65350 | chr2:43384329-43388234 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 43385477 | 43386677 | | chr2 | 43385938 | 43386506 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I043156 | chr2 | 43383741 | 43393336 |
|
Enhancer Sequence | CCCCATCACT GGGCTAAACG AATGACCCGC CACTCAGCAG GTGACGACTT ACTCCTCCTT 60
GGCCGGCCCT TCAGCTCCTC CTCCTCACCC ATCCTGACTC AGAGGCCTGT CAGCTGCCAC 120
TGCCCCCGAG GCCTGGCAGA TTTGGGTGGG AAGGAGCTAT CTGGGTGCCA GGACCTGAGG 180
GGCTGGCCAT GCCCTCACTC CTTACTGACC TGACCTTTAG CAGGGCCTCT GAGCATTCTC 240
TGATCTAGAA ATGCCACATG TACACGCATG TGTGTGCACA CACACACAAA CACCCACACA 300
CTCACACCCA GCCGCTCTAT GACCTGATGA AACAGTCTGG GTGCAGGGCT GAGGCAGGCC 360
AGGGAGGAGA GTTAGACTGA GCAAAAGCAG GATGTGTGTG GAGCAGCCTC CTGGCCTCTC 420
TCCCGCAGAG GCACTTCCTG GTACTGGAGG GCAAAGCGGC CCGGGGTTGG GAAAGAGACC 480
GGTGCTGCTT GCTCCCTCTC CAGAACAGGC ATTAATTCTG GCTGCCCCTT GGTATTGGCC 540
TCCAACTTTA TAGTTCTCTC CCTTTCTTTC TCTCTCTCTC TCCTACACAC ACCCCTCTAG 600
ACTCCTCCCC TGCACCTCCT CAAAATTTCT CACCCACCCT CACCCCACAG AAGGAGCATC 660
AAAGCCCCAC ATAGCCTCTG GCCTCTCTCA ACACCTAGGA GTTGAGATCA GGCCCTTGTG 720
GCCCAGTCTT GGGGACTTCC CCCTACCAGG GTTGGCCCTC TTGGGTCCAC GCCTCTTTGG 780
CTAGACTTCT GATCGCTCTG GCGGCCACTC CGCAGTTTCA CCACGCCTGC TCCTGCCTGC 840
AACACACAGA AGTTGGCAGT GACTCTGCAC TGCTCCCAGC ACCCCGGATG GCTCAGGGCT 900
GTGGCATTTT GTTTTCTTTC GTTTTTCGCC TTCATGTCTG TGCTGTTCAC TGTGCCTGAA 960
ATCCCCTCCC CGCTAACCCT CCTGCCCATA GCGTCAGTGG CCCACATGTC AGCACCCAGC 1020
ACTTACCACT AGCGAGGCTG TGTCCTATCC TCCTGACCAT GCCAATGAAA AAAGTCCCAT 1080
TAATTATACC CACTGTTGGC CGGGTGCGAT GGCTCTCACC TGTAATCCCA GCACTTTGGG 1140
AGGCCGAGGC AGAAGGATCA CTTGAGCTCA GGAGTTCAAG ACCAGCCTGG GCAACATGGC 1200
AAGCCCCATC TCTACAAACA ATGCAAAAAT TAGCCGGGTG TGGTGGCGTG CACCTGTAGT 1260
CCCAGTCCCA GCTACTTGGG AGGCTGAGGT GGGAGGATCA CTGGAGCCCT GGAGGTGGAG 1320
GTTGCTGTGA GCTGAGATCA CGCCACTGCA CTCCAGCCTG GGCAACTGAG GGACCTTGTC 1380
TCAAAAAAAA AAAAAAAAAA AAGATACCAT TGTTCAGAGG AGGAAGCTGA GCTGACAGAG 1440
GTCAAGGAAG ATGCATTTCT ACCCAGCTTT CAAGATTCAC TTTGGACATC ACCTTCCTCA 1500
GACTCTGCCT TCTCCTCTTC ACCGCCCCAC TACGCCCCAG GCAGGAGAAA 1550
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