Tag | Content |
---|
EnhancerAtlas ID | HS145-12478 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr2:43395640-43396860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr2:43396116-43396127 | CCACACCCTGC | + | 6.62 | RREB1 | MA0073.1 | chr2:43396606-43396626 | TGTCTGTGTGTGTGTTGTGG | - | 6.01 | RREB1 | MA0073.1 | chr2:43396608-43396628 | TCTGTGTGTGTGTTGTGGGG | - | 6.54 | ZNF263 | MA0528.1 | chr2:43396081-43396102 | TTTCCTTCCCTTTCTTCCTCT | - | 6.18 |
|
| Number of super-enhancer constituents: 42 | ID | Coordinate | Tissue/cell |
SE_03102 | chr2:43395315-43396058 | Bladder | SE_03102 | chr2:43396144-43397914 | Bladder | SE_09287 | chr2:43394591-43397814 | CD14 | SE_10736 | chr2:43394904-43398818 | CD19_Primary | SE_11722 | chr2:43394406-43403989 | CD20 | SE_11879 | chr2:43395778-43399784 | CD3 | SE_12501 | chr2:43396298-43396478 | CD34_adult | SE_13409 | chr2:43395012-43397907 | CD34_Primary_RO01536 | SE_14384 | chr2:43395704-43399804 | CD4_Memory_Primary_7pool | SE_16655 | chr2:43396048-43398828 | CD4_Naive_Primary_8pool | SE_16950 | chr2:43396103-43398624 | CD4p_CD225int_CD127p_Tmem | SE_17323 | chr2:43394585-43404415 | CD4p_CD25-_CD45RAp_Naive | SE_17875 | chr2:43395625-43407220 | CD4p_CD25-_CD45ROp_Memory | SE_18565 | chr2:43394941-43399939 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19552 | chr2:43395255-43399774 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20209 | chr2:43394960-43399771 | CD56 | SE_20901 | chr2:43395401-43399064 | CD8_Memory_7pool | SE_22349 | chr2:43394743-43399769 | CD8_primiary | SE_23059 | chr2:43394803-43398677 | Colon_Crypt_1 | SE_23724 | chr2:43394783-43398643 | Colon_Crypt_2 | SE_24685 | chr2:43394825-43398672 | Colon_Crypt_3 | SE_25333 | chr2:43394791-43398436 | DND41 | SE_26374 | chr2:43395142-43397631 | Duodenum_Smooth_Muscle | SE_26557 | chr2:43394921-43398727 | Esophagus | SE_27617 | chr2:43394694-43399793 | Fetal_Intestine | SE_28536 | chr2:43394603-43399798 | Fetal_Intestine_Large | SE_30898 | chr2:43394882-43398155 | Fetal_Thymus | SE_31392 | chr2:43394985-43398655 | Gastric | SE_34919 | chr2:43394920-43397426 | HeLa | SE_38828 | chr2:43394545-43397667 | HUVEC | SE_40066 | chr2:43395750-43397271 | K562 | SE_43203 | chr2:43394771-43398773 | Lung | SE_47826 | chr2:43395126-43397358 | Pancreas | SE_50052 | chr2:43394779-43398763 | Sigmoid_Colon | SE_52337 | chr2:43394808-43398777 | Small_Intestine | SE_53288 | chr2:43394791-43398735 | Spleen | SE_55101 | chr2:43394850-43397892 | Thymus | SE_56731 | chr2:43394807-43397647 | VACO_400 | SE_58412 | chr2:43352450-43425007 | Ly1 | SE_61450 | chr2:43354337-43468354 | Toledo | SE_62203 | chr2:43354169-43468733 | Tonsil | SE_65350 | chr2:43394818-43397799 | Pancreatic_islets |
|
| 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 |
GH02I043167 | chr2 | 43394741 | 43409195 |
|
Enhancer Sequence | TCAGAAGCGG GAGGCAGAAC AGGGGAAGGC GCTGGAGCCT GAAGGATGGA GCGGACCAAG 60 TGCAGAGGGG ATGGAGGGCA CTGCAGGCAG GAGGCACAGC GAGAAGAATG GCCTGGAGGG 120 TTGGATGGGG AACACGGGGT CCTAGAGACG GAAGCAGGGT CCAGGCTGTG AGTGGTGGGG 180 CCGCCTCAGC TGGGGAGTTA TGGTAAGGAT AAACAGAAGG GCTCTGGGGC CGCCCAGAGT 240 GCATACCCCC CAGGGTGCAG ACGGGGGAAC AGCAATTGTC TCTGAGGGGG ATCCTCACCT 300 CCCTATCTCA TCGGCCTAGG AGACAGGACC TCACTTGACT GGCCCACAGC CAGGCCCTGG 360 CTGTGTTGAC AAATGGGTCC TTCCCCCTGG CCTGGTGAGC TGAGATGTGG CATTGTTAAG 420 CTGCAAGTGA GTCACAGAAC TTTTCCTTCC CTTTCTTCCT CTCTGCCCTG CTTGTCCCAC 480 ACCCTGCTCA TTTTTTTTTT CTCTCTCTCT CTCTCTCTCT CACACACACA CACACACACA 540 CACACTTGCC TTTCAGAACC TGTGAACTAT AAATAAGTGC TTTATCACCA TAAATGACTT 600 GATCCAGGCT AGGGTCGTGA GGGGCTTGGC TCAGGTTCCT GGGCATGTGG ATACCTGCAG 660 AGTGGGTTCC TGAGCACGTG AGGGCACAAG CGTGCAGTCT CGGACAAGGT GGAGTCTCAA 720 TGTGTGAGCT TGCTGAGGCC AGGGCAGTGT CTGGGAAGGG AGTGGAGGCA TCTTTGTGTC 780 TGTGGGGTTG TGGTGGGAGG GAGGTTTCGG GGGCTGTGAG GCGAGCACAG GCGTGTGTGC 840 TGTCTATGCC CCCAAGGGGA CAGGGCGTGG GTGGAGAACG TATTTGTGCC CGAGGTGTGT 900 CCGCAGGGAT ATCCGTGTGG TGAGTGTGGG AGGAGGGGCG CTGGGCATGG AGGAAGTGTT 960 TCTGTCTGTC TGTGTGTGTG TTGTGGGGGT GGCGGGGATT GGCGGGGGTG GGTTGTGCCT 1020 GGCCAGCCAA CCTTTACATC TGGTTCTGCA GGATGTGAAA AGGTTTGTGA CTGAGGCCAG 1080 TGGCACACCC TCCAGTCGGA TCAGAGGGTT GGAGATAAAC CCAAGTGAGC AAGCATTGGT 1140 GGCTGTGGCC GTGTGGTGTC CCATTCCTGG GGGGCTCCAG GAGATAGGGA AGCTCATCTG 1200 ACTTCCTGAG GGCCTGGCAG 1220
|