Tag | Content |
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EnhancerAtlas ID | HS176-20335 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:43395120-43396930 |
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 |
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| 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_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_49954 | chr2:43396740-43397866 | RPMI-8402 | 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 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I043167 | chr2 | 43394741 | 43409195 |
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Enhancer Sequence | CAGTTAGGTG ACCTGGGCAA TCCCCAGGCC TCTCTAAGCC TCAGTTTCCT GAGCTAGTGG 60 AAGCCCCTAG GTCACAGGGC TATTGTAGGG ATGGGTGTGC TCCTGAGGAA AACTAGCATG 120 AGCTTGGCAC CAGGCAGGTG AGGCCATGTG CTGCTCTCTG GGCCCCCAGC TTCTGTCCCC 180 CAGACCCTGG TGTCAGACAG GACCTGGTGA GAAATCCTTG CGGCCCTAGC CTGCCTAAGC 240 TGTGGAGGGG CTTGTCCAGG ACCTGCCAGG CAGAGGCTGC AGAAGGGTTC ACTTGGCCTT 300 TTCAGTCCCT CTCAGTCCCT TACTGTCTGC CTCTCAAGAA CATCCTGGCA CTTGCTGCTC 360 CACAGCCCTG CTGGGGTCCT GGGTGGGACT TTCTGGGGGC AGAGGAAGAA ATTCCAGGGC 420 CTGCCCTTGA CGAGCTCATA GTCTAACTGG GAAGAGAGTA GTGGCTCACT ATCCAGAAAA 480 CATGGAAAAG AGACTGTGGT TTGGAGAAAG CAGGAAGCGT TCAGAAGCGG GAGGCAGAAC 540 AGGGGAAGGC GCTGGAGCCT GAAGGATGGA GCGGACCAAG TGCAGAGGGG ATGGAGGGCA 600 CTGCAGGCAG GAGGCACAGC GAGAAGAATG GCCTGGAGGG TTGGATGGGG AACACGGGGT 660 CCTAGAGACG GAAGCAGGGT CCAGGCTGTG AGTGGTGGGG CCGCCTCAGC TGGGGAGTTA 720 TGGTAAGGAT AAACAGAAGG GCTCTGGGGC CGCCCAGAGT GCATACCCCC CAGGGTGCAG 780 ACGGGGGAAC AGCAATTGTC TCTGAGGGGG ATCCTCACCT CCCTATCTCA TCGGCCTAGG 840 AGACAGGACC TCACTTGACT GGCCCACAGC CAGGCCCTGG CTGTGTTGAC AAATGGGTCC 900 TTCCCCCTGG CCTGGTGAGC TGAGATGTGG CATTGTTAAG CTGCAAGTGA GTCACAGAAC 960 TTTTCCTTCC CTTTCTTCCT CTCTGCCCTG CTTGTCCCAC ACCCTGCTCA TTTTTTTTTT 1020 CTCTCTCTCT CTCTCTCTCT CACACACACA CACACACACA CACACTTGCC TTTCAGAACC 1080 TGTGAACTAT AAATAAGTGC TTTATCACCA TAAATGACTT GATCCAGGCT AGGGTCGTGA 1140 GGGGCTTGGC TCAGGTTCCT GGGCATGTGG ATACCTGCAG AGTGGGTTCC TGAGCACGTG 1200 AGGGCACAAG CGTGCAGTCT CGGACAAGGT GGAGTCTCAA TGTGTGAGCT TGCTGAGGCC 1260 AGGGCAGTGT CTGGGAAGGG AGTGGAGGCA TCTTTGTGTC TGTGGGGTTG TGGTGGGAGG 1320 GAGGTTTCGG GGGCTGTGAG GCGAGCACAG GCGTGTGTGC TGTCTATGCC CCCAAGGGGA 1380 CAGGGCGTGG GTGGAGAACG TATTTGTGCC CGAGGTGTGT CCGCAGGGAT ATCCGTGTGG 1440 TGAGTGTGGG AGGAGGGGCG CTGGGCATGG AGGAAGTGTT TCTGTCTGTC TGTGTGTGTG 1500 TTGTGGGGGT GGCGGGGATT GGCGGGGGTG GGTTGTGCCT GGCCAGCCAA CCTTTACATC 1560 TGGTTCTGCA GGATGTGAAA AGGTTTGTGA CTGAGGCCAG TGGCACACCC TCCAGTCGGA 1620 TCAGAGGGTT GGAGATAAAC CCAAGTGAGC AAGCATTGGT GGCTGTGGCC GTGTGGTGTC 1680 CCATTCCTGG GGGGCTCCAG GAGATAGGGA AGCTCATCTG ACTTCCTGAG GGCCTGGCAG 1740 CCCCTCCTGC CCTCCTCAAG GTGGTCCATC TGCCACGCCA AGCCCAGCCA GAGAGAAGGG 1800 GCACCCGGAG 1810
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