Tag | Content |
---|
EnhancerAtlas ID | HS133-09176 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr14:50334030-50335810 |
| Number of super-enhancer constituents: 37 | ID | Coordinate | Tissue/cell |
SE_00765 | chr14:50333992-50336201 | Adipose_Nuclei | SE_09576 | chr14:50334033-50337802 | CD14 | SE_10599 | chr14:50334104-50337580 | CD19_Primary | SE_11096 | chr14:50333539-50339390 | CD20 | SE_12440 | chr14:50334282-50335987 | CD3 | SE_12710 | chr14:50334684-50334870 | CD34_adult | SE_13687 | chr14:50334042-50335876 | CD34_Primary_RO01536 | SE_14679 | chr14:50334123-50336212 | CD4_Memory_Primary_7pool | SE_15756 | chr14:50333996-50336021 | CD4_Memory_Primary_8pool | SE_16123 | chr14:50334427-50335886 | CD4_Naive_Primary_7pool | SE_16695 | chr14:50334068-50336069 | CD4_Naive_Primary_8pool | SE_18438 | chr14:50333984-50336198 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19324 | chr14:50334089-50335907 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20104 | chr14:50334006-50337438 | CD56 | SE_21237 | chr14:50334033-50336208 | CD8_Memory_7pool | SE_21722 | chr14:50334033-50336067 | CD8_Naive_7pool | SE_22278 | chr14:50333968-50336018 | CD8_Naive_8pool | SE_22837 | chr14:50333983-50336850 | CD8_primiary | SE_23303 | chr14:50334241-50334973 | Colon_Crypt_1 | SE_23303 | chr14:50335002-50335628 | Colon_Crypt_1 | SE_24603 | chr14:50334338-50334959 | Colon_Crypt_2 | SE_24603 | chr14:50335010-50335534 | Colon_Crypt_2 | SE_25036 | chr14:50334350-50336082 | Colon_Crypt_3 | SE_26328 | chr14:50334059-50336156 | Duodenum_Smooth_Muscle | SE_26732 | chr14:50333843-50335723 | Esophagus | SE_27777 | chr14:50334068-50336154 | Fetal_Intestine | SE_28725 | chr14:50333995-50336010 | Fetal_Intestine_Large | SE_29997 | chr14:50334173-50335973 | Fetal_Muscle | SE_34956 | chr14:50334024-50336109 | HeLa | SE_52966 | chr14:50334193-50335805 | Small_Intestine | SE_54002 | chr14:50334175-50335700 | Spleen | SE_55560 | chr14:50334310-50335555 | Thymus | SE_59312 | chr14:50327340-50367097 | Ly3 | SE_60830 | chr14:50327790-50364534 | DHL6 | SE_61265 | chr14:50327065-50374962 | HBL1 | SE_62348 | chr14:50327484-50374966 | Tonsil | SE_64446 | chr14:50334201-50336000 | NHEK |
|
| 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 |
GH14I049867 | chr14 | 50334045 | 50337750 |
|
Enhancer Sequence | TGGCTATATG GGGCTTTGCT TGTTCAAAAT GTAACCTCTA TACGGCCGCG CGCAGTGGCT 60 CACGCCTGTA ATCCTAGCAC TTTGTAAGGC CCCGGCAGGC GGATCACTTG AGGGCAGGAG 120 TTCGAGGCCA GCCTGGCCAA CATGGTGAAA CCCCATCTCT ACTAAAAATA CAAAAATTAG 180 CCTGGCCTGG TGGCGCGCGC CTGTAGTCCC AGTTATTCAG GAGGCTAAGG CAGGAGAATC 240 GCTTGAACCC GGGAAGAGGA GGTTGCAGTA AGCCGAGACG TGCAACTGCA TTCCAGTCTG 300 GGCAAGACTC CGTCTCAAAA AAAAAAAAAA AAAAAGTAAC CTGTATGAAA GTTAATTTTG 360 TGGCACTGAA CATTGGAGTA GATAATAACC TCATCTGAAA TGGGATGTCT CAATCTGTCT 420 ACAAAAAACT CCATGCCATA GAGCTCAAAA GTTTGTAAAT TAGTCCTTTG GAGACGTTAA 480 AGAGCATGGA GTCATACGAA AAGGCTTTCT GCCCTGGTAA GGGAAGAAAG CTTGTGGGCA 540 GGTTGAGTCT GGTCCTTGAG TTCTCAGCTC TCACCAGGGA AGGGGTACCA GACAAAGCTG 600 AGGCTGAACT TGAGCCGCAC AGGCCCTGAT TGCTGGGCCG TGAGAGAACA CCCGAGGAGG 660 GGGCCCAACG CACCTGAAGA AAAGACGACG TGGAGGTCAT AAACGACCAA GAGAAAGGGG 720 CGCACCGCGG ACACTATCGC CAGCCGGACC CCAGATCAAG AGAAATAGAA GAGGAGCCGG 780 GGTCTCCAAA CACTACAGGC TGGGGTCCCA GGGCAAGGGA CTGGGCCGCC GGCGGAAGCG 840 TCGGGGAGAG GCGGGACTGT CGGCGGGGTG TGGGAGAGGC GGGGCGTGGG AGAGGCGGGG 900 CGTGGGAGAG GCGGGGCCAC CAGCAAGTGG GCGGGCGGGA GGCGGGGCCG CAGTTGGGGT 960 GTGGAAGAGG TGGGGCAGCC AGCAACTGGG AGGGGAGGGA GGCGGGGCCG CCGGCGGGGC 1020 GCGGTGAAGA GGCAGGCTGC CAGAGTGCCT GGCCGACAAA TTACCCAGCG TGAGCTCGGT 1080 CACCTGGGTG TGGCGGTTCA ACCCTGAGCT ACGTCCTCCC ACGGCGCCCG GAGTTTCCCC 1140 ACCCTTGACA CAATGCCTAT TCGCAGCTCG CTGCAGCGGA GTCATCTACT GCTGCTGGCA 1200 GGATTTTCAT TGCGACGGGT TGTTATGTGC ATTTCAGGAC ATACCCCGTG GGTTGTCCCT 1260 GATTCAGTTA CATTTAATAA ACGAGCGGTG GATTAACCGG AATTACAGTT TGACAGAAAA 1320 CACGTTTTCT TCTCGACAAC ACCCTGCGTG TAGGAAGAGC CTTTAATATG GTTGATACAC 1380 AATATTTAAT CGATCCAGAA ACACATTTCT TGTGACAGGC TTTTAAATAT CAGAATAAAT 1440 CCTAAGAGTG AACAGTTGAA GTTACTTATC CAATGTTACA CTGCTAGGCC TATAAATAAA 1500 CTTGCGGGGT CTATTTTCTC CCATTTGAAT ATGCTTTGAT TTCCATATGA CAGTTCTGCC 1560 GAAATGTTTT GACATTTTAG ATCTTAGTAG AACTCCATTA CAACACGACT ATTTATTACG 1620 TTGATTCTGA TCTGACGTGT AATAAATCAT GTCCCCAAAC CAAAACTCCA TACATTAATA 1680 TCCTGATATT TAACACACTT TATCCAACTA TTGATTCTAT CTGTTCACAC CAATGTGGTA 1740 AAAGCTTTAT GTTGTATTTA ATTTATTCAT TTTGAAAATA 1780
|