Tag | Content |
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EnhancerAtlas ID | HS056-00535 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr1:43407240-43408890 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr1:43407593-43407608 | GCATGACTCAGCAGG | + | 6.75 | Nfe2l2 | MA0150.2 | chr1:43407591-43407606 | GAGCATGACTCAGCA | + | 7.66 | ZNF263 | MA0528.1 | chr1:43408088-43408109 | CCTTTTCCTCTTCTCTCCTCC | - | 6 |
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| Number of super-enhancer constituents: 47 | ID | Coordinate | Tissue/cell |
SE_01795 | chr1:43403674-43411142 | Aorta | SE_02447 | chr1:43405569-43410613 | Astrocytes | SE_04284 | chr1:43406405-43408666 | Brain_Anterior_Caudate | SE_05390 | chr1:43406422-43410832 | Brain_Cingulate_Gyrus | SE_06192 | chr1:43406287-43411226 | Brain_Hippocampus_Middle | SE_07319 | chr1:43406534-43411143 | Brain_Hippocampus_Middle_150 | SE_08269 | chr1:43406272-43411134 | Brain_Inferior_Temporal_Lobe | SE_10377 | chr1:43406726-43412417 | CD19_Primary | SE_11009 | chr1:43387831-43425728 | CD20 | SE_13825 | chr1:43406488-43407528 | CD34_Primary_RO01536 | SE_14471 | chr1:43395753-43414527 | CD4_Memory_Primary_7pool | SE_19657 | chr1:43406292-43410967 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20345 | chr1:43407577-43412424 | CD56 | SE_20799 | chr1:43405756-43409955 | CD8_Memory_7pool | SE_22754 | chr1:43406075-43412634 | CD8_primiary | SE_23189 | chr1:43406366-43410995 | Colon_Crypt_1 | SE_23904 | chr1:43407223-43410890 | Colon_Crypt_2 | SE_25177 | chr1:43406652-43411022 | Colon_Crypt_3 | SE_26580 | chr1:43395721-43413249 | Esophagus | SE_29267 | chr1:43400819-43410293 | Fetal_Intestine_Large | SE_31882 | chr1:43406451-43411068 | Gastric | SE_33837 | chr1:43401475-43412846 | HCC1954 | SE_34353 | chr1:43395339-43412997 | HCT-116 | SE_35049 | chr1:43400682-43411164 | HeLa | SE_36013 | chr1:43405529-43411011 | HMEC | SE_37191 | chr1:43404622-43414101 | HSMMtube | SE_38794 | chr1:43405440-43410875 | HUVEC | SE_39883 | chr1:43405665-43410931 | K562 | SE_41038 | chr1:43405665-43414583 | Left_Ventricle | SE_41620 | chr1:43406373-43411014 | LNCaP | SE_42796 | chr1:43405575-43411121 | Lung | SE_49782 | chr1:43407568-43410944 | Right_Ventricle | SE_50202 | chr1:43406339-43411463 | Sigmoid_Colon | SE_54088 | chr1:43406450-43408242 | Spleen | SE_55340 | chr1:43407386-43410138 | Thymus | SE_55821 | chr1:43405505-43410178 | u87 | SE_57045 | chr1:43406294-43410932 | VACO_400 | SE_57417 | chr1:43405825-43410963 | VACO_503 | SE_58269 | chr1:43407361-43407923 | VACO_9m | SE_58269 | chr1:43408012-43408449 | VACO_9m | SE_58561 | chr1:43388242-43430420 | Ly1 | SE_60624 | chr1:43388552-43428820 | DHL6 | SE_62392 | chr1:43388423-43425814 | Tonsil | SE_64094 | chr1:43405747-43410036 | HSMM | SE_64340 | chr1:43405657-43411071 | NHEK | SE_67781 | chr1:43405505-43410178 | u87 | SE_68708 | chr1:43406265-43410984 | H9 |
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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 |
GH01I042929 | chr1 | 43395541 | 43414526 |
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Enhancer Sequence | TCATTAAATC CAGTAGCTGT CAACCTTGGC TGCACATTCG AATTGGTTGG GAAGCTTTTA 60 ATTGAATGCC CAAACAGCAT CCCAGACCAA TTAAATCAGA ATCTGGGGGC GTTCTGGAAA 120 CCCCAATGTG CAACCAAGTG GAGAGCTCAA CCTCCCTCTG TTTCCTCCCA GCCTGTCTTA 180 CAGACTTTCC ATCTGTAAGG ATTCCCAAAG GGAGCCAGTT CTGAAGCACA CACTTTGGCA 240 AGAGCTGTCA AGAGCACTTA GCAAATGCAG GGCTTGGGGC TGGTCCAAGC ATGGGCCCAC 300 GGTCTCCATG CCCAGCAAAC TTGGAAAAGT CCTGTCACCT CCCCTGCAGC TGAGCATGAC 360 TCAGCAGGCC AAGCCTTCCT GGTGACTTGC TCCTCAGCAT CGGGCGTGGC CCCATAGCCA 420 CTGTCTGCCT ATTTGGAAGA AGCCCAGCTA ACTCTAGACA CTACCTGGTT CCCCCAAACA 480 GGACCCTGAT CTTTGGGAGT CACTGCACTC ACTTTCTAGC CCCATCCGTC TGGACAAGAA 540 ATGTGGTCCT GACGTGAGGA CTGCCCACTC TCATTTGGTC CTCTCTGGGA AGGTACAGAT 600 TTTTAAACGG GCAAGGCAGC TGGTTAGGAA GACAACCTGA GGCCATGGAA ACAACAGAGC 660 TTGGCTTCTG ACTCCAGCAT TCAATAGCTT TGTGACCTTG GGCCTGTCGG CCATTTCATC 720 TGCCTGGGCC TCAGTTTCCG GGTCTACAAA ATGGAAATCA CCACCCAATC TCATAAACAC 780 AAGCAAAATG CCTGGTACAG AGGAAGGGCT CAGTTTCCTT TCCTGTCCCT GCCTCCTACC 840 CCCTACCCCC TTTTCCTCTT CTCTCCTCCT TAATGCAAGT AGGCTGGGCT GGAGGAGATG 900 GTCTAGGTCC CTTCCCATCC TGACATTCAA GTAAACAAGT GAGGACAGAT CTAGGATGCA 960 CGGCAGGGAG GAGGAAGCCA GCACAGACCT TCACCCCCTG TGGCTCCCTA GGGCAAGACG 1020 CCATTTCTGC TTTGACTGCC ACAGGGCCTT CAGGGAGAGG ACGCGGTTTC AACCTACAAA 1080 TAAAGGAAGT GTGCTGCCTG TGGATGGGTA TGAGTGCAGG CTCAAGGACC ACCTGGCAGG 1140 CAGGTGTTGG ATACCAGCTC TGTCTCTGAC TTAGCTGGGT GATATTGGGC GGGTTTCCTC 1200 TCTCTGGCCG TTTCCCACAC CTGCAGGCTG GGAGTGGTGC CTGCTGCCTC CTGACAGTGC 1260 TGCAGTGAGC ATCAAGTGAG ACAAGCCCAT GAAAACCCTC TGCAGCCCCA GAATGCCACG 1320 GAAATGCAGC ATTATTGTAT TGAGCTTTGC TTTGAGTTTA TTATATCATC AAACATATTA 1380 TTAAATGACT GAGTTGGGTG GGGGGTTGGT CAAGAGGGCC TATACAAGAC CCCAGGATTC 1440 TGTGGGACCT GAGATTCTAG AATTCTGCCA CCCTGATTCC AAAGCAAGAG AAGAGTCTCT 1500 GACATGATCA GGGCCAGAAA ACTGGCTGGA GAGGCAGACA GTACAGTGCG TTCATATAAA 1560 TGACTCTAAT TCAGGTGGTG GCGTGAGACT GTGGGCATGT GTGATGTGCA ACAGAGCAGG 1620 CTGGTGTCCA TAAGCCAACG ATGGCACAGT 1650
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