Tag | Content |
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EnhancerAtlas ID | HS146-00446 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr1:43401680-43403240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:43402790-43402808 | TCTTCCTTCCCTGCTCCC | - | 6.18 | ZNF263 | MA0528.1 | chr1:43402781-43402802 | CCCTCTCCCTCTTCCTTCCCT | - | 6.31 | ZNF263 | MA0528.1 | chr1:43402786-43402807 | TCCCTCTTCCTTCCCTGCTCC | - | 6.9 |
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| Number of super-enhancer constituents: 44 | ID | Coordinate | Tissue/cell |
SE_01795 | chr1:43401101-43403350 | Aorta | SE_02447 | chr1:43401761-43403049 | Astrocytes | SE_04284 | chr1:43399877-43402347 | Brain_Anterior_Caudate | SE_04284 | chr1:43403029-43404220 | Brain_Anterior_Caudate | SE_05390 | chr1:43400269-43403582 | Brain_Cingulate_Gyrus | SE_06192 | chr1:43395065-43405505 | Brain_Hippocampus_Middle | SE_07319 | chr1:43400813-43402381 | Brain_Hippocampus_Middle_150 | SE_08269 | chr1:43400734-43404931 | Brain_Inferior_Temporal_Lobe | SE_10377 | chr1:43396392-43405534 | CD19_Primary | SE_11009 | chr1:43387831-43425728 | CD20 | SE_12470 | chr1:43400220-43403900 | CD3 | SE_12535 | chr1:43401724-43401911 | CD34_adult | SE_13825 | chr1:43401464-43405153 | CD34_Primary_RO01536 | SE_14471 | chr1:43395753-43414527 | CD4_Memory_Primary_7pool | SE_19657 | chr1:43396427-43405202 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20345 | chr1:43395492-43405550 | CD56 | SE_20799 | chr1:43396312-43405729 | CD8_Memory_7pool | SE_22754 | chr1:43395674-43405513 | CD8_primiary | SE_23189 | chr1:43399749-43406265 | Colon_Crypt_1 | SE_23904 | chr1:43401192-43405387 | Colon_Crypt_2 | SE_25177 | chr1:43399941-43405213 | Colon_Crypt_3 | SE_26580 | chr1:43395721-43413249 | Esophagus | SE_29267 | chr1:43400819-43410293 | Fetal_Intestine_Large | SE_31882 | chr1:43401274-43405435 | Gastric | SE_33837 | chr1:43401475-43412846 | HCC1954 | SE_34353 | chr1:43395339-43412997 | HCT-116 | SE_35049 | chr1:43400682-43411164 | HeLa | SE_36013 | chr1:43400628-43405505 | HMEC | SE_37191 | chr1:43401608-43403612 | HSMMtube | SE_39883 | chr1:43397369-43405479 | K562 | SE_42796 | chr1:43401554-43405089 | Lung | SE_50202 | chr1:43396219-43406255 | Sigmoid_Colon | SE_54088 | chr1:43400594-43405374 | Spleen | SE_55340 | chr1:43401594-43402708 | Thymus | SE_55821 | chr1:43399761-43405450 | u87 | SE_57045 | chr1:43396858-43405413 | VACO_400 | SE_58269 | chr1:43401710-43402795 | VACO_9m | SE_58561 | chr1:43388242-43430420 | Ly1 | SE_60624 | chr1:43388552-43428820 | DHL6 | SE_62392 | chr1:43388423-43425814 | Tonsil | SE_64094 | chr1:43401625-43404135 | HSMM | SE_64340 | chr1:43397259-43405516 | NHEK | SE_67781 | chr1:43399761-43405450 | u87 | SE_68708 | chr1:43401621-43403290 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 43402214 | 43402581 | chr1 | 43402778 | 43403133 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I042929 | chr1 | 43395541 | 43414526 |
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Enhancer Sequence | GCTGGCTGGA TGTGGCCCTC CTGCCAACCC TTGATCTAGG ATTCTAGACC ACTGCCAGGA 60 GGGGTATGCG TTTTGGAACC TCTGGCTGGT CTCACCATCC TTCCCTCTAG ACATTCCTTT 120 ACCCCAGGAG GACTAGGTCA GTTAGGTCAT CCCCAGCAGG GATCCCTGGG CCAGGTTTAG 180 GCTCGGTCTC AACTCTCCCT GTGCTCTACG GGATGCTATT GTGGGGAAGA AGGGGCTAAA 240 CTGCCAGCCA AGCTTTCAGC GCCAGTTACA AGGAGGAAAG GGCCAGCTTC TCCGGCTTAG 300 CCTCTCAGCC TGGCCTTCAC CCCTGTTCCT TGCCTGCCCC TGTCTTCCAG TTGGGGCTGG 360 CCCCACACTG CCCTTCCCAC AAGCTCTCAG CCCAGGGCCT TCATCTCCAC AGCAACTCTC 420 AGCCACACCC CAGGGTGAGC TGGGAGATTG GAGCCAGATG TTCCAGGTGG GGCTGGACAG 480 ATAACCCTGC CCACTGGGTC CCCTGGGGCC TCACTTTGGG GCCTGGGGGA AGAGGCCCAG 540 GTTGGGGCTA GAGCTGGGCC CCAACCCCCC TGCAGAGGGC TGGACCACCC AGGCTGCTTC 600 CCTGGAACAG CCCTGACATG GCTAGCCTCC AAACCAAGGC CAGGCCAGGC CAGGCCTCCC 660 GGTAGACAGA GGAATCATCC CACTGCCGTG GCCACACCCG AAGCCCTTCT CAGCTCTTGC 720 AATAAAGTGT CTCCTCTACC CCAACTATGA CTCACAAGGC ACACGCAGTG ACTCCCTCAT 780 ACGACCTAGA CACCTCACAC CTTTGCTTGG GCCTAATCAC CTTTCAGAAC ATGCACAGAT 840 ACTCCTCTGG AAAGCCTTCC TCCCGAGAAC CACCCCTCCC ACTCCACTGC AACTGGTTCT 900 CAAACAGAGA CGGCTTTGGT ACCCCATAGG ACATCTGCCA ATGCCCAGAG ACATTTTTGG 960 TTGCCACACT GGCTACTGGT ATCTAGAGGG CAGAAGCCAA GGATGCTGAT AAACATCCTC 1020 CAATGCATGG GACAGGCCTC TACAACACCA GCAGAAACAT CACAGTGCCA AGCTGAGAAA 1080 CCCTGCTCTA AGGGCGAAGC ACCCTCTCCC TCTTCCTTCC CTGCTCCCAC TGTGCTTGCT 1140 CGCATTTCCA TCATCGCCTT TAGAAGACTA ACTGTAAGGT ACCGTGTGCT CCCTGTACAG 1200 TAAACCTCAG CACGGAGATG GTCTGTCTGA TGCATCCATG TTGCTGGTGC CCAGCACGGT 1260 GGTGGAGGTG CAGAGTTGAC ACTAAATGAC CAACAAGCCA TGAATCTAAC TGAAGGGCTT 1320 GAGGGGTGAT GTGATATGAC AGGGTGTGAT GGTGTAAGAG ATTGTGCAAC TGTGTGTGGG 1380 AAACCTGAGA TGTTGGTACA TGACTGAGCT TGACTCAGCT CCAAAGTGAG ACCACACACT 1440 GCCAGCTAGG TGGCAGTTGT AGGTGAGTGA AAGGGTGTTT AGGTGCCCAT CTGGGACTGT 1500 GTCCATCTTC CACAATGGTC AAGGGCACAG ACTAGGGCCA GACTCCCCGG AGTTACATTG 1560
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