Tag | Content |
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EnhancerAtlas ID | HS194-00141 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr1:43401860-43403270 |
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: 43 | 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_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 | GCTCGGTCTC AACTCTCCCT GTGCTCTACG GGATGCTATT GTGGGGAAGA AGGGGCTAAA 60 CTGCCAGCCA AGCTTTCAGC GCCAGTTACA AGGAGGAAAG GGCCAGCTTC TCCGGCTTAG 120 CCTCTCAGCC TGGCCTTCAC CCCTGTTCCT TGCCTGCCCC TGTCTTCCAG TTGGGGCTGG 180 CCCCACACTG CCCTTCCCAC AAGCTCTCAG CCCAGGGCCT TCATCTCCAC AGCAACTCTC 240 AGCCACACCC CAGGGTGAGC TGGGAGATTG GAGCCAGATG TTCCAGGTGG GGCTGGACAG 300 ATAACCCTGC CCACTGGGTC CCCTGGGGCC TCACTTTGGG GCCTGGGGGA AGAGGCCCAG 360 GTTGGGGCTA GAGCTGGGCC CCAACCCCCC TGCAGAGGGC TGGACCACCC AGGCTGCTTC 420 CCTGGAACAG CCCTGACATG GCTAGCCTCC AAACCAAGGC CAGGCCAGGC CAGGCCTCCC 480 GGTAGACAGA GGAATCATCC CACTGCCGTG GCCACACCCG AAGCCCTTCT CAGCTCTTGC 540 AATAAAGTGT CTCCTCTACC CCAACTATGA CTCACAAGGC ACACGCAGTG ACTCCCTCAT 600 ACGACCTAGA CACCTCACAC CTTTGCTTGG GCCTAATCAC CTTTCAGAAC ATGCACAGAT 660 ACTCCTCTGG AAAGCCTTCC TCCCGAGAAC CACCCCTCCC ACTCCACTGC AACTGGTTCT 720 CAAACAGAGA CGGCTTTGGT ACCCCATAGG ACATCTGCCA ATGCCCAGAG ACATTTTTGG 780 TTGCCACACT GGCTACTGGT ATCTAGAGGG CAGAAGCCAA GGATGCTGAT AAACATCCTC 840 CAATGCATGG GACAGGCCTC TACAACACCA GCAGAAACAT CACAGTGCCA AGCTGAGAAA 900 CCCTGCTCTA AGGGCGAAGC ACCCTCTCCC TCTTCCTTCC CTGCTCCCAC TGTGCTTGCT 960 CGCATTTCCA TCATCGCCTT TAGAAGACTA ACTGTAAGGT ACCGTGTGCT CCCTGTACAG 1020 TAAACCTCAG CACGGAGATG GTCTGTCTGA TGCATCCATG TTGCTGGTGC CCAGCACGGT 1080 GGTGGAGGTG CAGAGTTGAC ACTAAATGAC CAACAAGCCA TGAATCTAAC TGAAGGGCTT 1140 GAGGGGTGAT GTGATATGAC AGGGTGTGAT GGTGTAAGAG ATTGTGCAAC TGTGTGTGGG 1200 AAACCTGAGA TGTTGGTACA TGACTGAGCT TGACTCAGCT CCAAAGTGAG ACCACACACT 1260 GCCAGCTAGG TGGCAGTTGT AGGTGAGTGA AAGGGTGTTT AGGTGCCCAT CTGGGACTGT 1320 GTCCATCTTC CACAATGGTC AAGGGCACAG ACTAGGGCCA GACTCCCCGG AGTTACATTG 1380 CAGCCTTGCC ACTTACTAGC TGTGTGTCCT 1410
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