Tag | Content |
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EnhancerAtlas ID | HS191-01001 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr1:43401620-43403060 |
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_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: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I042929 | chr1 | 43395541 | 43414526 |
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Enhancer Sequence | TCTCAACCTT GTAAAAATGT AAAAACCATT GTTAGCTCAT GGGTTGCACA AAAACAGGCT 60 GCTGGCTGGA TGTGGCCCTC CTGCCAACCC TTGATCTAGG ATTCTAGACC ACTGCCAGGA 120 GGGGTATGCG TTTTGGAACC TCTGGCTGGT CTCACCATCC TTCCCTCTAG ACATTCCTTT 180 ACCCCAGGAG GACTAGGTCA GTTAGGTCAT CCCCAGCAGG GATCCCTGGG CCAGGTTTAG 240 GCTCGGTCTC AACTCTCCCT GTGCTCTACG GGATGCTATT GTGGGGAAGA AGGGGCTAAA 300 CTGCCAGCCA AGCTTTCAGC GCCAGTTACA AGGAGGAAAG GGCCAGCTTC TCCGGCTTAG 360 CCTCTCAGCC TGGCCTTCAC CCCTGTTCCT TGCCTGCCCC TGTCTTCCAG TTGGGGCTGG 420 CCCCACACTG CCCTTCCCAC AAGCTCTCAG CCCAGGGCCT TCATCTCCAC AGCAACTCTC 480 AGCCACACCC CAGGGTGAGC TGGGAGATTG GAGCCAGATG TTCCAGGTGG GGCTGGACAG 540 ATAACCCTGC CCACTGGGTC CCCTGGGGCC TCACTTTGGG GCCTGGGGGA AGAGGCCCAG 600 GTTGGGGCTA GAGCTGGGCC CCAACCCCCC TGCAGAGGGC TGGACCACCC AGGCTGCTTC 660 CCTGGAACAG CCCTGACATG GCTAGCCTCC AAACCAAGGC CAGGCCAGGC CAGGCCTCCC 720 GGTAGACAGA GGAATCATCC CACTGCCGTG GCCACACCCG AAGCCCTTCT CAGCTCTTGC 780 AATAAAGTGT CTCCTCTACC CCAACTATGA CTCACAAGGC ACACGCAGTG ACTCCCTCAT 840 ACGACCTAGA CACCTCACAC CTTTGCTTGG GCCTAATCAC CTTTCAGAAC ATGCACAGAT 900 ACTCCTCTGG AAAGCCTTCC TCCCGAGAAC CACCCCTCCC ACTCCACTGC AACTGGTTCT 960 CAAACAGAGA CGGCTTTGGT ACCCCATAGG ACATCTGCCA ATGCCCAGAG ACATTTTTGG 1020 TTGCCACACT GGCTACTGGT ATCTAGAGGG CAGAAGCCAA GGATGCTGAT AAACATCCTC 1080 CAATGCATGG GACAGGCCTC TACAACACCA GCAGAAACAT CACAGTGCCA AGCTGAGAAA 1140 CCCTGCTCTA AGGGCGAAGC ACCCTCTCCC TCTTCCTTCC CTGCTCCCAC TGTGCTTGCT 1200 CGCATTTCCA TCATCGCCTT TAGAAGACTA ACTGTAAGGT ACCGTGTGCT CCCTGTACAG 1260 TAAACCTCAG CACGGAGATG GTCTGTCTGA TGCATCCATG TTGCTGGTGC CCAGCACGGT 1320 GGTGGAGGTG CAGAGTTGAC ACTAAATGAC CAACAAGCCA TGAATCTAAC TGAAGGGCTT 1380 GAGGGGTGAT GTGATATGAC AGGGTGTGAT GGTGTAAGAG ATTGTGCAAC TGTGTGTGGG 1440
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