Tag | Content |
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EnhancerAtlas ID | HS180-01433 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:43401660-43403300 |
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 | GGGTTGCACA AAAACAGGCT GCTGGCTGGA TGTGGCCCTC CTGCCAACCC TTGATCTAGG 60 ATTCTAGACC ACTGCCAGGA GGGGTATGCG TTTTGGAACC TCTGGCTGGT CTCACCATCC 120 TTCCCTCTAG ACATTCCTTT ACCCCAGGAG GACTAGGTCA GTTAGGTCAT CCCCAGCAGG 180 GATCCCTGGG CCAGGTTTAG GCTCGGTCTC AACTCTCCCT GTGCTCTACG GGATGCTATT 240 GTGGGGAAGA AGGGGCTAAA CTGCCAGCCA AGCTTTCAGC GCCAGTTACA AGGAGGAAAG 300 GGCCAGCTTC TCCGGCTTAG CCTCTCAGCC TGGCCTTCAC CCCTGTTCCT TGCCTGCCCC 360 TGTCTTCCAG TTGGGGCTGG CCCCACACTG CCCTTCCCAC AAGCTCTCAG CCCAGGGCCT 420 TCATCTCCAC AGCAACTCTC AGCCACACCC CAGGGTGAGC TGGGAGATTG GAGCCAGATG 480 TTCCAGGTGG GGCTGGACAG ATAACCCTGC CCACTGGGTC CCCTGGGGCC TCACTTTGGG 540 GCCTGGGGGA AGAGGCCCAG GTTGGGGCTA GAGCTGGGCC CCAACCCCCC TGCAGAGGGC 600 TGGACCACCC AGGCTGCTTC CCTGGAACAG CCCTGACATG GCTAGCCTCC AAACCAAGGC 660 CAGGCCAGGC CAGGCCTCCC GGTAGACAGA GGAATCATCC CACTGCCGTG GCCACACCCG 720 AAGCCCTTCT CAGCTCTTGC AATAAAGTGT CTCCTCTACC CCAACTATGA CTCACAAGGC 780 ACACGCAGTG ACTCCCTCAT ACGACCTAGA CACCTCACAC CTTTGCTTGG GCCTAATCAC 840 CTTTCAGAAC ATGCACAGAT ACTCCTCTGG AAAGCCTTCC TCCCGAGAAC CACCCCTCCC 900 ACTCCACTGC AACTGGTTCT CAAACAGAGA CGGCTTTGGT ACCCCATAGG ACATCTGCCA 960 ATGCCCAGAG ACATTTTTGG TTGCCACACT GGCTACTGGT ATCTAGAGGG CAGAAGCCAA 1020 GGATGCTGAT AAACATCCTC CAATGCATGG GACAGGCCTC TACAACACCA GCAGAAACAT 1080 CACAGTGCCA AGCTGAGAAA CCCTGCTCTA AGGGCGAAGC ACCCTCTCCC TCTTCCTTCC 1140 CTGCTCCCAC TGTGCTTGCT CGCATTTCCA TCATCGCCTT TAGAAGACTA ACTGTAAGGT 1200 ACCGTGTGCT CCCTGTACAG TAAACCTCAG CACGGAGATG GTCTGTCTGA TGCATCCATG 1260 TTGCTGGTGC CCAGCACGGT GGTGGAGGTG CAGAGTTGAC ACTAAATGAC CAACAAGCCA 1320 TGAATCTAAC TGAAGGGCTT GAGGGGTGAT GTGATATGAC AGGGTGTGAT GGTGTAAGAG 1380 ATTGTGCAAC TGTGTGTGGG AAACCTGAGA TGTTGGTACA TGACTGAGCT TGACTCAGCT 1440 CCAAAGTGAG ACCACACACT GCCAGCTAGG TGGCAGTTGT AGGTGAGTGA AAGGGTGTTT 1500 AGGTGCCCAT CTGGGACTGT GTCCATCTTC CACAATGGTC AAGGGCACAG ACTAGGGCCA 1560 GACTCCCCGG AGTTACATTG CAGCCTTGCC ACTTACTAGC TGTGTGTCCT TGCTTTAATT 1620 GCTTAACATT CCTGTGCCCC 1640
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