Tag | Content |
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EnhancerAtlas ID | HS047-19709 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:128165060-128166770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:128165606-128165624 | GCGTCCTTCCCGCCTTCC | - | 6.01 | KLF16 | MA0741.1 | chr2:128165572-128165583 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr2:128165812-128165823 | GGGGGCGTGGC | - | 6.62 | KLF5 | MA0599.1 | chr2:128165572-128165582 | GCCCCGCCCC | + | 6.02 | RREB1 | MA0073.1 | chr2:128166244-128166264 | GCCCCCACCACCACCACCCC | + | 6.45 | SP3 | MA0746.2 | chr2:128165811-128165824 | TGGGGGCGTGGCG | - | 6.57 | SP8 | MA0747.1 | chr2:128165811-128165823 | TGGGGGCGTGGC | - | 6.11 | TFAP2A | MA0003.3 | chr2:128165379-128165390 | AGCCTCAGGCA | + | 6.32 | ZNF263 | MA0528.1 | chr2:128165526-128165547 | TCCTCCTCCTCCTCCCCCACC | - | 6.27 | ZNF263 | MA0528.1 | chr2:128165532-128165553 | TCCTCCTCCCCCACCACCTCT | - | 6.49 | ZNF263 | MA0528.1 | chr2:128165472-128165493 | CTCCCTCCCTCCTTCTGCTCC | - | 6.59 | ZNF263 | MA0528.1 | chr2:128165529-128165550 | TCCTCCTCCTCCCCCACCACC | - | 7.31 | ZNF263 | MA0528.1 | chr2:128165580-128165601 | CCCTCCTCTTCCCCCTGCCCC | - | 7.81 | ZNF263 | MA0528.1 | chr2:128165523-128165544 | GCCTCCTCCTCCTCCTCCCCC | - | 8.62 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09644 | chr2:128164535-128166940 | CD14 | SE_23461 | chr2:128165153-128165765 | Colon_Crypt_1 | SE_23461 | chr2:128165766-128166677 | Colon_Crypt_1 | SE_24012 | chr2:128165266-128166623 | Colon_Crypt_2 | SE_24894 | chr2:128165065-128166599 | Colon_Crypt_3 | SE_28345 | chr2:128164776-128166852 | Fetal_Intestine | SE_29146 | chr2:128164682-128166773 | Fetal_Intestine_Large | SE_43376 | chr2:128165019-128166813 | Lung | SE_50833 | chr2:128165107-128166882 | Sigmoid_Colon | SE_52838 | chr2:128165093-128165615 | Small_Intestine | SE_52838 | chr2:128165639-128166869 | Small_Intestine |
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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 |
GH02I127406 | chr2 | 128164514 | 128166975 |
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Enhancer Sequence | ATACAGCAGG TTGCAACCTA TTAATAGATC ATAAAATCAG TTTAGTGTTT CATCATCATC 60 ATCAAAAACC ACCACCAACA ACAAAAAGAC CCAGAACAGA TAGTGTAAAG AGTGCATCCC 120 TGCATTCCTG TATAGGGAGA AATATGGTTT TGTGGAACCT TGTTGCGATG TAAAGTGTAC 180 TTCTTAAGAT AAATACAGGG TTGAGGTTTT TGAAATAAAG TTTGAACAGG ACCACCTTAA 240 GCCACAGTGT AGACTTTCCA TAGGCCAAAA CCTGGATCAC CAAGACAGTG TGCCCCAGGC 300 TGCAGGCCAC ACTCCTGGGA GCCTCAGGCA ACCTTGTGCA GGCCTGACTT CGAGACACTC 360 TGAGCATGAG CTGGTTCCTG GGTAGCCTCC CCTCTACCTC TCCCCGCTTG CCCTCCCTCC 420 CTCCTTCTGC TCCTGTCTCT CCTCATCCCC TCCCCGAGTT GCTGCCTCCT CCTCCTCCTC 480 CCCCACCACC TCTCCCCGTC TCCGAGTTGC CTGCCCCGCC CCCTCCTCTT CCCCCTGCCC 540 CTCTCCGCGT CCTTCCCGCC TTCCCCCTCC TCGTCTCCCC CCTCCCCGCC CGCGCCGTCT 600 GCGTCCCTCC CGGGCCCAGA CGCGGCGCGG TCAGGGGGCG CTGACTCACA GGCTGACTCA 660 GCTGCAGGCG CGCTGCCAGG CGACGCAGCG GGCGGGTGGC CGGGCGCCGG CGGGCTCGCA 720 GCCGGGCTGC TGGCAACGGT GCCGGCGGAG GTGGGGGCGT GGCGCGGGAT GGGCGGCGCG 780 GGCCCTGCCG TGGTACCGCC TGGCAGCGTC CACCCCGCCG CTGGGGCGCC CTGGAGGCTC 840 CTGGCCCTCC GTGGGGCCGT GACACCGGCG CTGCGGGGAG CGGTGGCCTC GCAGAGGCTG 900 GGCATGGGAG GACGGCCGCC CCGGGTAAAG GACAGGGCCC TGGAAACGCG GGTCTGCCGG 960 GAGCAGGGGA CAGGAAGGAG ACCGCGGCTC TCCCAGTCCT GCTGCCCCGG GCCTCCAGAC 1020 GGCCAGACTC TCCCCACACC GGCCTGGAGG GGGACGCGCC GACCCCAGCT GGGAGGGGTG 1080 GCTGGCTGCG TAGATCCGTT TGGGCCGCCT GCCTGGAAAG GCCCAGGTCC GGGCCTCGTC 1140 CTCCTCTTCA CACTCTCCCC CGATCTCCAA CCACCTTCAC CCTCGCCCCC ACCACCACCA 1200 CCCCCAGCTC CTCCTGGCCG CCTGCGGTCC AGCTGAGGCC CGCCTCCTCC AGGAAGTCTT 1260 CCTGGAGAGC CTGTCCTGGG TTAGGCCCGC CCAGAGCCAC CTGGGGCGAC TTATTTCATG 1320 GCACCTTCGA CCTTGCTCTC TGTCTGTTTT GTGTCTGGCT TCATCACCAA ACTGAGCCTC 1380 TTGGGGGCAG TGACCGGGTC TTAGGTCTTA GTTGGCCCTT AGGCGCTAGG GCTGAGAAGA 1440 CTTAGGCGGA CAGGAGATGA GACTGTGTAT TCGACGACAC ACTTTAGAGA TCCAGCCCGG 1500 AACACAGCCA TACCAGATTT TAAAAAAAGC CAACATAATA TAGCATGTTA AAAATTATTG 1560 TAGGCCGGGA GCGGTGGCCC ACGCCTGTAA TCCCAGCAAT TCAGGAGGCT GAGGCCGGAG 1620 GATCACTTGA GCTCAGGAGT TTGAGACCAG CCTAGGCAAC CAACATAGTG AGACTCCGTC 1680 TGTACAAAAA TGAAAAAAAA TTAGCCGAGC 1710
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