| Tag | Content |
|---|
EnhancerAtlas ID | HS191-21296 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr2:128164530-128165990 |
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 | | 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 |
|
| | 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 |
|
| | 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 |
| GH02I127406 | chr2 | 128164514 | 128166975 |
|
Enhancer Sequence | CATCCCCAGT GCCCTCCCAC CCCAGGTAAT CACAGTTACC AGGATTCAAT GCACATCCAA 60
ACACAAACAA ACACAAACCA TGGTGTGTTT ATTGCCCATG GAGGCTCTGT CTCAGGTCCC 120
TGGGAATCAT TGGGAGTTGT GGATCCCAGC ACTTTGGGAG GCTGAGGCAG GAGGATCGCT 180
TGAGCCCAGG AGTTTTTTGA GACCAGCTTG AACAACATAG TGAGACCCCA TCTCTACAAA 240
AAATTAAAAA ATTAGCCAGG TGTGGCGGTC CATGCCGGTA GTCCCAGCTA CTTGGGAGGC 300
TGAGGCAGGA TGATCACTTG CACCTGGGAC GTTGAGGCGG CAGTGAGCCG TGTTCGCGCC 360
ACTGCACTCC AGCCTGGGTG ACACTGCAAG ACCCTGTCTC AAAAAAAGTA GTCAAGGAGG 420
CTGAGAGCCA GGAAGCCTCT GGCCAGCAGG TGAGCAGGCC CTTTCCTGCT GCTGTGCATT 480
GTATTTAAGA GAAAAGACAG ATACGTCTGA TACCTTCAAA GGTGTTCTTC ATACAGCAGG 540
TTGCAACCTA TTAATAGATC ATAAAATCAG TTTAGTGTTT CATCATCATC ATCAAAAACC 600
ACCACCAACA ACAAAAAGAC CCAGAACAGA TAGTGTAAAG AGTGCATCCC TGCATTCCTG 660
TATAGGGAGA AATATGGTTT TGTGGAACCT TGTTGCGATG TAAAGTGTAC TTCTTAAGAT 720
AAATACAGGG TTGAGGTTTT TGAAATAAAG TTTGAACAGG ACCACCTTAA GCCACAGTGT 780
AGACTTTCCA TAGGCCAAAA CCTGGATCAC CAAGACAGTG TGCCCCAGGC TGCAGGCCAC 840
ACTCCTGGGA GCCTCAGGCA ACCTTGTGCA GGCCTGACTT CGAGACACTC TGAGCATGAG 900
CTGGTTCCTG GGTAGCCTCC CCTCTACCTC TCCCCGCTTG CCCTCCCTCC CTCCTTCTGC 960
TCCTGTCTCT CCTCATCCCC TCCCCGAGTT GCTGCCTCCT CCTCCTCCTC CCCCACCACC 1020
TCTCCCCGTC TCCGAGTTGC CTGCCCCGCC CCCTCCTCTT CCCCCTGCCC CTCTCCGCGT 1080
CCTTCCCGCC TTCCCCCTCC TCGTCTCCCC CCTCCCCGCC CGCGCCGTCT GCGTCCCTCC 1140
CGGGCCCAGA CGCGGCGCGG TCAGGGGGCG CTGACTCACA GGCTGACTCA GCTGCAGGCG 1200
CGCTGCCAGG CGACGCAGCG GGCGGGTGGC CGGGCGCCGG CGGGCTCGCA GCCGGGCTGC 1260
TGGCAACGGT GCCGGCGGAG GTGGGGGCGT GGCGCGGGAT GGGCGGCGCG GGCCCTGCCG 1320
TGGTACCGCC TGGCAGCGTC CACCCCGCCG CTGGGGCGCC CTGGAGGCTC CTGGCCCTCC 1380
GTGGGGCCGT GACACCGGCG CTGCGGGGAG CGGTGGCCTC GCAGAGGCTG GGCATGGGAG 1440
GACGGCCGCC CCGGGTAAAG 1460
|
