| Tag | Content |
|---|
EnhancerAtlas ID | HS034-17150 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:128164770-128165990 |
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 | AAATTAAAAA ATTAGCCAGG TGTGGCGGTC CATGCCGGTA GTCCCAGCTA CTTGGGAGGC 60
TGAGGCAGGA TGATCACTTG CACCTGGGAC GTTGAGGCGG CAGTGAGCCG TGTTCGCGCC 120
ACTGCACTCC AGCCTGGGTG ACACTGCAAG ACCCTGTCTC AAAAAAAGTA GTCAAGGAGG 180
CTGAGAGCCA GGAAGCCTCT GGCCAGCAGG TGAGCAGGCC CTTTCCTGCT GCTGTGCATT 240
GTATTTAAGA GAAAAGACAG ATACGTCTGA TACCTTCAAA GGTGTTCTTC ATACAGCAGG 300
TTGCAACCTA TTAATAGATC ATAAAATCAG TTTAGTGTTT CATCATCATC ATCAAAAACC 360
ACCACCAACA ACAAAAAGAC CCAGAACAGA TAGTGTAAAG AGTGCATCCC TGCATTCCTG 420
TATAGGGAGA AATATGGTTT TGTGGAACCT TGTTGCGATG TAAAGTGTAC TTCTTAAGAT 480
AAATACAGGG TTGAGGTTTT TGAAATAAAG TTTGAACAGG ACCACCTTAA GCCACAGTGT 540
AGACTTTCCA TAGGCCAAAA CCTGGATCAC CAAGACAGTG TGCCCCAGGC TGCAGGCCAC 600
ACTCCTGGGA GCCTCAGGCA ACCTTGTGCA GGCCTGACTT CGAGACACTC TGAGCATGAG 660
CTGGTTCCTG GGTAGCCTCC CCTCTACCTC TCCCCGCTTG CCCTCCCTCC CTCCTTCTGC 720
TCCTGTCTCT CCTCATCCCC TCCCCGAGTT GCTGCCTCCT CCTCCTCCTC CCCCACCACC 780
TCTCCCCGTC TCCGAGTTGC CTGCCCCGCC CCCTCCTCTT CCCCCTGCCC CTCTCCGCGT 840
CCTTCCCGCC TTCCCCCTCC TCGTCTCCCC CCTCCCCGCC CGCGCCGTCT GCGTCCCTCC 900
CGGGCCCAGA CGCGGCGCGG TCAGGGGGCG CTGACTCACA GGCTGACTCA GCTGCAGGCG 960
CGCTGCCAGG CGACGCAGCG GGCGGGTGGC CGGGCGCCGG CGGGCTCGCA GCCGGGCTGC 1020
TGGCAACGGT GCCGGCGGAG GTGGGGGCGT GGCGCGGGAT GGGCGGCGCG GGCCCTGCCG 1080
TGGTACCGCC TGGCAGCGTC CACCCCGCCG CTGGGGCGCC CTGGAGGCTC CTGGCCCTCC 1140
GTGGGGCCGT GACACCGGCG CTGCGGGGAG CGGTGGCCTC GCAGAGGCTG GGCATGGGAG 1200
GACGGCCGCC CCGGGTAAAG 1220
|
