| Tag | Content |
|---|
EnhancerAtlas ID | HS003-02372 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:153487760-153489020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:153488263-153488284 | GGAGGAGGACTGGAAAGGGGT | + | 6.3 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_02992 | chr1:153487818-153488496 | Bladder | | SE_23261 | chr1:153487446-153489480 | Colon_Crypt_1 | | SE_23926 | chr1:153487791-153489348 | Colon_Crypt_2 | | SE_25303 | chr1:153487485-153489518 | Colon_Crypt_3 | | SE_28418 | chr1:153487633-153489575 | Fetal_Intestine | | SE_36529 | chr1:153487745-153488859 | HMEC | | SE_52579 | chr1:153487618-153489518 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 153488459 | 153488748 | | chr1 | 153488088 | 153488813 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I153514 | chr1 | 153487077 | 153489449 |
|
Enhancer Sequence | ATCTATCATA GTGAATTCAT CTTGGCTTGT ATTTGTCTTT ATACCAATGC AGTCATGAAA 60
TGTTATTTTT AATATTTTTC TATGAAGGAA AGCGCCCACA GAGCCAAAAG TGCTGGGGCC 120
TGTGGAAGTC ATAAGGCCCT AGGTAACCCA TGAGGAACTC AGTCTCAGGC TTTGCATGCT 180
GCAGAGAATG ATCAGAATTG GAGGGCCCAT CCCTCCCTTC TCCTGGGTGT AGGACTGCAC 240
CGCCACCTGA AGCCTTCAGA GCCACGCAGC CTGGCTCAGG AAAGCTGCAT CTGCACTCTT 300
CAGTGCCAGG GAACTAAAGG CTGGGGCTTC CTATGCGAGG TGCAGAGCTC CCAGAGGAGC 360
AGGCACACAG ACCATGACAG GAGGCGGGGT AAGAGGCATT CATTGAAAGG TGCATCTGTG 420
TAGGATTCTT CCTAGCTGAA AACCCTAAAC TGAGCCTGGA GGCAGGAGAG GGGCTTTCTG 480
ATGCTGTGGC TCTTCCTTCC TGTGGAGGAG GACTGGAAAG GGGTCCCTTG GGGCCCTCCC 540
CAGCCTCCCT CATTCTTCTG GACAGAGGGC TGGGCTGCTG TCCCCTGGAC TTGGGGAGGA 600
CACAGGCAGG GAAGCTGGGT GCTCAGAGGA CAGAGAAAGG ATCTCCTTGG ACAGCCCACT 660
GAGCAATGGC AAGTGGCTCG CCAGGTTTCT CCTTCTCTGC TCCCTGCTCT CTTGTCACAC 720
CCTTCCTGGT ATGAAGCAAG ACAAGCTCCG GTAGTGAGCC CCTCCCTGAC TCCCTCGCCC 780
TAGGCACTGC CTATAATGGG GTGGGGCAAA ACAGCTCCCT TCTCCCAGCT TCCTCTTCAG 840
GCTCCACTGG GTCTGTCCCT GCTCACCACC TGGACTAGGT CCCTAGGTGT CAGGACAGCT 900
GGAGCTGTCT CCAGGTGTGT CATCATCACT GGCATCCTGG CCACCCAGGA GCCATACCTA 960
GGTATCCTAG ACCCCCTCTC TAGGCTCCAT CCTACCTCCT CCCACCCTGT TACCCTATAG 1020
CCAACAAACC CTGCATGTTC ATCCTTGGGC ACACGTCTGC CCTCTTCCTG CTACCCTACT 1080
CCACCCCAGG TCACATCCTC ATTCTCTCAC CGACCCAGGG CACCAGCCTC CTGGCGGGGG 1140
GCTCTGCCTC CACTCCAGGA CCCCTTCTCC AGGCTCCAGG TCTCCTTGAA GTCCAGGTTT 1200
TCATCACATC ACCATTCTGT TCAACCTTCA CCTACTTCAC GGCTTAGAGA TGAGGCTTTC 1260
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