| Tag | Content |
|---|
EnhancerAtlas ID | HS110-00248 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr1:153487850-153489080 |
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 | AGCGCCCACA GAGCCAAAAG TGCTGGGGCC TGTGGAAGTC ATAAGGCCCT AGGTAACCCA 60
TGAGGAACTC AGTCTCAGGC TTTGCATGCT GCAGAGAATG ATCAGAATTG GAGGGCCCAT 120
CCCTCCCTTC TCCTGGGTGT AGGACTGCAC CGCCACCTGA AGCCTTCAGA GCCACGCAGC 180
CTGGCTCAGG AAAGCTGCAT CTGCACTCTT CAGTGCCAGG GAACTAAAGG CTGGGGCTTC 240
CTATGCGAGG TGCAGAGCTC CCAGAGGAGC AGGCACACAG ACCATGACAG GAGGCGGGGT 300
AAGAGGCATT CATTGAAAGG TGCATCTGTG TAGGATTCTT CCTAGCTGAA AACCCTAAAC 360
TGAGCCTGGA GGCAGGAGAG GGGCTTTCTG ATGCTGTGGC TCTTCCTTCC TGTGGAGGAG 420
GACTGGAAAG GGGTCCCTTG GGGCCCTCCC CAGCCTCCCT CATTCTTCTG GACAGAGGGC 480
TGGGCTGCTG TCCCCTGGAC TTGGGGAGGA CACAGGCAGG GAAGCTGGGT GCTCAGAGGA 540
CAGAGAAAGG ATCTCCTTGG ACAGCCCACT GAGCAATGGC AAGTGGCTCG CCAGGTTTCT 600
CCTTCTCTGC TCCCTGCTCT CTTGTCACAC CCTTCCTGGT ATGAAGCAAG ACAAGCTCCG 660
GTAGTGAGCC CCTCCCTGAC TCCCTCGCCC TAGGCACTGC CTATAATGGG GTGGGGCAAA 720
ACAGCTCCCT TCTCCCAGCT TCCTCTTCAG GCTCCACTGG GTCTGTCCCT GCTCACCACC 780
TGGACTAGGT CCCTAGGTGT CAGGACAGCT GGAGCTGTCT CCAGGTGTGT CATCATCACT 840
GGCATCCTGG CCACCCAGGA GCCATACCTA GGTATCCTAG ACCCCCTCTC TAGGCTCCAT 900
CCTACCTCCT CCCACCCTGT TACCCTATAG CCAACAAACC CTGCATGTTC ATCCTTGGGC 960
ACACGTCTGC CCTCTTCCTG CTACCCTACT CCACCCCAGG TCACATCCTC ATTCTCTCAC 1020
CGACCCAGGG CACCAGCCTC CTGGCGGGGG GCTCTGCCTC CACTCCAGGA CCCCTTCTCC 1080
AGGCTCCAGG TCTCCTTGAA GTCCAGGTTT TCATCACATC ACCATTCTGT TCAACCTTCA 1140
CCTACTTCAC GGCTTAGAGA TGAGGCTTTC AAACATCTGT TTATTCCTAG AACCTTTCTT 1200
TAAAATAAAA CCTTATGAGG AAGCCTGATA 1230
|
