| Tag | Content |
|---|
EnhancerAtlas ID | HS184-15999 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:20335430-20336550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr2:20336017-20336028 | CCACACCCTGC | + | 6.62 | | ZNF263 | MA0528.1 | chr2:20335902-20335923 | GGGGGAAGCAGGAGAGGAGAG | + | 6.21 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23108 | chr2:20335434-20336559 | Colon_Crypt_1 | | SE_23761 | chr2:20335444-20336667 | Colon_Crypt_2 | | SE_24805 | chr2:20335404-20336639 | Colon_Crypt_3 | | SE_27030 | chr2:20335390-20336799 | Esophagus |
|
| | 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 |
| GH02I020135 | chr2 | 20335501 | 20336540 |
|
Enhancer Sequence | TGTTTCTCCC ACCTCAGCCT CCCCAAGTGC TGGGATTACA GACGAGAGCC ACCGCGCCTG 60
GCCTGAGAAA GGCTTTTTCT ATGCCACAGA GAAGTTGGGC TCCCAGTCAC GGGAGCAGCT 120
GCGGCCGGTT CCAGCAGGGG GCAGCTCTCA ATGACAGCTG AAGGGCATTG CATAGCCAGA 180
TGCGCACATG GCTTTTAGGA ACTGGGCTCT GCCTCCCCTG AAGTCTGTCT GAACCTGGGG 240
CATCACCGTC TCACCGGGCT GGGGCTTTGA TGCATCAGGC CCAGAGAAAG AAACTTGGTA 300
GAGGAGAGGA GGAAGGAGAT GCAACCTTCC AGGAAGCAGA AATGTTCAAG GACTCTCAAA 360
GGAAACTCCA GAAAACAAGG AGAGGCAGGA ATTGCCTTAT GATCGCTTCT AGCTCTATGT 420
CTCACCTTTG AAATAAAGCA TCTTCCTGGT CCCAGTGCAG AGACAGGTCC TGGGGGGAAG 480
CAGGAGAGGA GAGAATCAGC TCCTGTTCTC CTGTCTGCCT CAACTTCCCC AGGCCTACCC 540
AGCCCACCTG GGCTAGGACG GAGGTGCTGG CAGCCTCTCC CCATTAACCA CACCCTGCAG 600
GCTGAGGCGG GCAGGCTGAG GCGGGCAGGC TGGGGGCTGA GGAGACGCTC CTTCCCTGCA 660
TTCCATGGAC ATGGTGCCTT GGGCCAGGCT GCAGAGGCCG CAGGGCCTGG CATGTGCCCC 720
GTGAAACTGG CCCTGCAGTG AGGCGGGGGC AGTGGGGATG GATGAACTCA TTCTTTCCTC 780
GTCTGAGGCT GCTCTGATCG TAAAACCGTG GACGCTGAGC AAATGGCCCC AGGTGTGTGC 840
TCTCTCAGTT TCGCTGGGAT AATAGTCAGG AACAGCAAGA GGGTGACCTG GTTTCGATGG 900
AGCAGCTCCT GCTCTGGGCA CTACGTGGCT CTGCTGCCTC TGCTCTCCTG TCCTCTCCCC 960
ACCCCGTTTT GGAGGGCCAG GCCTTCACCA AAGCCTGAAG GAACCTCAGC AAGAGTGCAA 1020
AGGGGGTGCT GTCAGAGGTG CCCCAGGAAA AGACCCTTCT CCAGAGAGAG GCTCTGCGGA 1080
GAGGCCCGGG GTGCCTAGAG AGGGGAAAGC ACCCTGCACC 1120
|
