| Tag | Content |
|---|
EnhancerAtlas ID | HS095-20681 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr3:58456700-58457950 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr3:58457157-58457168 | CTTCTGGGAAA | + | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09926 | chr3:58455183-58462116 | CD14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 58457172 | 58457525 | | chr3 | 58457705 | 58457803 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I058469 | chr3 | 58455661 | 58459042 |
|
Enhancer Sequence | GCAGAGGTTC CCTAACCTTT CCTAAGCCTG AGTTTACTCA TGCAGAAAAT GCCAGGGTGG 60
ACTTGGAGGG TAGCTACAGG CCCTGTGAGC ACTAAGATTT CCTGAGACTT CGCTGCTGTC 120
CATGCCCCTC CCCTGTTTTG ACCTTTCCAA CAGACTGGAG GCTAGAATGA AGATAAGGAG 180
TACCATTTTT TTGTTAGGCA CTGGGAGACG GCCCAGACTT TGATATAGCA AAGGTTAATG 240
TTCTGTCATC TCAAAGATCC ATTTCCCCAG GCTGTCGGAA TGTAAATGTT AAGGTGATGA 300
AAATAGTGAA GCCTAGGTTC CGGCTCATTT GAGTCAGAGC CCCTCACCCC TCACAGTGCA 360
ACCCTGGTGC ACAGGGCCTC CTCTGTGGCC TGAACCTTCA TAAACTTGGG TTTAGGTTGT 420
CAGCACTGAT TTAAAGAGAT TTGCTTTGTT CAGTTTGCTT CTGGGAAAGA ACTGACATTC 480
ACAGCAGGGT TTGGGGGTTA AGAATGAAAC CTGAGCTGGC TTCTTCCCCA CTGGGTGTGT 540
GCAGAGTGAG TCAGATGTTT GCACAGAAGG CTGTGGTGTC AAATCAAATC CACAAATTTG 600
CAGGCCTTAT GCCTTTACCA CTTCAAACCG GAAAGGTGTT GCAACATAAC AGTTTTAATT 660
GCTAAACCCT AGCTGCAAAC CCAAATCTCT GGATTTAATA AGAATTGGGT GTGAAAGACT 720
GTGAACAGTG GCAGTTTTCT GCCAGGTGAG TTTATTTGTT CCTTCATTCC CTCATTTGCT 780
TCCTCGTTGG TGCCCAAGCC CACACCAAAG GCCTCTGGCC AGTCACTGCC TGCGCGCCCT 840
CCTCCTGATG ATGGACCTGT GGTCTCGCCT GTAGGTTTAC CTTCTTTCCT GCTCTTGGTT 900
GAGATTTGCG GACCTTTGTA TCCACTGTGG TCTCCTTGGA ACAAGCAACT GGAAATTCTT 960
CACACCAGCT ATGGCTGGTA GGAATTTCGG GCCACAACTC AGGTAGACAA AAAATAAAGC 1020
TTTCTTTTCT AGAACTTGAC TCTGGGTTCA GGTCTTTGCT GTGCCAGACT GGTATAAAAC 1080
CTCTAACCAT GGTCTTTGCC GGGCACATAC CCACTTCCCC AGCAACACGT ATTCACTGAG 1140
TTGCCCACCA TCCTTGGGGC TGAAGTAAGG CCATGATTAG GGAGGGAAAT GAATCTGGCT 1200
CTGTGTCATT GGTCCACATA GTTGGTCAAG GGATCTGTTG GTCTTGCTAA 1250
|
