| Tag | Content |
|---|
EnhancerAtlas ID | HS136-14422 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr3:195876590-195877710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr3:195877234-195877251 | TAGGTCACCGCGACCTT | + | 7.1 | | ESR1 | MA0112.3 | chr3:195877234-195877251 | TAGGTCACCGCGACCTT | - | 7.1 | | ESR2 | MA0258.2 | chr3:195877235-195877250 | AGGTCACCGCGACCT | + | 6.7 | | PPARG | MA0066.1 | chr3:195877233-195877253 | CTAGGTCACCGCGACCTTTT | + | 6.24 | | PPARG | MA0066.1 | chr3:195877232-195877252 | ACTAGGTCACCGCGACCTTT | - | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_34024 | chr3:195876545-195877823 | HCC1954 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 195877413 | 195877651 | | chr3 | 195876644 | 195877148 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I196149 | chr3 | 195876546 | 195877823 |
|
Enhancer Sequence | CAGTTAGCTG AGAGTGCGCC ACTGCACTCT AGCCTGGGCA ACAGAGTAAG ACTCTGTCTC 60
AAAAAAAAAA AAAAAAAAAA AGACTGAGAC TGCTGTTTGC CTTCATCAGC ACAGAAGCCG 120
CTAGTTAGGA ACCATTCTCC TAGCACACCC ACTCCCTGTG CTTCACAAAA GCAGGTCAAT 180
GTTTACAGAA GTCCCCTCTT CCCACGTCTT CTCATCTTCA GGGGAAACTG TTGCGAGGAA 240
CAGAGGACTG GAGAGACCAA TACGGGAAAC AGGAGGATGT TTATTTAAGG TGCACCAGCT 300
CAGAGGATTC GTATCCAAAA AGCTGAGCAT TGAACAAAGT CAGGGTTTAG CTTATATAGG 360
CCAGCGCAAA GGCTGTCAAT CACACAGTGA CAGCTTCTGT CATCTACAGC ATAACTAGTG 420
ACTTGGCACA ACCTGTGCCC TTGCATAGCG GGTAACCTTG CAGCTGAGGC AAAAGAAAAC 480
AGGAACTTAC AAATCTGACT AAGTACAAGC ATTGGCAAAC ATAGTCAGAA TTATTAGTTC 540
AGAGAAGGAG AGACAGTCAA GGAATTTGGT TTTGGGGATT TTTTGTTTTT CAACCATGCT 600
CGGGGGTGTC TGGAGCCTAT TCTTGCAGCT TTTGCTTCTC AGACTAGGTC ACCGCGACCT 660
TTTTATAGCC TTGCCTGTTA CTATCCTTAA AGTAAATAAA TGCAGTACTT ATGTTTCTTT 720
AAATTTCTGC CTCAAAACAA CACTAATTCT CCTGATTGTC TTTCATGACA GTTTCCAGAC 780
CTCTCACTTT TCTGGCTGTC TTTCCTGGAT GCTGAGTAAT GTCAAATGTG GCACTAAAAT 840
TCAGCACCCA GGGCTGAATG AAGCTTCAGG TGTGCCCCGA TCAGCCCAGA GGCCAGTGGC 900
ATGCTCAGCT CAATTCTGCT TGGCAGCAAA GCCACTTACA GATGCACTGG CTTTTCAAAC 960
GACTGAATGC ATTGTTGACT CTTACTCAGC TTGCAGCCAA TATCTTTTTT TATGTGAGCT 1020
GTCATCAAGC CAGGGATTCC TCATTCTCCA TTGGTGCAAC TGGCTCTTGA ACCTACATCA 1080
AGAACTTTGT CCGTGTTCAT TTCACATTGT AGGTCTTAGT 1120
|
