| Tag | Content |
|---|
EnhancerAtlas ID | HS059-33009 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr3:123976150-123977320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP4 | MA0691.1 | chr3:123976373-123976383 | AACAGCTGAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_01654 | chr3:123976104-123977799 | Aorta | | SE_54021 | chr3:123976157-123977628 | Spleen | | SE_54982 | chr3:123974671-123977588 | Stomach_Smooth_Muscle |
|
| | 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 |
| GH03I124256 | chr3 | 123975471 | 123977734 |
|
Enhancer Sequence | GAGAATCCTG AGCTTTATCC CAGACCAACA TTCATCAGAA TATCTGGAAG GCTTCCCCCA 60
AATCAGCATT TTTAAACAAG TGTTCTAGGT GATAAAGAAA GTCACTAAAG TTTGAGAAGC 120
ATTGGCATAA AGTGGTGAAA GTGCTTTTCT GAGATAGCAC AGGCTTACTA AGTGAAAACG 180
GCCCCAGTGG CATTTAATGA ACAAAAGAGG AAATGGTACA AGAAACAGCT GATCAATCAT 240
CCAGTCATTT GGTATACATT TATGACTTCT GGGCCCAAGA GCCCTGGAGA GTCTATGAAA 300
CAGAACACAG CTCAGTTTGA AGGGATTGTA ATTTATCACA AAGGGTGAGA ACCTGGCCAA 360
GGGGGCCTCA GGGGACCCAT GGCCCAGATG GGAAACTATA GGGCAGGGTG AGCACAGGGG 420
AGACAGGGCA GTGGCTGCCT TCTCCCTCTC AAGTAGCAGG TGTGGGAACA GGAAGGGGGT 480
CACCCACTGT TCTTTCCCCT CCTGAGGGGA TTTAAAAGTC TGCTTTGAAA AATATTTTTA 540
AATAAAAAAT AAGGATATAA AAGTCTGCTG CTCCAAACTT CACCCTCCTA TGCCCCCGTC 600
CTCACCATAC ACAATGCAAA CTTCTGCCCT TGAAAGTTTG ATTTGGGCTA ATAAATATCT 660
TTTAAAAGGT AAATCACCTA AAGGAAAAAA AGCAGGCTAC CTGTTAGTTA TGTTCCACTG 720
TAAACGGGTC TGCTCAAACT GCTGTCATTT GAGCACAGTG AATGAGAGAA CAGCCTTGGG 780
GAAGAGGGCA GGCTGGGGAG CAGCTGCGGG AGTTGGTTGG CCAGAGAGCA CCATGCAGAC 840
TCTGGCCACT GCTGGGGTTG GGGAGACAGA GCCAGGGGGT GGAAGTGCAC CACAAGCAGC 900
CTCTGATGTC TGTGGCACTT CCTGCTAATC ATTACAGAGA TTAACCAGGA AGACTGCTTC 960
CTTGCTCCAG CATTTATTCT GGCCCCAGCA CCCCACTGAA ATTTCCCTGA CTCAAGAGAC 1020
CGTGGCCTCT TGGTTGCTAA GTACAATAGT TCTGCTCTTA GTGAATGACC AGTCTCTCTG 1080
CAGCATTTGA CACTGTGGTT CCTCCTTGCA ATCCTCTCCT CCCTTATTTC TTTGACGTCA 1140
TTCCTCTCCT GGTTCTCTCT AACCTCTTCA 1170
|
