| Tag | Content |
|---|
EnhancerAtlas ID | HS182-16297 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr3:128000790-128002180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr3:128001210-128001226 | ATTTGTTTGCTTAAGC | - | 6.37 | | MYC | MA0147.3 | chr3:128000905-128000917 | CCCCACGTGCCC | + | 6.07 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41945 | chr3:127999233-128002747 | LNCaP |
|
| | 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 |
| GH03I128282 | chr3 | 128001741 | 128001950 |
|
Enhancer Sequence | GCTCTGGAGC CTGAATGGAT TTCTGACAGG AGAAGCTGAG GCTGTCCAGC CTGCCTTGGG 60
AACTTGGCTG CTTCACCAAG TGGGAGCTCT GAGACTCTCC CACAGGTCCC GTGCTCCCCA 120
CGTGCCCTTA CAGTTACCTG CCCACCAGGG CCCAGAGGAG GGGCTACCTG GAGCAAGGGT 180
GCCTGGACTG GGCCTCTGTC TTCCCCTGCT GTGAGCAGAG TTCTCACCTC CTGACCCCGA 240
CTTGGTCTAA CCCTGTGACC CACATGAAAT GCCAGCCACT GGTGGTGGGA AGTGGGTGGC 300
TGGTCTCTTC CAAGCCAGGA GTGCATCAGC TCCAGCCTCC TTCCCTGCTG CCGGCCTCGG 360
TTCACAGGGA GCCCTTTGAG GGGCTTTTTG ATGTGCACCA TGGATGTTTG GCTTGACCAA 420
ATTTGTTTGC TTAAGCATTG CTCTTGCCAG TTCATTCGGA CCTTCTCTTT CTTTTAAAAA 480
TATGCTGCTT GCCAAAGGTT ATTTTGGATC TGTTTTTGTT TATCAGGTAG AATTGTTCCA 540
GCGCAATTGA AAGCAGACCC ACATGTTGAC ACGCACTGGA GCTGCTTGCC AGGACACGTG 600
CACATGTGCA CACGCGCACA TGCAGAATAT GTGGCAGGCA TCTCATCGTG AGCCCTAGAG 660
TGTACACAGC TTAGGAAGGG GGACTGGGGA AGCTGCCCAT TTCACCGGGG ACTTGGTATG 720
TGAAGATTTT CATCATCTAG GTGCCAGCAC TGACAGACTT CAGGTGGGGA AAATCTAGGG 780
ACTGTTACCT CCTGGGAGAG GCAACCTGGT GAGTCTGAGT ACCTTGGGGT TAGGCTGGCT 840
CTGCCGCTGG TTGCCTGTCA TCCTTCCCTG CTCTGGCCTG GCTTCCTTCT CTGTGACTGA 900
TCTCCCGACT TCACAGGCTT TGTGCCAGGC TGTGGCTGAC GGCCTTCGGG AAGCAAGCAG 960
GGCTGGCCGG AAGTCAGCCA GAGTGAGGGA CTAGAGCGCT GGGCTCCCTA CAACTGTGCC 1020
TCCCTTTTAA GTGAGTAGCC TTTTCTTGGG AACACGGTTG GGTGCTTCCT GCCAGGAGGC 1080
CTGCAGTGGA TTTCTTCTGA AAACACAGCT CTTTCTCCCC ATCAGGACCT GCTGTGTATA 1140
AGCAGGCTGC TCAGAGGAGC CCTTTCAGGC ACTGGCTTTG GGCCTTGCTC CCTTGCCCCT 1200
TTGGGGCCCT GTGGCACCTG GAAACACACA GAGGGACTAG GCGGTTAAGG CTCGTCCTCT 1260
TTCCCATCCC AGGACAGCCC AGCAGAAAGC TTGAGGATAC TGATTCAGCT CCAGGTCTCA 1320
TTGAAGGGAG GACACTGTGT CCAGAGGGGT GGCTATGTTC GTTCGTTTGA TTATTATTAG 1380
TGATAGTAAC 1390
|
