| Tag | Content |
|---|
EnhancerAtlas ID | HS104-28170 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr18:60013620-60015030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr18:60014929-60014944 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr5a2 | MA0505.1 | chr18:60014937-60014952 | GAGTTCAAGGCCAGC | + | 8.25 | | RARA | MA0729.1 | chr18:60014929-60014947 | GAGGTCAGGAGTTCAAGG | + | 6.73 | | Zfx | MA0146.2 | chr18:60014905-60014919 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | 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 |
| GH18I062346 | chr18 | 60013689 | 60014872 |
|
Enhancer Sequence | GCATCTAAAA CAGAGAAAAG CATCTCAGAA GGGAGAGGTG TGGTGGCTTC TTTTAAGCAA 60
TTCTTCCTCA GTCCGCTGGG CTCAATGCAG CTTCCCTAAG ACTCTGTCAC CCAGTGAATA 120
CATGGGGAGC ATCTGATGTG TGTTACCCGG TGTCCACGGG GAGTGTTAGC AGGGCCCAGG 180
AAGCAAGTCC AAGTACAACC TTCCTGTCAC ACATCACCTC AATAACACAC TGGGACCTTC 240
TCATCGACCT CAGCCTCCTC ATAACCCCTT TGCTGGCCAG GGTGAGGTCA GAAAGGTCCG 300
TGATGGCTGT GTGCCCCACA CCCACTCAGC TAGCCTGGGC TTTCCTGGGT TTGGTGCTTT 360
CTTTATAAAG CTGCCTTCTA TAATGGAGCT ATTTTGAGGA TGCATGGCTT TTTCCAAGCC 420
ATATTATCTC TGCGCCCTCC ATCCGAGCAC TTTCATATGC AGATGAAGCC CTCCCCTGAC 480
TGCCTTTGTG ACACTGGGCT CCAGCTGGAC TGAAGGTCTC TTACTGCCTC CCAAGAGCTG 540
TTTCAGGCCT CATTGCCCCT GTTTGAACTG CTCATATTGT CCAAAGTCTT CCTACTTCCT 600
CCCACTACCT CCACCTGCCA GTTTCTGTTT CCTGGTCTGG CTGATTTCTA TTTATCCTGG 660
AAGGCTGATT ACTTACCACC TCCCTCAGGA AGCCATCCTG GCTGCTTCTG CTTCCTTCCT 720
ACTACTGCTG AGGTAGGGCC CATCTGGTAT GTGTTTCATT CCACTCTAAG ACCCTTGAGG 780
GGAAGGTTTG TGACTCTGTA TTCGACGACA CAGCAGGGAA CTTGCATGAA TCGCAAGTGT 840
GGTGTGCATA CGTGGATGTC TGTTCGGCTA AGCCCAGTTC TTCAGTTTCT GACATGACTG 900
CTTGTCAACA GGAGTGTGTG TTGTTTTTTG CTCACACCAA GAATGCTGAT CAGGAAAAGA 960
ACTTTTCTGT GGCAAACTGA TAAGAATCTC TGGGTGATTA TAGATGCCTG GGCTGCTCTG 1020
TTTTCTTTTG TTTTACTCAG ATGGGCAGAT TCAGAAATTG GTATTTGTCT TAGAATCATA 1080
CCGTTTTGAA CCAGAAGGGA ACCAGAGGCT GAGGAAGCTT AAACAGCTCC TGCAGTCCTT 1140
CAGGCAACAG GTAGTGAGGG CAGAGCCCAG GAAGCCCCTA CAACACCTTG CTTTCCCCGC 1200
TTTTTAAAAT TCTCTGTGTG TTTAACAAGT TAAAAGGTAA GCAGGCCGGG CGTGGTGGCT 1260
CAGGCTTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCGGGT GGATCACCTG AGGTCAGGAG 1320
TTCAAGGCCA GCCTGGCCAA CATGGTGAAA CCCCGTCTCT ACTAAAAATA CAAAAATTAG 1380
GTGGTGCGTG GCTATAGTCC CAGCTACTTG 1410
|
