| Tag | Content |
|---|
EnhancerAtlas ID | HS094-12052 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr14:21588220-21590220 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr14:21590166-21590179 | TTCTAGAAGTTTC | + | 6.25 | | IRF1 | MA0050.2 | chr14:21589703-21589724 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | Lhx3 | MA0135.1 | chr14:21588661-21588674 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr14:21588660-21588673 | AAATTAATTAATT | + | 6.92 | | Lhx3 | MA0135.1 | chr14:21588664-21588677 | TAATTAATTAAAT | + | 6 | | POU6F1 | MA0628.1 | chr14:21588662-21588672 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr14:21588662-21588672 | ATTAATTAAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAAAAATAAA GAAAACAAAT GCTGACCAGG TGCGGTGTCA TCCATATTTA GTCCCAGCTA 60
CACAGGAGTC TGAGGAGAGA GGATCACTTG AGCCCAGGAG TTTGAGGCCA GCCTGGGCAA 120
CATGGTGAGA CTCTGCGTCT AAAAAATAAA AATAGGGCCG GGCGCGGTGG CTCACGGCTG 180
TAATCCTAGC ACTTTGTGAG GCCGAGGCAG GCAGATAACC TGAGGTTAGG AGTTCGAGAC 240
CAGCCTGACC AACATGGAGA AACCCCGTCT CTACTAAAAA TACAAAATTA GCCAGGCATG 300
GTGGCACATG CCTGTAATCC CAGCTACTCG GGAGGCTGAA GCAGGAGAAT CGCTTGAACC 360
TGGGAGGTGG AGGTTGCGGT GAGCCGAGAT TGTGCCATTG CACTCCAGCC TGGGCAATAA 420
GAGCAAAACT CCGTCTCAAA AAATTAATTA ATTAAATAAA AATAAAAATA GGCCAGGCAT 480
GGTGGTTGAA AGGGCAGGGG AAAAAAGAAA TTTTTAAAAC ACCTCTTGCA TAGTTGTCTA 540
GCAGAGTCAA ATATGTGATT ATTGTAGGAG AGAAGTTCCT TTTGCTTTAA AGACAGGGTC 600
ACCCTTTGTC ACCCAGGCTG GAGTCCAGTG GTCCAATCGT AGTTCACTGC AGCCTTGAAC 660
TCCTGGCCTC AAGAGTTCCT CTTGCCTCGA TCCTCCCACT TAAACCTCCC AAGTAGCTGA 720
TTCTACAGGT ACCAGCCACC ATGCCTAGCT GAGGAATATC TTTCAAAAAG GGAAGAGAAT 780
GAGGACACCA CAAAATTATA TTAGAAGATA CAGACTAAAA GTTGCTTTTG CAATAAAGTT 840
GCTTTTGCAA CACACAGAGC CAGAGAGTTT AAAAATAACT CAGAAAAGGA GTAAGAGAAC 900
TGTTGTCCAA ATTTGTGGCC TCTGATTCTG GCTGGCCACT GGGTTGCAGG ACTAACGGGC 960
TGCAAGTGTG GTTTGTGTTC ACGAAAACGC CTTCGGAAAG GGTCTGGGGT AATAATAGTT 1020
ATGCACAATC ATGTAGTATC TATAATGATA ATAATAAAGA TACTCATATT GTTAATAACA 1080
ATACTTACAT AGACCTTTGT CATGCTTAGT ATTAACATAT ATTTGGCACT GTCCTAAGCA 1140
TTTTAGTGTT TTAATTCATT TAGTCCTCAC AGTACCCCTA AGAAGCAAGC ACTGTTATGA 1200
TCTCTGTTTT ACACATAAGA AAAATGAAGC ACAGGAAGGC TGAGTAATGT CTCAGATTAC 1260
TAATGTCACA TAACTAGTAA GCGACAGAGC CAATTTGTAA CCAGGTGATT TTACTCTGGA 1320
ATTCATGCTC TTAACCACTA TATTTTATAC TGCCTCTGCA GCCAAAATAT CCCCTCAGGC 1380
AGTAGTTCAC AAAGTGTAGT ATAGTCCTTC CAAGAAGTCT AGGAGGTCAA AAGTATTTTC 1440
ATAATAATGC CAAGATTTTT TTTTTCTTTT TTTCTTTTTT CTTTCTTTCT TTCTTTTTTT 1500
TTTTTTTTTG ACACAATCTC GCTCTGTTGC TCAGGCTGGA GTGCAGTGGT GCGATCTCAG 1560
CTCAGTGCCA TCTCCACCTC CTGGATTCAA GCGATTCTCA TGGCTCAGCC TCCTGAGCAG 1620
CTGGGACTAC AGGCATGCAC CACCACGCCC AGCTAATTTT TGTATTTTTT TGGTAAAGAT 1680
GGGATTTTGC CATGTTGGCC AGGTTGGTCT CGAGCTCCTG GCCTCAAGTG ATCTGCCTGC 1740
CTCGGTCTCC CGAAGTCCTG GGATTACAAG TGTGAGCCAT GGTGCCCTAC CTAATACCAC 1800
ATTTTTTTGT TTGTTTTGTT TCGTTTTGTT TTACCTATTT TACTTTCATT CTGAGTATGC 1860
AGAGGAGTTT TCCAGAGGCT ACAAGACATG TGATAACATC ATCACTCTAA TGGCTAATAG 1920
AAAATGTGCT TGTATAGTCT TGTATTTTCT AGAAGTTTCT ATGTAAACTC TTTGGGGTCC 1980
TGAAACCACA AAGTTTGAGA 2000
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