Tag | Content |
---|
EnhancerAtlas ID | HS165-13136 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr6:45648710-45650460 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr6:45648835-45648845 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr6:45648835-45648845 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr6:45648835-45648845 | AATGGAAAAT | - | 6.02 | Nkx3-2 | MA0122.3 | chr6:45649465-45649478 | TTAACCACTTAAT | + | 6.98 | RARA(var.2) | MA0730.1 | chr6:45649891-45649908 | TGACCTCCAGCTGACCC | - | 6.64 |
|
| 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 |
GH06I045681 | chr6 | 45649382 | 45650302 |
|
Enhancer Sequence | AAAGATCTCA AAGAGATATT TGTACACTTA TGTTCATAGC AGCATTGTTC ATGATAGCTA 60 AAATGCAGAC ACAACCCAAG TGTTCCTCTA CAGAAGAATG AATAAACAAA ATGGTATGTA 120 CATTCAATGG AAAATTATTC AGCCTTAAAA AGGAAGGAAA TTCTCACACA GGATACAACA 180 TGGATGAACC TTGAGGACAT TATGCTAAGT TAAATAAGAC AGTCACAAAA AGACAAATAC 240 TGTATGATTC CACTTATATG AGGTAATTAT TTGAGTATAA AATTACTAGA TCTAATCTAA 300 ATCTGCCAAT TACTATTCAA AATAATAGAG ATGGTGGTTG CCAGGGGATG GGGGCAATTG 360 AGAGTTATTG TTTAATGGGT AAATAATTCC AATTTTACAA GATGGAAAAA GTTCTGAAGA 420 TGGGTGGTGG TGATATTTAT ACAACATTAT GAATGAAGGT ATTAAAACCA CTGGAACTAT 480 ACACCCTGAA AAATCTTTAA GAGGTTAAAT TTTAAGTTAT GTGTATTTTA TCAAAATAAA 540 AAATTGGAAA CAATATTGTA AAGTTTTAAT AATCTAAAGA AAATTCTTCC TTTAGGGTGT 600 TATTCCCAAA AACGTGGTGT TGGTGTTCTA AATATCTAGG ATATTATTTT TATAATTTTA 660 AAACATGCAA TCATACTGCT GGGACATGAC TCTTTAAACA GCAGATCTTT GAGTGAATGT 720 GAATGTGATA AACTCTGCTT TCTAGAGAAT CCTTTTTAAC CACTTAATGC CTCTTTTAGC 780 TACTAGGTCT AAGAATCTAT AGAGAGGGGA TATGGCAGAG TGTAGAAATG ACCCTAATTA 840 TTCATCCCTC CTGTATCTAT GTCCTTCACC ATACACATCT GTATTGCTGT CCAATGCTGT 900 TTCTGAGCCT AATCATGGAC CTGTTTTGGC CAACAAGGTA AAGTGTAAGT ATCAGTTCCA 960 CATATAGAAC TTCAGAGACT GTGTGTGTTT CCTTTTGCTG TCTTGTGTAT CTGCCATTGC 1020 CATGACAACA CGCTCAAGCT AGCCGGCTGG AGGAAGAGAA ACTGAGCAGC AGAGCTGAGC 1080 CATCTCTGTT GCTCCAGTCA AAGCCAGTCT AGATCAGCCA ACTGCCAGCC GACTCTCACA 1140 CATATGAGTA AGCCCAGCCA AAATTAGCAG AGCCACTTAG CTGACCTCCA GCTGACCCTA 1200 GATGTTTACT GTTGCATGTC CCTGAGGTTT TTTTACTGCG AGGGAGCATT ATTGTGGAAG 1260 TAGATGACTG ATTTAGGGAA TTGCCTCATA TGCTTTTTTT TTTTTTTTAA TCACTCCTTT 1320 TCCCCTTGTT TCAATCAACT TGTCACAAAT ACATCTGAAC ATTGTTAGGT GTCTACCCAA 1380 TATCCACTCT CCTGCTTTTT CTTACTGCCA GAACCACATG CCCAGCTAAA AACCTACATT 1440 CTCTGGCTTC CTTTGTAGAA AGGAGTTGTC ATGTGACATT CCTTTGGCCA ATGAGAAGCA 1500 AGTGAAATAT TGAGTAGTTC CTTGAAGGAG GATGGGGAGT CCTTTTGCCC TTCTCCTTCT 1560 TCCTTTCTGG AATAAAAATC TGATGCTGGA AAATATTATG GCCCCAAGGA GCCAGCACAA 1620 GCTGAGAATG ATTGAGAGGA AAGCAGAAAG AGCTTGGGTC TCTGATGGTA TGACTACAGT 1680 ACCAGCCATG GGCTGCCTCC TTTTTCACTT CTAGCTACAT GTGAAAAAAA TAAGACTTCT 1740 CAACTAATTA 1750
|