| Tag | Content |
|---|
EnhancerAtlas ID | HS095-21219 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr3:124404050-124405640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr3:124404295-124404306 | TCAAGGTCATA | + | 6.62 | | Esrra | MA0592.2 | chr3:124404294-124404305 | GTCAAGGTCAT | + | 6.32 | | Esrrg | MA0643.1 | chr3:124404295-124404305 | TCAAGGTCAT | + | 6.02 | | Klf1 | MA0493.1 | chr3:124404055-124404066 | AGGGTGTGGCT | - | 6.02 | | Nr5a2 | MA0505.1 | chr3:124404291-124404306 | GAGGTCAAGGTCATA | + | 6.36 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr3 | 124404078 | 124404324 | | chr3 | 124404471 | 124404702 | | chr3 | 124404964 | 124405432 |
|
Enhancer Sequence | TCTGAAGGGT GTGGCTTGAA GACTTCCTGC CTGGCTTTGT TCTGACTCTC CATGCAGACC 60
GATTTATATT CCGCCACCAA GAGAAGGGAG CTGAGCTTAG TGGCTGCTTC CCTCTCCTGG 120
GAGAATTTTA AGAAGATCGT CCACAGCAGA TTCACATCTA TTATGCTTTT TGTTCCTTGC 180
AATTGCCCTG TGAAGTAAGT AGGGTAGAGT TTCTCACCCT CCTGGGGGAA ACATGTTCAG 240
GGAGGTCAAG GTCATACAGC TAATAAAAAG AGCAAGTCTT GATGGTGGTG CTTTGAGAGA 300
CCAAACTTAG CATGTGCTGT AGAGGAAGTC TACTCGTATG GCTCAAGTAC TTTCTTAACA 360
AGGGTCAGGC TCAGGCCCTC TTTTGCTGCA CATCTGTTTT AGGAGGAGAA TTTCTTCAAC 420
AACTTTTCAA ATCTCTTGAC TATTGGGATA ATTACTTGGC CTCACCCACG CCCTTTCTCA 480
ATGACTCAAG AGCCCAGCCA GAGCAACCAA GAAAGGAAGT CCAATTACAT GAGTTGGAAA 540
TGTCTGAACT GGTTTCTCAG GTCAACATAG TCACTCAGCA CGCCCTGTCA TGCATGTTCC 600
ATCGCACCCT CACCCTAGAC TGGGGGCCTA ACCCGTTTCG TTTACGTTGT ACACTAATGA 660
GATTACAAGG TACCATTGAC CCAGAAGTTC CTCTAAGAGC CTGCTATTGA AGAAGCAAAG 720
ACCATCACCC CCCAACCCCA CCCCCATGCT GTCAAAGTTC ACTCAGCGTG AGTTCCTAGT 780
CAGTTCAATT TCACACAATT TGATTAACAC AAGGCATTGC AGTGATTATT ATGGAGGACT 840
AACGAACAAT GTAAGATTGG TTCCCATGCT TAAGGCTTAA GAAGCATAAG AAGGAGGCAG 900
GTATAAATAA ATGCCCATGT TACACAGCAA ACTTTAAAAC CTGCTCTAAC AGTCATGGTG 960
AGGGACTGAT TAATCCTGCC TGGAGCCATT TATTCATTCT GTGGATATTT ATGCACCCAC 1020
TCAGGCACTG GGCTCACAAT AATAGTAGCT ACTACTTAGC AGTCTTTCCT GTGTAACTGG 1080
CTCTGTGCTG AGCTCCCAAC AACATCATCA CATAGGTACT ATTCGCGTTA TTCCCACTTT 1140
ATAGATGAGA AAACTGGAGC ACAGTGAGGT TAAGTGACTT TCCCAGGACT GTGTATTCTT 1200
AGGTAGCCTG TCTCCCAGGG AGCCTATGAG TGTGGTCATT GATTCACTGG GCAGCAGTGT 1260
GTGGGTTGGA TGAACTAATA GGATGTGGGC AGTCTTAGAG AAGGCAGAGG GTGAGGAGAG 1320
AGCATGAACA AAAGCCCTGA GGTGGGAGGT GCCTGGCACA TGCTGAGCAG GTATATGGTC 1380
TGAGTACCTG GGGTTAGTTA TGTAGGAAGA GCTGTAGGAG ATAAAGCCTG GCAGATGGGT 1440
TGAGACCAGA CAGACAACAA AGGCATGGAA GGACCTGCTA GGAAGCCAGG ACTTGATCCA 1500
TGGACTCCAA GGAACAGCAG TAGGTTTTAA GCAGTCCATA TGATTCGTCC TGTGCTTTAG 1560
GAAGGTAACC AGCATCTATG CAAACACTGG 1590
|
