| Tag | Content |
|---|
EnhancerAtlas ID | HS145-17883 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr3:124403070-124405290 |
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: 4 | Chromosome | Start | End |
| chr3 | 124403308 | 124403810 | | chr3 | 124403831 | 124404003 | | chr3 | 124404078 | 124404324 | | chr3 | 124404471 | 124404702 |
|
Enhancer Sequence | TTCTGGTTTT TCTGCTTGCT ATTCCCCCAC CTACACCATC CTGCGGCCAC TTGGTACCCC 60
ATCTCCAGGT TGATTTTAAC CTAAAACACA GATCCTGGCA GACGAGAAGA CCTAACTCCT 120
AGTGCCAATT TTTGTGTATA AGTGTGTTAT TCCATTTTCC AGCTCAATAA AAAGGAATAT 180
CATTTCTGCC CATCTTGGCT TTCCGAGGCT GAAGTGTAAC TTAAACAAAA ACCACAAAGG 240
CAGTATCACA TGGAAAACTG GAACAGGAGT CAAAAACCTG GATTCTAGTT TGGATACCGC 300
CAGCTATGAG ACTGCTGGCC AGTTAGCCTT TCTGAGCCCC AAGTTCCTCT GGAAAGTTGC 360
ACAGCTCCAA GTGTACAGGT GTTTATACAG TGATGTGTAA CCCTTTGAGC ACCATGCACG 420
TCTAAGGTGT GCTAACAAAG GACTTTGCTC TCCAGCACTT CTGACTTTGA AAACATTGAG 480
ATCCCGACCG AAGAGGACGT GGAAGATTCT GTGCTTTGGC CAGCAATTCA CTTTTCAGGG 540
GGTGTGGCGG GAATGGCCTG GGCAGATTTC CTTCTGAGAC TCAACTGGAG TGTCCACTCC 600
TGGCTCTGGG AAGTTTGAGC GGCCAGAGCT GGTACTTTTT TCCTTCCTCA AACCTACAGT 660
TCCCTGGCCC GCCTTTCATG TCCTCAGATC TGAAGAGCCA GCCTACTCCC CGCACCCCAC 720
TCCCCGCCAA CTACCACATC AGCTACTCTG GCCTCCTTAT CCTAGAGCTT CAAAATAACC 780
CGGCCAGACG GATTGAAGGA AACTTTTACA CCCCCAGCCA GGTGACCAAC CTCCTGGCAT 840
CCCCAGTGTG TGTCCACTGA TGCCTGGTTC CGCATTTTAT AAAAAGAATT TTTTCATGAA 900
AAGAACCCTT TGGATGAAAA GAAAGTGAAG CATCACATTC CTGTCGTTTT ATTTTTGCAA 960
AATATTTTCT TTGTAATATA TCTGAAGGGT GTGGCTTGAA GACTTCCTGC CTGGCTTTGT 1020
TCTGACTCTC CATGCAGACC GATTTATATT CCGCCACCAA GAGAAGGGAG CTGAGCTTAG 1080
TGGCTGCTTC CCTCTCCTGG GAGAATTTTA AGAAGATCGT CCACAGCAGA TTCACATCTA 1140
TTATGCTTTT TGTTCCTTGC AATTGCCCTG TGAAGTAAGT AGGGTAGAGT TTCTCACCCT 1200
CCTGGGGGAA ACATGTTCAG GGAGGTCAAG GTCATACAGC TAATAAAAAG AGCAAGTCTT 1260
GATGGTGGTG CTTTGAGAGA CCAAACTTAG CATGTGCTGT AGAGGAAGTC TACTCGTATG 1320
GCTCAAGTAC TTTCTTAACA AGGGTCAGGC TCAGGCCCTC TTTTGCTGCA CATCTGTTTT 1380
AGGAGGAGAA TTTCTTCAAC AACTTTTCAA ATCTCTTGAC TATTGGGATA ATTACTTGGC 1440
CTCACCCACG CCCTTTCTCA ATGACTCAAG AGCCCAGCCA GAGCAACCAA GAAAGGAAGT 1500
CCAATTACAT GAGTTGGAAA TGTCTGAACT GGTTTCTCAG GTCAACATAG TCACTCAGCA 1560
CGCCCTGTCA TGCATGTTCC ATCGCACCCT CACCCTAGAC TGGGGGCCTA ACCCGTTTCG 1620
TTTACGTTGT ACACTAATGA GATTACAAGG TACCATTGAC CCAGAAGTTC CTCTAAGAGC 1680
CTGCTATTGA AGAAGCAAAG ACCATCACCC CCCAACCCCA CCCCCATGCT GTCAAAGTTC 1740
ACTCAGCGTG AGTTCCTAGT CAGTTCAATT TCACACAATT TGATTAACAC AAGGCATTGC 1800
AGTGATTATT ATGGAGGACT AACGAACAAT GTAAGATTGG TTCCCATGCT TAAGGCTTAA 1860
GAAGCATAAG AAGGAGGCAG GTATAAATAA ATGCCCATGT TACACAGCAA ACTTTAAAAC 1920
CTGCTCTAAC AGTCATGGTG AGGGACTGAT TAATCCTGCC TGGAGCCATT TATTCATTCT 1980
GTGGATATTT ATGCACCCAC TCAGGCACTG GGCTCACAAT AATAGTAGCT ACTACTTAGC 2040
AGTCTTTCCT GTGTAACTGG CTCTGTGCTG AGCTCCCAAC AACATCATCA CATAGGTACT 2100
ATTCGCGTTA TTCCCACTTT ATAGATGAGA AAACTGGAGC ACAGTGAGGT TAAGTGACTT 2160
TCCCAGGACT GTGTATTCTT AGGTAGCCTG TCTCCCAGGG AGCCTATGAG TGTGGTCATT 2220
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