| Tag | Content |
|---|
EnhancerAtlas ID | HS095-20358 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr3:39054650-39055840 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr3:39055562-39055578 | AATTGTTTACACAGTG | - | 6.26 | | SPI1 | MA0080.4 | chr3:39054895-39054909 | AAAAAGAGGAAGAA | + | 6.14 | | SPIC | MA0687.1 | chr3:39054895-39054909 | AAAAAGAGGAAGAA | + | 7.01 | | ZNF410 | MA0752.1 | chr3:39055515-39055532 | CCCATTCCATAATACCT | + | 6.07 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 39055160 | 39055413 | | chr3 | 39055486 | 39055588 |
|
Enhancer Sequence | AAAACAACCA AATGAAAAAA AGTCATCAAT AATGCTACCA CTTAGAGATA ATGATCTTTA 60
GCAAATTACA TCATTAACAG TGTCTTCCAA TCCTTTTTCT TGGCAGGTAT AACAAACTAA 120
GTGATCCAAA AACACATTTT ACATGCTTAG TTCACACAAA CTTTCACATA CATAAAATTT 180
GTATATGCCA TAGTTGGAGC TATGCAGGAG ATCCAGTCCC TGCTGGAGAT GATGCTAGGA 240
CACAGAAAAA GAGGAAGAAA TTCTCTGGCT TCTGCCTTTT TTTTTTTTTT CCAGTCTCCC 300
AGTAGTGCCT CCCATTGGCT GAACCCAGCC AGAAGTCAGC TGACGTAAGA TCTTGGAAAA 360
TGCAGCCCAC AGCGGGGAAG CCCCAGGAAG TCACAGGAAG AAAGGGAGAG GCACAAACAA 420
GCACAGGATC AGCATAGCCC ACCCTTTTTG CTATTCAGCA TCCATTCTAA TCTTTCTGCC 480
CATACTTAAC TCTCATAAAA CAACCTTATG CTTCTACCTA ACATAAAATG TTAGGCGGAA 540
GATCTGTCCA ACAAATAAGG ATGTTCTTGC TCTCTCCCCA ACAAGGGGAA ACACAAAATC 600
TCATCTGTCA TGTTGTCCAC ATCAAATCTA AGATCTCCAA GGGATATGCA GCAACAGCAG 660
GTCTGGCTGT ATCTTCTCAT ACCTGGTTGC CATTGAATTA AAGTTAAGCA CCATTGAAAG 720
TCTTTGTGCA AAACCACAGG GAAAAGATGA AGGGCAGAGG CTTGGAATTA TTGGTTTAAA 780
TACACATAAC ACTGCAGCCT CAGTCCTCAG CTTCGTATCT GATCATGAAA CCATAGTTGA 840
TACTTATCAC ATCCTTTTTC CATTACCCAT TCCATAATAC CTTTGCCTTC GAGCAGAACC 900
TTGGCTGGTT GGAATTGTTT ACACAGTGAG GTGACCCACA CCTTCATTCT TTTTGGGTTT 960
TAGTCCTTAC TCGTCCTGAA TTTTTGTGGT CACTCTTACC CACCTCTTCC ACACTGACCT 1020
TTTCTACTGA ACATGCAAGT ATTAAGAGGT GCCCCAGGGA ATTCGTGATT CCAGACATGG 1080
TCTTCTCAGT CCTCATTGAG TAGAAATGCC TCCAATTCAA TGGAACTATT GTGTCTCCTG 1140
ATGTAAGCAT TCTGCTCTTG GGAATTAGGA CTTCTAGACC AGAAGTCAAG 1190
|
