| Tag | Content |
|---|
EnhancerAtlas ID | HS184-25335 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr5:167786680-167788290 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr5:167787855-167787868 | GAAGATTCTGGAA | - | 6.16 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 167786747 | 167787316 | | chr5 | 167787467 | 167788241 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH05I168359 | chr5 | 167786901 | 167787050 | | GH05I168361 | chr5 | 167787108 | 167787130 | | GH05I168360 | chr5 | 167787162 | 167790308 |
|
Enhancer Sequence | AGTTTTTTTT GTTTTTTCTT TTTTAACTCA CATATCACTT GTATGTGTAA AAAACCCACA 60
AAGGAATATA TGAGAAAAAT AAAACTCTGG TATTCCTACA GTGTCTTCCC ATTCAGAATC 120
CAGTTCTTCG GAGTAGCTTT TTAGCTGAGT TATTAATGTC TGTGCTTTTA ATATTGTCCT 180
TTGTGCCCTT AAGAGTGTTA GTCATACAGC CTTGTTATAA AGACCCACAA AAAGGGACTC 240
AAAGCTTGGC AATTCTGTAG AGGTAGCCAG CTTAAGAGTC CTGCTTTGGG AATGTTGCTA 300
AACAGGTCTG TTGCATACCT TCTCCACACC TTTCCACAAC CATTTGGTTC CTAGGGGTTA 360
AAAGTGCTTA CAACTTTATT GAGGAATTTT TGAATTCCTC AATGTCTTGT CTGTGGGATT 420
TTTATCCCAA GCCTGTAGCA CCCGTTCCAC CAGTGGCAGT GCTGATGCCT TTGATATATG 480
TGCACACACA GGCAGTGACA GCTCCATCAG GACTGCAGCC TAGGTGATAT CAGTTGTAAG 540
ATGTCAGTAG TAGTAGCATA CATCAGAGTT TCAGAAAATG CTGAATGTGT TTAAAAATGT 600
GCATCTTTTG GTGAAATAGG GTCTATGTAA GGGACATTGG ATAGTGCCTG GCATTTTGCA 660
AATACTCAAT GAAATTTTGC TTTTATTATT ATTATTGCTA TTACTATTAA GCCTCAGTTT 720
CCTGTTGGTG AAATTGGGGT GATTGTACCT GCCTCACAGA AATATTGTTA GAATAAAGGA 780
AGCGATCTAT TTTACATGGA GCATATGGTC CTGTGCCTAG TGCTTCACTG GCCTTAAGTG 840
GAAGCTGCCC TGACCTTTGG GACAGGTTGG CCAGGTATTA GACTAAAGCT GCAGAGGGTG 900
CCTTAGGGGT GTTAAATTCT AGCTTCCTCT GTTTTGCAGG TGGGAAAGAC CAAGAGAAAG 960
GGTTAAGGTC CAGCAACAGG AGTGCCTTGC CCAAGGGCAT CGTCAGGCTT CAAACCCAGA 1020
TCTCATCATT CTTCTTCCAG TGCTCTGTCT AAACCATGCA GTCTTGGGAG GGGCCCCAAG 1080
TCAGACAGGA TCTCAGAAAA GTCTTCACGG TCAATTCCAT TTCTAGAAGG ACCAGCTCCT 1140
CAAGCTGTGT GGTAAGGGTC AGAGCTCAAG GAGCAGAAGA TTCTGGAATG GCCAAATTCC 1200
AGGACAGGGT GAGCTGCTGC CTCTGCAGTT ACTGCTGATG AGGCTTCTAG ACAGCCCAGC 1260
ACCTGGGAAG AGCCCTTGGG AACCCAGCTC ATGAGGCTGG AAGGAATAAG GCTGGGAGTT 1320
GAGTGTCCCC AGAGTCCTAA ATACAGAAAG GAGTAGGGCT GCAGGCCTGC CTGGGGTTGT 1380
GTGCCAGGTG CTGTGTTGAG TCTTGTCCGT GCATGAATGA ATGCAAGAAC CTGGGAAGCA 1440
GGTTTTCTTG TCTGCTCTAT ACCTGCAGGA AAACTGAGGC TCAGACCTGG GGGAAGGAAT 1500
GGACTGAGAT TACACAGCTA GGAAGGATGG AACTGGGAGT CCTCTCTGGT TCTGTTGGCT 1560
TTTTCTTTAG GGCACAGAGC TTCCATAGCC TAACTCATAA TTCAGGAATG 1610
|
