| Tag | Content |
|---|
EnhancerAtlas ID | HS184-04554 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:101860190-101861830 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SCRT1 | MA0743.1 | chr10:101860484-101860499 | CACCACCTGTTGCCC | - | 6.22 |
|
| | 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 |
| GH10I100100 | chr10 | 101860401 | 101861311 |
|
Enhancer Sequence | TGGATTTTCA GTGTTCTCTG CAAACATCTT GCTCCTCCTC TCCAAATAAA TTCCCCTTAG 60
AACTCACCAC CCCCACATCC CCACCACACA CTGCTTCAGT CATGTCTCAC ATTTCAATAA 120
AAGTTCTGTA TAAACTGTAG AGTGCTATGT ATATGTTCAT TGTATTTATT AAATTCTTAT 180
TGGCTTGGCT AGAATAATTT CCCCATTTGC CAATTTTGTA GGGACCACAA ATGCAACCCA 240
TTTGAATCTG AATGCAGTGT CTCTTCACCC ATAGTTGCTC CTCTTGGGAA ATGGCACCAC 300
CTGTTGCCCA AGTCAAAAAC ACAGGAGCCA TTCTAAATTC TTCCTTCTCA CTCACTTCCC 360
ATGATTACTC ATTCACTAAG CCCTCTCCGT TTTCTGTGTT GATCCTCATA GCTGACCCTT 420
GCTTTCCCCA TCTCCTGCCA CGGCCTCGGT TCTGCTCTCA CTCATCCTTG CCTAGATCTT 480
GGTAACTGCC TCCCATCATC TATCTTCCTG CCAGGATTTG ACCCCCTTCC ACTGCACACA 540
TCATGCAGTC GCCACCATGA TCTTTCTTCA ATGCAAACCA CCTCTTGTCT ATTGCTCACC 600
CCTTCCTTCC ACTGTTTAGA TCCTTTATCG CTTCTCCTTT CTGCTCAGTT AAGCCCACAC 660
TTCCTCACAT GGCAAAGACC TGCCAGGCCC TGATGTTTCC TGCCTTCCCA GCATTACATG 720
CCCTGCTCCT CTCCAGCACC CCTCCCGCCT CCTAGTTATA CCTAACAAAT TGCAGTCTTC 780
AAAAGCCTCT GAGTTTTTGA ACATCTCCTC TCCCTCCAAT TAGAAGTTAG CTGACTCCTA 840
TTTGTGTTTT AGAATAAATC CAGGCATCAT TTTCTCTAAA CCTTTCCCAT CATTTGCCCT 900
GTGTCTGATT TTAGTGTCCT TCCCTTGTAT TTCCATAGAA CTCGGCACAT ATTTCTCTAC 960
AAACATTACA TTGTGCCATA ATTTTTGGCT TGTGACTTCC TTGATTAAAA TATAAGGTCC 1020
TTAAGGGCAG GGACCACATC TTATTTGTTT CTGGATTCCC AGTCCCTACT CTGTAGCTGG 1080
CATATAACAG GTATTCATGT TGAAAAGCAG TAACAAAGAA TAAACAGTCT CCTCTGCATT 1140
TATATTTTGT TGACTTTTTA GAACAGGGCA GGAAATGACT ACATGGAGTT CCAGAAACCT 1200
CGGCTCTTCC ATGTGCCCCC ACTAACTCTC CTTCCAACAG GGCAGTCGTT GGTTCAGTGA 1260
CATATTGACT CAGACTGCCC TCTAGCCAAT GGCAGCCACG CATGCATGGA CTCTGAATCT 1320
ATTCTGTGTA CCAGTGTTGC CTAATTTGCA AATAGCCTGT ACCTGTGTAA TCCTCTTTGT 1380
CGGGAGTGAA GTGGTTCTCC CTGCTTTTGA AAAAAGCTAA TGTGATGTAT GTTTACTGAT 1440
ATGACATCAA TGAGGATAAC AGGGTATCAA GCAGGAGGTT AACTGGAAAA GAGGAGCCTG 1500
GCTCTAAATG ATCTGGTCAC TTGGGATGGA GGGATTGCCA CATATCAGAC TTTGAGTAGC 1560
TCTATTAACA GGGTTAGTAA TGGCTATGGG CCAACATGTA GCGGGGCAAC TATATTTCAT 1620
TGATTCTAAG GCACTCCTTC 1640
|
