| Tag | Content |
|---|
EnhancerAtlas ID | HS037-00207 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr1:11415500-11416850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr1:11415613-11415626 | TTCTAGAACTTTC | + | 7.04 | | LBX2 | MA0699.1 | chr1:11416332-11416342 | GCCAATTAGC | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr1:11416819-11416834 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 11416000 | 11416400 | | chr1 | 11416400 | 11416650 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I011355 | chr1 | 11415181 | 11416790 |
|
Enhancer Sequence | GGACTGCATG CCACAGGGTG AGAGCCAGGC GCCGGCAGAT TTCTCGAGGC AGGTCGAGAG 60
CAAGAGTGGG ATGATGTGGA GGTGTGGGAG ATCAAAGGGG AGAGCACACT ATCTTCTAGA 120
ACTTTCTTCC TGCCACTCTG CCCCCTCTTT CATCCACCTG ATTCCTTCTG GGCCCCGTGC 180
CCCCCGGGCT GGGAGGGGAA CCTGGCCTAC TCCTTGGCAG TGCTGCCAGG GAGTCTCCAT 240
GACAACCCCA GCCCCCATCT GTGGGAGTGG AGCCCTCGGC TAGGGCCTCA AGGGAGTTGC 300
CTGGGTAACC GGGCTCCCTT GCCCCACTTC CCCGCCAACC AAACCTCCTC GGCCCCTCCC 360
CCTCTTTGCG ATGGGAGGGT GAGAGGATGG GGTCACCATG GAGACCCAGC TTCCCTCCCG 420
CTGCCCCCTT TCCAGAGCAG CTGTCACAGG ATGATGGTCG GGAGGAGACC TGGGAACGAG 480
GGTGTCTGCT GGCGAGGAGA CAAATGACCA AGACCCTCTC TCTGGCGGAG GAAGAGCATC 540
CTGGCTCTTT AAGAAGTGAC ACTTCTTGGG ATGTTTGGGG TGTTGAGTGC AACTCCTCTC 600
AGCCACCCCC TGCTGGAAGT CCTGGGCTCA GTGGAGCGGG CCTGGGCAAC GAGTTCTGGA 660
GCGGGGACCT TCTCCCTCCC TGCCTGGCTG TTCCCCTGCA GAGGAGCTGT GGCTCATTCA 720
GCAACGGAGA ACACTCAGGT GGTTAACGAG CATTTACTTC CCAAACGAGG AGACGGTTAC 780
ATGACTAGTT GTTGTTTTAT CTTGCTAATG AAAATACATA AAAAACAAAA TGGCCAATTA 840
GCAAGGCCAT TTGTTCCCAG GTCTTGGCTG TTTCTTTCTG GAGAGGGAAG CCATTCTCTG 900
GGTTGGGGCT GGCCCCTCAG TCAACTGTGG TGGCCTCTGA GGCCCCTCCC CCTCACTCCT 960
GCCCTTGTGG TCCCTGGTAC CCTTGCCTTT GATTTCTGAT GTGTGCCGCC AGCAGCCAGG 1020
AAACCCCTGC CGGTGTTCCC TGCCAACCCC CCTCTGTAGC CTTCTCATTC ATTTCTTTCT 1080
TTCTTTCTTT TTTTTTCTTT TCTTTTTTTT TTTTGGAGAT GGAGTCTCGC TTTGTTGCTC 1140
ACCAGGCTGG AGTGCAGTGG CGTGATCTCG GCTCACCGCA ACCTCCGCCT CCCAGGTTCA 1200
AGTGATTCTC CTGCCTCAGC CTCCCGAGTA GCTGGGATTA CAGGCATGCA CCACCACACC 1260
CAGCTAATTT TTGTATTTTT AGTAGAGATG GGGCTTCACC ATGTTGTCCA GGCTGGTCTT 1320
GAACTCCTGA CCTCAAGTGA TCCCCCCGAC 1350
|
