| Tag | Content |
|---|
EnhancerAtlas ID | HS067-00399 |
Organism | Homo sapiens |
Tissue/cell | GM18522 |
Coordinate | chr1:110872470-110873580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr1:110873512-110873527 | GGTTAATCTTTAACC | - | 6.26 | | HNF1B | MA0153.2 | chr1:110873513-110873526 | GTTAATCTTTAAC | - | 6.18 |
|
| | 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 |
| GH01I110330 | chr1 | 110873481 | 110873630 |
|
Enhancer Sequence | GAAAAAAAAA TCTGAAACAC TTCTGGACCC AAGCATTTTG GATAAGAGAT ACTCCATTTG 60
TTTTGTGCTT TATAGCTTCT TTTCCCATCT AGGATATAAG GTAGCATTAG GCATTGATTT 120
TATTGACATG TCTCTCGTCT ACTCTGGAAG AAATTCAACT TCTATAATTA AAAACTTGAT 180
AGCTAACTGG AATAAAGCGA ATTTTCTTAA GGTAAGGATA ATAAGAAAAC AAACAAAATG 240
CGTAATAAAC ATCATCTTAA ATGGAGAAAC GTTAGAAGTA CTCCTTTTAA AATTAGGAAT 300
AATAAGCCAG GTGCAGTTGC TCACACCTGT AATCCCAGCG CTCTGGGAGG CCGAGGCGGA 360
TGGATCACCT GAGGACAGCA GTTCGAGACC AGCCTGACCA AAGTGGTGAA ACCCCGTCTC 420
TACTAACGTA GCAGGATGAG CTGCAGACAA AACCCCTCAG ACACCAGGTT AAAGAAGGAA 480
GAGGCATTAT TCAGCTGGGA GCATCGGCAG AATTGCGTCT CAAGAACCGA GCTCCCCAAA 540
GAAAGAGTTC CTGGCCCTTT TAAGGGCTTA CAACTCTAAG AAGTCCACGT GAAAAGGTCG 600
TGATAGATTG AGCAAGCAAG AGGTGTGTGA CTATGTCCAC AAACACTAGC GGCAGGGGTA 660
AGCAAGGCAA GTATTTCTCT ATACCATTGT CTGTGATCTA TAGATAGCAC GAGCAGTTAG 720
GGTGGGTGTT AATCTTTTTT TTTTTTTTTT TAAGACAGAG TCTTGCTCTG TTGCCCAGGC 780
TGGAGTGCAG TGGCACAGTC TCGGCTCACT GCAAGCTCCG CCTCCCGGGT TCACGCCATT 840
CTCCTGTCTC AGCCTCCCGA GTAGCTGGGA CTACAGGTGC CTGCCACCAC GCCCAGCTAA 900
TTTTTTTTGT ATTTTTAGTA GAGACAGGGT TTCACCATGT TAGCCAGGAT GGTCTCGATC 960
TCCTGACCTC GTGATCCGCC CTCCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCACGAGC 1020
CACCATGCCT GGCCAGGGTG AGGGTTAATC TTTAACCTAC AGGCCTGGCC AGTGGCGCCG 1080
ATCAGTCTGT TATTTTTCAG TTTTTACTTC 1110
|
