| Tag | Content |
|---|
EnhancerAtlas ID | HS092-19940 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr16:89698970-89700290 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr16:89699049-89699060 | ACAGATAAGGA | - | 6.14 | | ZNF263 | MA0528.1 | chr16:89699356-89699377 | GCAGGAGGAGGAGGGAGGGGA | + | 6.15 | | ZNF263 | MA0528.1 | chr16:89699362-89699383 | GGAGGAGGGAGGGGAGAGCAG | + | 6.49 | | ZNF263 | MA0528.1 | chr16:89699359-89699380 | GGAGGAGGAGGGAGGGGAGAG | + | 9.53 |
|
| | 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 |
| GH16I089631 | chr16 | 89697242 | 89700208 |
|
Enhancer Sequence | GCTTTTCCAG CACTTTCCAG CACTCCTTGG AGCAGGACGC CGGCTTCCAT ATCCCAGCTA 60
AGGGCATTGC CCCAGCTGCA CAGATAAGGA GGGTGGGTCT GATTAGCAGA ACTGCCATTT 120
GCCCTGGCCA TGAGGCAGGC AGGGCCTCCC TCCCACTGAG AAACCAGAGG CCCCACCTTC 180
CCATCGTTTT CTCCAGCAAG AGTGGAGAGG GCTGGCGGGG CACAGTGGCT CACAGGTGTG 240
GTCCCAGCAC TTTGGGAGAC CGAGGTGGGA GGACTGCTTG AACCCAGAAG GTTGGGGGCT 300
GCAGTGAGCT GTGATTGCAC CCCTGCCCTC CAGCCTGGGC AACAGAGTGA GACCCTGTCT 360
CAAAAAGAAA AAAGAAAGGA GGGGCTGCAG GAGGAGGAGG GAGGGGAGAG CAGAGAGCTG 420
CCCCATTGCA GCCTGTCCCT CCAAGGGCGG CTCCTGGGGT CCTAGGAATC CCTACCCATC 480
CCAGGCTAAT GTCTGAGATG GGCCGCCTGC GTCCTCAGGC CAAGGAGTAA AGTCTCCTGG 540
GAGCCCTGCC CAGCCCCACC CAGGACAGTG CCCAGTGTAG GGTTGCACCT AGCGATGAGG 600
CTGCTGCCCG GGCAGGGTCC CTGGCTGGAG CTCATGGTTC CCTCAGCAAG TGCGTCCTGA 660
CCACCCACTC TGCTCCGAGG GCTGGGGAGA GGCCCGTGCC AGCCCAGGCT GTCATGTGGA 720
CTCGCTGTGG CCAGGGACAA CCTCGCTGAC GCAGGAGCTT TGGGAGAGAC TCACACCAGC 780
ATCAGGCGTG CGCCCGCCCA TCTGCCCAGG GGTGGGGCCG GAAAGCGTGC CAGGCTGGGC 840
TTGGGGGCAC TAGCCCAGGG GAGGTCAGGA ACGACTGGGA CCCAGGAAGG GCAGAGCCCT 900
CCCCTTCTTT CCCCTGAGGA GCTCCATGGG TGCATTCGCC TTGGAAAAGC TCATTGCGGG 960
CACATAGATT TGAGCTGGGT CACAGAAAGC AGAGCCCGCA GCTGGAAATG ATTAACAGTT 1020
ACTCATCTGC CTCTCCCAGC TGCCCTCCAA GGAAAGCACC AAGACACCCT CATGTTACAG 1080
ATGGGGAAAC TGAGACACAG AGGGAGCTGT CCTCAAGGAG AGCACCAAAA CACCCTCATG 1140
TTACAGATGG GGAAACTGAG ACACAGAGGG AGCTGTCCTC CAAGGAAGGC ACCAAGACAC 1200
CCTCATGTTA CAGATGGGGA AACTGAGGCA CAGGGATGGG TCTGGAAACT GCAAGTGGAG 1260
GGGCCCCTGT GGCCTCATCC CAGCGCACAC CCTCACAAGG CAGTCCCCCC GAGACAGGGG 1320
|
