| Tag | Content |
|---|
EnhancerAtlas ID | HS116-00544 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:21011510-21012530 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:21011984-21012005 | GCTTCCCCCCGTCCCTCCTTC | - | 6.57 |
|
| | 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 |
| GH01I020683 | chr1 | 21010345 | 21012897 |
|
Enhancer Sequence | CTCCTGAGTG TGAAGAGAAA CCCAGGTGGA GGTGGGAAGG CCGCCCCAAC CCCCGCCGAC 60
AGCTCCCAGG TGGCTCAATC CCAGACGGGG CCATTCCGCC TGCTGCAGCC CCGACAGATC 120
ACCTCCAGCT CAGGGACACC AGTGACACAA AAACACGCCC TGTTGAGTTC TTACTGCCGC 180
TATTCCCACT GACACCCCCA CGCTAGGAGG AAGGCTCCCA GCTTCCTCTC TCACCTCCCA 240
CAATCCAGTC TCCACAGGCA GCCAGGGCCA TCTTAAAATA GAAACCGATC ACATCCCGTT 300
CCCGATGAGC CCCATGTGAC TTCCCGTCAC GTTCGCAGGA AAGTCCACTT TCCTCCCTGC 360
CGGCTCCCTG CCTCCACGGC CTCCCCCGCC ACCGTGGCCT CCTTTTCCAT TGCTAAGAAA 420
GTCAAGGTCT TTCCAGCCAT AGGACCTTGG CACTTGCTAT CCCCTCTGCT TGCTGCTTCC 480
CCCCGTCCCT CCTTCACGCC TGGGTCCCAC CCCAGAGTCA CTTCCTAGCC AGGGCTGCCC 540
CGGCTGCTCC ATCTACGCCC TGCTGAGAGC CTGCTGCAGG CCCGGTGCCC AGCCCACACT 600
TGAGTCCAAA CTGTCTTCTT CCTCTATAAA TGTAGGGAGA TTTAAAGCTT CCTCTCCTTT 660
TGCTCCCCTG GGGTGTTCAA ATTGGGTTCC CCGATGGTGT CATAGGGGCC ACCAGCCCTG 720
ACCTGCAGCC CTCGTCCTTT GCACACACTG GGCCTCAATT CCTTTACACA AAGGGCGACA 780
AGGCTAAGGA AGGTTTGAAA GCCACCATCT AGAACAACAG GCCACTTTCA CTCCATAAGA 840
AGAAGATGAT GGTTCCTCCC ACTGCACACT GCCTGGCCAC GGGCCACAAG CCCGGGGAAG 900
GCTGGAGTTG TTGTTCTCAG CTCATGGATG AGGAAACTGA AGCTCAGGGA GGGAGAAGAC 960
AAGCTGGAGT TTCCCAGGAA GTTGAAGAGA ACCCCGTCCC CCACATGGAG GCCCGGGGAG 1020
|
