| Tag | Content |
|---|
EnhancerAtlas ID | HS059-01487 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:44228810-44229760 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr1:44228836-44228847 | TTAATTAAATC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 44229452 | 44229714 | | chr1 | 44229038 | 44229664 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043763 | chr1 | 44228701 | 44229826 |
|
Enhancer Sequence | TAGAATGTTT ACCAGTAGAG AACAAGTTAA TTAAATCATG GTTCCCCCAT CCGGTGAGTA 60
CTCTGCACCT GAAGATGAGG AGGCTCTGTA TACACTAATA TGAAAAGATT TCTGAAATAT 120
ACTGTTAGGT GTAAAAAAGC AAGGATGGGG AGTTTTCTTT GGGGCTTATA ATGTTTTAAA 180
CTTTTATCAT TGTTGTAAAT GGATGTAGCT GGTTGTTATA TTCCTTACAA TTACGAGATA 240
CTGGGTTCTT GGGTTTGTTT TTCTATGAGT TCTAGTATTC TGTTATTCTT TCTAACTTTC 300
TTATTATGAG CAATAGTTGG CATGGAGGAG TGGCGGATCA AATTTTTAGG TTATTAAATA 360
GGCTCCATTT CAAGCCAATC AGCGTTGCCT TCTGCTGTTT TGTGCCTGGC TGCCAAGTGC 420
CTTTATATGG TGTTTCAGCT TTTTAATGGA GCTTTGATAT GTAGCAGTCA CCCTGAGCCA 480
CAAGAGGGCA GAAGAACCTT TTGATTGCCA CAGGACAGAT TAGCGCTGGA ATGACTTCTG 540
GCAAAATCCT GCATGGAGTA GTTCTTCAAC TCACTTACTA GACCGTGGGC ATCCAAAGGC 600
AGGCCAGTGT CTAAGCCATC AGAGGAGGCA ATGGAGGGGT GAGAGGAGAG AGTGTGTGTT 660
TTGGAATCCT CTATATCTGC CTTATGTTCC AGGCTCCCCT GCAAATTACT TAGTGAACTA 720
TACTCCTTAC AGTGTTAACC TCTCTCAGAG CTTGAATATG CAAGACAGTA GAGGCATTAC 780
AACATAGTGG AACATAAGAG TTGAGGCTTT GGAATCCACC CCACCTAACG TTGAGTCCTG 840
GCTATGTGAC TTTGGGTCAT TTCTTAACTG TCATTTATTC AATGAGATAG TGTGTGTAGA 900
GCTCTTAGCA CTGTGTTGTG AACACTCAGA AAGTAACTGC TATAATTACA 950
|
