| Tag | Content |
|---|
EnhancerAtlas ID | HS176-01128 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:62587510-62588370 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:62588075-62588086 | ATGAGTCATCC | - | 6.62 | | JUN(var.2) | MA0489.1 | chr1:62588075-62588089 | ATGAGTCATCCTCC | - | 6.43 | | JUNB | MA0490.1 | chr1:62588075-62588086 | ATGAGTCATCC | - | 6.62 |
|
| | 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 |
| GH01I062121 | chr1 | 62587265 | 62588599 |
|
Enhancer Sequence | AAGCTGGAGT GCATGGTAAA ATAAAATTAC TTACAAAGAG AAAATTAATA AATTACAGGT 60
CACTGGAGAA AGGTCAGAAG TGTGTATACC TTCTATGGGA AAATTGGGCC AGTTAAAAGA 120
AAAAAAAAAG TGTGTATATC CTTGGGGGCA GGGTGGGACA AGGGGTCCTT TTAAGTCTTT 180
TGTTGAATGG AGGGTTATCT TTGATTAAGG TAGAAAAAAA TGTACAATGA AACACAAATG 240
ACTCAGCCGG GCCCGGTGGC TCATGCCTGT AATCTTAGCA CTTTGGGAGG CCAAGGCAGG 300
CGGATCACCT GAGGTCAGGA GTTTGAGAGC AGCCTGGCCA ACATGGAGAA ACCTCGCCTG 360
TACTAAAAAT ACAAAAATTA GCCGGGCATG GTGGCACATG CCTATAATCC CAGCTACTTG 420
GGAGGCTGAG GCAGGAGAAT CGCTTGAACC CAAGAGGCAG AGATGGCAGT GAGCTAAGAT 480
CGGACCACTG CACTCCAGCC TGGGCGACAG AGTGAGACTC CATCTAAAAA AAAAAAAAAA 540
AAAAAAACCA CACACACACA CAAAAATGAG TCATCCTCCA AGCATTTACT CACCATGTTC 600
CAGGCAGCTG CTGCTATATA GCCCATCCAC TTTTGTCAGA CCAAATGGTT ATGGCCACAT 660
TGATCTCAAA CAGAGAGCAC TTCTTTAAAA TAGAGGACAC AGCAGGCCGG GCACGGTGGC 720
TCACGCCTGT AATCCCAACA CTTTGGGAGG CCGAGGCAGG TGGATCACTT GAGGTCGAGA 780
GTTTGAGACC AGCCTGGCCA ACATGGTGAA ACCCCGTCTC TACTAAAAAT ACAAAAATTA 840
GCCGGGCGTG GTGGCAGGCA 860
|
