| Tag | Content |
|---|
EnhancerAtlas ID | HS175-26080 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr6:45864100-45865530 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr6:45864224-45864235 | TTCTTTGTTTT | - | 6.62 | | Spz1 | MA0111.1 | chr6:45864881-45864892 | GCTGCTACCCT | - | 6.02 | | ZNF263 | MA0528.1 | chr6:45865168-45865189 | GGGGGAGTAGGGAGGAGGGAG | + | 6.2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGATTGTAT AATCTCATAG ACAAGGAGCC TTCATAACTC CCTTCGGGAA ACTGAGGCCC 60
AGAAAGGAGC CTTGCTCAAG GGCACATGGT AATTTAATGA TGGACCTAAG AGTCAAATTC 120
TCGTTTCTTT GTTTTCAGTC CTGACTTCCT ACCTCTCCAG TCTAATACTC CATGCCTTTT 180
CCCACAAGGT AAAACTTACT GGGGGCTCTG GGTAGGTTAG CTACTAGACA TAAAAACAAA 240
AGAAATAAAT AAAAGCAGCA TAGGTCACAA CAACTTTGAG TGTAATGAGA TACTCTCATT 300
TACAATGTCA CTTCTCTGGA AGCTTCTCTG GAACAGGACT TAGTCTTCCT CAATACTAGG 360
CACAGTCACT GCCATCCTGT GCCCCTTGGT TTCTTCACAG AACCGTTAAG GAAACCAAGA 420
CACAGAGAGA TGATGTCTCC CATGCTCCCA GCTCTTGGTC AGCCTGGAGA GCAGATGCCC 480
TACATTCACA CAGTGGAAGC CTGGGACGCC TCCTGGGTGA GCAGTCTAAT GATCTAACTG 540
GCTATTAAAA AAACAACCAC CACAACCAAC TTGGCTAATA TACCACTTAG AATGCCTTGG 600
GCCACTCGTG GGGTAAAAGA AAATCACCAT CAAACAATCT GGGATGAATT ACAGAACAGG 660
AAATCCAGAG TTAGGACCAG TTTCAGGGTT TGTTGATTTA GCAACTCTGT GGTCACATCA 720
AGGACCCAGG TTCTGTCTCT GTCTCTTGCT GCGTTTTGCA GCATGTTGCC TTTGCCCTGA 780
GGCTGCTACC CTCTCAGGGT CCCCAGAGGA CGGCAGCACT TCCAGGCCTC ATACCCACAA 840
TCAGAAGCAG TGACCTAAGG AGTCACTTTC TTAACAACAA GGGGATATTT CTCAGAAGTT 900
CCTGAGTAAA TCTGCCTTCA CAATACTGGG CGGAACTTGG TCAGGAGCCC ACTTTGAAAC 960
CAACCACAGC CAGCAGGATG GCCCAGACCA TTTGTGCTTT ACTCTTGGAA CTGGGGATGA 1020
AATCACCCTC GCTCCAGTCA TCTGAGGGTG GGAGTGTGTG TGTAGGGTGG GGGAGTAGGG 1080
AGGAGGGAGG TGGTGGACTC CTGACCCAAT CAGAGCTCTG CCTGTGGAAG ATGGGAGTCG 1140
GGATGGTGGG GTGACCACCA GCTGCATCTA CTGCACCTGT CCTGAGACCC TAGCTGCCCC 1200
TCCCATCAAG ATCCACCCCT GGGTCTGCTG TTTCATTTCT TCCAAGGTAA TGAAGTGCTG 1260
TTATGACTAC CCTTTAGCAA TGTGAATGCT CATAGAAGTC TTCATCAGAC GTCACATTGG 1320
CTTCAGGTAA AGCTTACTAA GGACTCTGGG AACCTGAACC CAGAGTCAGT GATGTGGTGT 1380
TGAGAGTAGG GATTTCAGCC TAGGAACGCA AGCCACTGAG AGCCAACAGA 1430
|
