| Tag | Content |
|---|
EnhancerAtlas ID | HS178-13659 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr2:101219880-101221310 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox6 | MA0515.1 | chr2:101220580-101220590 | CCATTGTTTT | + | 6.02 |
|
| | 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 |
| GH02I100603 | chr2 | 101220085 | 101220198 |
|
Enhancer Sequence | AAAAAACCCC CAAAAAACAA AACCCAACAT AGGAACAAAA TACTGGGAGA TACTCAGGTG 60
GGTCATCCCG CCTATGTCTG GGGCCAGGCT GAGGTGGCTG GAAGATTGAG CTCAGCTGGG 120
ACTGTTGGCT GGAGCACCGG TGCACCCCTT GCGCATGGCT CTGGCTCTGC ATGTCACAGG 180
AGCCAGGTTC CAAGAGGAAG TGTCACAAGA GCAAGCAAAT GAAGAGCTCA AGAAGGTATG 240
TGGCCTTTTG TGACCTAGCC TGGGGCATCA CAGAGCATCA CACTCACTAC ATTCTAGAAG 300
TTGAAGCTGG CGCAAGTTGG CTGAGACTCG GGGGGAGAGG ACATAGAGCC CACTTCTCCA 360
TGACATTTGC TCGGACGGGG GGTCCCAACT GCCCCAATAG CTTTGGACAT CCCATGTGCA 420
TTGCTTGAAT GAGCAGGACC CCAGGGTTCT TCCAGAGGAG CAGAAGTCTC AGGTTGGTTT 480
TGTTCACTCT GCTGGGTACA CCTAACTGAA AGGACTCTAA GAACCCATGC CTCTTTCATA 540
GGGACTGCAG CTCAGGACTT TGAAGTGACT TGCAAAGGCC ACACCGCCAG GACCAGAGCC 600
TGCTTCTCCA TCCCTTCCTC CTGACACAGC CGCTGATAAA TGCCATTACC TGAATTCCAT 660
GCTGAGTTGC TATTCTTATC CCACGGAGGC TGCCTGTGTG CCATTGTTTT AATTACAGGC 720
TGTTATTTCA TTTGAAAAGT CAGCGATAGG ATTAAGGGTA CTGTCATTTT AAAAGCCAGA 780
TTCCTGGCCT AAAACCGCTC AGTGAATCAG AGGACAAATG TTCCCATTGT GCTGGTTAAA 840
AATAGGAGCA ATGGAAAAAG TGACAGAATG CGATGAATAC CATTAAAGTG TAATTACATT 900
TACTGTAGAT GTGAGCCTCA GGAAGAGTCT ATCCCAGGCA GGGAAGCTTG GTCAGAGCCT 960
GTGACATGAA AAACCCAAAG CCTCCGTGGA CGGCCCATTT CAGGTTTTGA GTGTTTATAC 1020
TGTATATTGT TACATATCGT TCTTGGGAGC CATCCACCTT ATTAGGGGTA CTTGAAAGAA 1080
CTGTGTCTTT CCAAAGGAAA ATAAGAACCA CGTAGCTCAC CTTGATTCTC AGAATGTAGC 1140
TTTCCTGTAT TTCTCATGAG GAACATTATA CAGTTTCTGT ATTTTTTGCC TCAATAGTCA 1200
AATGTAGTAG CTGAGTTGGA CATATCTGAA AGGCAGGGCT AATTTTTTTC TTTTAATGAA 1260
AACAGTTCGT GTTTTTCTAA TTTTAAAACA ACACATTCTT GCCATATAAT TTTTTTTTAA 1320
ATGTACAAAG AAAGTAAACG TTAGTCTAAA TCCAGCCACC CACAGATAAA GCACTACTAA 1380
CATTTTGGTG AATATCCTTT CAAACTACAA TCTTTATGTG GATTTATAGA 1430
|
