| Tag | Content |
|---|
EnhancerAtlas ID | HS113-03443 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:221840370-221841830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid5a | MA0602.1 | chr1:221840513-221840527 | TTTTTCAATATTGG | - | 6.72 | | FOXC1 | MA0032.2 | chr1:221841745-221841756 | TAAGTAAATAT | + | 6.14 | | FOXP1 | MA0481.2 | chr1:221841394-221841406 | ATCTGTTTACAT | - | 6.62 | | FOXP2 | MA0593.1 | chr1:221841395-221841406 | TCTGTTTACAT | - | 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 |
| GH01I221667 | chr1 | 221840377 | 221841590 |
|
Enhancer Sequence | AGTATCCAGC TGTTCCCACA CAATTTATTG AAAAGACTAT CTTTCCCCCA TCGAATTACT 60
TTGGTACCTC TGTCAAAAAC CGCTTGTCTA TATTTACTTT TATTTAAAGA GTCTGTAATT 120
TTTATGTGGC AAGTACTTTG GTTTTTTTCA ATATTGGTGT TTAAGATCTA TCAGGACAGG 180
ACAGAGGAGG CTTTATTCTA TGGCTAGCTT AAGCCCTGCT CTCAAGGCCA ACCATTTTGG 240
AGTTTCTAAC AAATGTTCCA GGTATTCAAT AATGTCTGTC TTCACTCTGG CTGTTTGGAA 300
ATGGAATATC CTCCTACTCT CTATGAACTC TGTGAATTAT TTAACTTACA GCTCTTTAGT 360
AGTTTTTCTT ATCCTGGCCT CATAGAGTTT TATTGGATGC AAGCTCAGCT TATTCAGGCA 420
AAGACTCAAG GGGATTCCTG GGCAAATGTT TGGAGTTATT TTTCTTAAAA ATTCCCTCTT 480
CTCTGCAACC CAGCCCTTCC AACTTGAGCT GCCTCGGTCT CCCTGAATTT GGTTTTACGT 540
CTCCTCACTC AGTGAGAGTG TTATGCTCTG CTTGTTCCCC CACTGTGCAT GCTAGTTCAG 600
AAAAGGTTCC CATGCAGAAA CCTCAGGTAA TTATGGGACT TGCCTTGTTA GTTTCCCTTA 660
TCTTATGAGT CACAGTCCTG CAGTTCCTAT TGCTCAAGAT CTGAACATGA TGTGTCATGT 720
GCTTTGTCCC ATATTCTAGT TGTTTACAGC AAAAGAGCAA ATCTAATATC AGTTATTCCA 780
TAGTGGCTAT AAGTGGAAGA TTTTGGAAAC AGTGCTTCTT GAATTGTTTC ATGTCTCCGC 840
ACTGTCAGAC ATACAAATTA CTGATAGCCT TGTTGGAAGG ATTGAATGGT AAGCATGCTT 900
TATAAATTAG AAATAGTAAA TTGCTCTGGA GAGATCTGAA GTTCCATCTC CATCAGAACT 960
ATTTGCTTAC ACTCTAAGAG TGATAAAAAC CTAGAGACAC CTTCCTTTCC TCTCCCCAGA 1020
GAGGATCTGT TTACATTTCA GAGCAGCAAG ATCTCTTTCA TTCTCCCCTC CCTTCAGGGC 1080
AGGTAAGACA CATGTGCCAG CCATCTTATA GAAGCTTCAA GCATCATAAA TAATCAATCA 1140
AGTATCAATA ATCAATATCA AATTTACCTA CTTGTGCAGC GGTTGCTTCA TAGGAGAGAA 1200
AACTAACATT AGTTTTCTCT CCTATGAAGC AACCGCTGCA CAAGTAGGTA AATTTGGCTC 1260
CCACTATGTT ACCCGCGAAA CAAGAATTGG GACATGGGGA ACTAGTGCTG CTAAGATTCT 1320
CTGAGTGAAT GATCTGTTTC TGACCCAGAG ACCTGTGTTG TCAGAAAAAA ATAGATAAGT 1380
AAATATAGGG AGATTTTTTT AAAGACTCTT TTAAAGTCTC TCGTGATTGT AAACTTAATC 1440
CATGCTCATA TTTAAAATCT 1460
|
