| Tag | Content |
|---|
EnhancerAtlas ID | HS053-08467 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr11:129600740-129602150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr11:129601121-129601132 | AAGCACTCAAG | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I129731 | chr11 | 129601384 | 129601709 | | GH11I129732 | chr11 | 129601899 | 129604263 |
|
Enhancer Sequence | TTATGTAAGT GACAGGTGTC CACTGAAGAG CTTTAAGGAG GCAAGTGACA CAGTCAGATT 60
GAGATCTGGA AAATCACCCT GGAAGATGGA CTGGAGAGGA GCCAAGTTGT GCATGGGTCG 120
GGAAATGGCA ATGAGGGGGC GACGGCAATA ATGCAGGTGA TAGGTCCGCA TATTGGAATC 180
TCTTCCGCAT GGAGATCCAG CAATGCCTCA CACAGTTTCA TTGCCCGGCA CACTGGTCTT 240
TGGGTCAGCA GCCTTCAGCT TCAGAGGATT TCCAGTAGAA AGTGAGAATA AACTTGCAAC 300
AAGAATGCAG AAGCTCCCGG AAAGAAATAT GCACTGACAA CCAGAGAGAA TGACTTGGAA 360
GGATAAAAAG CAGCTTTAGG AAAGCACTCA AGGAAAAAAC GCCAAGAAAA AGCCGAGCAG 420
AAATATCCCT CGCGTCCCAC AAAGAACTCT GTGCTGTATT CCCCAAGGAC ACTTCAGGAC 480
CCTCCGGGTA CCTGAGTTCC AGAGACTTCT GGCAGAAGGA CCTCCAGTCT CAAGGTCACT 540
TAACACGTTG CCTCAGAAGC CACTCTCCTG TGCGACCCCT AGCCCGCCAG GGTTTTCTCT 600
ATTGGCTGGC TCCGTTCGCT CTCCACACAG GTCATGAACA GAACTGACCT CCCTGACTCA 660
GCAGCTCTGA CAACATCTCT GCTCCAGAAG GTCAGGTTCC CTGGCAAGCA CCAGCACCCT 720
GGCCACGCCT GATGTCAAGA GAGAATGATG CATCCTCCTG AATGGTTTGG GCTGAATTGG 780
GAGACCAAGC CCTTGTCAGT CAAATGCCAA CAGGGCAGTT CTGAACCTGC CGGGCTGGGT 840
GAGTCATCAC CTTCATAAAA CAAAATACCC CAATAATTAA TACAGAACAA ATTAATTAAA 900
GGAAGTGAGA CCATTGCAGC ACCCACTGTG AACGGATGAT AATTATTTGC AAACACAGGG 960
AGAGGCTCAG TAAGCATCCA GACTCCTGCT TCACTGGCAA CGAACTAAGC CCTGAAATCC 1020
CACGCATCTA AAGGTCAGGA GGAAACGCAG AGCAGAACCC ACCCAGCCAA CTGCGAGACT 1080
GAAGCAGGTG AGGCCACAGC CCAGGCTTAG CCCTTTGCCT GATCATTTCA CCTGCATAAA 1140
AATTTCCAGC ACCTCTGTCC CTCAGTCATT TACAATTCCA ATCCCTCAGA GGAATAACCA 1200
CAAGCTTCTC CCTACATTTT TAACAGGAGA AGTGAACGTA AAGGGACACT AATCTTACAG 1260
AAGCCACGCG TCACTTCAGC TGAGGCCTCC CCACCTTTCC AAGCAGTGTC CTAGCCCTGG 1320
GCGACTACCC TCGTTCTCAG ACGTAGATCC ACCAGTGTCT GGACCAGATC CGAACGGCCT 1380
TGAATGAAAT GCCCTGTTTA CAGATGATTG 1410
|
