| Tag | Content |
|---|
EnhancerAtlas ID | HS129-10066 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr13:20484200-20485330 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Znf423 | MA0116.1 | chr13:20484927-20484942 | GAACCCCAGGGTGGC | - | 6.05 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 20484200 | 20485155 | | chr13 | 20484555 | 20484667 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I019910 | chr13 | 20484195 | 20485184 |
|
Enhancer Sequence | AAAAAAAATA CAAAAAATTA GCTGAGCGTG GTGGCGGGTG CCTGTAGTCC CAGCTACTCG 60
GGAGGCTGAG GCAGGAGAAT GGCGTGAACC CGGGAGGCGG AGCTTGCAGT GAGCCGAGAT 120
TGCGCCACTG CACTCCAGCC TGGGCAATGG AGCGAAACTC TGTCTTAAAA AAAAAAAAGT 180
TGTATTAGGC CAAATTTATT GTTATGAACC CATTAAGCAG AGATTCTGCA TTTAGTGTTG 240
CAGCTTTGGG AATTAGAAAG GGTTCTAACA GTTAGTTAGG TTGGTTGGCT GACACATGGA 300
CTATAAAGTG GCCCACAGTA AATGAACTTG AAATGCCAGA CCTATCTCGG TTTACTGAAG 360
GGAAAGGATT CAAAAGCTTA GAAAGATTGG AATGTTAGAG TGGATTTGTC ATTCAAGACT 420
TACTCATCCA TCCTGGGAGG GCCCTGTGGA CACACCTTTC TTTCTCTCTC TCTCTTTTTT 480
TTTTTTTTGA GACAGTCTCG CTGTCACCCA GGCTGAGTGC AGTGGTGTGA TCTTGGCTCA 540
CTGGAACTTC CTCCTCCCGG GCGTGAACCA CCGTGCCCAG CCTAGGACAC ACCTTTCATC 600
ATGACTCTGA GAAAACAAAT ATCTGAGGGG AGCCCCAACC CTGCGATCAC TCTTCTCTTT 660
AGGCCAGAAA TTATACTGGG AAATTACTGC CACTAAATTG GGAAACCTAA ATACAATGAG 720
AATAGTTGAA CCCCAGGGTG GCAGGTGCAA GGTGGATGTG GTTACTGTAA TGGACAGCAG 780
AGTCAAAGTG GCAATCCAAG TAGTCTAACT CTGGGAGACC TGTGGTGTCG GCAAGTTAAC 840
CACAGTGTTC TAGGAGTGAC ATAGATAGGA TGGTTACCAA ATTTTGACTT GGTCTGTAGA 900
CGCAGAAAAG CTCTAAGTCA GATGAACACA TGCCTAACCT GAATCATAAA AACAGAATCG 960
TAGCCCTTTA GTCAGTTCCC AGTCTTTTTT TTTTTTTTTT TTTTTGAGAC AGAGTCTCAC 1020
TCTGTTGTCC AGCTAATTTT GGCTGGAGTG CAGTGGTGGG ATCTCGGCTC ACTGCAAACT 1080
CCACCTCCCA GGTTCAAGCA ATTCTTGTGC CTCAGCCTCC CAAGTAGCTG 1130
|
