| Tag | Content |
|---|
EnhancerAtlas ID | HS082-38254 | Organism | Homo sapiens | Tissue/cell | HCASMC | Coordinate | chrX:67651860-67652700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIC | MA0161.2 | chrX:67652428-67652439 | TCTGCCAAGTA | - | 6.62 | | Nr5a2 | MA0505.1 | chrX:67652139-67652154 | ACTGACCTTGACCTA | - | 6.24 | | RARA(var.2) | MA0730.1 | chrX:67652130-67652147 | TGAACTTAGACTGACCT | - | 6.12 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATTATTCTTT CTTTTACTCC AAGCCTCCTA CCAACAAGCA GAAAAAAAAC CTCCACACAC 60
AATGGGGGAA GGAGAGAGCT TCCCACAGCT GAGTCAGCTG TGAGCACTGG AAAAGCGAAG 120
CTAGGTGAAG TTCCTTCAGC CCAGCAGCCC CCAACCCTAT CCCTATTTTA CTCCCTGGGG 180
GCTGGGCCCC TTGTGGCAGG GACTAAGTAG TCAGCTCTTT GTTCCACACT CAAGCAGAAT 240
TCAGTGGCAG GTGAAGCCAT CCAATAATCC TGAACTTAGA CTGACCTTGA CCTAAACCAT 300
AGCTCAGTGT GATAAAGAAA ATAATTCACT GGGGCAAAGG TGCTTTCCTT AAAAAATAAC 360
TTGCCATGGC GAATTTTTTA CTGCCCCCCA CACTTATCTG TAGCAACCAG AGACCAGGAC 420
AAAATTATTA TTCAAGCTGC TGACCTTAAT CCCCAATTGT TTAGGAGGTG CTGGGGCAGT 480
TCCTTGGTCA GCTTGGATGT CACTTTGCCC CAGACAGGGG TGCTGAATAT GTCTAACAGT 540
ACAGCAGATT GTCCCTTAAG AACAATCATC TGCCAAGTAA GGGTAATTGC TGAGCAAGAG 600
GGTCCCTGGC ACAGCTACGG ATCACGTCTT ATAAGGTCAA AACCACTAAA GGAAAAGGCC 660
CAAAGTTCTG GTTGTATCCA CCACTTTCCA CTTCTACTAT CTCCACTCCC CAAGTGTGGG 720
AAACCCATTT GCCTCAGAGA TCTGGGCTGG GAGTCACCCT GCAATCTCCC TTCCCCTGGT 780
GGTGTGGAAA GGCTTAAAGG CCAGACACAC CAGCTCAGAG AAACAGCTCA TCGAAGCCTT 840
|
| |
|
|
|
