| Tag | Content |
|---|
EnhancerAtlas ID | HS037-23136 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr21:19032250-19033680 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA(var.2) | MA0072.1 | chr21:19033572-19033586 | AGAAATTAGGTCAA | + | 6.05 |
|
| | 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 |
| GH21I017660 | chr21 | 19032901 | 19033050 |
|
Enhancer Sequence | GTCTCAAGTG CTGTGAAAGC ACTTCATGTA TTATTTCTCA TTCTTACATA GATCCTTCAA 60
GGGGAATGAC ATTTTTACTG CCTTTCCCAG TTGAATCTAA GACTCAGAGA AGGCCAGTAA 120
ATTCCATACA GCTAGAAAGC ATCAGTCAGG ATTTGAAGCC AGGTTGAACC CAGCATTTGA 180
ATCCATGCTC TTTCTACACT TGTAGTATAC CAACTCCTTT CATTCTCAGA ACTCACATAA 240
GGTCTGCATA TTACAGATAA GCTTATTCTA CAAGCATATT CTAGCAGCAT TATTGAATTT 300
TCATCTAGAG CTGTAATGTG GACTACTAAC CTAGATAGAA TCGAAATCCA TCTAGGATGG 360
ACTGGATGCT GAGACATATA ATGTTAGCTC TGTCCTTTTG GGAATTAGGT GACCAGTTTT 420
CCAAGCAAAT GTACTTGTCT CCTTAGGGCC ATTGGATCCT GGTGAGAACC TGGGAGAGTC 480
AAGATATCAT CAATGAGCAG CCTGGTTCTG AAATTCAGAA CCCCTCCTGA GTCTAACAAT 540
GGCAGAAAGC TCTTAACTTA TTCTTCATTT CCTTCTCTGC ATTCCTTACT CCCCAGATTT 600
AAAAACGACA CTCTCTCCAT GATATAATCA TGGGCAAGCA CTCTGAGTTG AGTGTCAGAG 660
GTATTTTATT TGTCTTGGGA AGATGTAAAT TCCTGGGTGT GTACAGATTC CAGTGGCTTT 720
CCGAGGGAAA GAGCATGCTG CTTTTCTTAA GAAAGGCCAC CAATGGGAAT GATTTCTGGT 780
GATGCAATGT TGATATTTTA GTACCATTCT AGAAAAGGGA AGAGGTGGGG TTTCTCTGGA 840
GCCAGATTAA CTCATAATTA GTTCTCACGC AGCCTGCTTA AGTAATTATG GTGAAACCAA 900
ATCACATTAC TTTTTTCTCC TGTTCCTGAT AAAAGCTTCA ACCCCACTCC TTCTGCCCCA 960
TAGGGCACTT GGCTGGCCAT CATACCCTAC ACTACAGGCA CTATTCTTCA GTTCTGTTTC 1020
CAGGCTACAA CTGTCACTGT GTAAAATAAG AAGTGTGGGG GAAAAATGTA CACCTCTCGG 1080
TCTCACTACT TCAGAGGCAC CTAGCAACCC TGTCTCCAGG CAGGCAGCAC GCATCTCCCT 1140
GGTAGTTTAC AGCCCACTCA CAGCAGAGGC GGCATGCTCT CTGCAAATAG CCTACGTCTT 1200
TGCTGGTGCC AGCTTGGCGG TGGGGTGGTG GTGTCATTTG GTGTCCTCAG GGACGTTTGG 1260
TTCTTGTTCT GGGAAGACTA GGGCAAAGCA ATGACTATTT CACCAAAACT GCCTGAGGGA 1320
TTAGAAATTA GGTCAAGCAG TTCTGTACTT GGGGTTGCAT TGTCTAAAAT CAAAAGCAAT 1380
GGTTTTTAAT CTTTGTTTTT CTCCAGTCTT TGGGACATTT CTGTCATAAA 1430
|
