| Tag | Content |
|---|
EnhancerAtlas ID | HS147-35236 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr6:11146010-11147030 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr6:11146758-11146773 | TGACCTCTCACCTTT | - | 6.51 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATACGGACTC AACAGGTTTG GGCTCACTGG GGTTCTAAAT CTGGATTGTC CAGCAAGGAG 60
GACTTGCACA GGGTTTGGAG GAAAGGTGCA TTTAACAAGA GCAAGTGGCC TGTGAGCAAT 120
GTGGTTGGAT TCCCAGGGGT TAATAGTAGA AACCTGCACC CCGTGTCCAC ATAGTCTGGA 180
AGGTGGTAGG TCTCTAATGA GGGTGGCTTG CGGATACTCG GTATCTGAAT GCTAAGCTCT 240
GGCTTTGGAA ACTGTAGCCA TGTTTTCTGT GGCCACCTTG GACCCAGGGA GTGATGCTTT 300
GAGCAGTAAG GTGGACCCCA TAGGGCCGGA TGACGAGCAT CTCAGTGACA GCGCTGACAA 360
CCTGAAGAGC GCAGGCTGTT GCTAAGTTTT CTGGATTGTG GAGGACCCTT CAGGCTCTTA 420
GGGAGAGGGA GATATGTTGC CAGTAATGAC TTACATTGAA TGTCTCACTA ACCCTGGTAA 480
GTAGACTCAG AGTCACATTT AATTTGATTG AGAAACAAAA CAAACCCAAA TACATAACAA 540
ATCTTGCACT GAGTGTTGTC AGGTTAACTC ATACTCATTA GTGATTACAT GTAAAAACAA 600
GTCCTCTGCT CCTGTCCAGA CCAAAAAATG AAACACAGAA AGAAGCCCAG GGCCCCGGCC 660
TGTTTTCTAG GCTGGTTCCT TCCTAGCCCA CACCATCCAT CCATCAGTCC TGCCCCATGC 720
TGCTGCAAAT GCCAGTCACC TTGCCTGGTG ACCTCTCACC TTTAACTCAA GGGCCACCTC 780
TTCCATGCAG CCTTCCCTGG TCCCCTGTAT CCTGTGGCTT TCCATTGGCA CCTCCAGGAG 840
ATCTCTCACT TGTCCCTCCT TCTAGGCAAG TGTTCTCAGC ATGCAGAATC ACCTGGGTGC 900
TTGCTAAGTG CAGATTCTTG GCCCTTTCTT ATTGAAATCC ACTGAATGAG AATCTCGGGA 960
GGTCTGGACT AAGAAGCTGT ATTTTTAATA TGTGTCCCTG CAGGTGATTA CTATCCTCTC 1020
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