| Tag | Content |
|---|
EnhancerAtlas ID | HS095-25528 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr6:11146080-11146990 | 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 | GGGTTTGGAG GAAAGGTGCA TTTAACAAGA GCAAGTGGCC TGTGAGCAAT GTGGTTGGAT 60
TCCCAGGGGT TAATAGTAGA AACCTGCACC CCGTGTCCAC ATAGTCTGGA AGGTGGTAGG 120
TCTCTAATGA GGGTGGCTTG CGGATACTCG GTATCTGAAT GCTAAGCTCT GGCTTTGGAA 180
ACTGTAGCCA TGTTTTCTGT GGCCACCTTG GACCCAGGGA GTGATGCTTT GAGCAGTAAG 240
GTGGACCCCA TAGGGCCGGA TGACGAGCAT CTCAGTGACA GCGCTGACAA CCTGAAGAGC 300
GCAGGCTGTT GCTAAGTTTT CTGGATTGTG GAGGACCCTT CAGGCTCTTA GGGAGAGGGA 360
GATATGTTGC CAGTAATGAC TTACATTGAA TGTCTCACTA ACCCTGGTAA GTAGACTCAG 420
AGTCACATTT AATTTGATTG AGAAACAAAA CAAACCCAAA TACATAACAA ATCTTGCACT 480
GAGTGTTGTC AGGTTAACTC ATACTCATTA GTGATTACAT GTAAAAACAA GTCCTCTGCT 540
CCTGTCCAGA CCAAAAAATG AAACACAGAA AGAAGCCCAG GGCCCCGGCC TGTTTTCTAG 600
GCTGGTTCCT TCCTAGCCCA CACCATCCAT CCATCAGTCC TGCCCCATGC TGCTGCAAAT 660
GCCAGTCACC TTGCCTGGTG ACCTCTCACC TTTAACTCAA GGGCCACCTC TTCCATGCAG 720
CCTTCCCTGG TCCCCTGTAT CCTGTGGCTT TCCATTGGCA CCTCCAGGAG ATCTCTCACT 780
TGTCCCTCCT TCTAGGCAAG TGTTCTCAGC ATGCAGAATC ACCTGGGTGC TTGCTAAGTG 840
CAGATTCTTG GCCCTTTCTT ATTGAAATCC ACTGAATGAG AATCTCGGGA GGTCTGGACT 900
AAGAAGCTGT 910
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